MARUO YOSHIHIRO 丸尾良浩

… Alternative Names

Researcher Number	80314160
Other IDs
External Links
Affiliation (Current)	2022: 滋賀医科大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2016 – 2020: 滋賀医科大学, 医学部, 教授 2015: 滋賀医科大学, 医学部, 講師 2008 – 2013: Shiga University of Medical Science, 医学部, 講師 2007: Shiga University of Medical Science, Undergraduate School of Medicine, Assistant Professor 2006: 滋賀医科大学, 医学部, 助手 2000 – 2004: 滋賀医科大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Pediatrics / Pediatrics / Embryonic/Neonatal medicine / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Biological Sciences / Medical sociology / Applied pharmacology / Embryonic/Neonatal medicine
Keywords	Principal Investigator ビリルビンUDP-グルクロン酸転移酵素 / 母乳性黄疸 / UGT1A1 / Gilbert症候群 / 体質性黄疸 / Crigler-Najjar症候群 / Dual oxidase 2 / 核黄疸 / 新生児高ビリルビン血症 / UGT1A3 … More Except Principal Investigator 遺伝子多型 / グルクロン酸転移酵素 / 薬物副作用 / 日本人 / propofol / 遺伝子解析 / UGT1 / 予知法 / 緩和医療 / 医療者と宗教者の協働 / 医学教育 / スピリチュアルペイン / ビハーラ活動 / 医療と宗教の協働 / 緩和医療教育 / 早期医学教育 / 宗教者の緩和教育 / 緩和病 / UDP-グルクロン酸転移酵素 / UGT1A9 / プロポフォール / 麻酔薬 / 副作用 / UDPグルクロン酸転移酵素 / UGTIA9 / グルクロン酵転移酵素 / Y486D / 遺伝子 / UDP-glucuronosyltransferases / polymorphism / T1A9 is / adverse effects of drugs / UGT1A1 / 臨床的核黄疸 / 早産児 / 慢性ビリルビン脳症 / 臨床的黄疸 / 未熟児医学 / 核黄疸 Less

新生児高ビリルビン血症の脳神経の発達にお及ぼす効果についての研究Principal Investigator
- Principal Investigator
  
  丸尾良浩
- Project Period (FY)
  2018 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Shiga University of Medical Science
Is genetics a risk factor for clinical kernicterus in preterm infants?
- Principal Investigator
  
  YANAGI TAKAHIDE
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Shiga University of Medical Science
Making of the management method for breast milk jaundice using transgenic micePrincipal Investigator
- Principal Investigator
  
  MARUO YOSHIHIRO
- Project Period (FY)
  2015 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Shiga University of Medical Science
The exhaustive analysis for congenital hypothyroidism using the next generation sequencerPrincipal Investigator
- Principal Investigator
  
  MARUO YOSHIHIRO
- Project Period (FY)
  2012 – 2013
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Shiga University of Medical Science
Practical study on palliative medicine education through teachers for medicine-Religionist Collaboration
- Principal Investigator
  
  BANBA Tadao
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Medical sociology
- Research Institution
  Shiga University of Medical Science
Analysis of genetic basis of hereditary unconjugated hyperbilirubinemias and diagnostic criteriaPrincipal Investigator
- Principal Investigator
  
  MARUO Yoshihiro
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Shiga University of Medical Science
Effect of polymorphism of UDP-glucuronosyltransferase(UGT1A9)on drug metabolism
- Principal Investigator
  
  SATO Hiroshi
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Applied pharmacology
- Research Institution
  Shiga University of Medical Science
母乳性黄疽の原因の解明と安全な管理法を確立するための研究Principal Investigator
- Principal Investigator
  
  丸尾良浩
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Young Scientists (A)
- Research Field
  
  Pediatrics
- Research Institution
  Shiga University of Medical Science
グルクロン酸転移酵素多型による薬物副作用の予知法開発に関する研究
- Principal Investigator
  
  佐藤浩
- Project Period (FY)
  2001
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas (C)
- Review Section
  
  Biological Sciences
- Research Institution
  Shiga University of Medical Science
グルクロン酸転移酵素多型による薬物副作用の予知法開発に関する研究
- Principal Investigator
  
  SATO Hiroshi
- Project Period (FY)
  2000
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas (C)
- Review Section
  
  Biological Sciences
- Research Institution
  Shiga University of Medical Science

[Book] 大関武彦、古川漸、横田俊一郎、水口雅編、今日の小児治療指針第15版2012
- Author(s)
  丸尾良浩
- Publisher
  新生児黄疸
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] Fasting-associated urticaria and/or anaphylaxis: A case report2021
- Author(s)
  Kunitsu Tomoaki、Ueba Satoko、Nakajima Ryo、Nonomura Kazuo、Maruo Yoshihiro、Hide Michihiro
- Journal Title
  
  Allergology International
  
  Volume: 70 Issue: 2 Pages: 271-273
- DOI
  10.1016/j.alit.2020.09.006
- NAID
  130008024403
- ISSN
  1323-8930, 1440-1592
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07818, KAKENHI-PROJECT-18K08298
[Journal Article] Atypical Familial Mediterranean Fever in a Japanese Boy with Heterozygous MEFV p.Ser503Cys Exon 5 Variant2021
- Author(s)
  Sato Tomonobu、Takezaki Shunichiro、Goto Takeru、Ishikawa Shinichi、Oura Kazumi、Takahata Asuka、Shiraishi Haruki、Maruo Yuji、Sato Norio、Suganuma Takashi、Mikawa Makoto
- Journal Title
  
  Case Reports in Pediatrics
  
  Volume: 2021 Pages: 1-6
- DOI
  10.1155/2021/6650226
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07818
[Journal Article] Auditory brainstem response in preterm infants with bilirubin encephalopathy2021
- Author(s)
  Okumura Akihisa、Kitai Yukihiro、Arai Hiroshi、Hayakawa Masahiro、Maruo Yoshihiro、Kusaka Takashi、Kunikata Tetsuya、Kumada Satoko、Morioka Ichiro
- Journal Title
  
  Early Human Development
  
  Volume: 154 Pages: 105319-105319
- DOI
  10.1016/j.earlhumdev.2021.105319
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07818, KAKENHI-PROJECT-19K08341
[Journal Article] Neonatal Jaundice in Preterm Infants with Bilirubin Encephalopathy2021
- Author(s)
  Okumura Akihisa、Ichimura Shintaro、Hayakawa Masahiro、Arai Hiroshi、Maruo Yoshihiro、Kusaka Takashi、Kunikata Tetsuya、Kumada Satoko、Morioka Ichiro
- Journal Title
  
