MacDonald ME - Search Results

1

MacDonald ME, Gines S, Gusella JF, Wheeler VC. MacDonald ME, et al. Neuromolecular Med. 2003;4(1-2):7-20. doi: 10.1385/NMM:4:1-2:7. Neuromolecular Med. 2003. PMID: 14528049 Review.

2

The Huntington's disease candidate region exhibits many different haplotypes.

MacDonald ME, Novelletto A, Lin C, Tagle D, Barnes G, Bates G, Taylor S, Allitto B, Altherr M, Myers R, et al. MacDonald ME, et al. Nat Genet. 1992 May;1(2):99-103. doi: 10.1038/ng0592-99. Nat Genet. 1992. PMID: 1302016 Review.

3

A dinucleotide repeat polymorphism at the D4S127 locus.

Taylor SA, Barnes GT, MacDonald ME, Gusella JF. Taylor SA, et al. Among authors: macdonald me. Hum Mol Genet. 1992 May;1(2):142. doi: 10.1093/hmg/1.2.142-a. Hum Mol Genet. 1992. PMID: 1339471 No abstract available.

4

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

5

A recombination event that redefines the Huntington disease region.

Snell RG, Thompson LM, Tagle DA, Holloway TL, Barnes G, Harley HG, Sandkuijl LA, MacDonald ME, Collins FS, Gusella JF, et al. Snell RG, et al. Among authors: macdonald me. Am J Hum Genet. 1992 Aug;51(2):357-62. Am J Hum Genet. 1992. PMID: 1386495 Free PMC article.

6

Radiation hybrid map spanning the Huntington disease gene region of chromosome 4.

Altherr MR, Plummer S, Bates G, MacDonald M, Taylor S, Lehrach H, Frischauf AM, Gusella JF, Boehnke M, Wasmuth JJ. Altherr MR, et al. Genomics. 1992 Aug;13(4):1040-6. doi: 10.1016/0888-7543(92)90017-m. Genomics. 1992. PMID: 1387106 Free article.

7

The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p.

Youngman S, Bates GP, Williams S, McClatchey AI, Baxendale S, Sedlacek Z, Altherr M, Wasmuth JJ, MacDonald ME, Gusella JF, et al. Youngman S, et al. Among authors: macdonald me. Genomics. 1992 Oct;14(2):350-6. doi: 10.1016/s0888-7543(05)80225-3. Genomics. 1992. PMID: 1427851

8

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. Among authors: macdonald me. Genomics. 1992 Dec;14(4):1118-20. doi: 10.1016/s0888-7543(05)80145-4. Genomics. 1992. PMID: 1478658 No abstract available.

9

Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4.

Allitto BA, McClatchey AI, Barnes G, Altherr M, Wasmuth J, Frischauf AM, MacDonald ME, Gusella J. Allitto BA, et al. Among authors: macdonald me. Mol Cell Probes. 1992 Dec;6(6):513-20. doi: 10.1016/0890-8508(92)90048-3. Mol Cell Probes. 1992. PMID: 1480191

10

Linkage, but not gene order, of homologous loci, including alpha-L-iduronidase (Idua), is conserved in the Huntington disease region of the mouse and human genomes.

Koizumi T, MacDonald M, Búcan M, Hopwood JJ, Morris CP, Scott HS, Gusella JF, Nadeau JH. Koizumi T, et al. Mamm Genome. 1992;3(1):23-7. doi: 10.1007/BF00355837. Mamm Genome. 1992. PMID: 1533802

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