Gregg RG - Search Results

1

Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology.

Wilson GR, Sim JC, McLean C, Giannandrea M, Galea CA, Riseley JR, Stephenson SE, Fitzpatrick E, Haas SA, Pope K, Hogan KJ, Gregg RG, Bromhead CJ, Wargowski DS, Lawrence CH, James PA, Churchyard A, Gao Y, Phelan DG, Gillies G, Salce N, Stanford L, Marsh AP, Mignogna ML, Hayflick SJ, Leventer RJ, Delatycki MB, Mellick GD, Kalscheuer VM, D'Adamo P, Bahlo M, Amor DJ, Lockhart PJ. Wilson GR, et al. Among authors: gregg rg. Am J Hum Genet. 2014 Dec 4;95(6):729-35. doi: 10.1016/j.ajhg.2014.10.015. Epub 2014 Nov 26. Am J Hum Genet. 2014. PMID: 25434005 Free PMC article.

2

The structure of the gene encoding the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3).

Hogan K, Gregg RG, Powers PA. Hogan K, et al. Among authors: gregg rg. Genomics. 1996 Feb 1;31(3):392-4. doi: 10.1006/geno.1996.0066. Genomics. 1996. PMID: 8838325

3

A cysteine-for-arginine substitution (R614C) in the human skeletal muscle calcium release channel cosegregates with malignant hyperthermia.

Hogan K, Couch F, Powers PA, Gregg RG. Hogan K, et al. Among authors: gregg rg. Anesth Analg. 1992 Sep;75(3):441-8. doi: 10.1213/00000539-199209000-00022. Anesth Analg. 1992. PMID: 1510267

4

Linkage mapping of the human gene for the alpha 1 subunit of the cardiac DHP-sensitive Ca2+ channel (CACNL1A1) to chromosome 12p13.2-pter using a dinucleotide repeat.

Powers PA, Gregg RG, Hogan K. Powers PA, et al. Among authors: gregg rg. Genomics. 1992 Sep;14(1):206-7. doi: 10.1016/s0888-7543(05)80312-x. Genomics. 1992. PMID: 1330882 No abstract available.

5

Assignment of the human gene for the beta subunit of the voltage-dependent calcium channel (CACNLB1) to chromosome 17 using somatic cell hybrids and linkage mapping.

Gregg RG, Powers PA, Hogan K. Gregg RG, et al. Genomics. 1993 Jan;15(1):185-7. doi: 10.1006/geno.1993.1029. Genomics. 1993. PMID: 8381767

6

Skeletal muscle and brain isoforms of a beta-subunit of human voltage-dependent calcium channels are encoded by a single gene.

Powers PA, Liu S, Hogan K, Gregg RG. Powers PA, et al. Among authors: gregg rg. J Biol Chem. 1992 Nov 15;267(32):22967-72. J Biol Chem. 1992. PMID: 1385409 Free article.

7

G to A polymorphism in the CACNLG gene.

Olckers A, Jedlicka AE, Powers PA, Hogan K, Gregg RG, Levitt RC. Olckers A, et al. Among authors: gregg rg. Hum Mol Genet. 1993 Dec;2(12):2198. doi: 10.1093/hmg/2.12.2198-a. Hum Mol Genet. 1993. PMID: 8111396 No abstract available.

8

Molecular characterization of the gene encoding the gamma subunit of the human skeletal muscle 1,4-dihydropyridine-sensitive Ca2+ channel (CACNLG), cDNA sequence, gene structure, and chromosomal location.

Powers PA, Liu S, Hogan K, Gregg RG. Powers PA, et al. Among authors: gregg rg. J Biol Chem. 1993 May 5;268(13):9275-9. J Biol Chem. 1993. PMID: 8387489 Free article.

9

Dinucleotide repeat polymorphism at the D10S178 locus.

Couch FJ, Gregg RG, McCarthy TV, Hogan K. Couch FJ, et al. Among authors: gregg rg. Nucleic Acids Res. 1992 Mar 25;20(6):1431. Nucleic Acids Res. 1992. PMID: 1561111 Free PMC article. No abstract available.

10

Dinucleotide repeat polymorphism at the D10S179 locus.

Couch FJ, McCarthy TV, Hogan K, Gregg RG. Couch FJ, et al. Among authors: gregg rg. Nucleic Acids Res. 1992 Mar 25;20(6):1431. Nucleic Acids Res. 1992. PMID: 1561112 Free PMC article. No abstract available.

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