McClatchey AI - Search Results

1

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: mcclatchey ai. 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.

2

Detection by PCR of the VNTR polymorphism at D4S95.

Allitto BA, Horn GT, Altherr MR, Richards B, McClatchey AI, Wasmuth JJ, Gusella JF. Allitto BA, et al. Among authors: mcclatchey ai. Nucleic Acids Res. 1991 Jul 25;19(14):4015. doi: 10.1093/nar/19.14.4015-a. Nucleic Acids Res. 1991. PMID: 1677758 Free PMC article.

3

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

4

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: mcclatchey ai. Genomics. 1992 Oct;14(2):350-6. doi: 10.1016/s0888-7543(05)80225-3. Genomics. 1992. PMID: 1427851

5

The genomic structure of the human skeletal muscle sodium channel gene.

McClatchey AI, Lin CS, Wang J, Hoffman EP, Rojas C, Gusella JF. McClatchey AI, et al. Hum Mol Genet. 1992 Oct;1(7):521-7. doi: 10.1093/hmg/1.7.521. Hum Mol Genet. 1992. PMID: 1339144

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: mcclatchey ai. Genomics. 1992 May;13(1):75-80. doi: 10.1016/0888-7543(92)90204-6. Genomics. 1992. PMID: 1533609 Free article.

7

The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid beta-protein gene.

Tanzi RE, St George-Hyslop PH, Haines JL, Polinsky RJ, Nee L, Foncin JF, Neve RL, McClatchey AI, Conneally PM, Gusella JF. Tanzi RE, et al. Among authors: mcclatchey ai. Nature. 1987 Sep 10-16;329(6135):156-7. doi: 10.1038/329156a0. Nature. 1987. PMID: 2888020

8

Modification of the Na+ current conducted by the rat skeletal muscle alpha subunit by coexpression with a human brain beta subunit.

Cannon SC, McClatchey AI, Gusella JF. Cannon SC, et al. Among authors: mcclatchey ai. Pflugers Arch. 1993 Apr;423(1-2):155-7. doi: 10.1007/BF00374974. Pflugers Arch. 1993. PMID: 7683789

9

Protease inhibitor domain encoded by an amyloid protein precursor mRNA associated with Alzheimer's disease.

Tanzi RE, McClatchey AI, Lamperti ED, Villa-Komaroff L, Gusella JF, Neve RL. Tanzi RE, et al. Among authors: mcclatchey ai. Nature. 1988 Feb 11;331(6156):528-30. doi: 10.1038/331528a0. Nature. 1988. PMID: 2893290

10

The cloning and expression of a sodium channel beta 1-subunit cDNA from human brain.

McClatchey AI, Cannon SC, Slaugenhaupt SA, Gusella JF. McClatchey AI, et al. Hum Mol Genet. 1993 Jun;2(6):745-9. doi: 10.1093/hmg/2.6.745. Hum Mol Genet. 1993. PMID: 8394762

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