Pericak-Vance MA - Search Results

1

Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.

van der Walt JM, Nicodemus KK, Martin ER, Scott WK, Nance MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Mastaglia F, Stajich JM, McLaurin AC, Middleton LT, Scott BL, Schmechel DE, Pericak-Vance MA, Vance JM. van der Walt JM, et al. Am J Hum Genet. 2003 Apr;72(4):804-11. doi: 10.1086/373937. Epub 2003 Feb 28. Am J Hum Genet. 2003. PMID: 12618962 Free PMC article.

2

Apolipoprotein E is present in hippocampal neurons without neurofibrillary tangles in Alzheimer's disease and in age-matched controls.

Han SH, Hulette C, Saunders AM, Einstein G, Pericak-Vance M, Strittmatter WJ, Roses AD, Schmechel DE. Han SH, et al. Exp Neurol. 1994 Jul;128(1):13-26. doi: 10.1006/exnr.1994.1108. Exp Neurol. 1994. PMID: 8070517

3

Apolipoprotein E is localized to the cytoplasm of human cortical neurons: a light and electron microscopic study.

Han SH, Einstein G, Weisgraber KH, Strittmatter WJ, Saunders AM, Pericak-Vance M, Roses AD, Schmechel DE. Han SH, et al. J Neuropathol Exp Neurol. 1994 Sep;53(5):535-44. doi: 10.1097/00005072-199409000-00013. J Neuropathol Exp Neurol. 1994. PMID: 8083695

4

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.

Strittmatter WJ, Saunders AM, Schmechel D, Pericak-Vance M, Enghild J, Salvesen GS, Roses AD. Strittmatter WJ, et al. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1977-81. doi: 10.1073/pnas.90.5.1977. Proc Natl Acad Sci U S A. 1993. PMID: 8446617 Free PMC article.

5

Ocular motility in North Carolina autosomal dominant ataxia.

Small KW, Pollock SC, Vance JM, Stajich JM, Pericak-Vance M. Small KW, et al. J Neuroophthalmol. 1996 Jun;16(2):91-5. doi: 10.3109/01658109609009667. J Neuroophthalmol. 1996. PMID: 8797163

6

Chorea-acanthocytosis: genetic linkage to chromosome 9q21.

Rubio JP, Danek A, Stone C, Chalmers R, Wood N, Verellen C, Ferrer X, Malandrini A, Fabrizi GM, Manfredi M, Vance J, Pericak-Vance M, Brown R, Rudolf G, Picard F, Alonso E, Brin M, Németh AH, Farrall M, Monaco AP. Rubio JP, et al. Am J Hum Genet. 1997 Oct;61(4):899-908. doi: 10.1086/514876. Am J Hum Genet. 1997. PMID: 9382101 Free PMC article.

7

Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.

Othmane KB, Johnson E, Menold M, Graham FL, Hamida MB, Hasegawa O, Rogala AD, Ohnishi A, Pericak-Vance M, Hentati F, Vance JM. Othmane KB, et al. Genomics. 1999 Dec 15;62(3):344-9. doi: 10.1006/geno.1999.6028. Genomics. 1999. PMID: 10644431

8

Genome-wide scan for adult onset primary open angle glaucoma.

Wiggs JL, Allingham RR, Hossain A, Kern J, Auguste J, DelBono EA, Broomer B, Graham FL, Hauser M, Pericak-Vance M, Haines JL. Wiggs JL, et al. Hum Mol Genet. 2000 Apr 12;9(7):1109-17. doi: 10.1093/hmg/9.7.1109. Hum Mol Genet. 2000. PMID: 10767336

9

Linkage of the CCR5 Delta 32 mutation with a functional polymorphism of CD45RA.

Liao HX, Montefiori DC, Patel DD, Lee DM, Scott WK, Pericak-Vance M, Haynes BF. Liao HX, et al. J Immunol. 2000 Jul 1;165(1):148-57. doi: 10.4049/jimmunol.165.1.148. J Immunol. 2000. PMID: 10861047

10

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.

Baxter RV, Ben Othmane K, Rochelle JM, Stajich JE, Hulette C, Dew-Knight S, Hentati F, Ben Hamida M, Bel S, Stenger JE, Gilbert JR, Pericak-Vance MA, Vance JM. Baxter RV, et al. Nat Genet. 2002 Jan;30(1):21-2. doi: 10.1038/ng796. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743579

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