MacDonald ME - Search Results

1

A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study.

Li JL, Hayden MR, Almqvist EW, Brinkman RR, Durr A, Dodé C, Morrison PJ, Suchowersky O, Ross CA, Margolis RL, Rosenblatt A, Gómez-Tortosa E, Cabrero DM, Novelletto A, Frontali M, Nance M, Trent RJ, McCusker E, Jones R, Paulsen JS, Harrison M, Zanko A, Abramson RK, Russ AL, Knowlton B, Djoussé L, Mysore JS, Tariot S, Gusella MF, Wheeler VC, Atwood LD, Cupples LA, Saint-Hilaire M, Cha JH, Hersch SM, Koroshetz WJ, Gusella JF, MacDonald ME, Myers RH. Li JL, et al. Among authors: macdonald me. Am J Hum Genet. 2003 Sep;73(3):682-7. doi: 10.1086/378133. Epub 2003 Aug 1. Am J Hum Genet. 2003. PMID: 12900792 Free PMC article.

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

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.

5

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.

6

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

7

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

8

Detection by PCR of a VNTR polymorphism at D4S43.

Horn GT, McClatchey AI, Richards B, MacDonald ME, Gusella JF. Horn GT, et al. Among authors: macdonald me. Nucleic Acids Res. 1991 Sep 11;19(17):4772. doi: 10.1093/nar/19.17.4772. Nucleic Acids Res. 1991. PMID: 1679922 Free PMC article.

9

Complex patterns of linkage disequilibrium in the Huntington disease region.

MacDonald ME, Lin C, Srinidhi L, Bates G, Altherr M, Whaley WL, Lehrach H, Wasmuth J, Gusella JF. MacDonald ME, et al. Am J Hum Genet. 1991 Oct;49(4):723-34. Am J Hum Genet. 1991. PMID: 1680285 Free PMC article.

10

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. Among authors: macdonald me. Somat Cell Mol Genet. 1991 Sep;17(5):481-8. doi: 10.1007/BF01233172. Somat Cell Mol Genet. 1991. PMID: 1684879

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