Ogata T - Search Results

1

Identification and functional characterization of two novel NPR2 mutations in Japanese patients with short stature.

Amano N, Mukai T, Ito Y, Narumi S, Tanaka T, Yokoya S, Ogata T, Hasegawa T. Amano N, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2014 Apr;99(4):E713-8. doi: 10.1210/jc.2013-3525. Epub 2014 Jan 28. J Clin Endocrinol Metab. 2014. PMID: 24471569

2

Short stature in a girl with partial monosomy of the pseudoautosomal region distal to DXYS15: further evidence for the assignment of the critical region for a pseudoautosomal growth gene(s).

Ogata T, Yoshizawa A, Muroya K, Matsuo N, Fukushima Y, Rappold G, Yokoya S. Ogata T, et al. J Med Genet. 1995 Oct;32(10):831-4. doi: 10.1136/jmg.32.10.831. J Med Genet. 1995. PMID: 8558568 Free PMC article.

3

Skeletal features and growth patterns in 14 patients with haploinsufficiency of SHOX: implications for the development of Turner syndrome.

Kosho T, Muroya K, Nagai T, Fujimoto M, Yokoya S, Sakamoto H, Hirano T, Terasaki H, Ohashi H, Nishimura G, Sato S, Matsuo N, Ogata T. Kosho T, et al. Among authors: ogata t. J Clin Endocrinol Metab. 1999 Dec;84(12):4613-21. doi: 10.1210/jcem.84.12.6289. J Clin Endocrinol Metab. 1999. PMID: 10599728

4

Novel mutations of the autoimmune regulator gene in two siblings with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.

Ishii T, Suzuki Y, Ando N, Matsuo N, Ogata T. Ishii T, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2000 Aug;85(8):2922-6. doi: 10.1210/jcem.85.8.6726. J Clin Endocrinol Metab. 2000. PMID: 10946904 Review.

5

Novel and recurrent EBP mutations in X-linked dominant chondrodysplasia punctata.

Ikegawa S, Ohashi H, Ogata T, Honda A, Tsukahara M, Kubo T, Kimizuka M, Shimode M, Hasegawa T, Nishimura G, Nakamura Y. Ikegawa S, et al. Among authors: ogata t. Am J Med Genet. 2000 Oct 2;94(4):300-5. doi: 10.1002/1096-8628(20001002)94:4<300::aid-ajmg7>3.0.co;2-3. Am J Med Genet. 2000. PMID: 11038443 Review.

6

Clinical and molecular studies in 15 females with ring X chromosomes: implications for r(X) formation and mental development.

Matsuo M, Muroya K, Adachi M, Tachibana K, Asakura Y, Nakagomi Y, Hanaki K, Yokoya S, Yoshizawa A, Igarashi Y, Hanew K, Matsuo N, Ogata T. Matsuo M, et al. Among authors: ogata t. Hum Genet. 2000 Nov;107(5):433-9. doi: 10.1007/s004390000377. Hum Genet. 2000. PMID: 11140940

7

GATA3 abnormalities and the phenotypic spectrum of HDR syndrome.

Muroya K, Hasegawa T, Ito Y, Nagai T, Isotani H, Iwata Y, Yamamoto K, Fujimoto S, Seishu S, Fukushima Y, Hasegawa Y, Ogata T. Muroya K, et al. Among authors: ogata t. J Med Genet. 2001 Jun;38(6):374-80. doi: 10.1136/jmg.38.6.374. J Med Genet. 2001. PMID: 11389161 Free PMC article.

8

Micropenis and the AR Gene: mutation and CAG repeat-length analysis.

Ishii T, Sato S, Kosaki K, Sasaki G, Muroya K, Ogata T, Matsuo N. Ishii T, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2001 Nov;86(11):5372-8. doi: 10.1210/jcem.86.11.7999. J Clin Endocrinol Metab. 2001. PMID: 11701709 Clinical Trial.

9

Female gonadal development in XX patients with distal 9p monosomy.

Ogata T, Muroya K, Ohashi H, Mochizuki H, Hasegawa T, Kaji M. Ogata T, et al. Eur J Endocrinol. 2001 Nov;145(5):613-7. doi: 10.1530/eje.0.1450613. Eur J Endocrinol. 2001. PMID: 11720880 Clinical Trial.

10

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

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