医療関係者・学生向け 研究実績

2010年

【和文】

  •   1. 緒方勤:生殖補助医療とインプリンティング異常.Horm Front Gynecol 17 (12)(特集:エピジェネティクス・ゲノムインプリンティング):361-368, 2010.
  •   2. 中村美智子,深見真紀,宮戸真美,須川史啓,緒方勤,野々村克也.Mamld1は、マウスライディッヒ腫瘍細胞において、ステロイド合成酵素遺伝子Cyp17a1の発現調節を介し、テストステロン産生に関わっている.日小児泌会誌(印刷中).
  •   3. 緒方勤:内分泌撹乱物質:特に性分化・発達にたいする影響について.Pediatric Endocrinology Reviews抄訳シリーズ.No. 3. ジャパンメディアートパブリッシング 2-3, 2010.
  •   4. 緒方勤:性分化異常症:P450 oxidoreductase (POR)異常症.新川詔夫,緒方勤(監)ビジュアル疾患解説:遺伝病とターナー症候群.日本ケミカルリサーチ No. 5, pp10-12, 2009.
  •   5. 田中葉子, Paravee K, 緒方勤:良好な成長率を維持している抗GH抗体陰性の成長ホルモン単独欠損症IA型(IGHD IA)の1例.ホルモンと臨 58(増刊号内分泌クリニカルカンファレンス51): 22-27, 2010.
  •   6. 勝島由利子、山澤一樹,緒方勤、勝島史夫:成長ホルモン分泌不全を来し、H19-DMRの低メチル化を認めたSilver-Russell症候群の1例.ホルモンと臨 91-96, 2010.
  •   7. 深見真紀,伊達木澄人,緒方勤:中枢性性腺機能低下症.Horm Front Gynecol 17 (2)(目で見る生殖内分泌疾患の診断と治療): 4-8, 2010.
  •   8. 佐藤直子,緒方勤:Prokineticin signaling pathwayとKallmann症候群.医のあゆみ233 (9)(第5土曜特集:G蛋白質共役受容体研究―疾患解明とシグナル制御の新時代): 934-938, 2010.
  •   9. 大関武彦:メタボリックシンドロームの基本概念。小児科診療 73: 177-184, 2010.
  • 10. 中川祐一,大関武彦:生活習慣と思春期。思春期学 28: 45-48, 2010.
  • 11. 中川祐一:出生前因子. 小児科診療73(2):205-210, 2010.
  • 12. Lustig R, 大関武彦:Meet-the-Professor:視床下部性肥満の研究から、NAFLDと小児肥満、メタボリックシンドロームの本態としてのミトコンドリア機能障害の研究。Adiposcience 6: 286-295, 2010.

