MIYAMOTO Toshinobu 宮本敏伸

Researcher Number	70360998
External Links
Affiliation (based on the past Project Information) *help	2022: 獨協医科大学, 医学部, 准教授 2009 – 2020: Asahikawa Medical College, 医学部, 講師 2007 – 2009: Asahikawa Medical College, 医学部, 助教 2003 – 2006: Asahikawa Medical College, Dept.of OB/GYN, Staff, 医学部, 助手
Review Section/Research Field	Principal Investigator Obstetrics and gynecology / Basic Section 56040:Obstetrics and gynecology-related Except Principal Investigator Obstetrics and gynecology / Obstetrics and gynecology
Keywords	Principal Investigator mutation / azoospermia / 無精子症 / MA / SCOS / SNP / 減数分裂 / male infertility / 生殖医学 / 不妊症 … More / meiosis / CDK2 / 機能解析 / genetics / azoopsermia / 原因遺伝子 / Male infertility / Meiotic Arrest / male ifertility / gene / habitual abortion / PLK4 / SEPTIN12 / HOP2 / MEISETZ / 遺伝子 / SPATA17 / PARP-2 / spermatogenesis / FK506 binding domain / 遺伝子変異 / imprinting / FKBP6 / Meisez / Hop2 … More Except Principal Investigator 無精子症 / 男性不妊 / 減数分裂異常 / 精子形成 / 遺伝子 / CDK2 / MEISEZ / HOP2 / SNP / SYCP3 / Mbx / LHX / 減数分裂 / meiosis / azoospermia / Mutation / FKBP6 / MEI1 / HOP / 原因遺伝子 / Azoospermia / Homeobox gene / Development / 悪性腫瘍 / 発生 / 遺伝子発現 / 小眼症 / ホメオボックス / 奇形 / 流産 / LIM / ホメオボックス遺伝子 / 発生学 / Plk4 / Sin 3A / RAD21L / ETV5 / セルトリセルオンリー / セルトリ細胞症候群 / セルトリ細胞 Less

ヒト男性不妊症および不育症の病態解明および臨床医学への応用Principal Investigator
- Principal Investigator
  
  宮本敏伸
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56040:Obstetrics and gynecology-related
- Research Institution
  Dokkyo Medical University
Analysis of the genes causing male infertility in humanPrincipal Investigator
- Principal Investigator
  
  宮本敏伸
- Project Period (FY)
  2019 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56040:Obstetrics and gynecology-related
- Research Institution
  Asahikawa Medical College
idetification of the genes causing male infertility and habitual abortion by next generation sequencing in humanPrincipal Investigator
- Principal Investigator
  
  MIYAMOTO TOSHINOBU
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Asahikawa Medical College
Analysis of genes related to human azoospermia using a reverse genetics method
- Principal Investigator
  
  SENGOKU Kazuo
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Asahikawa Medical College
Analysis of human azoospermia and POF and its clinical advancePrincipal Investigator
- Principal Investigator
  
  MIYAMOTO TOSHINOBU
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Asahikawa Medical College
Investigation of the mechanisms of spermatogenesis using a comprehensive analysis of genes related to human azoospermia
- Principal Investigator
  
  SENGOKU Kazuo
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Asahikawa Medical College
Analysis of the factors on male infertility and habitual abortion & their Applications to clinical medicinePrincipal Investigator
- Principal Investigator
  
  MIYAMOTO Toshinobu
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Asahikawa Medical College
Comprehensive analysis of genes related to human azoospermia
- Principal Investigator
  
  SENGOKU Kazuo
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Asahikawa Medical College
Identification of the genes causing azoospermia in human and analysis of the mechanism in spermatogenesisPrincipal Investigator
- Principal Investigator
  
  MIYAMOTO Toshinobu
- Project Period (FY)
  2007 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Asahikawa Medical College
新たなヒト無精子症の原因遺伝子の単離およびその機能解析Principal Investigator
- Principal Investigator
  
  宮本敏伸
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Asahikawa Medical College
Identification of the genes causing azoospermia in humans and analysis of protein function and the mechanism of the spermatogenesis
- Principal Investigator
  
  ISHIKAWA Mutsuo
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Asahikawa Medical College
Analysis of LHX gene on human development
- Principal Investigator
  
  ISHIKAWA Mutsuo
- Project Period (FY)
  2001 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Asahikawa Medical College

[Book] Fertility Preservation ～妊孕性温存のすべて～2021
- Author(s)
  宮本敏伸、宇津野泰弘
- Total Pages
  6
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-19K09770
[Book] ARTラボ必携　生殖補助医療の必須知識とラボテクニックの伝承2021
- Author(s)
  宮本敏伸、宇津野泰弘
- Total Pages
  6
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-19K09770
[Book] 生殖補助医療(ART)-胚培養の理論と実際2017
- Author(s)
  宮本敏伸
- Total Pages
  5
- Publisher
  近代出版
- Data Source
  KAKENHI-PROJECT-16K11077
[Book] VII培養室業務の実際：精液調整法、生殖補助医療(ART)-胚培養の理論と実際2016
- Author(s)
  宮本敏伸
- Total Pages
  5
- Publisher
  日本卵子学会
- Data Source
  KAKENHI-PROJECT-25462547
[Journal Article] Population Attributable Fractions of Modifiable Risk Factors for Nonsyndromic Orofacial Clefts: A Prospective Cohort Study From the Japan Environment and Children’s Study2021
- Author(s)
  Sato Y, Yoshioka E, Saijo Y, Miyamoto T, Sengoku K, Azuma H, Tanahashi Y, Ito Y, Kobayashi S, Minatoya M, Ait Bamai Y, Yamazaki K, Itoh S, Miyashita C, Araki A, Kishi R; Japan Environment and Children’s Study (JECS) Group.
- Journal Title
  
  Journal of Epidemiology
  
  Volume: 31 Issue: 4 Pages: 272-279
- DOI
  10.2188/jea.JE20190347
- NAID
  130008021560
- ISSN
  0917-5040, 1349-9092
- Year and Date
  2021-04-05
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09770
[Journal Article] Factors correlating with serum birch pollen IgE status in pregnant women in Hokkaido, Japan: The Japan Environment and Children's Study (JECS)2020
- Author(s)
  Saijo Y, Yoshioka E, Sato Y, Miyamoto T, Sengoku K, Ito Y, Itoh S, Miyashita C, Araki A, Kishi R; Japan Environment and Children's Study Group.
- Journal Title
  
  World Allergy Organ J.
  
  Volume: 13: Issue: 6 Pages: 100128-100128
- DOI
  10.1016/j.waojou.2020.100128
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09770
[Journal Article] Trajectories of the Psychological Status of Mothers of Infants With Nonsyndromic Orofacial Clefts: A Prospective Cohort Study From the Japan Environment and Children's Study2020
- Author(s)
  Sato Y, Yoshioka E, Saijo Y, Miyamoto T, Sengoku K, Azuma H, Tanahashi Y, Ito Y, Kobayashi S, Minatoya M, Bamai YA, Yamazaki K, Ito S, Miyashita C, Araki A, Kishi R; Japan Environment and Children’s Study (JECS) Group.
- Journal Title
  
  Cleft Palate Craniofac J.
  
  Volume: - Issue: 3 Pages: 369-377
- DOI
  10.1177/1055665620951399
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09770
[Journal Article] The poly(A) polymerase beta gene may not be associated with azoospermia caused by Sertoli-cell-only syndrome in Japanese patients by comparing patients and normal controls.2019
- Author(s)
  Miyamoto T, Shin T, Iijima M, Minase G, Okada H, Saijo Y, Sengoku K.
- Journal Title
  
  J Obstet Gynaecol.
  
