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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
LMNA mutations in atypical Werner's syndrome.
Chen L, Lee L, Kudlow BA, Dos Santos HG, Sletvold O, Shafeghati Y, Botha EG, Garg A, Hanson NB, Martin GM, Mian IS, Kennedy BK, Oshima J. Chen L, et al. Among authors: Oshima J. Lancet. 2003 Aug 9;362(9382):440-5. doi: 10.1016/S0140-6736(03)14069-X. Lancet. 2003. PMID: 12927431
Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.
Nakura J, Miki T, Ye L, Mitsuda N, Zhao Y, Kihara K, Yu CE, Oshima J, Fukuchi KI, Wijsman EM, Schellenberg GD, Martin GM, Murano Si, Hashimoto K, Fujiwara Y, Ogihara T. Nakura J, et al. Among authors: Oshima J. Genomics. 1996 Aug 15;36(1):130-41. doi: 10.1006/geno.1996.0433. Genomics. 1996. PMID: 8812424
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
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
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