Kosaki Kenjiro 小崎健次郎

… Alternative Names

KOSAKI Kenjiro 小崎健次郎

小さき健次郎コサキケンジロウ

Less

Researcher Number	30234743
Other IDs
Affiliation (Current)	2025: 慶應義塾大学, 医学部(信濃町), 教授
Affiliation (based on the past Project Information) *help	2011 – 2017: 慶應義塾大学, 医学部, 教授 2007 – 2010: Keio University, School of Medicine, Associate professor 2007: 慶應義塾大学, 医学研究科, 准教授 2002 – 2006: KEIO UNIVERSITY, SCHOOL OF MEDICINE, DEPARTMENT OF PEDIATRICS, ASSOCIATE PROFESSOR, 医学部, 助教授 2002 – 2003: KEIO UNIVERSITY, PEDIATRICS, ASSISTANT PROFESSOR, 医学部, 講師 … More 1999 – 2002: 慶應義塾大学, 医学部, 専任講師 2000: KEIO UNIVERSITY, SCHOOL OF MEDICINE, ASSISTANT PROFESSOR, 医学部, 専任講師 2000: 慶應義塾大学, 医学部, 講師 Less
Review Section/Research Field	Principal Investigator Pediatrics / Embryonic/Neonatal medicine / Laboratory medicine / Pediatrics Except Principal Investigator Pediatrics / Laboratory medicine / Obstetrics and gynecology / Obstetrics and gynecology / Gastroenterology / Pediatrics / Pediatric surgery
Keywords	Principal Investigator マイクロアレイ / 先天異常 / バイオインフォマティクス / ダイオキシン受容体 / ゲノム / ダイオキシン / teratogen / brain / microarray / endocrine disruptors … More / TCDD / dioxin / ヒト完全長cDNA配列 / CONGENITAL MALFORMATIONS / MUTATION ANALYSIS / LEFT-RIGHT AXIS / SITUS AMBIGUUS / SITUS INVERSUS / 遺伝子変異 / 先天性心疾患 / 変異解析 / 左右軸 / 内臓錯位 / 内臓逆位 / アレイCGH / 遺伝子診断 / 先天異常症候群 / 検査の感度 / アレイ / 遺伝子 / エンハンサー / 多発奇形症候群 / ニワトリ胚 / 発生生物学 / 内分泌撹乱因子 / 環境因子 / 催奇形因子 / 奇形 / 多型 / 環境ホルモン / 内分泌撹乱物質 / ミクロペニス / 連関解析 … More Except Principal Investigator 細胞周期 / 神経発生 / 大脳皮質発生 / エピジェネティクス / 遺伝子検査学 / 大脳皮質 / マウス / 神経前駆細胞 / MMP-8 / cell cycle / neuronal progenitor cells / p27Kip1 / TCDD / endometriosis / 子宮筋腫 / 子宮内膜症 / ダイオキシン / H.pylori / SNP / SHOX / 臨床的有用性 / 臨床的妥当性 / 分析的妥当性 / 精度管理 / 遺伝学的検査 / acetylation / mice / cerebral cortical histogenesis / epigenetics / アセチル化 / 子宮腺筋症 / LXA4R / neonate / E2 gene / maple syrup urine disease / Philippine / 新生児 / E2遺伝子 / メープルシロップ尿症 / フィリピン / differentiation / mouse / in utero exposure / cortical histogenesis / p27Kipl / 分化誘導 / 胎内曝露 / leiomyoma / dioxin / atrophic gastritis / cytokine / antral predominant gastritis / corpus predominant gastritis / TLR4 / polymorphism / endotoxin (LPS) / 胃粘膜上皮細胞 / 細胞遊走 / 画像処理 / 細胞欠損領域を作製する器具 / エンドトキシン / 萎縮性胃炎 / サイトカイン / Corpus predominant gastritis / Antrum predominant gastritis / Toll様受容体 / 遺伝子多型 / エンドトキシン(LPS) / LYMPHOEDEMA / GONADAL FUNCTION / SHORT STATURE / TURNER SKELETAL FEATURES / HAPLOINSUFFICIENCY / SEX CHROMOSOME / X染色体短腕欠失 / 量効果 / Langer type skeletal dysplasia / dyscondrosteosis / 下肢長比 / 座高 / 成長パターン / リンパ浮腫 / 性腺機能 / 特発性低身長 / ターナー骨格徴候 / 半量不全 / 性染色体 / 神経幹細胞 / 小児神経 / エピゲノム / メチル化 / 次世代シーケンサー / 網羅的遺伝子解析 / 神経堤幹細胞 / 腸管グリア / hypoganglionosis / ヒルシュスプルング病類縁疾患 / ヒルシュスプルング病 / 神経堤細胞 / 再生医療 / 幹細胞 / 分化 / 発生 / 腸管神経 / 小児神経学 / エピジェネティック / オリゴDNAアレイCGH法 / ラッセル・シルバー症候群 / ゲノムDNAアレイCGH / オリゴDNAアレイCGH / 子宮内発育遅延 / ラッセルシルバー症候群 / 先天異常学 / 遺伝 / 稀少疾患 / ヒストン脱アセチル化 / ガイドライン / OECD / 標準化 Less

