Vance JM - Search Results

1

Mechanisms of disease: a molecular genetic update on hereditary axonal neuropathies.

Züchner S, Vance JM. Züchner S, et al. Among authors: vance jm. Nat Clin Pract Neurol. 2006 Jan;2(1):45-53. doi: 10.1038/ncpneuro0071. Nat Clin Pract Neurol. 2006. PMID: 16932520 Review.

2

Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities.

Loprest LJ, Pericak-Vance MA, Stajich J, Gaskell PC, Lucas AM, Lennon F, Yamaoka LH, Roses AD, Vance JM. Loprest LJ, et al. Among authors: vance jm. Neurology. 1992 Mar;42(3 Pt 1):597-601. doi: 10.1212/wnl.42.3.597. Neurology. 1992. PMID: 1549221

3

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

Vance JM, Barker D, Yamaoka LH, Stajich JM, Loprest L, Hung WY, Fischbeck K, Roses AD, Pericak-Vance MA. Vance JM, et al. Genomics. 1991 Apr;9(4):623-8. doi: 10.1016/0888-7543(91)90355-i. Genomics. 1991. PMID: 1674726

4

Hereditary motor and sensory neuropathies.

Vance JM. Vance JM. J Med Genet. 1991 Jan;28(1):1-5. doi: 10.1136/jmg.28.1.1. J Med Genet. 1991. PMID: 1999826 Free PMC article. Review. No abstract available.

5

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17.

Vance JM, Nicholson GA, Yamaoka LH, Stajich J, Stewart CS, Speer MC, Hung WY, Roses AD, Barker D, Pericak-Vance MA. Vance JM, et al. Exp Neurol. 1989 May;104(2):186-9. doi: 10.1016/s0014-4886(89)80013-5. Exp Neurol. 1989. PMID: 2707366

6

The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family.

Burke JR, Wingfield MS, Lewis KE, Roses AD, Lee JE, Hulette C, Pericak-Vance MA, Vance JM. Burke JR, et al. Among authors: vance jm. Nat Genet. 1994 Aug;7(4):521-4. doi: 10.1038/ng0894-521. Nat Genet. 1994. PMID: 7951323

7

Partitioned pulsed-field gel electrophoresis-PCR (PPF-PCR): a new method for pulsed-field mapping for STS and microsatellites.

Denton PH, Cullen JB, Loeb D, Lucas A, Nunes K, Hulett C, Vance JM. Denton PH, et al. Among authors: vance jm. Nucleic Acids Res. 1994 May 11;22(9):1776-7. doi: 10.1093/nar/22.9.1776. Nucleic Acids Res. 1994. PMID: 8202390 Free PMC article.

8

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

Ben Othmane K, Hentati F, Lennon F, Ben Hamida C, Blel S, Roses AD, Pericak-Vance MA, Ben Hamida M, Vance JM. Ben Othmane K, et al. Among authors: vance jm. Hum Mol Genet. 1993 Oct;2(10):1625-8. doi: 10.1093/hmg/2.10.1625. Hum Mol Genet. 1993. PMID: 8268915

9

Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.

Othmane KB, Loeb D, Hayworth-Hodgte R, Hentati F, Rao N, Roses AD, Ben Hamida M, Pericak-Vance MA, Vance JM. Othmane KB, et al. Among authors: vance jm. Genomics. 1995 Jul 20;28(2):286-90. doi: 10.1006/geno.1995.1143. Genomics. 1995. PMID: 8530038

10

Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH.

Burke JR, Enghild JJ, Martin ME, Jou YS, Myers RM, Roses AD, Vance JM, Strittmatter WJ. Burke JR, et al. Among authors: vance jm. Nat Med. 1996 Mar;2(3):347-50. doi: 10.1038/nm0396-347. Nat Med. 1996. PMID: 8612237

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