Cheng SV - Search Results

1

Recombination events suggest potential sites for the Huntington's disease gene.

MacDonald ME, Haines JL, Zimmer M, Cheng SV, Youngman S, Whaley WL, Wexler N, Bucan M, Allitto BA, Smith B, et al. MacDonald ME, et al. Among authors: cheng sv. Neuron. 1989 Aug;3(2):183-90. doi: 10.1016/0896-6273(89)90031-7. Neuron. 1989. PMID: 2576211

2

Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease gene.

Cheng SV, Martin GR, Nadeau JH, Haines JL, Bucan M, Kozak CA, MacDonald ME, Lockyer JL, Ledley FD, Woo SL, et al. Cheng SV, et al. Genomics. 1989 Apr;4(3):419-26. doi: 10.1016/0888-7543(89)90349-2. Genomics. 1989. PMID: 2523855

3

Clustering of multiallele DNA markers near the Huntington's disease gene.

MacDonald ME, Cheng SV, Zimmer M, Haines JL, Poustka A, Allitto B, Smith B, Whaley WL, Romano DM, Jagadeesh J, et al. MacDonald ME, et al. Among authors: cheng sv. J Clin Invest. 1989 Sep;84(3):1013-6. doi: 10.1172/JCI114222. J Clin Invest. 1989. PMID: 2569477 Free PMC article.

4

A DNA segment encoding two genes very tightly linked to Huntington's disease.

Gilliam TC, Bucan M, MacDonald ME, Zimmer M, Haines JL, Cheng SV, Pohl TM, Meyers RH, Whaley WL, Allitto BA, et al. Gilliam TC, et al. Among authors: cheng sv. Science. 1987 Nov 13;238(4829):950-2. doi: 10.1126/science.2890209. Science. 1987. PMID: 2890209

5

The alpha-subunit of the skeletal muscle sodium channel is encoded proximal to Tk-1 on mouse chromosome 11.

Ambrose C, Cheng S, Fontaine B, Nadeau JH, MacDonald M, Gusella JF. Ambrose C, et al. Mamm Genome. 1992;3(3):151-5. doi: 10.1007/BF00352459. Mamm Genome. 1992. PMID: 1352160

6

Molecular genetics of Huntington's disease.

Gusella JF, Gilliam TC, Tanzi RE, MacDonald ME, Cheng SV, Wallace M, Haines J, Conneally PM, Wexler NS. Gusella JF, et al. Among authors: cheng sv. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:359-64. doi: 10.1101/sqb.1986.051.01.043. Cold Spring Harb Symp Quant Biol. 1986. PMID: 2884064

7

Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere.

Gilliam TC, Tanzi RE, Haines JL, Bonner TI, Faryniarz AG, Hobbs WJ, MacDonald ME, Cheng SV, Folstein SE, Conneally PM, et al. Gilliam TC, et al. Among authors: cheng sv. Cell. 1987 Aug 14;50(4):565-71. doi: 10.1016/0092-8674(87)90029-8. Cell. 1987. PMID: 2886227

8

Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17.

Cheng SV, Nadeau JH, Tanzi RE, Watkins PC, Jagadesh J, Taylor BA, Haines JL, Sacchi N, Gusella JF. Cheng SV, et al. Proc Natl Acad Sci U S A. 1988 Aug;85(16):6032-6. doi: 10.1073/pnas.85.16.6032. Proc Natl Acad Sci U S A. 1988. PMID: 2901095 Free PMC article.

9

Molecular genetics of human chromosome 4.

Gusella JA, Gilliam TC, MacDonald ME, Cheng SV, Tanzi RE. Gusella JA, et al. Among authors: cheng sv. J Med Genet. 1986 Jun;23(3):193-9. doi: 10.1136/jmg.23.3.193. J Med Genet. 1986. PMID: 2941587 Free PMC article.

10

Chromosomal localization of the mouse homolog of the Huntington's disease linked G8 (D4S10) marker.

Cheng SV, Gross Lugo T, Tanzi RE, Whitney JB 3rd, Fournier RE, Gusella JF. Cheng SV, et al. DNA. 1987 Oct;6(5):401-7. doi: 10.1089/dna.1987.6.401. DNA. 1987. PMID: 2890502

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