  Neonatology
  
  Volume: - Pages: 1-9
- DOI
  10.1159/000513785
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07818, KAKENHI-PROJECT-19K08341
[Journal Article] Gm14230 controls Tbc1d24-cytoophidia and neuronal cellular juvenescence2021
- Author(s)
  Morimune Takao、Tano Ayami、Tanaka Yuya、Yukiue Haruka、Yamamoto Takefumi、Tooyama Ikuo、Maruo Yoshihiro、Nishimura Masaki、Mori Masaki
- Journal Title
  
  PLoS ONE
  
  Volume: 16 Pages: 1-14
- DOI
  10.1371/journal.pone.0248517
- NAID
  120007034814
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07788, KAKENHI-PROJECT-18K07818, KAKENHI-PROJECT-19K21585, KAKENHI-PUBLICLY-19H04774
[Journal Article] Ketogenic diet for refractory epilepsy with MEHMO syndrome: Caution for acute necrotizing pancreatitis2021
- Author(s)
  Mori Mioko、Kumada Tomohiro、Inoue Kenji、Nozaki Fumihito、Matsui Katsuyuki、Maruo Yoshihiro、Yamada Mamiko、Suzuki Hisato、Kosaki Kenjiro、Shibata Minoru
- Journal Title
  
  Brain and Development
  
  Volume: 43 Pages: 724-728
- DOI
  10.1016/j.braindev.2021.02.002
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07818
[Journal Article] A nationwide survey of bilirubin encephalopathy in preterm infants in Japan2020
- Author(s)
  Okumura Akihisa、Morioka Ichiro、Arai Hiroshi、Hayakawa Masahiro、Maruo Yoshihiro、Kusaka Takashi、Kunikata Tetsuya、Kumada Satoko
- Journal Title
  
  Brain and Development
  
  Volume: 42 Pages: 730-737
- DOI
  10.1016/j.braindev.2020.06.010
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07818, KAKENHI-PROJECT-18K07890, KAKENHI-PROJECT-19K08341
[Journal Article] Rotor Syndrome: Glucuronidated Bile Acidemia From Defective Reuptake by Hepatocytes2020
- Author(s)
  Kimura Akihiko、Kagawa Tatehiro、Takei Hajime、Maruo Yoshihiro、Sakugawa Hiroshi、Sasaki Takahiro、Murai Tsuyoshi、Naritaka Nakayuki、Takikawa Hajime、Nittono Hiroshi
- Journal Title
  
  Hepatology Communications
  
  Volume: 5 Pages: 629-633
- DOI
  10.1002/hep4.1660
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07818
[Journal Article] Citrullinated fibrinogen is a target of auto-antibodies in interstitial lung disease in mice with collagen-induced arthritis2020
- Author(s)
  Sato Tomomi、Satooka Hiroki、Ichioka Satoko、Maruo Yoshihiro、Hirata Takako
- Journal Title
  
  International Immunology
  
  Volume: - Pages: 533-545
- DOI
  10.1093/intimm/dxaa021
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K15183, KAKENHI-PROJECT-18K07818, KAKENHI-PROJECT-19K07621
[Journal Article] Histamine depolarizes rat intracardiac ganglion neurons through the activation of TRPC non-selective cation channels2020
- Author(s)
  Aya Sato, Shiho Arichi, Fumiaki Kojima, Toru Hayashi, Tatsuko Ohba, Dennis Lawrence Cheung, Kei Eto, Madoka Narushima, Hideji Murakoshi, Yoshihiro Maruo, Yuichi Kadoya, Junichi Nabekura, Hitoshi Ishibashi.
- Journal Title
  
  European journal of Pharmacology
  
  Volume: 886 Pages: 173536-173536
- DOI
  10.1016/j.ejphar.2020.173536
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08604, KAKENHI-PROJECT-18K07818, KAKENHI-PROJECT-19K07287, KAKENHI-PROJECT-17H01530, KAKENHI-PUBLICLY-19H05434
[Journal Article] Learning disability and myoclonic epilepsy associated with apparently synonymous but splice‐disrupting JMJD1C variant that led to 21bp deletion of the transcript2020
- Author(s)
  Yamada Mamiko、Sokoda Tatsuyuki、Uehara Tomoko、Suzuki Hisato、Takenouchi Toshiki、Yagihashi Tatsuhiko、Maruo Yoshihiro、Kosaki Kenjiro
- Journal Title
  
  American Journal of Medical Genetics Part A
  
  Volume: 182 Pages: 3064-3067
- DOI
  10.1002/ajmg.a.61892
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07818, KAKENHI-PROJECT-19K17342
[Journal Article] 母乳性黄疸と体質性黄疸2019
- Author(s)
  丸尾良浩
- Journal Title
  
  周産期医学
  
  Volume: 49 Pages: 217-221
- Data Source
  KAKENHI-PROJECT-18K07818
[Journal Article] Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol-3-OH kinase δ syndrome type 12019
- Author(s)
  Okano T, Imai K, Tsujita Y, Mitsuiki N, Yoshida K, Kamae C, Maruo Y, et al.
- Journal Title
  
  J Allergy Clin Immunol
  
  Volume: 143 Pages: 266-275
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09710
[Journal Article] X-linked Charcot-Marie-Tooth disease type 5 with recurrent weakness after febrile illness.2019
- Author(s)
  Nishikura N, Yamagata T, Morimune T, Matsui J, Sokoda T, Sawai C, Sakaue Y, Higuchi Y, Hashiguchi A, Takashima H, Takeuchi Y, Maruo Y.
- Journal Title
  
  Brain Dev
  
  Volume: 41 Pages: 201-204
- DOI
  10.1016/j.braindev.2018.08.006
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07818
[Journal Article] Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol-3-OH kinase δ syndrome type 12019
- Author(s)
  Okano T, Imai K, ..., Nonoyama S, Morio T. et al.
- Journal Title
  
  J Allergy Clin Immunol.
  
