Nakura J - Search Results

1

Isolation of DNA clones revealing restriction fragment length polymorphisms in the human genome.

Nishisho I, Miki T, Tateishi H, Takai S, Motomura K, Nakura J, Kumahara Y, Mori T, Honjo T. Nishisho I, et al. Among authors: nakura j. Jinrui Idengaku Zasshi. 1986 Sep;31(3):249-58. doi: 10.1007/BF01870755. Jinrui Idengaku Zasshi. 1986. PMID: 2882041 No abstract available.

2

Mapping of the genes around MEN2A locus using pulsed-field gel electrophoresis.

Tanaka N, Miki T, Yamamoto M, Nakura J, Okazaki M, Miya A, Mori T, Takai S. Tanaka N, et al. Among authors: nakura j. Jinrui Idengaku Zasshi. 1990 Dec;35(4):325-30. doi: 10.1007/BF01883755. Jinrui Idengaku Zasshi. 1990. PMID: 1982737

3

[Genetic analysis of hereditary diseases using PFLPs of DNA base sequence].

Miki T, Nakura J, Kumahara Y, Takai S, Tateishi H, Nishisho I, Mori T. Miki T, et al. Among authors: nakura j. Rinsho Byori. 1985 Nov;33 Spec No 65:151-9. Rinsho Byori. 1985. PMID: 2869164 Review. Japanese. No abstract available.

4

Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers.

Takemoto Y, Miki T, Nakura J, Nishikawa K, Kamino K, Takeda S, Kuzu K, Osame M, Nakagawa M, Higuchi I, et al. Takemoto Y, et al. Among authors: nakura j. Jinrui Idengaku Zasshi. 1989 Sep;34(3):189-94. doi: 10.1007/BF01900720. Jinrui Idengaku Zasshi. 1989. PMID: 2576756

5

Dinucleotide repeat polymorphism at the D8S1054.

Mitsuda N, Nakura J, Ye L, Takahashi-Fujii A, Ishino Y, Miki T, Ogihara T. Mitsuda N, et al. Among authors: nakura j. Jpn J Hum Genet. 1995 Jun;40(2):215-6. doi: 10.1007/BF01883580. Jpn J Hum Genet. 1995. PMID: 7663003 No abstract available.

6

Three dinucleotide repeat polymorphisms at the D8S1217, D8S1220, and D8S1221 loci.

Mitsuda N, Nakura J, Ye L, Miki T, Ogihara T. Mitsuda N, et al. Among authors: nakura j. Jpn J Hum Genet. 1995 Sep;40(3):283-5. doi: 10.1007/BF01876189. Jpn J Hum Genet. 1995. PMID: 8527805 No abstract available.

7

Two dinucleotide repeat polymorphisms at the D8S1444 and D8S1445 loci.

Nakura J, Ye L, Takahashi-Fujii A, Ishino Y, Kato I, Miki T, Ogihara T. Nakura J, et al. Jpn J Hum Genet. 1996 Jun;41(2):261-3. doi: 10.1007/BF01875988. Jpn J Hum Genet. 1996. PMID: 8771993 No abstract available.

8

Association of ACE I/D polymorphism with cardiovascular risk factors.

Uemura K, Nakura J, Kohara K, Miki T. Uemura K, et al. Among authors: nakura j. Hum Genet. 2000 Sep;107(3):239-42. doi: 10.1007/s004390000358. Hum Genet. 2000. PMID: 11071385

9

A BglII polymorphism for pKNB46 [D19S73].

Nishikawa K, Miki T, Takemoto Y, Kamino K, Nakura J, Takai S, Ogihara T. Nishikawa K, et al. Among authors: nakura j. Nucleic Acids Res. 1990 Feb 11;18(3):692. doi: 10.1093/nar/18.3.692. Nucleic Acids Res. 1990. PMID: 1968630 Free PMC article.

10

A case of first trimester prenatal diagnosis of 21-hydroxylase deficiency with human complement C4 cDNA probe.

Nakura J, Miki T, Nishikawa K, Takemoto Y, Kamino K, Takai S, Hayashi K, Ogihara T. Nakura J, et al. Endocrinol Jpn. 1990 Oct;37(5):615-8. doi: 10.1507/endocrj1954.37.615. Endocrinol Jpn. 1990. PMID: 1982260 Free article.

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