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

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

1

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

2

Molecular genetics of human chromosome 21.

Watkins PC, Tanzi RE, Cheng SV, Gusella JF. Watkins PC, et al. J Med Genet. 1987 May;24(5):257-70. doi: 10.1136/jmg.24.5.257. J Med Genet. 1987. PMID: 2884319 Free PMC article. Review.

3

Homozygotes for Huntington's disease.

Wexler NS, Young AB, Tanzi RE, Travers H, Starosta-Rubinstein S, Penney JB, Snodgrass SR, Shoulson I, Gomez F, Ramos Arroyo MA, et al. Wexler NS, et al. Nature. 1987 Mar 12-18;326(6109):194-7. doi: 10.1038/326194a0. Nature. 1987. PMID: 2881213 Free article.

4

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.

5

Molecular approaches to hereditary diseases of the nervous system: Huntington's disease as a paradigm.

Wexler NS, Rose EA, Housman DE. Wexler NS, et al. Annu Rev Neurosci. 1991;14:503-29. doi: 10.1146/annurev.ne.14.030191.002443. Annu Rev Neurosci. 1991. PMID: 1827708 Review. No abstract available.

6

Genetic linkage map of human chromosome 21.

Tanzi RE, Haines JL, Watkins PC, Stewart GD, Wallace MR, Hallewell R, Wong C, Wexler NS, Conneally PM, Gusella JF. Tanzi RE, et al. Genomics. 1988 Aug;3(2):129-36. doi: 10.1016/0888-7543(88)90143-7. Genomics. 1988. PMID: 2906323

7

Molecular genetic strategies to investigate Huntington's disease.

Gilliam TC, Gusella JF, Lehrach H. Gilliam TC, et al. Adv Neurol. 1988;48:17-29. Adv Neurol. 1988. PMID: 2891255 Review. No abstract available.

8

Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.

Whaley WL, Michiels F, MacDonald ME, Romano D, Zimmer M, Smith B, Leavitt J, Bucan M, Haines JL, Gilliam TC, et al. Whaley WL, et al. Nucleic Acids Res. 1988 Dec 23;16(24):11769-80. doi: 10.1093/nar/16.24.11769. Nucleic Acids Res. 1988. PMID: 2905444 Free PMC article.

9

New DNA markers in the Huntington's disease gene candidate region.

Lin CS, Altherr M, Bates G, Whaley WL, Read AP, Harris R, Lehrach H, Wasmuth JJ, Gusella JF, MacDonald ME. Lin CS, et al. Somat Cell Mol Genet. 1991 Sep;17(5):481-8. doi: 10.1007/BF01233172. Somat Cell Mol Genet. 1991. PMID: 1684879

10

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.

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