  Volume: 印刷中 Pages: 266-275
- DOI
  10.1016/j.jaci.2018.04.032
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09640, KAKENHI-PROJECT-17K10099, KAKENHI-PROJECT-18K07814, KAKENHI-PROJECT-18K07818, KAKENHI-PLANNED-15H05909, KAKENHI-PROJECT-19H05656, KAKENHI-PROJECT-17H04233
[Journal Article] Pregnancy outcome of Japanese patients with GCK-MODY.2019
- Author(s)
  Hosokawa Yuki、Higuchi Shinji、Kawakita Rie、Hata Ikue、Urakami Tatsuhiko、Isojima Tsuyoshi、Takasawa Kei、Matsubara Yohei、Mizuno Haruo、Maruo Yoshihiro、Matsui Katsuyuki、Aizu Katsuya、Jinno Kazuhiko、Araki Shunsuke、Fujisawa Yasuko、Osugi Koji、Tono Chikako、Takeshima Yasuhiro、Yorifuji Tohru
- Journal Title
  
  J Diabetes Investig
  
  Volume: N/A Pages: 1586-1589
- DOI
  10.1111/jdi.13046
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07887, KAKENHI-PROJECT-18K07895, KAKENHI-PROJECT-18K07818
[Journal Article] X-linked Charcot-Marie-Tooth disease type 5 with recurrent weakness after febrile illness2019
- Author(s)
  Nishikura N, Yamagata T, Morimune T, Matsui J, Sokoda T, Sawai C, Sakaue Y, Higuchi Y, Hashiguchi A, Takashima H, Takeuchi Y, Maruo Y
- Journal Title
  
  Brain Dev
  
  Volume: 41 Pages: 201-204
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09710
[Journal Article] The juvenility-associated long noncoding RNA Gm14230 maintains cellular juvenescence.2019
- Author(s)
  Tano Ayami、Kadota Yosuke、Morimune Takao、Jam Faidruz Azura、Yukiue Haruka、Bellier Jean-Pierre、Sokoda Tatsuyuki、Maruo Yoshihiro、Tooyama Ikuo、Mori Masaki
- Journal Title
  
  J Cell Sci
  
  Volume: 132 Pages: 1-1
- DOI
  10.1242/jcs.227801
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08853, KAKENHI-PROJECT-18K07788, KAKENHI-PROJECT-18K07818
[Journal Article] The histological findings in transposition of the great artery with severe persistent pulmonary hypertension of the newborn2018
- Author(s)
  Hoshino S, Somura J, Furukawa O, Yanagi T, Maruo Y
- Journal Title
  
  J Cardiol Cases
  
  Volume: 2018 Pages: 159-162
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09710
[Journal Article] Postnatal developmental changes in the sensitivity of L-type Ca2+ channel to inhibition by verapamil in a mouse heart model.2018
- Author(s)
  Sagawa H, Hoshino S, Yoshioka K, Ding WG, Omatsu-Kanbe M, Nakagawa M, Maruo Y, Matsuura H.
- Journal Title
  
  Pediatr Res
  
  Volume: 83 Pages: 1207-1217
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07818
[Journal Article] Postnatal developmental changes in the sensitivity of L-type Ca2+ channel to inhibition by verapamil in a mouse heart model.2018
- Author(s)
  Sagawa Hironori、Hoshino Shinsuke、Yoshioka Kengo、Ding Wei-Guang、Omatsu-Kanbe Mariko、Nakagawa Masao、Maruo Yoshihiro、Matsuura Hiroshi
- Journal Title
  
  Pediatr Res
  
  Volume: in press Pages: 1207-1217
- DOI
  10.1038/pr.2018.46
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-18K15706, KAKENHI-PROJECT-15K09710
[Journal Article] The histological findings in transposition of the great artery with severe persistent pulmonary hypertension of the newborn2018
- Author(s)
  Hoshino Shinsuke、Somura Junpei、Furukawa Ouki、Yanagi Takahide、Maruo Yoshihiro
- Journal Title
  
  Journal of Cardiology Cases
  
  Volume: 17 Pages: 159-162
- DOI
  10.1016/j.jccase.2018.01.003
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07818
[Journal Article] Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia2017
- Author(s)
  Aiso M, Yagi M, Tanaka A, Miura K, Miura R, Arizumi T, Takamori Y, Nakahara S, Maruo Y, Takikawa H
- Journal Title
  
  Internal Medicine
  
  Volume: 56 Issue: 6 Pages: 661-664
- DOI
  10.2169/internalmedicine.56.7362
- NAID
  130005450367
- ISSN
  0918-2918, 1349-7235
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09710
[Journal Article] Development of rhabdomyolysis in a child after norovirus gastroenteritis.2017
- Author(s)
  Maruo Y, Nishigawa G, Irie M, Yoshihara K, Matsumoto T, Minagi S.
- Journal Title
  
  J Appl Biomater Funct Mater
  
  Volume: 15 Pages: 93-100
- DOI
  10.5301/jabfm.5000303
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26462920, KAKENHI-PROJECT-15K09710, KAKENHI-PROJECT-26462884, KAKENHI-PROJECT-26462950, KAKENHI-PROJECT-16K20455, KAKENHI-PROJECT-15K11159
[Journal Article] Bilirubin Uridine Diphosphate-glucuronosyltransferase Polymorphism as a Risk Factor for Prolonged Hyperbilirubinemia in Japanese Preterm Infants.2017
- Author(s)
  Yanagi Takahide、Nakahara Sayuri、Maruo Yoshihiro
- Journal Title
  
  Journal of Pediatrics
  
  Volume: 190 Pages: 159-162
- DOI
  10.1016/j.jpeds.2017.07.014
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09710, KAKENHI-PROJECT-16K10088
[Journal Article] Successful every-other-day liothyronine therapy for severe resistance to thyroid hormone beta with a novel THRB mutation; case report.2016
- Author(s)
  Maruo Y, Mori A, Morioka Y, Sawai C, Mimura Y, Matui K, Takeuchi Y.
- Journal Title
  
  BMC Endocr Disord
  
  Volume: 16 Pages: 1-1
- DOI
  10.1186/s12902-015-0081-7
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25860909, KAKENHI-PROJECT-15K09710
[Journal Article] Steroid Pulse Therapy for Kawasaki Disease Complicated with Myocarditis.2016
- Author(s)
  Sato T, Somura J, Maruo Y.
- Journal Title
  
  Indian Pediatr
  
  Volume: 53 Pages: 1015-1016
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09710
[Journal Article] Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.2016
- Author(s)
  Maruo Y, Nakahara S, Yanagi T, Nomura A, Mimura Y, Matsui K, Sato H, Takeuchi Y
- Journal Title
  
  J Gastroenterol Hepatol
  
  Volume: 31 Pages: 403-408
- DOI
  10.1111/jgh.13071
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09710
[Journal Article] Natural course of congenital hypothyroidism by dual oxidase 2 mutations from the neonatal period through puberty.2016
- Author(s)
  Maruo Y, Nagasaki K, Matsui K, Mimura Y, Mori A, Fukami M, Takeuchi Y
- Journal Title
  
  Eur J Endocrinol
  
  Volume: 174 Pages: 453-463
- DOI
  10.1530/eje-15-0959
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09710
[Journal Article] Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency.2016
- Author(s)
  Tsujita Y, et al.
- Journal Title
  