Study on quality, usefulness and ELSI of genetic testing including NGS analysis.
- Principal Investigator
  
  KOSUGI SHINJI
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Laboratory medicine
- Research Institution
  Kyoto University
Roles of epigenetic mechanism on cerebral cortical histogenesis in congenital malformation syndrome
- Principal Investigator
  
  TAKAHASHI TAKAO
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Keio University
Effects of abnormal histone methylation on cell cycle kinetics of neuronal progenitor cells
- Principal Investigator
  
  MITSUHASHI TAKAYUKI
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Keio University
Evaluation of quality and usefullness of genetics testing-clinical application of next generation sequencer.
- Principal Investigator
  
  KOSUGI SHINJI
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Laboratory medicine
- Research Institution
  Kyoto University
Gene analyses and neural crest stem cell therapy in Hirschsprung's disease and allied disorders.
- Principal Investigator
  
  SHIMOJIMA Naoki
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatric surgery
- Research Institution
  Keio University
ROLES OF EPIGENETIC MECHANISM IN HOMEOSTATIC CELL-CYCLE CONTROL IN NEURONAL STEM CELLS
- Principal Investigator
  
  TAKAHASHI TAKAO
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Keio University
The high resolution oligonucleotide microarray for the chromosomaland epigenetic alterations in Russell-Silver syndrome
- Principal Investigator
  
  YOSHIHASHI Hiroshi
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Keio University
Research on validity and utility of molecular genetic testing.
- Principal Investigator
  
  KOSUGI Shinji
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Laboratory medicine
- Research Institution
  Kyoto University
Detection of intragenic deletions by array CGH analysisPrincipal Investigator
- Principal Investigator
  
  KOSAKI Kenjiro
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Laboratory medicine
- Research Institution
  Keio University
EPIGENETIC REGULATION OF CELL CYCLE KINETICS OF MURINE NEURONAL STEM CELLS BY HISTONE DEACETYLASE
- Principal Investigator
  
  TAKAHASHI Takao
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Keio University
Study on the standardization and quality assurance of genetic testing
- Principal Investigator
  
  KOSUGI Shinji
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Laboratory medicine
- Research Institution
  Kyoto University
多発奇形症候群責任遺伝子群の組織特異的発現機構の解明:比較ゲノム学的検討Principal Investigator
- Principal Investigator
  
  小崎健次郎
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Keio University
Epigenetic mechanisms in cell cycle regulation of neuronal stem rolls
- Principal Investigator
  
  TAKAHASHI Takao
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Keio University
Molecular epidemiolojial study on maple syrup urine disease in Philippine.
- Principal Investigator
  
  MATSUO Masafumi
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
Gene expression analysis in endometrium of steroid withdrawal model and endometriotic lesion.
- Principal Investigator
  
  ASADA Hironori
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Keio University
Toxic effects of in utero exposure to dioxins on cerebral histogenesis: quantitative analysis using mathematical model of cerebral histogenesis.
- Principal Investigator
  
  TAKAHASHI Takao
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Keio University
Genome-wide screening of dioxin-responsive genesPrincipal Investigator
- Principal Investigator
  
  KOSAKI Kenjiro
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Keio University
The association of polymorphism in dioxin related genes with leiomyoma and endometriosis
- Principal Investigator
  
  ASADA Hironori
- Project Period (FY)
  2002 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  KEIO UNIVERSITY
先天異常とダイオキシン受容体関連蛋白の多型との相関:性腺機能障害と口蓋裂Principal Investigator
- Principal Investigator
  
