Martin GM - Search Results

1

Schellenberg GD, Bird TD, Wijsman EM, Moore DK, Martin GM. Schellenberg GD, et al. Among authors: martin gm. Biomed Pharmacother. 1989;43(7):463-8. doi: 10.1016/0753-3322(89)90106-6. Biomed Pharmacother. 1989. PMID: 2531010 Review.

2

Trypsin inhibitor activities of fibroblasts increase with age of donor and are unaltered in familial Alzheimer's disease.

Hearn MG, Edland SD, Ogburn CE, Smith AC, Bird TD, Martin GM, Fukuchi K. Hearn MG, et al. Among authors: martin gm. Exp Gerontol. 1994 Nov-Dec;29(6):611-23. doi: 10.1016/0531-5565(94)90074-4. Exp Gerontol. 1994. PMID: 9435914

3

The Seattle Alzheimer's disease data set.

Wijsman EM, Bird TD, Martin GM, Schellenberg GD. Wijsman EM, et al. Among authors: martin gm. Genet Epidemiol. 1993;10(6):365-9. doi: 10.1002/gepi.1370100606. Genet Epidemiol. 1993. PMID: 8314028 Review.

4

Genetic association and linkage analysis of the apolipoprotein CII locus and familial Alzheimer's disease.

Schellenberg GD, Boehnke M, Wijsman EM, Moore DK, Martin GM, Bird TD. Schellenberg GD, et al. Among authors: martin gm. Ann Neurol. 1992 Feb;31(2):223-7. doi: 10.1002/ana.410310214. Ann Neurol. 1992. PMID: 1349467

5

APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.

Schellenberg GD, Anderson L, O'dahl S, Wisjman EM, Sadovnick AD, Ball MJ, Larson EB, Kukull WA, Martin GM, Roses AD, et al. Schellenberg GD, et al. Among authors: martin gm. Am J Hum Genet. 1991 Sep;49(3):511-7. Am J Hum Genet. 1991. PMID: 1679288 Free PMC article.

6

Evidence for etiologic heterogeneity in Alzheimer's disease.

Bird TD, Schellenberg GD, Wijsman EM, Martin GM. Bird TD, et al. Among authors: martin gm. Neurobiol Aging. 1989 Sep-Oct;10(5):432-4; discussion 446-8. doi: 10.1016/0197-4580(89)90085-7. Neurobiol Aging. 1989. PMID: 2812202

7

Lack of detectable radiation hypersensitivity in lymphoblastoid cells from multiple pedigrees of familial Alzheimer disease.

Bryant EM, Bird TD, Ogburn CE, Traylor GH, Lampe TH, Martin GM. Bryant EM, et al. Among authors: martin gm. Alzheimer Dis Assoc Disord. 1993 Summer;7(2):88-97. doi: 10.1097/00002093-199307020-00004. Alzheimer Dis Assoc Disord. 1993. PMID: 8347332

8

Positional cloning of the Werner's syndrome gene.

Yu CE, Oshima J, Fu YH, Wijsman EM, Hisama F, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD. Yu CE, et al. Among authors: martin gm. Science. 1996 Apr 12;272(5259):258-62. doi: 10.1126/science.272.5259.258. Science. 1996. PMID: 8602509

9

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: martin gm. Am J Hum Genet. 1996 Jun;58(6):1286-302. Am J Hum Genet. 1996. PMID: 8651307 Free PMC article.

10

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. Among authors: martin gm. Am J Hum Genet. 1997 Feb;60(2):330-41. Am J Hum Genet. 1997. PMID: 9012406 Free PMC article.

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