  J Allergy Clin Immunol
  
  Volume: 138 Pages: 1672-1680
- DOI
  10.1016/j.jaci.2016.03.055
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26221308, KAKENHI-PROJECT-16H05355, KAKENHI-PROJECT-15H06186, KAKENHI-PROJECT-26293244, KAKENHI-PROJECT-26461570, KAKENHI-PROJECT-15K09640, KAKENHI-PROJECT-15K09710, KAKENHI-PROJECT-16K15528
[Journal Article] Contribution of UGT1A1 variations to chemotherapy-induced unconjugated hyperbilirubinemia in pediatric leukemia patients.2016
- Author(s)
  Nomura A, Maruo Y, Taga T, Takeuchi Y.
- Journal Title
  
  Pediatr Res
  
  Volume: 202 Pages: 252-257
- DOI
  10.1038/pr.2016.75
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09710
[Journal Article] Neonatal Meckel diverticulum: Obstruction due to a short mesodiverticular band.2015
- Author(s)
  Kunitsu T, Koshida S, Tanaka K, Nakahara S, Yanagi T, Maruo Y,
- Journal Title
  
  Pediatr Int
  
  Volume: 57 Pages: 1007-1009
- DOI
  10.1111/ped.12694
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08548, KAKENHI-PROJECT-15K08803, KAKENHI-PROJECT-15K09710, KAKENHI-PROJECT-26670497
[Journal Article] Two Different UGT1A1 Mutations causing Crigler-Najjar Syndrome types I and II in an Iranian Family.2015
- Author(s)
  Maruo Y, Behnam M, Ikushiro S, Nakahara S, Nouri N, Salehi M.
- Journal Title
  
  J Gastrointestin Liver Dis.
  
  Volume: 24 Pages: 523-526
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09710
[Journal Article] Role of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia2015
- Author(s)
  Fujiwara R, Maruo Y, Chen S, Tukey RH
- Journal Title
  
  Toxicology and Applied Pharmacology
  
  Volume: 289 Pages: 124-132
- DOI
  10.1016/j.taap.2015.08.018
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09710, KAKENHI-PROJECT-26870562
[Journal Article] A novel large deletion (exons 12, 13) and a missense mutation (p.G46R) in the PAH in a Japanese patient with phenylketonuria.2015
- Author(s)
  Maruo Y, Suzaki M, Matsui K, Mimura Y, Mori A, Shintaku H, Takeuchi Y.
- Journal Title
  
  World J Pediatr
  
  Volume: 11 Pages: 181-184
- DOI
  10.1007/s12519-015-0020-8
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09710, KAKENHI-PROJECT-26670497
[Journal Article] Escherichia coli O121:H19 infection identified on microagglutination assay and PCR.2015
- Author(s)
  Sakai T, Sawai T, Shimizu Y, Morimune T, Okuda Y, Maruo Y, Iyoda S, Takeuchi Y.
- Journal Title
  
  Pediatr Int
  
  Volume: 57 Pages: 1001-1003
- DOI
  10.1111/ped.12699
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09710, KAKENHI-PROJECT-26670497
[Journal Article] Bilirubin Uridine Diphosphate-Glucuronosyltransferase Variation Is a Genetic Basis of Breast Milk Jaundice2014
- Author(s)
  Maruo Y, Morioka Y, Fujito H, Nakahara S, Yanagi T, Matsui K, Mori A, Sato H, Tukey RH, Takeuchi Y.
- Journal Title
  
  J Pediatr.
  
  Volume: may Pages: 36-41
- DOI
  10.1016/j.jpeds.2014.01.060
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-24659495, KAKENHI-PROJECT-26670497
[Journal Article] Molecular and clinical characterization of glucokinase maturity-onset diabetes of the young (GCK-MODY) in Japanese patients2014
- Author(s)
  Kawakita R, Hosokawa Y, Fujimaru R, Tamagawa N, Urakami T, Takasawa K, Moriya K, Mizuno H, Maruo Y, Takuwa M, Nagasaka H, Nishi Y, Yamamoto Y, Aizu K, Yorifuji T.
- Journal Title
  
  Diabet Med.
  
  Volume: mar Pages: 1357-1362
- DOI
  10.1111/dme.12487
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24659495, KAKENHI-PROJECT-26461535
[Journal Article] Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus2013
- Author(s)
  Yorifuji T, Fujimaru R, Hosokawa Y, Tamagawa N, Shiozaki M, Aizu K, Jinno K, Maruo Y, Nagasaka H, Tajima T, Kobayashi K, Urakami T.
- Journal Title
  
  Pediatr Diabetes
  
  Volume: 14(3) Pages: 230-230
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] UDP-グルクロン酸転移酵素1型ファミリー共通エクソン変異(p.P364L)の薬物代謝に及ぼす影響2012
- Author(s)
  三村由卯、丸尾良浩、森岡依子、佐藤浩、竹内義博
- Journal Title
  
  日本小児臨床薬理学会雑誌
  
  Volume: 25巻 Pages: 129-134
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] Compound heterozygote of a novel missense mutation (p.K402T) and a double missense mutation (p.[G71R;Y486D]) in type II Crigler-Najjar syndrome2011
- Author(s)
  Maruo Y, Ozgenc F, Mimura Y, Ota Y, Matsui K, Takahashi H, Mori A, Taga T, Takano T, Sato H, Takeuchi Y.
- Journal Title
  
  J Pediatr Gastroenterol Nutr
  
  Volume: 52(3) Pages: 362-5
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] Inhibitory Effect of 5_-Pregnane-3_, 20_-Diol on Transcriptional Activity and Enzyme Activity of Human Bilirubin UDP-Gluouronosyltransferase2011
- Author(s)
  YOSHIHIRO MARUO, HIROSHI SATO, et al
- Journal Title
  
  Pediatr Res
  
  Volume: 70-5 Pages: 453-57
- DOI
  10.1203/pdr.0b013e31822f242e
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590561
[Journal Article] Inhibitory Effect of 5_-Pregnane-3_, 20_-Diol on Transcriptional Activity and Enzyme Activity of Human Bilirubin UDP-Glucuronosyltransferase2011
- Author(s)
  YOSHIHIRO MARUO, HIROSHI SATO, et al
- Journal Title
  
  Pediatr Res
  
  Volume: 70-5 Pages: 453-457
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590561
[Journal Article] Dual oxidase 2(DUOX2)の両アレル変異による一過性甲状腺機能低下症の8例2011
- Author(s)
  丸尾良浩、三村由卯、森岡依子、松井克之、森麻美、佐藤浩、竹内義博
- Journal Title
  