  小崎健次郎
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Keio University
Toll-like receptor polymorphism and H.pylori-associated gastric mucosal lesions
- Principal Investigator
  
  SUZUKI Hidekazu
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Gastroenterology
- Research Institution
  KEIO UNIVERSITY
CLARIFICATION OF CLINICAL ROLE AND GROWTH REGULATION MECHANISM OF THE SHOX GENE ON THE HUMAN PSEUDOAUTOSOMAL REGION
- Principal Investigator
  
  MATSUO Nobutake
- Project Period (FY)
  2000 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  NATIONAL CENTER FOR CHILD HEALTH AND DEVELOPMENT
  Keio University
MOLECULAR GENETICS OF HUMAN LEFT-RIGHT AXIS MALFORMATIONSPrincipal Investigator
- Principal Investigator
  
  KOSAKI Kenjiro
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  KEIO UNIVERSITY

All 2017 2016 2012 2011 2010 2009 2008 2007 2006 2005 2004 2003 2002 Other

All Journal Article Presentation

[Journal Article] Hydrocephalus with Hirschsprung disease : Severe end of X-linked hydrocephalus spectrum2012
- Author(s)
  Takenouchi T, Nakazawa M, Kanemura Y, Shimozato S, Yamasaki M, Takahashi T, Kosaki K
- Journal Title
  
  American Journal of Medical Genetics
  
  Volume: 158 Issue: 4 Pages: 812-815
- DOI
  10.1002/ajmg.a.35245
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590638
[Journal Article] Ophthalmic features of CHARGE syndrome with CHD7 mutations. 158A(3) : 514-82012
- Author(s)
  Nishina S, Kosaki R, Yagihashi T, Azuma N, Okamoto N, Hatsukawa Y, Kurosawa K, Yamane T, Mizuno S, Tsuzuki K, Kosaki K
- Journal Title
  
  American Journal of Medical Genetics
  
  Volume: 158 Issue: 3 Pages: 514-518
- DOI
  10.1002/ajmg.a.34400
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590638, KAKENHI-PROJECT-22591975, KAKENHI-PROJECT-24659770
[Journal Article] Ophthalmic features of CHARGE syndrome with CHD7 mutations2012
- Author(s)
  Nishina S, Kosaki R, Yagihashi T, Azuma N, Okamoto N, Hatsukawa Y, Kurosawa K, Yamane T, Mizuno S, Tsuzuki K, Kosaki K.
- Volume
  158巻
- Pages
  514-518
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590638
[Journal Article] Hydrocephalus with Hirschsprung disease : Severe end of X-linked hydrocephalus spectrum2012
- Author(s)
  Takenouchi T, Nakazawa M, Kanemura Y, Shimozato S, Yamasaki M, Takahashi T, Kosaki K.
- Journal Title
  
  American Journal of Medical Genetics
  
  Volume: 158巻 Pages: 812-815
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590638
[Journal Article] Role of rare cases in deciphering the mechanisms of congenital anomalies : CHARGE syndrome research. Kosaki K.2011
- Author(s)
  Kenjiro Kosaki
- Journal Title
  
  Congenital Anomalies
  
  Volume: 51 Pages: 12-15
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590638
[Journal Article] In utero exposure to dioxin causes neocortical dysgenesis through the actions of p27^<Kip1>2010
- Author(s)
  Mitsuhashi T, Yonemoto J, Sone H, Kosuge Y, Kosaki K, Takahashi T
- Journal Title
  
  Proc Natl Acad Sci USA 107(37)
  
  Pages: 16331-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390299
[Journal Article] In utero exposure to dioxin causes neocortical dysgenesis through the actions of p27Kip1.2010
- Author(s)
  Mitsuhashi T, Yonemoto J, Sone H, Kosuge Y, Kosaki K, Takahashi T.
- Journal Title
  
  Proc Natl Acad Sci USA
  
  Volume: 107 Pages: 16331-16335
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390299
[Journal Article] Two distinctive classic genetic syndromes, 22q11.2 deletion syndrome and Angelman syndrome, occurring within the same family.2009
- Author(s)
  Kosaki R, Migita O, Takahashi T, Kosaki K
- Journal Title
  
