Yamagata H - Search Results

1

[A case of Hashimoto's thyroiditis associated with renal tubular acidosis, Sjögren syndrome and empty sella syndrome].

Yoshiiwa A, Nabata T, Morimoto S, Sakaguchi K, Yamagata H, Fukuo K, Ogihara T. Yoshiiwa A, et al. Among authors: yamagata h. Nihon Naibunpi Gakkai Zasshi. 1992 Nov 20;68(11):1215-23. doi: 10.1507/endocrine1927.68.11_1215. Nihon Naibunpi Gakkai Zasshi. 1992. PMID: 1468597 Review. Japanese.

2

[Molecular genetics of myotonic dystrophy--population genetics of the CTG repeat expansion of the MTPK gene].

Yamagata H, Miki T, Ogihara T. Yamagata H, et al. Nihon Rinsho. 1997 Dec;55(12):3205-9. Nihon Rinsho. 1997. PMID: 9436437 Review. Japanese.

3

[Molecular genetics of myotonic dystrophy].

Miki T, Yamagata H, Ogihara T. Miki T, et al. Among authors: yamagata h. Rinsho Shinkeigaku. 1995 Dec;35(12):1479-81. Rinsho Shinkeigaku. 1995. PMID: 8752436 Review. Japanese.

4

[Advances in molecular genetics of myotonic dystrophy].

Yamagata H, Yamanaka N, Miki T, Ogihara T. Yamagata H, et al. Nihon Rinsho. 1993 Sep;51(9):2474-80. Nihon Rinsho. 1993. PMID: 8411731 Review. Japanese.

5

[A case of mild-type myotonic dystrophy with dementia and severe arteriosclerosis obliterans].

Horiki M, Morishima A, Yamagata H, Rakugi H, Ikegami H, Miki T, Ogihara T. Horiki M, et al. Among authors: yamagata h. Nihon Ronen Igakkai Zasshi. 1998 Feb;35(2):136-8. doi: 10.3143/geriatrics.35.136. Nihon Ronen Igakkai Zasshi. 1998. PMID: 9584492 Free article. Japanese.

6

[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.

7

Association of CTG repeats and the 1-kb Alu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation.

Yamagata H, Miki T, Nakagawa M, Johnson K, Deka R, Ogihara T. Yamagata H, et al. Hum Genet. 1996 Feb;97(2):145-7. doi: 10.1007/BF02265255. Hum Genet. 1996. PMID: 8566943

8

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.

9

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.

10

Xylose (glucose) isomerase gene from the thermophile Clostridium thermohydrosulfuricum; cloning, sequencing, and expression in Escherichia coli.

Dekker K, Yamagata H, Sakaguchi K, Udaka S. Dekker K, et al. Among authors: yamagata h. Agric Biol Chem. 1991 Jan;55(1):221-7. Agric Biol Chem. 1991. PMID: 1368665 Free article.

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