Takahashi T - Search Results

1

Severe craniosynostosis with Noonan syndrome phenotype associated with SHOC2 mutation: clinical evidence of crosslink between FGFR and RAS signaling pathways.

Takenouchi T, Sakamoto Y, Miwa T, Torii C, Kosaki R, Kishi K, Takahashi T, Kosaki K. Takenouchi T, et al. Among authors: takahashi t. Am J Med Genet A. 2014 Nov;164A(11):2869-72. doi: 10.1002/ajmg.a.36705. Epub 2014 Aug 13. Am J Med Genet A. 2014. PMID: 25123707

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: takahashi t. Teratology. 2002 Jan;65(1):10-8. doi: 10.1002/tera.1093. Teratology. 2002. PMID: 11835227

3

Complete mutation analysis panel of the 39 human HOX genes.

Kosaki K, Kosaki R, Suzuki T, Yoshihashi H, Takahashi T, Sasaki K, Tomita M, McGinnis W, Matsuo N. Kosaki K, et al. Among authors: takahashi t. Teratology. 2002 Feb;65(2):50-62. doi: 10.1002/tera.10009. Teratology. 2002. PMID: 11857506

4

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: takahashi t. J Clin Endocrinol Metab. 2003 Jul;88(7):3431-6. doi: 10.1210/jc.2002-021415. J Clin Endocrinol Metab. 2003. PMID: 12843198

5

Position-specific expression of Hox genes along the gastrointestinal tract.

Yahagi N, Kosaki R, Ito T, Mitsuhashi T, Shimada H, Tomita M, Takahashi T, Kosaki K. Yahagi N, et al. Among authors: takahashi t. Congenit Anom (Kyoto). 2004 Mar;44(1):18-26. doi: 10.1111/j.1741-4520.2003.00004.x. Congenit Anom (Kyoto). 2004. PMID: 15008896

6

[Effect of post-exposure prophylaxis with oseltamivir for those in contacts with influenza patients in pediatric wards].

Shinjoh M, Sato S, Sugaya N, Mitamura K, Takeuchi Y, Kosaki K, Takahashi T. Shinjoh M, et al. Among authors: takahashi t. Kansenshogaku Zasshi. 2004 Mar;78(3):262-9. doi: 10.11150/kansenshogakuzasshi1970.78.262. Kansenshogaku Zasshi. 2004. PMID: 15103909 Japanese.

7

Absent inner dynein arms in a fetus with familial hydrocephalus-situs abnormality.

Kosaki K, Ikeda K, Miyakoshi K, Ueno M, Kosaki R, Takahashi D, Tanaka M, Torikata C, Yoshimura Y, Takahashi T. Kosaki K, et al. Among authors: takahashi d, takahashi t. Am J Med Genet A. 2004 Sep 1;129A(3):308-11. doi: 10.1002/ajmg.a.30177. Am J Med Genet A. 2004. PMID: 15326634

8

Hyperinsulinemic hypoglycemia in a newborn infant with trisomy 13.

Tamame T, Hori N, Homma H, Yoshida R, Inokuchi M, Kosaki K, Takahashi T, Hasegawa T. Tamame T, et al. Among authors: takahashi t. Am J Med Genet A. 2004 Sep 1;129A(3):321-2. doi: 10.1002/ajmg.a.30147. Am J Med Genet A. 2004. PMID: 15326637 No abstract available.

9

A major influence of CYP2C19 genotype on the steady-state concentration of N-desmethylclobazam.

Kosaki K, Tamura K, Sato R, Samejima H, Tanigawara Y, Takahashi T. Kosaki K, et al. Among authors: takahashi t. Brain Dev. 2004 Dec;26(8):530-4. doi: 10.1016/j.braindev.2004.02.010. Brain Dev. 2004. PMID: 15533655

10

Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFB.

Goto T, Aramaki M, Yoshihashi H, Nishimura G, Hasegawa Y, Takahashi T, Ishii T, Fukushima Y, Kosaki K. Goto T, et al. Among authors: takahashi t. Congenit Anom (Kyoto). 2004 Dec;44(4):225-9. doi: 10.1111/j.1741-4520.2004.00043.x. Congenit Anom (Kyoto). 2004. PMID: 15566413

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