  Am J Med Genet 149A
  
  Pages: 702-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390299
[Journal Article] Effects of the CYP2D6*10 alleles and co-medication with CYP2D6-dependent drugs on risperidone metabolism in patients with schizophrenia.2009
- Author(s)
  Yagihashi T, Mizuno M, Chino B, Sato Y, Sakuma K, Takebayashi T, Takahashi T, Kosaki K
- Journal Title
  
  Hum Psychopharmacol. 24
  
  Pages: 301-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390299
[Journal Article] Caudal regression and tracheoesophageal malformation induced by adriamycin : A novel chick model of VATER association.2009
- Author(s)
  Naito Y, Kimura T, Aramaki M, Izumi K, Okada Y, Suzuki H, Takahashi T, Kosaki K
- Journal Title
  
  Pediatr Res 65
  
  Pages: 607-12
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390299
[Journal Article] Split hand foot malformation with whorl-like pigmentary pattern : Phenotypic expression of somatic mosaicism for the p63 mutation.2008
- Author(s)
  Kosaki R, Naito Y, Torii C, Takahashi T, Nakajima T, Kosaki K
- Journal Title
  
  Am J Med Genet 146
  
  Pages: 2574-2577
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390299
[Journal Article] Embryonic expression profile of chicken CHD7, the ortholog of the causative gene for CHARGE syndrome2007
- Author(s)
  Aramaki, M, Kimura, T, Udaka, T, Kosaki, R, Mitsuhashi, T, Okada, Y, Takahashi, T, Kosaki, K
- Journal Title
  
  Birth Defects Res A Clin Mol Teratol 79
  
  Pages: 50-57
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390302
[Journal Article] 遺伝子検査ネットワーク.2007
- Author(s)
  沼部博直, 松原洋一, 小崎健次郎, 小杉眞司
- Journal Title
  
  臨床検査 51
  
  Pages: 1621-1623
- Data Source
  KAKENHI-PROJECT-19590556
[Journal Article] (2007)遺伝子診断を取り巻く最近の動向2007
- Author(s)
  沼部博直、松原洋一、小崎健次郎、小杉眞司
- Journal Title
  
  遺伝子検査ネットワーク臨床検査 51(12)
  
  Pages: 1621-1623
- Data Source
  KAKENHI-PROJECT-19590556
[Journal Article] Identification of a prosencephalic-specific enhancer of SALL1:Comparative genomic approach using the chick embryo2007
- Author(s)
  Izumi, K., Aramaki, M., Kimura, T., Naito, Y., Udaka, T., Uchikawa, M., Kondoh, H., Suzuki, H., Cho, G. Okada, Y., Takahashi, T., Golden, JA., Kosaki, K.
- Journal Title
  
  Pediatric Research 61
  
  Pages: 660-665
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18659307
[Journal Article] Genome-wide screening of dioxin-responsive genes in fetal brain : bioinformatic and experimental approaches2006
- Author(s)
  Fujita, H, Samejima, H, Kitagawa, N, Mitsuhashi, T, Washio, T, Yonemoto, J, Tomita, M, Takahashi, T, Kosaki, K
- Journal Title
  
  Congenital Anomaly 46
  
  Pages: 135-143
- NAID
  10027385612
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18390302
[Journal Article] DHPLC in clinical molecular diagnostic services.2005
- Author(s)
  Kosaki K, et al.
- Journal Title
  
  Mol Genet Metab.(Review) 86(1-2)
  
  Pages: 117-123
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16591685
[Journal Article] DHPLC in clinical molecular diagnostic services.2005
- Author(s)
  Kosaki K, et al.
- Journal Title
  
  Mol Genet Metab. 86・1_2
  
  Pages: 117-23
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16591685
[Journal Article] Marfanoid Habitus With Abnormal Situs.2004
- Author(s)
  Kosaki K, Bird LM, Maeda J, Higuchi M, Jones MC, Matsumoto M.
- Journal Title
  
  American Journal of Medical Genetics 127A
  
  Pages: 310-312
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591162
[Journal Article] Position-specific expression of Hox genes along the gastrointestinal tract.2004
- Author(s)
  Yahagi N, Kosaki R, Ito T, Mitsuhashi T, Shimada H, Tomita M, Takahashi T, Kosaki K.
- Journal Title
  