  Volume: 39 Pages: 434-436
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] Association Between Maternal Serum Folate Concentrations in the First Trimester and the Risk of Birth Defects: The Hokkaido Study of Environment and Children's Health.2019
- Author(s)
  Ito K, Hanaoka T, Tamura N, Sasaki S, Miyashita C, Araki A, Ito S, Minakami H, Cho K, Endo T, Baba T, Miyamoto T, Sengoku K, Tamakoshi A, Kishi R.
- Journal Title
  
  J Epidemiol.
  
  Volume: 29 Pages: 164-171
- NAID
  130007624300
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] The relationship between prenatal psychological stress and placental abruption in Japan, The Japan Environment and Children's Study (JECS).2019
- Author(s)
  Kawanishi Y, Yoshioka E, Saijo Y, Itoh T, Miyamoto T, Sengoku K, Ito Y, Ito S, Miyashita C, Araki A, Endo T, Cho K, Minakami H, Kishi R
- Journal Title
  
  PLoS One
  
  Volume: 14 Issue: 7 Pages: e0219379-e0219379
- DOI
  10.1371/journal.pone.0219379
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09770
[Journal Article] Association Between Maternal Serum Folate Concentrations in the First Trimester and the Risk of Birth Defects: The Hokkaido Study of Environment and Children’s Health2019
- Author(s)
  Ito Kumiko、Hanaoka Tomoyuki、Tamura Naomi、Sasaki Seiko、Miyashita Chihiro、Araki Atsuko、Ito Sachiko、Minakami Hisanori、Cho Kazutoshi、Endo Toshiaki、Baba Tsuyoshi、Miyamoto Toshinobu、Sengoku Kazuo、Tamakoshi Akiko、Kishi Reiko
- Journal Title
  
  Journal of Epidemiology
  
  Volume: 29 Issue: 4 Pages: 164-171
- DOI
  10.2188/jea.JE20170185
- NAID
  130007624300
- ISSN
  0917-5040, 1349-9092
- Year and Date
  2019-04-05
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16H02645, KAKENHI-PROJECT-19K09770, KAKENHI-PROJECT-19H01071
[Journal Article] 【内分泌症候群(第3版)-その他の内分泌疾患を含めて-】女性性機能　その他　乳汁漏出症2019
- Author(s)
  千石一雄, 宮本敏伸, 水無瀬学, 水無瀬萌
- Journal Title
  
  日本臨床 (0047-1852)別冊内分泌症候群III
  
  Volume: III Pages: 262-266
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] The poly(A) polymerase beta gene may not be associated with azoospermia caused by Sertoli-cell-only syndrome in Japanese patients by comparing patients and normal controls.2019
- Author(s)
  Miyamoto T, Shin T, Iijima M, Minase G, Okada H, Saijo Y, Sengoku K.
- Journal Title
  
  J Obstet Gynaecol.
  
  Volume: 39 Issue: 3 Pages: 434-436
- DOI
  10.1080/01443615.2018.1504205
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09770, KAKENHI-PROJECT-19K18550
[Journal Article] CUL4B mutations are uncommon in Japanese patients with Sertoli-cell-only syndrome and azoospermia.2018
- Author(s)
  Miyamoto T, Iijima M, Shin T, Minase G, Ueda H, Okada H, Sengoku K.
- Journal Title
  
  J Obstet Gynaecol.
  
  Volume: 38 Issue: 2 Pages: 293-294
- DOI
  10.1080/01443615.2017.1336755
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] Prevalence and Risk of Birth Defects Observed in a Prospective Cohort Study: The Hokkaido Study on Environment and Children's Health.2018
- Author(s)
  Hanaoka T, Tamura N, Ito K, Sasaki S, Araki A, Ikeno T, Miyashita C, Ito S, Minakami H, Cho K, Endo T, Baba T, Miyamoto T, Sengoku K, Kishi R
- Journal Title
  
  J Epidemiol
  
  Volume: 28 Pages: 125-132
- NAID
  130006434072
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] 【不妊・不育症医療の最前線】不妊の診断・治療(女性)2018
- Author(s)
  千石一雄, 宮本敏伸, 水無瀬萌
- Journal Title
  
  臨床検査
  
  Volume: 62 Pages: 626-632
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] An association study of the single-nucleotide polymorphism c190C>T (Arg64Cys) in the human testis-specific histone variant, H3t, of Japanese patients with Sertoli cell-only syndrome.2018
- Author(s)
  Miyamoto T, Iijima M, Shin T, Minase G, Ueda H, Saijo Y, Okada H, Sengoku K.
- Journal Title
  
  Asian J Androl.
  
  Volume: 20 Pages: 527-528
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] CUL4B mutations are uncommon in Japanese patients with Sertoli-cell-only syndrome and azoospermia.2018
- Author(s)
  Miyamoto T, Iijima M, Shin T, Minase G, Ueda H, Okada H, Sengoku K.
- Journal Title
  
  J Obstet Gynaecol
  
  Volume: 38 Pages: 293-294
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] An atypical case of SPG56/CYP2U1-related spastic paraplegia presenting with delayed myelination.2017
- Author(s)
  Minase G, Miyatake S, Nabatame S, Arai H, Koshimizu E, Mizuguchi T, Nakashima M, Miyake N, Saitsu H, Miyamoto T, Sengoku K, Matsumoto N.
- Journal Title
  
  J Hum Genet.
  
  Volume: 62 Issue: 11 Pages: 997-1000
- DOI
  10.1038/jhg.2017.77
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11077, KAKENHI-PROJECT-17K15630, KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-16H05357
[Journal Article] Naturally Conceived Heterotopic Pregnancy Treated with Abdominal Wall-lifting Laparoscopic Salpingectomy Using Spinal Anaesthesia2017
- Author(s)
  Nakanishi K, Miyamoto T, Murakami K, Ono M, Nozawa A, Sengoku K, Kitamura S
- Journal Title
  
  Journal of Obstetrics and Gynecology
  
  Volume: in press
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] Prenatal diagnosis of a body stalk anomaly by a combination of ultrasonography and foetal magnetic resonance imaging.2017
- Author(s)
  Ueda H, Miyamoto T, Minase G, Sengoku K.
- Journal Title
  
  J Obstet Gynaecol.
  
  Volume: 37 Issue: 7 Pages: 946-947
- DOI
  10.1080/01443615.2017.1306842
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] Human Male Infertility and its Genetic Causes2017
- Author(s)
  Miyamoto T, Minase G, Shin T, Ueda H, Okada H, Sengoku K
- Journal Title
  
  Reprod Med Biol
  
  Volume: in press
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] Human male infertility and its genetic causes.2017
- Author(s)
  Miyamoto T, Minase G, Shin T, Ueda H, Okada H, Sengoku K.
- Journal Title
  
  Reprod Med Biol.
  