  ホルモンと臨床
  
  Volume: 59巻 Pages: 1057-1062
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] Epstein-Barr virus-related lymphoproliferative disorder, cytomegalovirus reactivation, and varicella zoster virus encephalitis during treatment of medulloblastoma2011
- Author(s)
  Ohta M, Taga T, Nomura A, Kato H, Takano T, Maruo Y, Takeuchi Y, Ishida M, Ohta S.
- Journal Title
  
  J Med Virol
  
  Volume: 83(9) Pages: 1582-4
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] Effect of common exon variant (p.P364L) on drug glucuronidation by the human UDP-glucuronosyltransferase 1 family2011
- Author(s)
  Mimura Y, Maruo Y, Ohta Y, Sato H, Takeuchi Y.
- Journal Title
  
  Basic Clin Pharmacol Toxicol
  
  Volume: 109(6) Pages: 486-93
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] Inhibitory effect of 5β-pregnane-3α,20β-diol on transcriptional activity and enzyme activity of human bilirubin UDP-glucuronosyltransferase2011
- Author(s)
  Ota Y, Maruo Y, Matsui K, Mimura Y, Sato H, Takeuchi Y.
- Journal Title
  
  Pediatr Res
  
  Volume: 70(5) Pages: 453-7
- Data Source
  KAKENHI-PROJECT-24659495
[Journal Article] Phase II drug metabolism and individual drug therapy2010
- Author(s)
  Maruo Y, Sato H, 他
- Journal Title
  
  Curr Pharmacogenom Personal Med. (submitted)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590561
[Journal Article] Combined effect regulatory polymorphisms transcription of UGT1A1 as a cause of Gilbert syndrome2010
- Author(s)
  SATOH H, MARUO Y, 他
- Journal Title
  
  BMC Gastroenterology(電子ジャーナル)
  
  Volume: 10-57 Pages: 1-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590561
[Journal Article] Hereditary spherocytosis in 3 children coexisting with UDP-glucuronyl transferase 1A1 deficiency2009
- Author(s)
  Shiota M, Asada J, Nishida H, Kumakura A, Yoshioka T, Hata A, Watanabe K, Maruo Y, et.al.
- Journal Title
  
  J Pediatr Hematol Oncol. 31
  
  Pages: 121-3
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] 体質性黄疸2008
- Author(s)
  丸尾良浩
- Journal Title
  
  小児内科
  
  Pages: 40638-40643
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Transient congenital hypothyroidism caused by biallelic mutations of the dual oxidase 2 (DUOX2) gene in Japanese patients detected by a neonatal screening program2008
- Author(s)
  Yoshihiro Maruo, Hiroko Takahashi, lkumi Soeda, et al.
- Journal Title
  
  J Clin Endoclinol Metab 93
  
  Pages: 4261-4267
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Conformational change of UGT1A1 by a novel missense mutation (p.L131P) causing Crigler-Najjar syndrome type2008
- Author(s)
  H., Takahashi, Y., Maruo, A., Mori, M., Iwai, H., Sato, Y., Takeuchi
- Journal Title
  
  Pediatr Gastroenterol Nutr CONCERNED, YEAR 46(3)
  
  Pages: 308-311
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590508
[Journal Article] Effect of D256N and Y483D on propofol glucuronidation by human UDP-glucuronosyltransferase (UGT1A9)2008
- Author(s)
  Hiroko Takahashi, Yoshihiro Maruo, Asami Mori, et.al.
- Journal Title
  
  Basic Clin Pharmacol Toxicol 103
  
  Pages: 394-398
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Conformational change of UGT1A1 by a novel missense mutation (P. L131P) causing Crigler-Najiar syndrome type l2008
- Author(s)
  Yoshihiro Maruo, Ishwar Chander Verma, Katsuyuki Matsui, et al.
- Journal Title
  
  J Pediatr Gastroenterol Nutr 46
  
  Pages: 308-311
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Effect of D256N and Y483D on propofol glucuronidation by human UDP-glucuronosyltransferase (UGT1A9)2008
- Author(s)
  Hiroko Takahashi, Yoshihiro Maruo, Asami Mori, et al.
- Journal Title
  
  Basic Clin Pharmacol Toxicol 103
  
  Pages: 394-398
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Conformational Change of UGT1A1 by a Novel Missense Mutation (p.L131P) Causing Crigler-Najjar Syndrome Type I2008
- Author(s)
  Yoshihiro Maruo, Ishwar Chander Verma, Katsuyuki Matsui, et.al.
- Journal Title
  
  J Pediatr Gastroenterol nutr 46
  
  Pages: 308-311
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] 消化器疾患体質性黄疸2008
- Author(s)
  丸尾良浩
- Journal Title
  
  小児内科 40
  
  Pages: 638-643
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Transient congenital hypothyroidism caused by biallelic mutations of the dual oxidase 2(DUOX2)gene in Japanese patients detected by aneonatal screening program2008
- Author(s)
  Yoshihiro Maruo, Hiroko Takahashi, Ikumi Soeda, et.al.
- Journal Title
  
  J Clin Endoclinol Metab 93
  
  Pages: 4261-4267
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Conformational Change of UGT1A1 by a Novel Missense Mutation (p.L131P) Ca using Crigler-Najjar Syndrome Type I2008
- Author(s)
  Maruo Y, et. al.
- Journal Title
  
  Journal of Pediatric Gastroenterology and Nutrition 46
  
  Pages: 308-311
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Conformational change of UGT1A1 by a novel missense mutation (p.L131P)causing Crigler-Najjar syndrome type I.2008
- Author(s)
  Maruo Y, et. al.
- Journal Title
  
  J Pediatr Gastroenterol Nutr 46
  
  Pages: 308-311
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590508
[Journal Article] 体質性黄疽の病態と遺伝子異常2007
- Author(s)
  丸尾良浩
- Journal Title
  
  小児科診療 70
  
  Pages: 930-935
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome2007
- Author(s)
  Sugita K, Maruo Y, et. al.
- Journal Title
  
  Pediatric International 49
  
  Pages: 540-542
- NAID
  10019815055
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] 遺伝性非抱合型高ビリルビン血症(特集)2007
- Author(s)
  丸尾良浩
- Journal Title
  
  周産期医学 (0386-9881)37巻10 号
  
  Pages: 1323-1327
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome2007
- Author(s)
  Sugita K, Maruo Y, Kurosawa H, Tsuchioka A, Fujiwara T, Mori A, Ideguchi H, eguchi M
- Journal Title
  
  Pediatr Int 49
  
  Pages: 540-2
- NAID
  10019815055
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] 体質性黄疸の病態と遺伝子異常(特集)2007
- Author(s)
  丸尾良浩
- Journal Title
  