  Congenital Anomalies 44
  
  Pages: 18-26
- NAID
  10018085417
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15390327
[Journal Article] In utero dioxin (TCDD) exposure causes neocortical dysgenesis : coordinate regulation of probability of cell cycle exit and laminar fate of neocortical neurons.2004
- Author(s)
  Mitsuhashi T, Yonemoto J, Kosuge Y, Kosaki K, Tohyama C, Takahashi T.
- Journal Title
  
  Soc Neurosci Abstr(online) 30
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15390327
[Journal Article] Absent inner dynein arms in a fetus with familial hydrocephalus-situs abnormality.2004
- Author(s)
  Kosaki K, Ikeda K, Miyakoshi K, Ueno M, Kosaki R, Takahashi D, Tanaka M, Torikata C, Yoshimura Y, Takahashi T.
- Journal Title
  
  American Journal of Medical Genetics 129
  
  Pages: 308-311
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591162
[Journal Article] Marfanoid habitus with abnormal situs.2004
- Author(s)
  Kosaki K, Bird LM, Maeda J, Higuchi M, Jones MC, Matsumoto M.
- Journal Title
  
  Am J Med Genet 15(3)
  
  Pages: 310-312
- Data Source
  KAKENHI-PROJECT-16591685
[Journal Article] Premature ovarian failure in a female with proximal symphalangism and Nogginmutation.2004
- Author(s)
  Kosaki K, Sato S, Hasegawa T, Matsuo N, Suzuki T, Ogata T.
- Journal Title
  
  Fertil Steril 81(4)
  
  Pages: 1137-1139
- Data Source
  KAKENHI-PROJECT-16591685
[Journal Article] Position-specific expression of Hox genes along the gastrointestinal tract.2004
- Author(s)
  Yahagi N, Kosaki R, Ito T, Mitsuhashi T, Shimada H, Tomita M, Takahashi T, Kosaki K.
- Journal Title
  
  Congenital Anomalies 44
  
  Pages: 18-26
- NAID
  10018085417
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591162
[Journal Article] Genitourinary anomaly in congenital varicella syndrome : case report and review.2004
- Author(s)
  Fujita H, Yoshii A, Maeda J, Kosaki K, Shishido, Nakai H, Awazu M.
- Journal Title
  
  Pediatr Nephrol 19(5)
  
  Pages: 554-557
- Data Source
  KAKENHI-PROJECT-16591685
[Journal Article] Absent inner dynein arms in a fetus with familial hydrocephalus-situs abnormality.2004
- Author(s)
  Kosaki K, Ikeda K, Miyakoshi K, Ueno M, Kosaki R, Takahashi D, Tanaka M, Torikata C Yoshimura Y, Takahashi T.
- Journal Title
  
  American Journal of Medical Genetics 129
  
  Pages: 308-311
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591162
[Journal Article] Absent inner dynein arms in a fetus with familial hydrocephalus-situs abnormality.2004
- Author(s)
  Kosaki K, Ikeda K, Miyakoshi K, Ueno M, Kosaki R, Takahashi D, Tanaka M, Torikata C, Yoshimura Y, Takahashi T.
- Journal Title
  
  American Journal of Medical Genetics 129A
  
  Pages: 308-311
- Data Source
  KAKENHI-PROJECT-15591162
[Journal Article] EYA1 mutation in a newborn female presenting with cardiofacial syndrome.2004
- Author(s)
  Shimasaki N, Watanabe K, Hara M, Kosaki K.
- Journal Title
  
  Pediatr Cardiol 25(4)
  
  Pages: 411-413
- Data Source
  KAKENHI-PROJECT-16591685
[Journal Article] Premature ovarian failure in a female with proximal symphalangism and NOG mutation.2004
- Author(s)
  Kosaki K, Sato S, Hasegawa T, Matsuo N, Suzuki T, Ogata T.
- Journal Title
  
  Fertility 81
  
  Pages: 1137-1139
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591162
[Journal Article] Absent inner dynein arms in a fetus with familial hydrocephalus-situs abnormality.2004
- Author(s)
  Kosaki K, Ikeda K, Miyakoshi K, Ueno M, Kosaki R, Takahashi D, Tanaka M, Torikata C, Yoshimura Y, Takahashi T.
- Journal Title
  
  Am J Med Genet 129A
  
  Pages: 308-311
- Data Source
  KAKENHI-PROJECT-16591685
[Journal Article] Premature ovarian failure in a female with proximal symphalangism and NOG mutation.2004
- Author(s)
  Kosaki K, Sato S, Hasegawa T, Matsuo N, Suzuki T, Ogata T.
- Journal Title
  