  Volume: 16 Issue: 2 Pages: 81-88
- DOI
  10.1002/rmb2.12017
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] Naturally conceived heterotopic pregnancy treated with abdominal wall-lifting laparoscopic salpingectomy using spinal anaesthesia.2017
- Author(s)
  Nakanishi K, Miyamoto T, Murakami K, Ono M, Nozawa A, Sengoku K, Kitamura S.
- Journal Title
  
  J Obstet Gynaecol
  
  Volume: 37 Issue: 8 Pages: 1104-1105
- DOI
  10.1080/01443615.2017.1322047
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] Prenatal diagnosis of a body stalk anomaly by a combination of ultrasonography and foetal magnetic resonance imaging2017
- Author(s)
  Ueda H, Miyamoto T, Minase G, Sengoku K
- Journal Title
  
  Journal of Obstetrics and Gynecology
  
  Volume: in press
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] Single-nucleotide polymorphism in the human RAD21L gene may be a genetic risk factor for japanese patients with azoospermia cause by meiotic arrest and Sertoli cell-only syndrome2017
- Author(s)
  Minase G, Miyamoto T, Miyagawa Y, Iijima M, Ueda H, Saijo Y, Namiki M, Sengoku K
- Journal Title
  
  Human Fertility
  
  Volume: - Issue: 3 Pages: 217-220
- DOI
  10.1080/14647273.2017.1292004
- NAID
  120006510212
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26462469, KAKENHI-PROJECT-16K11077, KAKENHI-PROJECT-17K11198
[Journal Article] Single-nucleotide polymorphisms in ETV5: A risk factor for Sertoli cell-only syndrome in Japanese men?2017
- Author(s)
  Hiroto Ueda, Gaku Minase, Toshinobu Miyamoto, Masashi Iijima, Yasuaki Saijo3, Mitsuko Nakashima, Naomichi Matsumoto, Mikio Namiki and Kazuo Sengoku
- Journal Title
  
  Clinical Experimental Obstet Gynecol
  
  Volume: -
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26462469
[Journal Article] A PLK4 mutation causing azoospermia in a man with Sertoli cell-only syndrome.2016
- Author(s)
  Miyamoto T, Bando Y, Koh E, Tsujimura A, Miyagawa Y, Iijima M, Namiki M, Shiina M, Ogata K, Matsumoto N, Sengoku K.
- Journal Title
  
  Andrology
  
  Volume: 4 Pages: 75-81
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] The Association between Prenatal Yoga and the Administration of Ritodrine Hydrochloride during Pregnancy: An Adjunct Study of the Japan Environment and Children's Study.2016
- Author(s)
  Kawanishi Y, Saijo Y, Yoshioka E, Nakagi Y, Yoshida T, Miyamoto T, Sengoku K, Ito Y, Miyashita C, Araki A, Kishi R.
- Journal Title
  
  PLoS One.
  
  Volume: 11
- NAID
  120005907002
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] Rectal perforation after incision of the vaginal canal following incorrect insertion of a Vagi-Pipe into the rectum during total laparoscopic hysterectomy2016
- Author(s)
  Okamoto Ｓ, Nakanishi K, Ono M, Nozawa A, Kitarura S, Miyamoto T, Sengoku K
- Journal Title
  
  Journal of Obstetrics and Gynecology
  
  Volume: 36 Pages: 992-993
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-16K11077
[Journal Article] A PLK4 mutation causing azoospermia in a man with Sertoli cell only syndrome2016
- Author(s)
  Miyamoto T, Bando Y, Tsujimura A, Miyagawa Y, Iijima M, Namiki M, Shina M ,Ogata K, Matsumoto N, Sengoku K
- Journal Title
  
  Andrology
  
  Volume: 4 Issue: 1 Pages: 24-81
- DOI
  10.1111/andr.12113
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26462469, KAKENHI-PROJECT-25462547
[Journal Article] Male infertility and its genetic causes2015
- Author(s)
  Miyamoto T, Minase G, Okabe K, Ueda H, Sengoku K
- Journal Title
  
  J Obstet Gynaecol Res
  
  Volume: 41 Issue: 10 Pages: 15001-15005
- DOI
  10.1111/jog.12765
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26462469, KAKENHI-PROJECT-25462547
[Journal Article] SIN3A mutations are rare in men with azoospermia2015
- Author(s)
  Miyamoto T, Koh E, Tsujimura A, Miyagawa Y, Minase G, Ueda Y,Namiki M,Sengoku K
- Journal Title
  
  Andrologia
  
  Volume: 47 Issue: 9 Pages: 1083-1085
- DOI
  10.1111/and.12379
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26462469, KAKENHI-PROJECT-25462547
[Journal Article] Prenatal diagnosis of congenital imperforate hymen with hydrocolpos.2015
- Author(s)
  Nakajima E, Ishigouoka T, Yoshida T, Sato T, Miyamoto T, Shirai M, Sengoku K.
- Journal Title
  
  J Obstet Gynaecol.
  
  Volume: 35 Issue: 3 Pages: 311-313
- DOI
  10.3109/01443615.2014.951608
- Data Source
  KAKENHI-PROJECT-25462547
[Journal Article] Single-nucleotide polymorphisms in the LRWD1 gene may be a genetic risk factor for Japanese patients with Sertoli cell-only syndrome2014
- Author(s)
  Miyamoto T, Koh E, Tsujimura A, Miyagawa Y, Saijo Y,Namiki M, Sengoku K
- Journal Title
  
  Andrologia
  
  Volume: 48 Pages: 273-276
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23592388
[Journal Article] Single-nucleotide polymorphisms in the LRWD1 gene may be a genetic risk factor for Japanese patients with Sertoli cell-only syndrome.2014
- Author(s)
  Miyamoto T, Koh E, Tsujimura A, Miyagawa Y, Saijo Y, Namiki M, Sengoku K
- Journal Title
  
  Andrologia
  
  Volume: 46 Pages: 273-276
- Data Source
  KAKENHI-PROJECT-25462547
[Journal Article] Single-nucleotide polymorphisms in the LRWD1 gene may be a genetic risk factor for Japanese patients with Sertoli cell-only syndrome2014
- Author(s)
  Miyamoto T, Koh E, Tsujimura A, Miyagawa Y, Saijo Y, Namiki M, Sengoku K
- Journal Title
  
  Andorologia
  
  Volume: 48(3) Pages: 273-276
- Data Source
  KAKENHI-PROJECT-23592388
[Journal Article] Study of the vulvar skin in healthy Jananese women : components of the stratum corneum and microbes2013
- Author(s)
  Miyamoto T, Akiba S, Sato N, Fujimura T, TakagiY, Kitahara T, Takema Y, Iizuka H, Sengoku K
- Journal Title
  
  Int J Dermatol
  
  Volume: 53(12) Pages: 1500-1505
- Data Source
  KAKENHI-PROJECT-23592388
[Journal Article] Ten years of progress in the Hokkaido birth cohort study on environment and children's health: cohort profile--updated 2013.2013
- Author(s)
  Kishi R, , Goudarzi H, Azumi K, Kanazawa A, Otake Y, Yila TA, Ait Bamai Y, Cong S, Baba T, Braimoh TS, Ban S, Washino N, Konishi K, Kato S, Uno A, Limpar M, Minakami H, Nonomura K, Mitsui T, Endo T, Baba T, Sengoku K, Saijo Y, Yoshioka E, Miyamoto T et al
- Journal Title
  
  Environ Health Prev Med.
  
