Barnes G - Search Results

1

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: barnes g. Mol Cell Probes. 1992 Dec;6(6):513-20. doi: 10.1016/0890-8508(92)90048-3. Mol Cell Probes. 1992. PMID: 1480191

2

Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat.

Ambrose CM, Duyao MP, Barnes G, Bates GP, Lin CS, Srinidhi J, Baxendale S, Hummerich H, Lehrach H, Altherr M, Wasmuth J, Buckler A, Church D, Housman D, Berks M, Micklem G, Durbin R, Dodge A, Read A, Gusella J, MacDonald ME. Ambrose CM, et al. Among authors: barnes g. Somat Cell Mol Genet. 1994 Jan;20(1):27-38. doi: 10.1007/BF02257483. Somat Cell Mol Genet. 1994. PMID: 8197474

3

A dinucleotide repeat polymorphism at the D4S127 locus.

Taylor SA, Barnes GT, MacDonald ME, Gusella JF. Taylor SA, et al. Among authors: barnes gt. 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

Mouse Huntington's disease gene homolog (Hdh).

Barnes GT, Duyao MP, Ambrose CM, McNeil S, Persichetti F, Srinidhi J, Gusella JF, MacDonald ME. Barnes GT, et al. Somat Cell Mol Genet. 1994 Mar;20(2):87-97. doi: 10.1007/BF02290678. Somat Cell Mol Genet. 1994. PMID: 8009370

5

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. Among authors: barnes g. Nat Genet. 1992 May;1(2):99-103. doi: 10.1038/ng0592-99. Nat Genet. 1992. PMID: 1302016 Review.

6

Sequence-tagged sites (STSs) spanning 4p16.3 and the Huntington disease candidate region.

Gusella JF, Altherr MR, McClatchey AI, Doucette-Stamm LA, Tagle D, Plummer S, Groot N, Barnes G, Hummerich H, Collins FS, et al. Gusella JF, et al. Among authors: barnes g. Genomics. 1992 May;13(1):75-80. doi: 10.1016/0888-7543(92)90204-6. Genomics. 1992. PMID: 1533609 Free article.

7

Reduced penetrance of the Huntington's disease mutation.

McNeil SM, Novelletto A, Srinidhi J, Barnes G, Kornbluth I, Altherr MR, Wasmuth JJ, Gusella JF, MacDonald ME, Myers RH. McNeil SM, et al. Among authors: barnes g. Hum Mol Genet. 1997 May;6(5):775-9. doi: 10.1093/hmg/6.5.775. Hum Mol Genet. 1997. PMID: 9158152

8

Differential expression of normal and mutant Huntington's disease gene alleles.

Persichetti F, Carlee L, Faber PW, McNeil SM, Ambrose CM, Srinidhi J, Anderson M, Barnes GT, Gusella JF, MacDonald ME. Persichetti F, et al. Among authors: barnes gt. Neurobiol Dis. 1996;3(3):183-90. doi: 10.1006/nbdi.1996.0018. Neurobiol Dis. 1996. PMID: 8980018

9

Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains.

Persichetti F, Srinidhi J, Kanaley L, Ge P, Myers RH, D'Arrigo K, Barnes GT, MacDonald ME, Vonsattel JP, Gusella JF, et al. Persichetti F, et al. Among authors: barnes gt. Neurobiol Dis. 1994 Dec;1(3):159-66. doi: 10.1006/nbdi.1994.0019. Neurobiol Dis. 1994. PMID: 9173995 Free article.

10

Exon trapping and sequence-based methods of gene finding in transcript mapping of human 4p16.3.

Pribill I, Barnes GT, Chen J, Church D, Buckler A, Baxendale S, Bates GP, Lehrach H, Gusella MJ, Duyao MP, Ambrose CM, Gusella JF, MacDonald ME. Pribill I, et al. Among authors: barnes gt. Somat Cell Mol Genet. 1997 Nov;23(6):413-27. doi: 10.1007/BF02673751. Somat Cell Mol Genet. 1997. PMID: 9661704

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