  Fertility and Sterility 81
  
  Pages: 1137-1139
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591162
[Journal Article] Effects of in utero exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in the neural progenitor cells (NPC) of the developing murine neocortex.2003
- Author(s)
  Mitsuhashi T, Yonemoto J, Sone H, Kosaki K, Tohyama C, Takahashi T.
- Journal Title
  
  Soc Neurosci Abstr(online) 29
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15390327
[Journal Article] Characterization of the human arylhydrocarbon receptor repressor (AHRR) gene and association between micropenis and Pro186Ala polymorphism in the AHRR gene.2002
- Author(s)
  Fujita H, Kosaki R, Yoshihashi H, Ogata T, Tomita M, Takahashi T, Matsuo N, Kosaki K.
- Journal Title
  
  Teratology 65(1)
  
  Pages: 10-18
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-12470171
[Journal Article] Characterization of the aryl hydrocarbon receptor repressor gene and association of its Pro185Ala polymorphism with micropenis.2002
- Author(s)
  Fujita H, Kosaki K, Matsuo N, et al.
- Journal Title
  
  Teratology 65(1)
  
  Pages: 10-8
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-12470171
[Journal Article] OEIS complex With del(3)(q12.2q13.2).
- Author(s)
  Kosaki R, Kosaki K, Kawashima N, Ueoka K, Fukuhara Y, Kosuga M, Honna, T, Okuyama T.
- Journal Title
  
  American Journal of Medical Genetics (印刷中)
- Data Source
  KAKENHI-PROJECT-15591162
[Journal Article] OEIS compelx With del(3)(q12.2q13.2).
- Author(s)
  Kosaki R, Fukuhara Y, Kosuga M, Okuyama T, Kawashima N, Honna T, Ueoka K, Kosaki K.
- Journal Title
  
  American Journal of Medical Genetics (in print)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591162
[Journal Article] OEIS compelx With del(3)(q12.2q13.2).
- Author(s)
  Kosaki R, Fukuhara Y, Kosuga M, Okuyama T, Kawashima N, Honna T, Ueoka K, Kosaki K.
- Journal Title
  
  American Journal of Medical Genetics (印刷中)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591162
[Journal Article] Identification of a prosencephalic-specific enhancer of SALL1 : Comparative genomic approach using the chick embryo.
- Author(s)
  Izumi, K., Aramaki, M., Kimura, T., Naito, Y., Udaka, T., Uchikawa, M., Kondoh, H., Suzuki, H., Cho, G., Okada, Y., Takahashi, T., Golden, JA., Kosaki, K.
- Journal Title
  