  Volume: 18 Pages: 429-50
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25462547
[Journal Article] Study of the vulnar skin in healthy Japanese wpmen Component of the stratum corneum and microbes2013
- Author(s)
  Miyamoto T, Akiba S, Sato N, Fujimura T, Takagi Y, Kitahara T, Takema Y, Iizuka H, Sengoku K
- Journal Title
  
  Int J Dermatol
  
  Volume: 52 Pages: 1500-1505
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23592388
[Journal Article] Single-nucleotide polymorphisms in the LRWD1 gene may be a genetic risk factor for Japanese patients with Sertoli cell-only syndrome2013
- Author(s)
  Miyamoto T, Koh E, Tsujimura A, Miyagawa Y, Saijo Y, Namiki M, Sengoku K
- Journal Title
  
  Andrologia
  
  Volume: 46 Issue: 3 Pages: 273-276
- DOI
  10.1111/and.12077
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Pathogenic mutations in two families with congenital cataract identified with whole-exome sequencing2013
- Author(s)
  Kondo Y, Saitsu H, Miyamoto T, Lee BJ, Nishiyama K, Nakashima M, Tsurusaki Y, Doi H, Miyake N, Kim JH, Yu YS, Matsumoto N
- Journal Title
  
  Mol Vis
  
  Volume: 19 Pages: 384-9
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Clinicopathologic risk factors for recurrence of ovarian endometrioma following laparoscopic cystectomy2013
- Author(s)
  Sengoku K, Miyamoto T, Horikawa M, Katayama H, Nishiwaki K, Kato Y, Kawanishi Y, Saijo Y.
- Journal Title
  
  Acta Obstet Gynecol Scand
  
  Volume: 92(3) Issue: 3 Pages: 278-84
- DOI
  10.1111/aogs.12051
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591811, KAKENHI-PROJECT-23592388
[Journal Article] Pathogenic mutations in two families with congenital cataract identified with whole-exome sequencing.2013
- Author(s)
  Kondo Y, Saitsu H,Miyamoto T, Lee BJ, Nishiyama K, Nakashima M, Tsurusaki Y, Doi H, Miyake N, Kim JH, Yu YS, Matsumoto N
- Journal Title
  
  Mol Vis.
  
  Volume: 19 Pages: 384-389
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25462547
[Journal Article] Sigle-nucleotide polymorphisms in the SEPTIN 12 gene may be a genetic risk factor for Japanese patients with Sertoli cell-only syndrome2012
- Author(s)
  Miyakawa K, Miyamoto T, Koh E, Tsujimura A, Miyagawa Y, Saijo Y, Namiki M, Sengoku K
- Journal Title
  
  J Androl
  
  Volume: 33(3) Pages: 483-487
- Data Source
  KAKENHI-PROJECT-23592388
[Journal Article] Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men2012
- Author(s)
  Miyamoto T, et al.
- Journal Title
  
  J Assist Reprod Genet
  
  Volume: 29 Pages: 47-51
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Single-nucleotide polymorphisms in the SEPTIN12 gene may be a genetic risk factor for Japanese patients with Sertoli cell-only syndrome2012
- Author(s)
  Miyakawa H, Miyamoto T, Koh E, Tsujimura A, Miyagawa Y, Saijo Y, Namiki M, Sengoku K.
- Journal Title
  
  J Androl
  
  Volume: 53(3) Pages: 483-7
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men.2012
- Author(s)
  Miyamoto T
- Journal Title
  
  J Assist Reprod Genet.
  
  Volume: 29 Issue: 1 Pages: 47-51
- DOI
  10.1007/s10815-011-9679-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591811, KAKENHI-PROJECT-22591812
[Journal Article] Single-nucleotide polymorphisms in HORMAD1 may be a risk factor for azoospermia caused by meiotic arrest in Japanese patients2012
- Author(s)
  Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Horikawa M, Saijo Y, Sengoku K.
- Journal Title
  
  Asian J Androl
  
  Volume: 14(4) Pages: 580-3
- NAID
  120006580771
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Single-nucleotide polymorphisms in HORMAD1 may be a risk factor for azoospermia caused by meiotic arrest in Japanese patients2012
- Author(s)
  Miyamoto T, et al.
- Journal Title
  
  Asian J Androl
  
  Volume: 14 Issue: 4 Pages: 580-583
- DOI
  10.1038/aja.2011.180
- NAID
  120006580771
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591811, KAKENHI-PROJECT-22591812
[Journal Article] Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men2012
- Author(s)
  Toshinobu Miyamoto & Akira Tsujimura & Yasushi Miyagawa & Eitetsu Koh & Mikio Namiki & Michiharu Horikawa & Yasuaki Saijo & Kazuo Sengoku
- Journal Title
  
  J Assist Reprod Genet
  
  Volume: 29 Pages: 47-51
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23592388
[Journal Article] Study of the vulvar skin in healthy Japanese women: components of the stratum corneum and microbes2012
- Author(s)
  Miyamoto T, Akiba S, Sato N, Fujimura T, Takagi Y, Kitahara T, Takema Y, Iizuka H, Sengoku K.
- Journal Title
  
  Int J Dermatol
  
  Volume: 52 Issue: 12 Pages: 1500-1505
- DOI
  10.1111/j.1365-4632.2012.05582.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Single-nucleotide polymorphisms in HORMAD1 gene may be a risk factor for azoospermia caused by meiotic arrest in Japanese patients2012
- Author(s)
  Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Horikawa M, Saijo Y, Sengoku K
- Journal Title
  
  Asian J Androl
  
  Volume: 14(4) Pages: 580-583
- Data Source
  KAKENHI-PROJECT-23592388
[Journal Article] Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men2012
- Author(s)
  Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Horikawa M, Saijo Y, Sengoku K.
- Journal Title
  
  J Assist Reprod Genet
  
  Volume: 29(1) Pages: 47-51
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Male infertility and its causes in human2012
- Author(s)
  Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Sengoku K
- Journal Title
  
  Adv Urol
- Data Source
  KAKENHI-PROJECT-23592388
[Journal Article] Male infertility and its causes in human2012
- Author(s)
  Miyamoto T, et al.
- Journal Title
  
  Adv Urol
  
  Volume: 2012 Pages: 384520-384520
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Male infertility and its causes in human2012
- Author(s)
  Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Sengoku K.
- Journal Title
  
  Adv Urol 2012
  
  Volume: 2012 Pages: 384520-384520
- DOI
  10.1155/2012/384520
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] A family of oculofaciocardiodental syndrome (OFCD) with a novel BCOR mutation and genomic rearrangements involving NHS2012
- Author(s)
  Kondo Y, Saitsu H, Miyamoto T, Nishiyama K, Tsurusaki Y, Doi H, Miyake N, Ryoo NK, Kim JH, Yu YS, Matsumoto N
- Journal Title
  
  J Hum Genet
  
  Volume: 57(3) Pages: 197-201
- NAID
  10030712110
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Single nucleotide polymorphisms in the UBR2 gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest2011
- Author(s)
  Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Namiki M, Horikawa M, Saijo Y, Sengoku K
- Journal Title
  
  J Assist Reprod Genet
  
  Volume: 28(8) Pages: 743-746
- Data Source
  KAKENHI-PROJECT-23592388
[Journal Article] Single nucleotide polymorphism in the UBR2 gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest2011
- Author(s)
  Miyamoto T, et al.
- Journal Title
  
  J Assist Reprod Genet
  
  Volume: 28 Pages: 743-746
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Single-Nucleotide Polymorphisms in the SEPTIN12 Gene May Be a Grenetic Risk Factor for Japanese Patients with Sertoli Cell-Only Syndrome2011
- Author(s)
  Miyakawa H, Miyamoto T, et al.
- Journal Title
  
  J Androl
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] 不妊への対応PCOSにおける排卵誘発法と問題点】経口薬2010
- Author(s)
  千石一雄、佐藤恒、宮本敏伸
- Journal Title
  
  産婦人科の実際
  
  Volume: 64 Pages: 157-161
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Current concepts of human azoospermia and its causes2010
- Author(s)
  T.Miyamoto, T.Tsujimmura, K.Sengoku, et al
- Journal Title
  
