Oshima J - Search Results

1

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.

Goddard KA, Yu CE, Oshima J, Miki T, Nakura J, Piussan C, Martin GM, Schellenberg GD, Wijsman EM. Goddard KA, et al. Among authors: oshima j. Am J Hum Genet. 1996 Jun;58(6):1286-302. Am J Hum Genet. 1996. PMID: 8651307 Free PMC article.

2

Candidate gene for the chromosome 1 familial Alzheimer's disease locus.

Levy-Lahad E, Wasco W, Poorkaj P, Romano DM, Oshima J, Pettingell WH, Yu CE, Jondro PD, Schmidt SD, Wang K, et al. Levy-Lahad E, et al. Among authors: oshima j. Science. 1995 Aug 18;269(5226):973-7. doi: 10.1126/science.7638622. Science. 1995. PMID: 7638622

3

Regulation of c-fos expression in senescing Werner syndrome fibroblasts differs from that observed in senescing fibroblasts from normal donors.

Oshima J, Campisi J, Tannock TC, Martin GM. Oshima J, et al. J Cell Physiol. 1995 Feb;162(2):277-83. doi: 10.1002/jcp.1041620213. J Cell Physiol. 1995. PMID: 7822435

4

Integrated mapping analysis of the Werner syndrome region of chromosome 8.

Oshima J, Yu CE, Boehnke M, Weber JL, Edelhoff S, Wagner MJ, Wells DE, Wood S, Disteche CM, Martin GM, et al. Oshima J, et al. Genomics. 1994 Sep 1;23(1):100-13. doi: 10.1006/geno.1994.1464. Genomics. 1994. PMID: 7829057 Free article.

5

Homozygosity mapping of the Werner syndrome locus (WRN).

Nakura J, Wijsman EM, Miki T, Kamino K, Yu CE, Oshima J, Fukuchi K, Weber JL, Piussan C, Melaragno MI, et al. Nakura J, et al. Among authors: oshima j. Genomics. 1994 Oct;23(3):600-8. doi: 10.1006/geno.1994.1548. Genomics. 1994. PMID: 7851888

6

Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome.

Yu CE, Oshima J, Goddard KA, Miki T, Nakura J, Ogihara T, Poot M, Hoehn H, Fraccaro M, Piussan C, et al. Yu CE, et al. Among authors: oshima j. Am J Hum Genet. 1994 Aug;55(2):356-64. Am J Hum Genet. 1994. PMID: 8037212 Free PMC article.

7

Dinucleotide repeat polymorphism at the D8S131 locus.

Yu CE, Anderson L, Oshima J, Schellenberg GD. Yu CE, et al. Among authors: oshima j. Hum Mol Genet. 1994 Jan;3(1):211. Hum Mol Genet. 1994. PMID: 8162035 No abstract available.

8

Dinucleotide repeat polymorphism at the FGFR1 gene.

Yu CE, Anderson L, Oshima J, Schellenberg GD. Yu CE, et al. Among authors: oshima j. Hum Mol Genet. 1994 Jan;3(1):212. Hum Mol Genet. 1994. PMID: 8162037 No abstract available.

9

Dinucleotide repeat polymorphisms at the GSR gene.

Yu CE, Anderson L, Oshima J, Schellenberg GD. Yu CE, et al. Among authors: oshima j. Hum Mol Genet. 1994 Jan;3(1):212. Hum Mol Genet. 1994. PMID: 8162038 No abstract available.

10

Evidence against DNA polymerase beta as a candidate gene for Werner syndrome.

Chang M, Burmer GC, Sweasy J, Loeb LA, Edelhoff S, Disteche CM, Yu CE, Anderson L, Oshima J, Nakura J, et al. Chang M, et al. Among authors: oshima j. Hum Genet. 1994 May;93(5):507-12. doi: 10.1007/BF00202813. Hum Genet. 1994. PMID: 8168825

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