【英文】

  •   1. Dateki S, Kosaka K, Hasegawa K, Tanaka H, Azuma N, Yokoya S, Muroya K, Adachi M, Tajima T, Motomura K, Kinoshita E, Moriuchi H, Sato N, Fukami M, Ogata T*. Heterozygous OTX2 mutations are associated with variable pituitary phenotype. J Clin Endocrinol Metab 95 (2): 756-764, 2010. (IF = 6.202)
  •   2. Fukami M, Maruyama T, Dateki S, Sato N, Yoshimura Y, Ogata T*. Hypothalamic dysfunction in a female with isolated hypogonadotropic hypogonadism and compound heterozygous TACR3 mutations and clinical manifestation in her heterozygous mother. Horm Res Peadiatr 73 (6): 477-481, 2010. (IF = 1.730)
  •   3. Muroya K, Mochizuki T, Fukami M, Iso M, Fujita K, Ogata T*. Diabetes mellitus in a Japanese girl with HDR syndrome and GATA3 mutation. Endocr J 157 (2): 171-174, 2010. (IF = 1.806)
  •   4. Fukami M*, Nagai T, Mochizuki H, Muroya K, Yamada G, Takitani K, Ogata T. Anorectal and urinary anomalies and aberrant retinoic acid metabolism in cytochrome P450 oxidoreductase deficiency. Mol Genet Metab 100 (3): 269-273, 2010. (IF = 2.897)
  •   5. Ashkenazi-Hoffnung L, Lebenthal Y, Wyatt AW, Ragge NK, Dateki S, Fukami M, Ogata T, Phillip M*, Gat-Yablonski G. A novel loss of function mutation in OTX2 is associated with phenotypically variable anophthalmia and isolated growth hormone deficiency. Hum Genet 127 (6): 721-729, 2010. (IF = 4.523)
  •   6. Iijima K*, Nozu K, Kamei K, Nakayama M, Ito S, Matsuoka K, Ogata T, Kaito H, Nakanishi K, Mastuo M. Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation. Pediatr Nephrol 25 (10): 2165-2170, 2010. (IF = 2.425)
  •   7. Dateki S, Fukami M, Uematsu A, Kaji M, Iso M, Ono M, Mizota M, Yokoya S, Motomura K, Kinoshita E, Moriuchi H, Ogata T*. Mutation and gene copy number analyses of six pituitary transcription factor genes in 71 patients with combined pituitary hormone deficiency: identification of a single patient with LHX4 deletion. J Clin Endocrinol Metab 95 (8): 4043-4047, 2010. (IF = 6.202)
  •   8. Kagami M, O'Sullivan MJ, Green AJ, Watabe Y, Arisaka O, Masawa N, Matsuoka K, Fukami M, Matsubara K, Kato F, Ferguson-Smith AC, Ogata T*. The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers. PLoS Genet 6 (6): e1000992, 2010. (IF = 9.532)
  •   9. Yamazawa K, Nakabayashi K, Kagami M, Sato T, Saitoh S, Horikawa R, Hizuka N, Ogata T*. Parthenogenetic chimaerism/mosaicism with a Silver-Russell Syndrome-like Phenotype. J Med Genet 47 (11): 782-785, 2010. (IF = 5.751)
  • 10. Kato H, Yoshida R, Tsukamoto K, Suga H, Eto H, Higashino T, Araki J, Ogata T, Yoshimura K*: Familial cases of atypical clinical features genetically diagnosed as LEOPARD syndrome (multiple lentigines syndrome). Int J Dermatol 49 (10): 1146-1151, 2010. (IF = 1.177)
  • 11. Hiraoka M*, Takahashi H, Orimo H, Hiraoka M, Ogata T, Azuma N: Genetic screening of Wnt signaling factors in advanced retinopathy of prematurity. Mol Vis 16 (12): 2572-2577, 2010. (IF = 2.541)
  • 12. Matsubara K, Iwamoto H, Yoshida A, Ogata T*: Semen analysis and successful paternity by intracytoplasmic sperm injection in a man with steroid 5a-reductase-2 deficiency. Fertil Steril 94 (7): 2770.e7-2770.e10, 2010. (IF = 3.970)
  • 13. Suzumori N*, Ogata T, Mizutani E, Hattori Y, Matsubara K, Kagami M, Suguhara-Ogasawara M: Prenatal diagnosis of paternal uniparental disomy 14: delineation of further patient. Am J Med Genet A 152A (12): 3189-3192, 2010. (IF = 2.404)
  • 14. Yamazawa K, Ogata T, Ferguson-Smith AC*: Uniparental disomy and human disease: an overview. Am J Med Genet C (Seminars in Medical Genetics) 154C (3): 329-334, 2010. (IF = 2.404)
  • 15. Ogata T, Matsubara K, Nagata E, Sano S, Murakami N, Nagai T: Advanced maternal age and the development of Prader-Willi syndrome resulting from upd(15)mat through non-disjunction at meiosis 1. Journal of Mammalian Ova Research (JMOR)
  • 16. Okada T, Ohzeki T, Nakagawa Y, Sugihara S, Arisaka O: Impact of leptin and leptin receptor gene polymorphisms on serum lipids in Japanese obese children. Acta Paediatr Feb 23, 2010. [1.768]
  • 17. Ishikawa T, Iwashima S, Ohzeki T:Effect of Cibenzoline on Biventricular Pressure Gradients in a Pediatric Patient with Hypertrophic Obstructive Cardiomyopathy. Pediatr Cardiol 2010 Feb 7.[1.151]
  • 18. Iwashima S, Ishikawa T, Ohzeki T:Delayed Enhancement Cardiac Magnetic Resonance Imaging in Propionic Acidemia. Pediatr Cardiol 2010. [1.151]
  • 19. Sano S, Nakagawa Y, Iwashima S, Ishikawa T, Satake E, Matsushita R, Nagata E, Yamaguchi R, Nakanishi T, Ohzeki T : Change of adrenocortical hormones and lipids in Kawasaki disease、Endocrine Journal : 57:643: Suppl. 2: 2010.
  • 20. Matusita R, Nakagawa Y, Sakai A, Nagata E, Satake E , Sano S, Yamaguchi R, Fujisawa Y, Nakanishi T, Nakano T, Ohzeki T : Circadian rhythm of ACTH in X-linked adrenal hypoplasia congenital (AHC)、Endocrine Journal : 57:643: Suppl. 2: 2010.
  • 21. Nagata E, Nakagawa Y, Yamaguch R, Sai S, Fujisawa Y, Ohzeki T : Sex differences in fetal programming of metabolic syndrome in rats : Endocrine Journal : 57:438: Suppl. 2: 2010.
  • 22. Fujisawa Y, Matsumura F, Wen Li, Patric Wong, Christoph Vogel, Hsing-Jien Kung, Nakagawa Y, Ohzeki T: AH receptor activation by ETK tyrosine kinase in ER alpha-negative MCF10AT1 breast cancer cells : Endocrine Journal : 57:578: Suppl. 2: 2010.
  • 23. Sano S, Nakagawa Y, Iwashima S, Ishikawa T, Satake E, Matsushita R, Nagata E, Yamaguchi R, Nakanishi T, Ohzeki T. Dynamics of endogenous glucocorticoid secretion and its metabolism in Kawasaki disease. Steroids. 2010 Dec;75(12):848-52. Epub 2010 Jun 19.
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