  Reprod Med Biol
  
  Volume: 9 Pages: 121-127
- NAID
  10027050484
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591902
[Journal Article] Current concepts of human azoospermia and its causes.2010
- Author(s)
  Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Sato H, et al.
- Journal Title
  
  Reprod Med Biol
  
  Volume: 9 Pages: 121-127
- NAID
  10027050484
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] 不妊と遺伝因子2010
- Author(s)
  宮本敏伸、佐藤恒、千石一雄
- Journal Title
  
  産婦人科の実際
  
  Volume: 59 Pages: 1959-1967
- Data Source
  KAKENHI-PROJECT-22591811
[Journal Article] Current concepts of human azoospermia and its causes2010
- Author(s)
  T Miyamoto, A Tsujimura, Y Miyagawa, E Koh, H Sato, M Namiki, K Sengoku
- Journal Title
  
  Reprod Med Biol 9
  
  Pages: 121-127
- NAID
  10027050484
- Data Source
  KAKENHI-PROJECT-20591902
[Journal Article] A single nucleotide polymorphism in SPATA17 may be a genetic risk factor for Japanese patients with meiotic arrest.2009
- Author(s)
  宮本敏伸, Tsujimura A, et al.
- Journal Title
  
  Asian J Androl 11
  
  Pages: 623-628
- NAID
  120006580770
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] LMTK2 and PARP-2 gene polymorphism and azoospermia secondary to meiotic arrest2009
- Author(s)
  N.Sakugawa, T.Miyamoto, K.Sengoku, et al.
- Journal Title
  
  J Assist Reprod Genet 26
  
  Pages: 1113-1118
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591902
[Journal Article] ヒト無精子症とその要因(総説)2009
- Author(s)
  宮本敏伸, ら
- Journal Title
  
  北海道産科婦人科学会会誌 53
  
  Pages: 21-26
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] LMTK2 and PARP-2 gene polymorphism and azoospermia secondary to meiotic arrest2009
- Author(s)
  Sakugawa N, Miyamoto T, Tsujimura A, Koh E, Miyagawa Y, Sato H, Namiki M, Okuyama A, Sengoku K.
- Journal Title
  
  J Assist Reprod Genet 26
  
  Pages: 545-552
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] A single nucleotide polymorphism in SPATA17 may be a genetic risk factor for Japanese patients with meiotic arrest2009
- Author(s)
  Miyamoto T, Tsujimura T, Miyagawa Y, Koh E, Sakugawa N, Miyakawa H, Sato H, Namiki M, Okuyama A, Sengoku K
- Journal Title
  
  Asian J Androl 11(5)
  
  Pages: 623-28
- NAID
  120006580770
- Data Source
  KAKENHI-PROJECT-20591902
[Journal Article] A single nucleotide polymorophism in SPATA17 may be a genetic factor for Japanese patients with meiotic arrest2009
- Author(s)
  T.Miyamoto, T.Tsujimmura, K.Sengoku, et al
- Journal Title
  
  Asian J Androl 11
  
  Pages: 623-628
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591902
[Journal Article] LMTK2 and PARP-2 gene polymorphism and azoospermia secondary to meiotic arrest.2009
- Author(s)
  Sakugawa N, 宮本敏伸, 他
- Journal Title
  
  J Assist Reprod Genet 26
  
  Pages: 545-552
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] A single nucleotide polymorphism in SPATA17 may be a genetic risk factor for Japanese patients with meiotic arrest2009
- Author(s)
  Miyamoto T, Tsujimura A, Miyagawa Y, Koh E, Sakugawa N, Miyakawa H, Sato H, Namiki M, Okuyama A, Sengoku K.
- Journal Title
  
  Asian J Androl. 11
  
  Pages: 623-628
- NAID
  120006580770
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] ヒト無精子症とその要因 (総説)2009
- Author(s)
  宮本敏伸, 佐藤恒, 佐久川直子, 宮川博栄, 千石一雄
- Journal Title
  
  北海道産科婦人科学会会誌 53
  
  Pages: 21-26
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest2008
- Author(s)
  Miyamoto T, Koh E, Sakugawa N, Sato H, Hayashi H, Namiki M, Sengoku K.
- Journal Title
  
  J Assist Reprod Genet. 25
  
  Pages: 553-7
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] Isolation of the human ePAB and ePABP2 cDNAs and analysis of the expression patterns2008
- Author(s)
  Sakugawa N, Miyamoto T, Sato H, Ishikawa M, Horikawa M, Hayashi H, Ishikawa M, Sengoku K.
- Journal Title
  
  J Assist Reprod Genet 25
  
  Pages: 215-21
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] Isolation of the human ePAB and ePABP2 cDNAs and analys is of the expression patterns2008
- Author(s)
  Sakugawa N, Miyamoto T, et,al.
- Journal Title
  
  J Assit Reprod. Genet 25
  
  Pages: 215-21
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest2008
- Author(s)
  Miyamoto T, et.al.
- Journal Title
  
  J Assit Reprod Genet 25
  
  Pages: 553-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] Isolatiom of the human ePAB and ePABP2 cDNAs and analysis of the expression patterns2008
- Author(s)
  N.Sakugawa, T.Miyamoto, H.Sato, M.Ishikawa, M.Horikawa, H.Hayashi, M.Ishikawa, K.Sengoku
- Journal Title
  
  J Assist Reprod Genet 25
  
  Pages: 215-221
- Data Source
  KAKENHI-PROJECT-20591902
[Journal Article] Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest2008
- Author(s)
  T.Miyamoto, E.Koh, N.Sakugawa, H.Sato, H.Hayashi, M.Namiki, K.Sengoku
- Journal Title
  
  J Assist Reprod Gene 25
  
  Pages: 553-557
- Data Source
  KAKENHI-PROJECT-20591902
[Journal Article] Two single nucleotide polymorphism in PRDM9 (MEISETZ) gene maybe a genetic risk factor for Japanese patients with azoospermia by meiotic arrest2008
- Author(s)
  Miyamoto T, Koh E, Sakugawa N, Sato H, Hayashi H, Namiki M, Sengoku K
- Journal Title
  
  J Assist Reprod Genet 25
  
  Pages: 553-557
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591902
[Journal Article] Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract2007
- Author(s)
  Miyamoto T, Yu YS, Sato H, Hayashi H, Sakugawa N, Ishikawa M, Sengoku K.
- Journal Title
  
  Turk J Pediatr 49
  
  Pages: 334-6
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] Three-dimensional magnetic resonance imaging after Ultrasonography for assessment of fetal gastroschisis2006
- Author(s)
  Sasaki Y, Miyamoto T et al.
- Journal Title
  
  Magn Reson Imaging 24・2
  
  Pages: 201-203
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest.2006
- Author(s)
  Sato H, Miyamoto T, Ishikawa M et al.
- Journal Title
  
  J Hum Genet 51
  
  Pages: 533-540
- NAID
  10017608347
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Is a genetic defect in FKBP6 a common cause of azoospermia?2006
- Author(s)
  Miyamoto T, Ishikawa M et al.
- Journal Title
  
  Cell Mol Biol Lett 11
  
  Pages: 557-569
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Is a genetic defect in FKBP6 a common cause of azoospermia?2006
- Author(s)
  Miyamoto T et al.
- Journal Title
  
  Cell Mol Biol Lett 11
  
  Pages: 557-569
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] 精子形成遺伝子2006
- Author(s)
  宮本敏伸他
- Journal Title
  