  小児科診療 70
  
  Pages: 930-935
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] 産科における新生児管理(特集)2007
- Author(s)
  柳貴英, 丸尾良浩, 楠田聡
- Journal Title
  
  周産期医学 (0386-9881)37巻10号
  
  Pages: 1275-1280
- Data Source
  KAKENHI-PROJECT-19591248
[Journal Article] Crigler-Najjar Syndrome type II caused by a homozygous triple mutation of UGTlAl.2006
- Author(s)
  Maruo et al.
- Journal Title
  
  Journal of Pediatric Gastroenterology and Nutrition 42
  
  Pages: 236-236
- Data Source
  KAKENHI-PROJECT-18590508
[Journal Article] Polymorphism of UDP-glucuronosyltransferase and drug metabolism2005
- Author(s)
  Yoshihiro Maruo, Masaru Iawai, Asami Mori, et al.
- Journal Title
  
  Current Drug Metabolism 6
  
  Pages: 91-99
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] わが国におけるGilbert症候群とCrigler-Najjar症候群の臨床診断と遺伝子型2004
- Author(s)
  丸尾良浩
- Journal Title
  
  小児科 45
  
  Pages: 2339-2345
- NAID
  40019867237
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] A novel mechanism for the inhibition of hyaluronan biosynthesis by 4-methylumbelliferone2004
- Author(s)
  Ikuko Kakizaki, Kaoru Kojima, Yoshihiro Maruo, et al.
- Journal Title
  
  Journal of Biological Chemistry 279
  
  Pages: 33281-33289
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 asa a principle cause of Gilbert syndrome2004
- Author(s)
  Yoshihiro Maruo, Carlos D'Addario, Asami Mori, et al.
- Journal Title
  
  Human Mutation 115
  
  Pages: 525-526
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] Six novel UDP-glucurinisyltransferase (UGT1A3) polymorphisms with varying activity2004
- Author(s)
  Masaru Iwai, Yoshihiro Maruo, Masaki Ito, et al.
- Journal Title
  
  Journal of Human Mutation 49
  
  Pages: 123-128
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] Genetic polymorphism of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert syndrome as well as in healthy Japanese patinets2004
- Author(s)
  Keisuke Takeuchi, Yoshinao Kobayashi, Yoshihiro Maruo, et al.
- Journal Title
  
  Journal of Gastroenterology and Hepatology 19
  
  Pages: 1023-1028
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] 母乳性黄疸の中でGilbert症候群を疑う例はどのような特徴があるか?2004
- Author(s)
  丸尾良浩
- Journal Title
  
  小児内科 36
  
  Pages: 1244-1246
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] Gilbert症候群と血液疾患2004
- Author(s)
  丸尾良浩, 太田茂
- Journal Title
  
  日本小児血液学会誌 18
  
  Pages: 601-608
- NAID
  10014291451
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] Co-occurrence of three different mutations in the bilirubin UDP-glucurinisyltransferase gene in a Chinese family with Crigler-Najjar syndrome type I and Gilbert's syndrome2003
- Author(s)
  Yoshihiro Maruo, KKH Poon, Masaki Ito, et al.
- Journal Title
  
  Clinical Genetics 64
  
  Pages: 1-5
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] A novel missense mutation of bilirubin UDP-glucurinisyltransferase gene in a Turkish patient with Crigler-Najjar syndrome type I2003
- Author(s)
  Yoshihiro Maruo, Erkin Serdaroglu, Masaki Ito, et al.
- Journal Title
  
  Journal of Pediatric Gastroenterology and Nutrition 37
  
  Pages: 627-630
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] Liver resection in patients with Gilbert's syndrome2003
- Author(s)
  Junichi Arita, Sugawara Yasuhiko, Yoshihiko Maruo, et al.
- Journal Title
  
  Surgery 134
  
  Pages: 835-837
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] Effect of D256N and Y483D on propofol glucuronidation by human UDP-glucuronsyltransferase(UGT1A9)
- Author(s)
  H., Takahashi, Y., Maruo, A., Mori, M., Iwai, H., Sato, Y., Takeuchi
- Journal Title
  
  Basic & Clinical Pharmacology & Toxicology CONCERNED, YEAR (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590508
[Journal Article] Conformational change of UGT1A1 by a novel missense mutation (p.L131P) causing Crigler-Najjar syndrome type l
- Author(s)
  Maruo Y, et. al.
- Journal Title
  
  Pediatr Gastroenterol Nutr (掲載確定)(印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590508
[Journal Article] UDP-glucuronosyltransferase1A4 polymorphisms in a Japanese population and kinetics of clozanine glucuronidation
- Author(s)
  Asami Mori, Yoshihiro Maruo, Masaru Iwai, et al.
- Journal Title
  
  Drug Metabolism and Disposition (In press)
- Data Source
  KAKENHI-PROJECT-14704032
[Journal Article] A novel large deletion (exons 12, 13) and a missense mutation (p.G46R) in the PAH in a Japanese patient with phenylketonuria
- Author(s)
  Maruo Y, Suzaki M, Matui K, Mimura Y, Mori A, Shintaku H, Takeuchi Y.
- Journal Title
  