  Pediatric Research (In press)
- Data Source
  KAKENHI-PROJECT-18659307
[Presentation] BRCA1/2遺伝子再構成は中等度以上のリスクを有する日本人遺伝性乳がん卵巣がん症例では稀である。2017
- Author(s)
  菅野康吉、高井響子、清水千佳子、田辺記子、吉田輝彦、青木大輔、増田健太、小崎健次郎、田中屋宏爾、矢形寛、青木美紀子、山内英子、大住省三、金子景香、小杉眞司、野水整、赤間孝典、織田信弥、黄瀬恵美子、古庄知己
- Organizer
  日本人類遺伝学会　第62回大会
- Data Source
  KAKENHI-PROJECT-15K08646
[Presentation] Cross-sectional study to identify Japanese HBOC kindred at the maximum risk categories suitable for expedited genetic screening.2016
- Author(s)
  Kokichi Sugano, Chikako Shimizu, Teruhiko Yoshida, Daisuke Aoki, Kenta Masuda, Kenjiro Kosaki, Kouji Tanakaya, Hiroshi Yagata, Mikiko Aoki, Shozo Ohsumi, Keika Kaneko, Shinji Kosugi, Tadashi Nomizu, Shinya Oda, Tomoki Koshou.
- Organizer
  The 6th Internationa Symposium of Hereditary Breast and Ovarian Cancer.
- Place of Presentation
  Montreal
- Year and Date
  2016-05-10
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08646
[Presentation] 診療利用の段階を迎えたアレイCGH :遺伝相談における活用のポイント2011
- Author(s)
  小崎健次郎
- Organizer
  日本人類遺伝学会第56回大会
- Place of Presentation
  幕張メッセ国際会議場
- Year and Date
  2011-11-12
- Data Source
  KAKENHI-PROJECT-21590638
[Presentation] 診療利用の段階を迎えたアレイCGH:遺伝相談における活用のポイント2011
- Author(s)
  小崎健次郎
- Organizer
  日本人類遺伝学会日本人類遺伝学会第56回大会
- Place of Presentation
  幕張メッセ国際会議場
- Year and Date
  2011-11-12
- Data Source
  KAKENHI-PROJECT-21590638
[Presentation] Two sibs with mulibrey nanism reported from Japan.2011
- Author(s)
  Yoshihashi H, Oomori S, Satoh S, Torii C, Kosaki K
- Organizer
  The 61th Annual Meeting of The American Society of Human Genetics 12th International Congress of Human Genetics
- Place of Presentation
  Montreal, Canada
- Data Source
  KAKENHI-PROJECT-22591146
[Presentation] In utero exposure to dioxin causes neocortical dysgenesis through the actions of p27Kip12011
- Author(s)
  Mitsuhashi T, Yonemoto J, Sone H, Kosuge Y, Kosaki K, Takahashi T
- Organizer
  The 41st annual meeting for Society for Neuroscience
- Place of Presentation
  Washington, D.C., USA
- Year and Date
  2011-11-14
- Data Source
  KAKENHI-PROJECT-23390276
[Presentation] 稀少遺伝性疾患に対する遺伝子診断ネットワーク構築の試み2007
- Author(s)
  松原洋一、福嶋義光、小崎健次郎、堤正好、成澤邦明、青木継稔、鎌谷直之、山口清次、小杉眞司、奥山虎之、櫻井晃洋、呉繁夫
- Organizer
  日本人類遺伝学会第52回大会
- Place of Presentation
  京王プラザホテル(東京都)
- Data Source
  KAKENHI-PROJECT-19590556

1. MITSUHASHI Takayuki (80338110)

# of Collaborated Projects: 8 results

# of Collaborated Products: 9 results
2. TAKAHASHI Takao (80171495)

# of Collaborated Projects: 6 results

# of Collaborated Products: 12 results
3. KOSUGI Shinji (50252432)

# of Collaborated Projects: 4 results

# of Collaborated Products: 5 results
4. YONEMOTO Junzo (30072664)

# of Collaborated Projects: 3 results

# of Collaborated Products: 3 results
5. SAKURAI Akihiro (70262706)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
6. MATSUO Nobutake (50173802)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
7. TOI Masakazu (10207516)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
8. YOSHIHASHI Hiroshi (60286531)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
9. MATSUBARA Yoich (00209602)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
10. NUMABE Hironao (00237801)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
11. NOMURA Fumio (80164739)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
12. SAKAI Yoshiharu (60273455)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
13. SEKINE Akihiro (30425631)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
14. ASADA Hironori (60231883)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
15. YOSHIMURA Yasunori (10129736)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
16. SUGANO Koukichi (00171124)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. SHIMOJIMA Naoki (30317151)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. KURODA Tatsuo (60170130)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. SHIBATE Shinsuke (70407089)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. OKANO Hideyuki (60160694)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. KUDO Jun (80178003)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. FUJIMURA Takumi (80573443)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
23. KOSAKI Rika (50234745)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
24. OGATA Tsutomu (40169173)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
25. HASEGAWA Tomonobu (20189533)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
26. SUZUKI Hidekazu (70255454)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
27. MATSUO Masafumi (10157266)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
28. NISHIO Hisahide (80189258)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
29. TAKESHIMA Yasuhiro (40281141)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
30. MARUYAMA Tetsuo (10209702)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
31. 勝又規行 (10260340)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
32. 森沢猛 (30379375)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
33. 奥山虎之

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

Kosaki Kenjiro 小崎 健次郎

KOSAKI Kenjiro 小崎 健次郎

小さき 健次郎 コサキ ケンジロウ

Research Projects

Research Products

Co-Researchers

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Detection of intragenic deletions by array CGH analysisPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

多発奇形症候群責任遺伝子群の組織特異的発現機構の解明:比較ゲノム学的検討Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Principal Investigator

Project Period (FY)

Kosaki Kenjiro 小崎健次郎

KOSAKI Kenjiro 小崎健次郎

小さき健次郎コサキケンジロウ