  産婦人科の実際 55・2
  
  Pages: 159-164
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] Is a genetic defect in FKBP6 a common cause of azoospermia?2006
- Author(s)
  Miyamoto T, Ishikawa M, et al.
- Journal Title
  
  Cell Mol Biol Lett 11
  
  Pages: 557-569
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Polymorphic alleles of the human MEI1 gene are associated With human azoospermia by meiotic arrest.2006
- Author(s)
  Sato H, Miyamoto T, Ishikawa M, et al.
- Journal Title
  
  J Hum Genet 51
  
  Pages: 533-540
- NAID
  10017608347
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest.2006
- Author(s)
  Sato H, Miyamoto T et al.
- Journal Title
  
  J Hum Genet 51
  
  Pages: 533-540
- NAID
  10017608347
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] GATM, the human ortholog of the mouse imprinted Gatm gene, escapes genomic imprinting in placenta2005
- Author(s)
  Miyamoto T, Ishikawa M et al.
- Journal Title
  
  Genetics and Molecular Biology 28・1
  
  Pages: 44-45
- NAID
  110004037390
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] GATM, the human ortholog of the mouse imprinted Gatm gene, escapes genomic imprinting in placenta2005
- Author(s)
  Miyamoto T et al.
- Journal Title
  
  Genetics and Molecular Biology 28・1
  
  Pages: 44-45
- NAID
  110004037390
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] The human transcript induced in spermatogenesis 50.2004
- Author(s)
  Sasaki Y, Miyamoto T, Sengoku K, Ishikawa M et al.
- Journal Title
  
  Reprod Med Biol 3
  
  Pages: 237-243
- NAID
  10014259263
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Integrins are not involved in the process of human sperm-oolemmal fusion.2004
- Author(s)
  Sengoku K, Takuma N, Miyamoto T, Ishikawa M et al.
- Journal Title
  
  Human Reprod 19(3)
  
  Pages: 639-644
- NAID
  120003161705
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] GATM, the human ortholog of the mouse imprinted Gatm gene, escapes genomic imprinting in placenta.2004
- Author(s)
  Miyamoto T, Sengoku K et al.
- Journal Title
  
  Genet and Mol Biol (in press)
- NAID
  110004037390
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] GATM, the human ortholog of the mouse imprinted Gatm gene, escapes genomic imprinting in placenta.2004
- Author(s)
  Miyamoto T, Sengoku K, Ishikawa M et al.
- Journal Title
  
  Genet and Mol Biol (in press)
- NAID
  110004037390
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Nuclear Dynamics of Parthenogenesis of Human oocytes : Effect of Oocyte A ging in vitro.2004
- Author(s)
  Sengoku K, Takuma N, Miyamoto T et al.
- Journal Title
  
  Gynecol Obstet Invest 58
  
  Pages: 155-159
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] The human transcript induced in spermatogenesis 50.2004
- Author(s)
  Sasaki Y, Miyamoto T et al.
- Journal Title
  
  Reprod Med Biol 3
  
  Pages: 237-243
- NAID
  10014259263
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] Integrins are not involved in the process of human sperm-oolemmal fusion.2004
- Author(s)
  Sengoku K, Takuma N, Miyamoto T et al.
- Journal Title
  
  Human Reprod 19(3)
  
  Pages: 639-644
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] Isolation and Expression analysis of the testis-specific gene, human OPPO1.2004
- Author(s)
  Miyamoto T et al.
- Journal Title
  
  J Assist Reprod Genet 21(4)
  
  Pages: 129-134
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] Nuclear Dynamics of Parthenogenesis of Human oocytes : Effect of Oocyte Aging in vitro.2004
- Author(s)
  Sengoku K, Takuma N, Miyamoto T, Ishikawa M et al.
- Journal Title
  
  Gynecol Obstet Invest 58
  
  Pages: 155-159
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Isolation and Expression analysis of the testis-specific gene, human OPPO1.2004
- Author(s)
  Miyamoto T, Sengoku K, Ishikawa M et al.
- Journal Title
  
  J Assist Reprod Genet 21(4)
  
  Pages: 129-134
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest
- Author(s)
  Sato H, Miyamoto T, Ishikawa M et al.
- Journal Title
  
  Journal of Human Genetics (in press)
- NAID
  10017608347
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract.
- Author(s)
  Miyamoto T, Ishikawa M et al.
- Journal Title
  
  Turk J Pediatr (in press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest
- Author(s)
  Sato H, Miyamoto T et al.
- Journal Title
  
  Journal of Human Genetics (in press)
- NAID
  10017608347
- Data Source
  KAKENHI-PROJECT-16790934
[Journal Article] Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract.
- Author(s)
  Miyamoto T, Ishikawa M, et al.
- Journal Title
  
  Turk J Pediatr (in presss)
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Single Nucleotide Polymorphism in the SPATA17 gene may be a genetic risk factor for Japanese patients with meiotic arrest
- Author(s)
  Miyamoto, et.al.
- Journal Title
  
  Asian J Andrology (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591887
[Journal Article] Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract.
- Author(s)
  Miyamoto T, Ishikawa M et al.
- Journal Title
  
  Turk J Pediatr (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390471
[Journal Article] Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract.
- Author(s)
  Miyamoto T et al.
- Journal Title
  
