119 related articles for article (PubMed ID: 7916735)
1. Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32.
Gregg RG; Couch F; Hogan K; Powers PA
Genomics; 1993 Jan; 15(1):107-12. PubMed ID: 7916735
[TBL] [Abstract][Full Text] [Related]
2. 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
Genomics; 1993 Jan; 15(1):185-7. PubMed ID: 8381767
[TBL] [Abstract][Full Text] [Related]
3. Assignment of the human gene for the alpha 1 subunit of the cardiac DHP-sensitive Ca2+ channel (CCHL1A1) to chromosome 12p12-pter.
Powers PA; Gregg RG; Lalley PA; Liao M; Hogan K
Genomics; 1991 Jul; 10(3):835-9. PubMed ID: 1653763
[TBL] [Abstract][Full Text] [Related]
4. Localization of the gene encoding the alpha 2/delta subunit (CACNL2A) of the human skeletal muscle voltage-dependent Ca2+ channel to chromosome 7q21-q22 by somatic cell hybrid analysis.
Powers PA; Scherer SW; Tsui LC; Gregg RG; Hogan K
Genomics; 1994 Jan; 19(1):192-3. PubMed ID: 8188232
[No Abstract] [Full Text] [Related]
5. 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
Genomics; 1996 Feb; 31(3):392-4. PubMed ID: 8838325
[TBL] [Abstract][Full Text] [Related]
6. Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36.
Su YR; Klanke CA; Houseal TW; Linn SC; Burk SE; Varvil TS; Otterud BE; Shull GE; Leppert MF; Menon AG
Genomics; 1994 Aug; 22(3):605-9. PubMed ID: 8001971
[TBL] [Abstract][Full Text] [Related]
7. Cloning of the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3).
Hogan K; Powers PA; Gregg RG
Genomics; 1994 Dec; 24(3):608-9. PubMed ID: 7713519
[No Abstract] [Full Text] [Related]
8. Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families.
Fontaine B; Vale-Santos J; Jurkat-Rott K; Reboul J; Plassart E; Rime CS; Elbaz A; Heine R; Guimarães J; Weissenbach J
Nat Genet; 1994 Mar; 6(3):267-72. PubMed ID: 8012389
[TBL] [Abstract][Full Text] [Related]
9. Refined localization of the alpha 1-subunit of the skeletal muscle L-type voltage-dependent calcium channel (CACNL1A3) to human chromosome 1q32 by in situ hybridization.
Iles DE; Segers B; Olde Weghuis D; Suijkerbuijk R; Mikala G; Schwartz A; Wieringa B
Genomics; 1994 Feb; 19(3):561-3. PubMed ID: 8188298
[TBL] [Abstract][Full Text] [Related]
10. Isolation and characterization of a human pseudogene for the regulatory subunit RI alpha of cAMP-dependent protein kinases and its sublocalization on chromosome 1.
Solberg R; Sandberg M; Spurkland A; Jahnsen T
Genomics; 1993 Mar; 15(3):591-7. PubMed ID: 8468054
[TBL] [Abstract][Full Text] [Related]
11. Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel.
Mikami A; Imoto K; Tanabe T; Niidome T; Mori Y; Takeshima H; Narumiya S; Numa S
Nature; 1989 Jul; 340(6230):230-3. PubMed ID: 2474130
[TBL] [Abstract][Full Text] [Related]
12. Molecular cloning of human hippocalcin cDNA and chromosomal mapping of its gene.
Takamatsu K; Kobayashi M; Saitoh S; Fujishiro M; Noguchi T
Biochem Biophys Res Commun; 1994 Apr; 200(1):606-11. PubMed ID: 8166736
[TBL] [Abstract][Full Text] [Related]
13. The gene for the alpha 1 subunit of the skeletal muscle dihydropyridine-sensitive calcium channel (Cchl1a3) maps to mouse chromosome 1.
Chin H; Krall M; Kim HL; Kozak CA; Mock B
Genomics; 1992 Dec; 14(4):1089-91. PubMed ID: 1335956
[TBL] [Abstract][Full Text] [Related]
14. The human L35a ribosomal protein (RPL35A) gene is located at chromosome band 3q29-qter.
Colombo P; Read M; Fried M
Genomics; 1996 Feb; 32(1):148-50. PubMed ID: 8786106
[TBL] [Abstract][Full Text] [Related]
15. Chromosome assignment by polymerase chain reaction techniques: assignment of the oncogene FGF-5 to human chromosome 4.
Dionne CA; Kaplan R; Seuánez H; O'Brien SJ; Jaye M
Biotechniques; 1990 Feb; 8(2):190-4. PubMed ID: 2317376
[TBL] [Abstract][Full Text] [Related]
16. Human bradykinin B2 receptor: nucleotide sequence analysis and assignment to chromosome 14.
Powell SJ; Slynn G; Thomas C; Hopkins B; Briggs I; Graham A
Genomics; 1993 Feb; 15(2):435-8. PubMed ID: 7916737
[TBL] [Abstract][Full Text] [Related]
17. Assignment of the human type I IMP dehydrogenase gene (IMPDH1) to chromosome 7q31.3-q32).
Gu JJ; Kaiser-Rogers K; Rao K; Mitchell BS
Genomics; 1994 Nov; 24(1):179-81. PubMed ID: 7896275
[TBL] [Abstract][Full Text] [Related]
18. Structure of the human gene (COX6A2) for the heart/muscle isoform of cytochrome c oxidase subunit VIa and its chromosomal location in humans, mice, and cattle.
Bachman NJ; Riggs PK; Siddiqui N; Makris GJ; Womack JE; Lomax MI
Genomics; 1997 May; 42(1):146-51. PubMed ID: 9177785
[TBL] [Abstract][Full Text] [Related]
19. A cluster of three novel Ca2+ channel gamma subunit genes on chromosome 19q13.4: evolution and expression profile of the gamma subunit gene family.
Burgess DL; Gefrides LA; Foreman PJ; Noebels JL
Genomics; 2001 Feb; 71(3):339-50. PubMed ID: 11170751
[TBL] [Abstract][Full Text] [Related]
20. Molecular cloning of human G alpha q cDNA and chromosomal localization of the G alpha q gene (GNAQ) and a processed pseudogene.
Dong Q; Shenker A; Way J; Haddad BR; Lin K; Hughes MR; McBride OW; Spiegel AM; Battey J
Genomics; 1995 Dec; 30(3):470-75. PubMed ID: 8825633
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
