Akira Hishinuma
Department of Clinical Laboratory Medicine
Dokkyo University School of Medicine
Mibu, Tochigi
Japan
Name/email consistency: high
- Haplotype analysis reveals founder effects of thyroglobulin gene mutations C1058R and C1977S in Japan. Hishinuma, A., Fukata, S., Nishiyama, S., Nishi, Y., Oh-Ishi, M., Murata, Y., Ohyama, Y., Matsuura, N., Kasai, K., Harada, S., Kitanaka, S., Takamatsu, J., Kiwaki, K., Ohye, H., Uruno, T., Tomoda, C., Tajima, T., Kuma, K., Miyauchi, A., Ieiri, T. J. Clin. Endocrinol. Metab. (2006)
- High incidence of thyroid cancer in long-standing goiters with thyroglobulin mutations. Hishinuma, A., Fukata, S., Kakudo, K., Murata, Y., Ieiri, T. Thyroid (2005)
- TTF-2 stimulates expression of 17 genes, including one novel thyroid-specific gene which might be involved in thyroid development. Hishinuma, A., Ohmika, N., Namatame, T., Ieiri, T. Mol. Cell. Endocrinol. (2004)
- Polymorphism of the polyalanine tract of thyroid transcription factor-2 gene in patients with thyroid dysgenesis. Hishinuma, A., Ohyama, Y., Kuribayashi, T., Nagakubo, N., Namatame, T., Shibayama, K., Arisaka, O., Matsuura, N., Ieiri, T. Eur. J. Endocrinol. (2001)
- A novel missense mutation (G2320R) in thyroglobulin causes hypothyroidism in rdw rats. Hishinuma, A., Furudate, S., Oh-Ishi, M., Nagakubo, N., Namatame, T., Ieiri, T. Endocrinology (2000)