  Turk J Pediatr (in press)
- Data Source
  KAKENHI-PROJECT-16790934
[Patent] でリケ－トエリアのかぶれ判定方法2016
- Inventor(s)
  千石一雄、宮本敏伸　他
- Industrial Property Rights Holder
  旭川医科大学
- Industrial Property Rights Type
  特許
- Filing Date
  2016-11-29
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] ヒトSCOSにおけるヒトH3T遺伝子の解析2019
- Author(s)
  宮本敏伸, 水無瀬学, 水無瀬萌, 千石一雄
- Organizer
  日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-19K09770
[Presentation] 当院における腹腔鏡下手術での工夫2019
- Author(s)
  水無瀬学, 水無瀬萌, 宮本敏伸, 千石一雄
- Organizer
  日本生殖医学会
- Data Source
  KAKENHI-PROJECT-19K09770
[Presentation] ヒトSCOSの原因遺伝子としてのヒトH3T遺伝子の解析2019
- Author(s)
  宮本敏伸, 水無瀬学, 水無瀬萌, 千石一雄
- Organizer
  日本産婦人科学会
- Data Source
  KAKENHI-PROJECT-19K09770
[Presentation] 非対称性子宮奇形の2例2019
- Author(s)
  水無瀬萌, 林なつき, 水崎恵, 水無瀬学, 寳田健平, 市川英俊, 北香, 高橋知昭, 宮本敏伸, 加藤育民, 片山英人, 千石一雄
- Organizer
  日本産婦人科学会
- Data Source
  KAKENHI-PROJECT-19K09770
[Presentation] 当院における腹腔鏡下筋腫核出術での工夫2019
- Author(s)
  水無瀬萌, 水無瀬学, 宮本敏伸, 千石一雄
- Organizer
  日本産科婦人科内視鏡学会
- Data Source
  KAKENHI-PROJECT-19K09770
[Presentation] 気胸の管理が必要となった希少部位子宮内膜症の2症例2018
- Author(s)
  水無瀬学, 加藤育民, 水無瀬萌, 宮本敏伸, 水崎恵, 高橋知昭, 千石一雄
- Organizer
  日本女性医学学会
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] 腹腔鏡とMRIで診断し得た重複子宮・腟中隔の1症例2018
- Author(s)
  水無瀬萌, 宮本敏伸, 林なつき, 西脇邦彦, 千石一雄
- Organizer
  日本生殖医学会
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] 日本人Sertoli Cell Only Syndrome患者におけるGALNTL5変異との関連について2018
- Author(s)
  水無瀬学, 宮本敏伸, 千石一雄
- Organizer
  北日本産科婦人科学会
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] マタニティヨガ実践と切迫早産,早産との関連に関する検討(エコチル調査北海道追加調査)(2018
- Author(s)
  川西康之, 岸玲子, 吉岡英治, 西條泰明, 吉田貴彦, 宮本敏伸, 千石一雄, 伊藤善也, 伊藤佐智子, 宮下ちひろ, 荒木敦子
- Organizer
  日本産科婦人科学会
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] GALNTL5遺伝子の変異は日本人Sertoli Cell Only Syndromeの原因遺伝子の可能性がある2018
- Author(s)
  水無瀬学, 宮本敏伸, 岡田弘, 慎武, 飯島将司, 千石一雄
- Organizer
  日本生殖医学会
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] 減数分裂停止及びSertoli cell-only syndromeに起因する日本人無精子症患者におけるヒトRAD21L1遺伝子の解析に関する検討2018
- Author(s)
  水無瀬学, 上田寛人, 宮本敏伸, 千石一雄
- Organizer
  日本産科婦人科学会
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] 日本人SCOS患者におけるヒトETV5遺伝子の検討2017
- Author(s)
  宮本敏伸
- Organizer
  北海道生殖医学会総会
- Place of Presentation
  札幌市
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] 当院における腹腔鏡下子宮筋腫核出術の後方視的検討　術後妊娠例を中心に2017
- Author(s)
  水無瀬萌, 竹内肇, 寳田健平, 市川英俊, 北香, 高橋知昭, 加藤育民, 片山英人, 西脇邦彦, 宮本敏伸, 千石一雄
- Organizer
  日本産科婦人科学会
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] ヒトCUL4B遺伝子の変異は日本人Sertoli Cell only Syndromeにおいては稀である2017
- Author(s)
  宮本敏伸, 安孫子公香, 千石一雄
- Organizer
  日本生殖医学会
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] 日本人セルトリセルオンリーシンドローム患者におけるヒトETV5遺伝子の一塩基多型解析に関する研究2017
- Author(s)
  上田寛人, 水無瀬学, 宮本敏伸, 千石一雄
- Organizer
  日本産婦人科学会
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] 日本人SCOS患者におけるヒトETV5遺伝子の検討2017
- Author(s)
  宮本敏伸, 上田寛人, 水無瀬学, 安孫子公香, 千石一雄
- Organizer
  北海道生殖医学会
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] 男性不妊症原因遺伝子群2016
- Author(s)
  宮本敏伸
- Organizer
  日本アンドロロジー学会
- Place of Presentation
  前橋市
- Year and Date
  2016-06-23
- Invited
- Data Source
  KAKENHI-PROJECT-25462547
[Presentation] 男性不妊症と遺伝学的素因2016
- Author(s)
  宮本敏伸
- Organizer
  精子研究会
- Place of Presentation
  秋田市
- Year and Date
  2016-06-03
- Invited
- Data Source
  KAKENHI-PROJECT-25462547
[Presentation] 男性不妊症原因遺伝子群2016
- Author(s)
  宮本敏伸
- Organizer
  日本アンドロロジー学会学術総会
- Place of Presentation
  前橋
- Invited
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] 男性不妊症と遺伝学的素因2016
- Author(s)
  宮本敏伸
- Organizer
  第４７回精子研究会
- Place of Presentation
  秋田市
- Invited
- Data Source
  KAKENHI-PROJECT-16K11077
[Presentation] ヒトSCOSにおけるヒトPLK4遺伝子の解析2014
- Author(s)
  宮本敏伸、千石一雄
- Organizer
  北海道生殖医学会学術講演会
- Place of Presentation
  札幌市
- Data Source
  KAKENHI-PROJECT-25462547
[Presentation] ヒトSertoli cell-only syndrome (SCOS) におけるヒトLRWD1遺伝子の解析2013
- Author(s)
  宮本敏伸、千石一雄
- Organizer
  日本産婦人科学会学術講演会
- Place of Presentation
  札幌市
- Data Source
  KAKENHI-PROJECT-25462547
[Presentation] ヒトSertoli cell-only syndrome (SCOS) におけるヒトLRWD1遺伝子の解析2013
- Author(s)
  宮本敏伸、千石一雄
- Organizer
  日本生殖医学会学術講演会
- Place of Presentation
  神戸市
- Data Source
  KAKENHI-PROJECT-25462547
[Presentation] ヒトSertoli cell-only syndrome (SCOS) におけるヒトLRWD1遺伝子の解析2013
- Author(s)
  宮本敏伸、千石一雄
- Organizer
  日本産科婦人科学会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-23592388
[Presentation] Sertoli-ceii-only syndromeによる無精子症患者群とヒトSEPTIN12遺伝子の多型解析2013
- Author(s)
  宮川博栄、宮本敏伸、千石一雄
- Organizer
  北日本産科婦人科学会
- Data Source
  KAKENHI-PROJECT-23592388
[Presentation] ヒトSertoli cell-only syndrome (SCOS)におけるヒトLRWD1遺伝子の解析2013
- Author(s)
  宮本敏伸、宮川博栄、千石一雄
- Organizer
  日本産科婦人科学会
- Data Source
  KAKENHI-PROJECT-23592388
[Presentation] ヒト無精子症におけるヒトSEPTIN12遺伝子の解析2012
- Author(s)
  宮本敏伸
- Organizer
  日本産婦人科学会総会
- Place of Presentation
  横浜市
- Data Source
  KAKENHI-PROJECT-22591811
[Presentation] ヒト精子形成過程におけるヒト SEPTIN12 遺伝子の解析2012
- Author(s)
  宮本敏伸,宮川博栄,千石一雄
- Organizer
  日本産婦人科学会
- Data Source
  KAKENHI-PROJECT-22591811
[Presentation] ヒト無精子症におけるヒトHOMAD1遺伝子の解析2012
- Author(s)
  宮本敏伸
- Organizer
  日本生殖医学会総会
- Place of Presentation
  長崎市
- Data Source
  KAKENHI-PROJECT-22591811
[Presentation] ヒト精子形成過程におけるヒト SEPTIN12 遺伝子の解析2012
- Author(s)
  宮本敏伸,宮川博栄,岡部公香,千石一雄
- Organizer
  日本生殖医学会
- Data Source
  KAKENHI-PROJECT-22591811
[Presentation] ヒト精子形成過程におけるヒト HOMAD1 遺伝子の解析2011
- Author(s)
  宮本敏伸,宮川博栄,岡部公香,千石一雄
- Organizer
  日本産婦人科学会
- Data Source
  KAKENHI-PROJECT-22591811
[Presentation] ヒト無精子症原因候補遺伝子であるSEPTIN12遺伝子の解析2011
- Author(s)
  宮本敏伸
- Organizer
  第56回日本生殖医学会学術講演会・総会
- Place of Presentation
  横浜市
- Year and Date
  2011-12-08
- Data Source
  KAKENHI-PROJECT-22591811
[Presentation] ヒト精子形成過程におけるヒト SEPTIN12 遺伝子の解析2011
- Author(s)
  宮本敏伸,宮川博栄,岡部公香,千石一雄
- Organizer
  日本生殖医学会
- Data Source
  KAKENHI-PROJECT-22591811
[Presentation] ヒト精子形成過程におけるヒト SEPTIN12 遺伝子の解析2011
- Author(s)
  宮本敏伸,宮川博栄,千石一雄
- Organizer
  日本産婦人科学会
- Data Source
  KAKENHI-PROJECT-22591811
[Presentation] ヒト精子形成過程におけるヒト HOMAD1 遺伝子の解析2011
- Author(s)
  宮本敏伸,宮川博栄,岡部公香,千石一雄
- Organizer
  日本生殖医学会
- Data Source
  KAKENHI-PROJECT-22591811
[Presentation] 教育講演:男性不妊とその要因2010
- Author(s)
  宮本敏伸
- Organizer
  日本生殖医学会
- Place of Presentation
  金沢市
- Year and Date
  2010-11-11
- Data Source
  KAKENHI-PROJECT-19591887
[Presentation] 新たなヒト無精子症原因候補遺伝子であるSPATA17遺伝子の解析2010
- Author(s)
  宮本敏伸、佐藤恒,千石一雄
- Organizer
  日本生殖医学会北海道地方会
- Data Source
  KAKENHI-PROJECT-20591902
[Presentation] 当教室において同定されたヒト無精子症に関わる遺伝子群2010
- Author(s)
  宮本敏伸,佐藤恒,佐久川直子,千石一雄
- Organizer
  日本産科婦人科学会
- Data Source
  KAKENHI-PROJECT-20591902
[Presentation] 男性不妊とその要因2010
- Author(s)
  宮本敏伸
- Organizer
  日本生殖医学会
- Data Source
  KAKENHI-PROJECT-20591902
[Presentation] 当教室において同定されたヒト無精子症に関わる遺伝子群2010
- Author(s)
  宮本敏伸
- Organizer
  第62回日本産婦人科学会学術講演会
- Place of Presentation
  東京国際フォーラム(東京)
- Year and Date
  2010-04-24
- Data Source
  KAKENHI-PROJECT-22591811
[Presentation] シンポジウム:造精機能障害と常染色体上の遺伝子解析2010
- Author(s)
  宮本敏伸
- Organizer
  RMB研究会シンポジウム
- Place of Presentation
  東京
- Year and Date
  2010-01-23
- Data Source
  KAKENHI-PROJECT-19591887
[Presentation] 教育講演:ヒト無精子症に関わる遺伝子の解析2009
- Author(s)
  宮本敏伸
- Organizer
  日本産婦人科学会北日本連合地方部会
- Place of Presentation
  札幌市
- Year and Date
  2009-08-29
- Data Source
  KAKENHI-PROJECT-19591887
[Presentation] シンポジウム : ヒト無精子症に関わる遺伝子の解析2009
- Author(s)
  宮本敏伸
- Organizer
  日本アンドロロジー学会
- Place of Presentation
  富山
- Data Source
  KAKENHI-PROJECT-19591887
[Presentation] 新たなヒト無精子症原因候補遺伝子であるSPATA17遺伝子の解析2009
- Author(s)
  宮本敏伸、佐久川直子, ら
- Organizer
  日本産婦人科学会
- Place of Presentation
  京都市
- Year and Date
  2009-04-04
- Data Source
  KAKENHI-PROJECT-19591887
[Presentation] ヒト無精子症におけるヒトBREK2遺伝子及びPARP-2遺伝子の解析2009
- Author(s)
  宮本敏伸,佐久川直子,佐藤恒,千石一雄
- Organizer
  日本生殖医学会
- Data Source
  KAKENHI-PROJECT-20591902
[Presentation] 教育講演 : ヒト無精子症に関わる遺伝子の解析2009
- Author(s)
  宮本敏伸
- Organizer
  日本産婦人科学会北日本連合地方部会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-19591887
[Presentation] 教育講演 : 男性不妊とその要因2009
- Author(s)
  宮本敏伸
- Organizer
  日本生殖医学会
- Place of Presentation
  金沢
- Data Source
  KAKENHI-PROJECT-19591887
[Presentation] シンポジウム:ヒト無精子症に関わる遺伝子の解析2009
- Author(s)
  宮本敏伸
- Organizer
  日本アンドロロジー学会
- Place of Presentation
  富山市
- Year and Date
  2009-07-03
- Data Source
  KAKENHI-PROJECT-19591887
[Presentation] ヒト無精子症原因遺伝子であるヒトMEISETZ遺伝子の解析2008
- Author(s)
  宮本敏伸
- Organizer
  日本産婦人科学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-19591887
[Presentation] ヒト無精子症におけるヒトLMTK2遺伝子及びPARP-2遺伝子の解析2008
- Author(s)
  宮本敏伸、佐久川直子,千石一雄
- Organizer
  日本生殖医学会
- Data Source
  KAKENHI-PROJECT-20591902
[Presentation] ヒト無精子症原因候補遺伝子であるヒトMEISEZ遺伝子,CDK2遺伝子およびHOP2遺伝子の解析、他27題2007
- Author(s)
  宮本敏伸、佐藤恒、佐久川直子、堀川道晴、千石一雄
- Organizer
  第59回日本産科婦人科学会学術講演会
- Place of Presentation
  京都国際会議場
- Data Source
  KAKENHI-PROJECT-19591887
[Presentation] シンポジウム : ヒト無精子症原因遺伝子群2007
- Author(s)
  宮本敏伸
- Organizer
  日本内分泌学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-19591887

