NS22031/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

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Subject: NS22031/NS/NINDS NIH HHS/United States[Grants and - PubMed

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Results by year

Year	Number of Results
1986	1
1987	8
1988	6
1989	4
1990	4
1991	9
1992	3
1993	4
1995	2
1999	1
2024	0

42 results

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Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism.

Leeflang EP, Tavaré S, Marjoram P, Neal CO, Srinidhi J, MacFarlane H, MacDonald ME, Gusella JF, de Young M, Wexler NS, Arnheim N. Leeflang EP, et al. Hum Mol Genet. 1999 Feb;8(2):173-83. doi: 10.1093/hmg/8.2.173. Hum Mol Genet. 1999. PMID: 9931325

Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum.

Leeflang EP, Zhang L, Tavaré S, Hubert R, Srinidhi J, MacDonald ME, Myers RH, de Young M, Wexler NS, Gusella JF, et al. Leeflang EP, et al. Hum Mol Genet. 1995 Sep;4(9):1519-26. doi: 10.1093/hmg/4.9.1519. Hum Mol Genet. 1995. PMID: 8541834

Normal and expanded Huntington's disease gene alleles produce distinguishable proteins due to translation across the CAG repeat.

Persichetti F, Ambrose CM, Ge P, McNeil SM, Srinidhi J, Anderson MA, Jenkins B, Barnes GT, Duyao MP, Kanaley L, et al. Persichetti F, et al. Mol Med. 1995 May;1(4):374-83. Mol Med. 1995. PMID: 8521295 Free PMC article.

Molecular genetics of Huntington's disease.

Gusella JF, MacDonald ME, Ambrose CM, Duyao MP. Gusella JF, et al. Arch Neurol. 1993 Nov;50(11):1157-63. doi: 10.1001/archneur.1993.00540110037003. Arch Neurol. 1993. PMID: 8215974 Review.

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group.

[No authors listed] [No authors listed] Cell. 1993 Mar 26;72(6):971-83. doi: 10.1016/0092-8674(93)90585-e. Cell. 1993. PMID: 8458085

A genetic linkage map of chromosome 21: a look at meiotic phenomena.

Haines JL, Guillemette W, Rosen D, Brown R Jr, Donaldson D, Patterson D. Haines JL, et al. Prog Clin Biol Res. 1993;384:51-61. Prog Clin Biol Res. 1993. PMID: 8115407 Review.

A genetic linkage map of the chromosome 4 short arm.

Locke PA, MacDonald ME, Srinidhi J, Gilliam TC, Tanzi RE, Conneally PM, Wexler NS, Haines JL, Gusella JF. Locke PA, et al. Somat Cell Mol Genet. 1993 Jan;19(1):95-101. doi: 10.1007/BF01233958. Somat Cell Mol Genet. 1993. PMID: 8096345

An 86-bp VNTR within IDUA is the basis of the D4S111 polymorphic locus.

Scott HS, Nelson PV, MacDonald ME, Gusella JF, Hopwood JJ, Morris CP. Scott HS, et al. Genomics. 1992 Dec;14(4):1118-20. doi: 10.1016/s0888-7543(05)80145-4. Genomics. 1992. PMID: 1478658 No abstract available.

Construction of a GT polymorphism map of human 9q.

Kwiatkowski DJ, Henske EP, Weimer K, Ozelius L, Gusella JF, Haines J. Kwiatkowski DJ, et al. Genomics. 1992 Feb;12(2):229-40. doi: 10.1016/0888-7543(92)90370-8. Genomics. 1992. PMID: 1339384

Chromosome 21 genetic linkage data set based on the Venezuelan reference pedigree.

Haines JL, Trofatter JA, Tanzi RE, Watkins P, Wexler NS, Conneally PM, Gusella JF. Haines JL, et al. Cytogenet Cell Genet. 1992;59(2-3):88-9. doi: 10.1159/000133208. Cytogenet Cell Genet. 1992. PMID: 1346592 No abstract available.

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