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Polymorphism of the polyalanine tract of thyroid transcription factor-2 gene in patients with thyroid dysgenesis.
Published in:
European Journal of Endocrinology, 2001, v. 145, n. 4, p. 385, doi. 10.1530/eje.0.1450385
By:
- Hishinuma, Akira;
- Ohyama, Yoshihide;
- Kuribayashi, Takeo;
- Nagakubo, Narumi;
- Namatame, Takashi;
- Shibayama, Keiko;
- Arisaka, Osamu;
- Matsuura, Nobuo;
- Ieiri, Tamio
Publication type:
Article
Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene.
Published in:
Pediatrics International, 2005, v. 47, n. 1, p. 105, doi. 10.1111/j.1442-200x.2005.02020.x
By:
- Shibayama, Keiko;
- Ohyama, Yoshihide;
- Hishinuma, Akira;
- Yokota, Yukifumi;
- Kazahari, Koji;
- Kazahari, Mayumi;
- Ieiri, Tamio;
- Matsuura, Nobuo
Publication type:
Article
Haplotype Analysis Reveals Founder Effects of Thyroglobulin Gene Mutations C1058R and C1977S in Japan.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 8, p. 3100, doi. 10.1210/jc.2005-2702
By:
- Akira Hishinuma;
- Shuji Fukata;
- Soroku Nishiyama;
- Yoshikazu Nishi;
- Masamichi Oh-Ishi;
- Yoshiharu Murata;
- Yoshihide Ohyama;
- Nobuo Matsuura;
- Kikuo Kasai;
- Shohei Harada;
- Sachiko Kitanaka;
- Junta Takamatsu;
- Kohji Kiwaki;
- Hidemi Ohye;
- Takashi Uruno;
- Chisato Tomoda;
- Toshihiro Tajima;
- Kanji Kuma;
- Akira Miyauchi;
- Tamio Ieiri
Publication type:
Article
High Prevalence of T354P Sodium/Iodide Symporter Gene Mutation in Japanese Patients with Iodide Transport Defect Who Have Heterogeneous Clinical Pictures.
Published in:
Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 11, p. 4123, doi. 10.1210/jc.83.11.4123
By:
- SHINJI KOSUGI;
- YUICHI SATO;
- MATSUDA, AKIRA;
- YOSHIHIDE OHYAMA;
- KENJI FUJIEDA;
- HIROAKI INOMATA;
- TORU KAMEYA;
- OSAMU ISOZAKI;
- JHIANG, SISSY M.
Publication type:
Article

Found: 4

Polymorphism of the polyalanine tract of thyroid transcription factor-2 gene in patients with thyroid dysgenesis.

Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene.

Haplotype Analysis Reveals Founder Effects of Thyroglobulin Gene Mutations C1058R and C1977S in Japan.

High Prevalence of T354P Sodium/Iodide Symporter Gene Mutation in Japanese Patients with Iodide Transport Defect Who Have Heterogeneous Clinical Pictures.