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Two dinucleotide repeat polymorphisms at the D8S1442 and D8S1443 loci.
Nakura J, Ye L, Kihara K, Yamagata H, Kamino K, Nakamura Y, Miki T, Ogihara T. Nakura J, et al. Among authors: yamagata h. Jpn J Hum Genet. 1995 Sep;40(3):281-2. doi: 10.1007/BF01876188. Jpn J Hum Genet. 1995. PMID: 8527804 No abstract available.
The DYRK1A gene, encoded in chromosome 21 Down syndrome critical region, bridges between beta-amyloid production and tau phosphorylation in Alzheimer disease.
Kimura R, Kamino K, Yamamoto M, Nuripa A, Kida T, Kazui H, Hashimoto R, Tanaka T, Kudo T, Yamagata H, Tabara Y, Miki T, Akatsu H, Kosaka K, Funakoshi E, Nishitomi K, Sakaguchi G, Kato A, Hattori H, Uema T, Takeda M. Kimura R, et al. Among authors: yamagata h. Hum Mol Genet. 2007 Jan 1;16(1):15-23. doi: 10.1093/hmg/ddl437. Epub 2006 Nov 29. Hum Mol Genet. 2007. PMID: 17135279
Characteristics of dynamic mutation in Japanese myotonic dystrophy.
Yamagata H, Miki T, Yamanaka N, Takemoto Y, Kanda F, Takahashi K, Inui T, Kinoshita M, Nakagawa M, Higuchi I, et al. Yamagata H, et al. Jpn J Hum Genet. 1994 Sep;39(3):327-35. doi: 10.1007/BF01874051. Jpn J Hum Genet. 1994. PMID: 7841443
Detection of a premutation in Japanese myotonic dystrophy.
Yamagata H, Miki T, Sakoda S, Yamanaka N, Davies J, Shelbourne P, Kubota R, Takenaga S, Nakagawa M, Ogihara T, et al. Yamagata H, et al. Hum Mol Genet. 1994 May;3(5):819-20. doi: 10.1093/hmg/3.5.819. Hum Mol Genet. 1994. PMID: 8081369 No abstract available.
[DNA diagnosis of myotonic dystrophy in a family].
Kihara K, Yamagata H, Miki T, Ogihara T. Kihara K, et al. Among authors: yamagata h. Rinsho Shinkeigaku. 1993 Mar;33(3):266-70. Rinsho Shinkeigaku. 1993. PMID: 8334788 Japanese.
423 results