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The prevalence of mitochondrial gene mutations in childhood diabetes in Japan.
Matsuura N, Suzuki S, Yokota Y, Kazahari K, Kazahari M, Toyota T, Hirai M, Okuno A, Harada S, Fukushima N, Koike A, Ito Y, Hotsubo T. Matsuura N, et al. Among authors: hotsubo t. J Pediatr Endocrinol Metab. 1999 Jan-Feb;12(1):27-30. doi: 10.1515/jpem.1999.12.1.27. J Pediatr Endocrinol Metab. 1999. PMID: 10392345
Analysis of the steroidogenic acute regulatory protein (StAR) gene in Japanese patients with congenital lipoid adrenal hyperplasia.
Nakae J, Tajima T, Sugawara T, Arakane F, Hanaki K, Hotsubo T, Igarashi N, Igarashi Y, Ishii T, Koda N, Kondo T, Kohno H, Nakagawa Y, Tachibana K, Takeshima Y, Tsubouchi K, Strauss JF 3rd, Fujieda K. Nakae J, et al. Among authors: hotsubo t. Hum Mol Genet. 1997 Apr;6(4):571-6. doi: 10.1093/hmg/6.4.571. Hum Mol Genet. 1997. PMID: 9097960
Familial short stature is associated with a novel dominant-negative heterozygous insulin-like growth factor 1 receptor (IGF1R) mutation.
Kawashima Y, Hakuno F, Okada S, Hotsubo T, Kinoshita T, Fujimoto M, Nishimura R, Fukushima T, Hanaki K, Takahashi S, Kanzaki S. Kawashima Y, et al. Among authors: hotsubo t. Clin Endocrinol (Oxf). 2014 Aug;81(2):312-4. doi: 10.1111/cen.12317. Epub 2013 Sep 30. Clin Endocrinol (Oxf). 2014. PMID: 24033502 No abstract available.
29 results