AG08303/AG/NIA NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1991	1
1992	1
1993	1
1994	5
1995	1
1996	3
1997	3
2024	0

1

The Werner syndrome protein is a DNA helicase.

Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA. Gray MD, et al. Nat Genet. 1997 Sep;17(1):100-3. doi: 10.1038/ng0997-100. Nat Genet. 1997. PMID: 9288107

2

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.

3

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. Am J Hum Genet. 1994 Aug;55(2):356-64. Am J Hum Genet. 1994. PMID: 8037212 Free PMC article.

4

Abiotrophic gene action in Homo sapiens: potential mechanisms and significance for the pathobiology of aging.

Martin GM. Martin GM. Genetica. 1993;91(1-3):265-77. doi: 10.1007/BF01436003. Genetica. 1993. PMID: 8125275 Review.

5

Homozygous and compound heterozygous mutations at the Werner syndrome locus.

Oshima J, Yu CE, Piussan C, Klein G, Jabkowski J, Balci S, Miki T, Nakura J, Ogihara T, Ells J, Smith M, Melaragno MI, Fraccaro M, Scappaticci S, Matthews J, Ouais S, Jarzebowicz A, Schellenberg GD, Martin GM. Oshima J, et al. Hum Mol Genet. 1996 Dec;5(12):1909-13. doi: 10.1093/hmg/5.12.1909. Hum Mol Genet. 1996. PMID: 8968742

6

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. Hum Genet. 1994 May;93(5):507-12. doi: 10.1007/BF00202813. Hum Genet. 1994. PMID: 8168825

7

Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

Yu CE, Oshima J, Wijsman EM, Nakura J, Miki T, Piussan C, Matthews S, Fu YH, Mulligan J, Martin GM, Schellenberg GD. Yu CE, et al. Am J Hum Genet. 1997 Feb;60(2):330-41. Am J Hum Genet. 1997. PMID: 9012406 Free PMC article.

8

Recurrence risk of a new dominant mutation in children of unaffected parents.

Wijsman EM. Wijsman EM. Am J Hum Genet. 1991 Apr;48(4):654-61. Am J Hum Genet. 1991. PMID: 2014793 Free PMC article.

9

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. Genomics. 1994 Oct;23(3):600-8. doi: 10.1006/geno.1994.1548. Genomics. 1994. PMID: 7851888

10

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

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