  World J Pediatr
  
  Volume: (in press)
- Data Source
  KAKENHI-PROJECT-24659495
[Patent] UGT1A3核酸配列の変異検査法2004
- Inventor(s)
  丸尾良浩, 岩井勝
- Industrial Property Rights Holder
  丸尾良浩, 岩井勝, 高山正法
- Industrial Property Number
  2004-189133
- Filing Date
  2004-06-28
- Data Source
  KAKENHI-PROJECT-14704032
[Patent] UGT1核酸配列の変異検査法2004
- Inventor(s)
  丸尾良浩, 佐藤浩
- Industrial Property Rights Holder
  丸尾良浩, 佐藤浩, 高山正法
- Industrial Property Number
  2004-217376
- Filing Date
  2004-07-26
- Data Source
  KAKENHI-PROJECT-14704032
[Patent] UGT1A4核酸配列の変異検査法2004
- Inventor(s)
  丸尾良浩, 森麻美
- Industrial Property Rights Holder
  丸尾良浩, 森麻美, 高山正法
- Industrial Property Number
  2004-295291
- Filing Date
  2004-10-07
- Data Source
  KAKENHI-PROJECT-14704032
[Presentation] Tissue‐specific Humanized Models Expressing Human UGT1A12020
- Author(s)
  Mennillo E, Yang X, Weber A, Chen S, MaruoY, Tukey RH.
- Organizer
  Experimental Biology 2020 Meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07818
[Presentation] ビリルビンUDP-グルクロン酸転移酵素と新生児黄疸2018
- Author(s)
  丸尾良浩
- Organizer
  第５回大阪小児科医会総会・教育セミナー
- Invited
- Data Source
  KAKENHI-PROJECT-18K07818
[Presentation] ビリルビンUDP-グルクロン酸転移酵素と新生児黄疸2018
- Author(s)
  丸尾良浩
- Organizer
  第５回大阪小児科医会総会・教育セミナー
- Invited
- Data Source
  KAKENHI-PROJECT-15K09710
[Presentation] ビリルビンUDP-グルクロン酸転移酵素と黄疸2017
- Author(s)
  丸尾良浩
- Organizer
  第44回日本小児栄養消化器肝臓学会
- Invited
- Data Source
  KAKENHI-PROJECT-15K09710
[Presentation] Bilirubin UDP-Glucuronosyltransferase Variation Is a Genetic Basis of Breast Milk Jaundice.2015
- Author(s)
  Maruo Y, Yanagi T, Tukey RH
- Organizer
  Pediatric Academic Societies, annual Meeting
- Place of Presentation
  San Diego, USA
- Year and Date
  2015-04-25
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09710
[Presentation] Neonatal Hemochromatosis detected by galactosemia at newborn screening.2015
- Author(s)
  Takashima K, Maruo Y, Tsutsui H, Yanagi T, Kasahara M, Takeuchi Y.
- Organizer
  North American Society for Pediatric Gastroenterology, Hepatology and Nutrition, Annual Meeting.
- Place of Presentation
  Washington DC, USA.
- Year and Date
  2015-10-07
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09710
[Presentation] Bilirubin Uridine Diphospahate-glucuronosyltransferase polymorpshism is a risk factor for prolonged unconjugated hyperbilirubinema in preterm infants.2015
- Author(s)
  Yanagi T, Nakahara S, Maruo Y
- Organizer
  Pediatric Academic Societies, annual Meeting
- Place of Presentation
  San Diego, USA
- Year and Date
  2015-04-25
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09710
[Presentation] Dual oxidase 2 (DUOX2)異常症の臨床像の解明 23例の解析より2014
- Author(s)
  丸尾良浩、長崎啓祐、森麻美、松井克之、三村由卯、深見真紀、竹内義博
- Organizer
  第117回日本小児科学会学術集会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] Dual oxidase 2 (DUOX2)異常症の臨床像の解明23例の解析より2014
- Author(s)
  丸尾良浩、長崎啓祐、森麻美、松井克之、三村由卯、深見真紀、竹内義博
- Organizer
  第117回日本小児科学会学術集会
- Place of Presentation
  名古屋市(口演・一般)
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] 先天性甲状腺機能低下症に対する次世代シーケンサーを用いたターゲットリシーケンス解析2013
- Author(s)
  長崎啓祐、丸尾良浩、佐藤英利、小川洋平、菊池透、浅見直、深見真紀
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] 先天性甲状腺機能低下症に対する次世代シーケンサーを用いたターゲットリシーケンス解析2013
- Author(s)
  長崎啓祐、丸尾良浩、佐藤英利、小川洋平、菊池透、浅見直、深見真紀
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京(口演・一般)
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] 小児の成長発達と内分泌2013
- Author(s)
  丸尾良浩
- Organizer
  第199回大阪小児科学会
- Place of Presentation
  大阪市(シンポジウム)
- Year and Date
  2013-09-29
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] AVP遺伝子に変異を認めた家族性中枢性尿崩症の2家系2013
- Author(s)
  丸尾良浩、森宗孝夫、國津智彬、松井克之、森麻美、三村由卯、竹内義博
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京(ポスター・一般)
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] AVP遺伝子に変異を認めた家族性中枢性尿崩症の２家系2013
- Author(s)
  丸尾良浩、森宗孝夫、國津智彬、松井克之、森麻美、三村由卯、竹内義博
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] Hutcinson-Gilford-Progeria Syndromeに認められた甲状腺機能低下症の検討2012
- Author(s)
  丸尾良浩、川北理恵、松井克之、森麻美、森岡依子、西尾友宏、岡本暢之、宮下文、西澤嘉四郎、竹内義博
- Organizer
  第115回日本小児科学会学術集会
- Place of Presentation
  福岡市(ポスター、一般)
- Data Source
  KAKENHI-PROJECT-24659495
[Presentation] Differential diagnosis of Gilbert syndrome and Crigler-Najjar syndrome type II based on genotypes ofUGT1A12008
- Author(s)
  Yoshihiro Maruo
- Organizer
  The 12th International Glucuronidation and UGT Workshop
- Place of Presentation
  Quebec City, Canada
- Year and Date
  2008-07-25
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] Differential daiagnosis of Gilbert syndrome and Crigler-Najjar syndrome type II based on genotypes of UGT1A1.2008
- Author(s)
  Maruo Y, Mori A, Takahashi H, et al.
- Organizer
  11th International Workshop on Glucuronidation
- Place of Presentation
  Quebecc City, Canada
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] 母乳性黄疸の遺伝的背景の解明106例の解析2008
- Author(s)
  丸尾良浩, 高橋浩子, 森麻美, 等
- Organizer
  第111回日本小児科学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] Combined effect of regulatory polymorphisms of Gilbert syndrome on transcription of UGT1A12008
- Author(s)
  Matsui K, Maruo Y, Sato H, Takeuchi Y
- Organizer
  The 12^<th> International Glucuronidation and UGT Workshop
- Place of Presentation
  Quebec City, Canada
- Year and Date
  2008-07-26
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] 発現実験を用いたプレグナンジオールのビリルビUDP-グルクロン酸転移酵素阻害の検討2008
- Author(s)
  丸尾良浩, 三村由卯, 太田依子, 等
- Organizer
  第111回日本小児科学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] Effectof D256N and Y486D on propofol glucuronidation by human UDP-glucuronosyltransf erase (UGT1A9)2008
- Author(s)
  Ota Y, Takahashi H, Maruo Y, et.al.
- Organizer
  The 12^<th> International Glucuronidation and UGT Workshop
- Place of Presentation
  Quebec City, Canada
- Year and Date
  2008-07-26
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] Dual oxidase 2 (DUOX2)遺伝子のbiallelic mutationによる-過性甲状腺機能低下症の8例と8つの新規変異2008
- Author(s)
  丸尾良浩, 森麻美, 高橋浩子, 松井克之, 三村由卯, 太田依子, 佐藤浩, 竹内義博.
- Organizer
  第42回日本小児内分泌学会
- Place of Presentation
  米子
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] 寛解導入時の遷延する高ビリルビン血症からGilbert症候群と診断されたALLの1例2008
- Author(s)
  合井久美子, 本名浩子, 廣瀬衣子, 黒田格, 犬飼岳史, 杉田完爾, 高橋和也, 佐藤和正, 丸尾良浩
- Organizer
  第111回日本小児科学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] Effect of D256N and Y486D on propofol glucuronidation by human UDP-glucuronosyltransferase (UGT1A9)2008
- Author(s)
  Ota Y, Takahashi H, Maruo Y, et al.
- Organizer
  11th International Workshop on Glucuronidation
- Place of Presentation
  Quebecc City, Canada
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] UDP-glucuronosyltransferase 1A4 polymorphisms in a Japanese population and kinetics of clozapine glucuronidation2008
- Author(s)
  Mori A, Maruo Y, Iwai M, et.al.
- Organizer
  The 12^<th> International Glucuronidationand UGT Workshop
- Place of Presentation
  Quebecc City, Canada
- Year and Date
  2008-07-26
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] Combined effect of regulatory polymorphisms of Gilbert syndrome on transcription of UGT1A1.2008
- Author(s)
  Matsui K, Maruo Y, Sato H, Takeuchi Y.
- Organizer
  11th International Workshop on Glucuronidation
- Place of Presentation
  Quebecc City, Canada
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] UDP-glucuronosyltransferase 1A4 polymorphisms in a Japanese population and kinetics of clozapine glucuronidation.2008
- Author(s)
  Mori A, Maruo Y, Iwai M, et al.
- Organizer
  11th International Workshop on Glucuronidation
- Place of Presentation
  Quebecc City, Canada
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] -過性甲状腺機能低下症家系にみられたDual oxidase 2 (DUOX2)新規変異2008
- Author(s)
  丸尾良浩, 森麻美, 高橋浩子, 等
- Organizer
  第59回日本小児科学会滋賀地方会
- Place of Presentation
  大津
- Year and Date
  2008-05-18
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] トルコ人Crigler-Najjar症候群II型にみられたビリルビンUDP-グルクロン酸転移酵素(UGTIAI)遺伝子の新規変異.2008
- Author(s)
  丸尾良浩1), Funda Ozgenc2), 三村由卯, 等
- Organizer
  P450&UGT研究会
- Place of Presentation
  博多
- Data Source
  KAKENHI-PROJECT-19591248
[Presentation] 遺伝性非抱合型ビリルビン型(Gilbert症候群、Crigler-Najjar症候群)の遺伝子様式は147例の解析より2007
- Author(s)
  丸尾良浩
- Organizer
  日本小児栄養消化器肝臓学会
- Place of Presentation
  山形市
- Year and Date
  2007-11-15
- Data Source
  KAKENHI-PROJECT-19591248

