Hasegawa T - Search Results

1

CXorf6 is a causative gene for hypospadias.

Fukami M, Wada Y, Miyabayashi K, Nishino I, Hasegawa T, Nordenskjöld A, Camerino G, Kretz C, Buj-Bello A, Laporte J, Yamada G, Morohashi K, Ogata T. Fukami M, et al. Among authors: hasegawa t. Nat Genet. 2006 Dec;38(12):1369-71. doi: 10.1038/ng1900. Epub 2006 Nov 5. Nat Genet. 2006. PMID: 17086185

2

Characterization of the aryl hydrocarbon receptor repressor gene and association of its Pro185Ala polymorphism with micropenis.

Fujita H, Kosaki R, Yoshihashi H, Ogata T, Tomita M, Hasegawa T, Takahashi T, Matsuo N, Kosaki K. Fujita H, et al. Among authors: hasegawa t. Teratology. 2002 Jan;65(1):10-8. doi: 10.1002/tera.1093. Teratology. 2002. PMID: 11835227

3

Novel mutation of TBX3 in a Japanese family with ulnar-mammary syndrome: implication for impaired sex development.

Sasaki G, Ogata T, Ishii T, Hasegawa T, Sato S, Matsuo N. Sasaki G, et al. Among authors: hasegawa t. Am J Med Genet. 2002 Jul 15;110(4):365-9. doi: 10.1002/ajmg.10447. Am J Med Genet. 2002. PMID: 12116211

4

PTPN11 (protein-tyrosine phosphatase, nonreceptor-type 11) mutations in seven Japanese patients with Noonan syndrome.

Kosaki K, Suzuki T, Muroya K, Hasegawa T, Sato S, Matsuo N, Kosaki R, Nagai T, Hasegawa Y, Ogata T. Kosaki K, et al. Among authors: hasegawa t, hasegawa y. J Clin Endocrinol Metab. 2002 Aug;87(8):3529-33. doi: 10.1210/jcem.87.8.8694. J Clin Endocrinol Metab. 2002. PMID: 12161469

5

Giant seminoma in a patient with 5 alpha-reductase type 2 deficiency.

Sasaki G, Nakagawa K, Hashiguchi A, Hasegawa T, Ogata T, Murai M. Sasaki G, et al. Among authors: hasegawa t. J Urol. 2003 Mar;169(3):1080-1. doi: 10.1097/01.ju.0000047621.66463.29. J Urol. 2003. PMID: 12576851 No abstract available.

6

Micropenis and the 5alpha-reductase-2 (SRD5A2) gene: mutation and V89L polymorphism analysis in 81 Japanese patients.

Sasaki G, Ogata T, Ishii T, Kosaki K, Sato S, Homma K, Takahashi T, Hasegawa T, Matsuo N. Sasaki G, et al. Among authors: hasegawa t. J Clin Endocrinol Metab. 2003 Jul;88(7):3431-6. doi: 10.1210/jc.2002-021415. J Clin Endocrinol Metab. 2003. PMID: 12843198

7

Mental retardation in a boy with congenital adrenal hypoplasia: a clue to contiguous gene syndrome involving DAX1 and IL1RAPL.

Sasaki R, Inamo Y, Saitoh K, Hasegawa T, Kinoshita E, Ogata T. Sasaki R, et al. Among authors: hasegawa t. Endocr J. 2003 Jun;50(3):303-7. doi: 10.1507/endocrj.50.303. Endocr J. 2003. PMID: 12940459 Free article.

8

Longitudinal auxological study in a female with SHOX (short stature homeobox containing gene) haploinsufficiency and normal ovarian function.

Fukami M, Matsuo N, Hasegawa T, Sato S, Ogata T. Fukami M, et al. Among authors: hasegawa t. Eur J Endocrinol. 2003 Oct;149(4):337-41. doi: 10.1530/eje.0.1490337. Eur J Endocrinol. 2003. PMID: 14514349

9

Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

Sato N, Katsumata N, Kagami M, Hasegawa T, Hori N, Kawakita S, Minowada S, Shimotsuka A, Shishiba Y, Yokozawa M, Yasuda T, Nagasaki K, Hasegawa D, Hasegawa Y, Tachibana K, Naiki Y, Horikawa R, Tanaka T, Ogata T. Sato N, et al. Among authors: hasegawa t, hasegawa d, hasegawa y. J Clin Endocrinol Metab. 2004 Mar;89(3):1079-88. doi: 10.1210/jc.2003-030476. J Clin Endocrinol Metab. 2004. PMID: 15001591

10

Premature ovarian failure in a female with proximal symphalangism and Noggin mutation.

Kosaki K, Sato S, Hasegawa T, Matsuo N, Suzuki T, Ogata T. Kosaki K, et al. Among authors: hasegawa t. Fertil Steril. 2004 Apr;81(4):1137-9. doi: 10.1016/j.fertnstert.2003.08.054. Fertil Steril. 2004. PMID: 15066478 Free article.

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