1. SENGOKU Kazuo (30163124)

# of Collaborated Projects: 9 results

# of Collaborated Products: 99 results
2. ISHIKAWA Mutsuo (20002131)

# of Collaborated Projects: 3 results

# of Collaborated Products: 16 results
3. TAKUMA Naoyuki (10312464)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. YAMASHITA Tsuyoshi (30271787)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 藤ノ木政勝 (30316583)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 茂木絵美 (60595031)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

MIYAMOTO Toshinobu 宮本 敏伸

Research Projects

Research Products

Co-Researchers

ヒト男性不妊症および不育症の病態解明および臨床医学への応用Principal Investigator

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Review Section

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Analysis of the genes causing male infertility in humanPrincipal Investigator

Principal Investigator

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Review Section

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idetification of the genes causing male infertility and habitual abortion by next generation sequencing in humanPrincipal Investigator

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Analysis of genes related to human azoospermia using a reverse genetics method

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Analysis of human azoospermia and POF and its clinical advancePrincipal Investigator

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Investigation of the mechanisms of spermatogenesis using a comprehensive analysis of genes related to human azoospermia

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Analysis of the factors on male infertility and habitual abortion & their Applications to clinical medicinePrincipal Investigator

Principal Investigator

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Comprehensive analysis of genes related to human azoospermia

Principal Investigator

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Identification of the genes causing azoospermia in human and analysis of the mechanism in spermatogenesisPrincipal Investigator

Principal Investigator

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新たなヒト無精子症の原因遺伝子の単離およびその機能解析Principal Investigator

Principal Investigator

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Research Institution

Identification of the genes causing azoospermia in humans and analysis of protein function and the mechanism of the spermatogenesis

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Analysis of LHX gene on human development

Principal Investigator

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Research Institution

[Book] Fertility Preservation ～妊孕性温存のすべて～2021

Author(s)

Total Pages

Publisher

MIYAMOTO Toshinobu 宮本敏伸

[Book] ARTラボ必携　生殖補助医療の必須知識とラボテクニックの伝承2021

[Journal Article] 【内分泌症候群(第3版)-その他の内分泌疾患を含めて-】女性性機能　その他　乳汁漏出症2019