1. SATO Hiroshi (90090430)

# of Collaborated Projects: 5 results

# of Collaborated Products: 10 results
2. YANAGI TAKAHIDE (70418755)

# of Collaborated Projects: 3 results

# of Collaborated Products: 9 results
3. MATSUI Katsuyuki (60595924)

# of Collaborated Projects: 2 results

# of Collaborated Products: 13 results
4. BANBA Tadao (40079819)

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5. HAYASHIMA Osamu (60108272)

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6. NAGAKKURA Norihiro (60437142)

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7. YOKOO Michiyo (00336158)

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8. MORI Asami (70437151)

# of Collaborated Projects: 1 results

# of Collaborated Products: 11 results
9. 藤原亮一 (40631643)

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10. 荒井洋 (50501194)

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11. 森岡一朗 (80437467)

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12. 中原小百合 (30599204)

# of Collaborated Projects: 1 results

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13. Tukey Robert H

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
14. SATO Yoshiaki

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# of Collaborated Products: 3 results
15. KOSHIDA Shigeki

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# of Collaborated Products: 1 results
16. IMAI Kohsuke

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# of Collaborated Products: 2 results
17. OKADA Satoshi

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# of Collaborated Products: 1 results
18. OHARA osamu

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# of Collaborated Products: 1 results
19. ASANO takaki

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# of Collaborated Products: 2 results
20. ISOJIMA Tsuyoshi

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# of Collaborated Products: 1 results
21. KOJIMA Fumiaki

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# of Collaborated Products: 1 results
22. YAMAMOTO Yukiyo

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# of Collaborated Products: 1 results
23. 澤井ちひろ

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24. 奥村彰久

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25. 早川昌弘

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26. 竹内義博

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27. 秀道広

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28. 小川誠司

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29. 野々山恵章

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30. 松浦博

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31. 丁維光

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32. 星野真介

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33. 里岡大樹

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34. 平田多佳子

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35. 満生紀子

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36. 金兼弘和

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37. 依藤亨

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38. 石橋仁

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39. 鍋倉淳一

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40. 村越秀治

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41. 森雅樹

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42. 西村正樹

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43. BELLIER Jean-Pierre

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44. 丸尾幸憲

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45. 西川悟郎

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46. 入江正郎

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47. 皆木省吾

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48. 吉原久美子

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49. 長岡紀幸

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MARUO YOSHIHIRO 丸尾 良浩

MARUO Yoshihiro 丸尾 良浩

丸尾 良浩 マルオ ヨシヒロ

Research Projects

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Co-Researchers

新生児高ビリルビン血症の脳神経の発達にお及ぼす効果についての研究Principal Investigator

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Is genetics a risk factor for clinical kernicterus in preterm infants?

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Making of the management method for breast milk jaundice using transgenic micePrincipal Investigator

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The exhaustive analysis for congenital hypothyroidism using the next generation sequencerPrincipal Investigator

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Practical study on palliative medicine education through teachers for medicine-Religionist Collaboration

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Analysis of genetic basis of hereditary unconjugated hyperbilirubinemias and diagnostic criteriaPrincipal Investigator

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Effect of polymorphism of UDP-glucuronosyltransferase(UGT1A9)on drug metabolism

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母乳性黄疽の原因の解明と安全な管理法を確立するための研究Principal Investigator

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グルクロン酸転移酵素多型による薬物副作用の予知法開発に関する研究

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グルクロン酸転移酵素多型による薬物副作用の予知法開発に関する研究

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[Book] 大関武彦、古川漸、横田俊一郎、水口雅編、今日の小児治療指針第15版2012

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[Journal Article] Fasting-associated urticaria and/or anaphylaxis: A case report2021

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[Journal Article] Atypical Familial Mediterranean Fever in a Japanese Boy with Heterozygous MEFV p.Ser503Cys Exon 5 Variant2021

Author(s)

MARUO YOSHIHIRO 丸尾良浩

MARUO Yoshihiro 丸尾良浩

丸尾良浩マルオヨシヒロ