156 related articles for article (PubMed ID: 12119109)
1. Physical mapping and characterization of the human Na,K-ATPase isoform, ATP1A4.
Keryanov S; Gardner KL
Gene; 2002 Jun; 292(1-2):151-66. PubMed ID: 12119109
[TBL] [Abstract][Full Text] [Related]
2. Molecular cloning and characterization of porcine Na⁺/K⁺-ATPase isoform α4.
Larsen K; Henriksen C; Kristensen KK; Momeni J; Farajzadeh L
Biochimie; 2019 Mar; 158():149-155. PubMed ID: 30633937
[TBL] [Abstract][Full Text] [Related]
3. The Na,K-ATPase alpha4 gene (Atp1a4) encodes a ouabain-resistant alpha subunit and is tightly linked to the alpha2 gene (Atp1a2) on mouse chromosome 1.
Underhill DA; Canfield VA; Dahl JP; Gros P; Levenson R
Biochemistry; 1999 Nov; 38(45):14746-51. PubMed ID: 10555956
[TBL] [Abstract][Full Text] [Related]
4. A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
Fernandez DM; Hand CK; Sweeney BJ; Parfrey NA
Headache; 2008 Jan; 48(1):101-8. PubMed ID: 18184292
[TBL] [Abstract][Full Text] [Related]
5. The transcription factor CREMtau and cAMP regulate promoter activity of the Na,K-ATPase alpha4 isoform.
Rodova M; Nguyen AN; Blanco G
Mol Reprod Dev; 2006 Nov; 73(11):1435-47. PubMed ID: 16894555
[TBL] [Abstract][Full Text] [Related]
6. Genomic organization of the human ATP1AL1 gene encoding a ouabain-sensitive H,K-ATPase.
Sverdlov VE; Kostina MB; Modyanov NN
Genomics; 1996 Mar; 32(3):317-27. PubMed ID: 8838794
[TBL] [Abstract][Full Text] [Related]
7. Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene.
White KE; Lorenz B; Evans WE; Meitinger T; Strom TM; Econs MJ
Gene; 2000 Apr; 246(1-2):347-56. PubMed ID: 10767557
[TBL] [Abstract][Full Text] [Related]
8. Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine.
Vanmolkot KR; Kors EE; Turk U; Turkdogan D; Keyser A; Broos LA; Kia SK; van den Heuvel JJ; Black DF; Haan J; Frants RR; Barone V; Ferrari MD; Casari G; Koenderink JB; van den Maagdenberg AM
Eur J Hum Genet; 2006 May; 14(5):555-60. PubMed ID: 16538223
[TBL] [Abstract][Full Text] [Related]
9. Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine.
Tonelli A; Gallanti A; Bersano A; Cardin V; Ballabio E; Airoldi G; Redaelli F; Candelise L; Bresolin N; Bassi MT
Clin Genet; 2007 Dec; 72(6):517-23. PubMed ID: 17877748
[TBL] [Abstract][Full Text] [Related]
10. Evolution of the Na,K- and H,K-ATPase beta subunit gene family: structure of the murine Na,K-ATPase beta 2 subunit gene.
Shyjan AW; Canfield VA; Levenson R
Genomics; 1991 Oct; 11(2):435-42. PubMed ID: 1663071
[TBL] [Abstract][Full Text] [Related]
11. Human homologue of a gene mutated in the slow Wallerian degeneration (C57BL/Wld(s)) mouse.
Fernando FS; Conforti L; Tosi S; Smith AD; Coleman MP
Gene; 2002 Feb; 284(1-2):23-9. PubMed ID: 11891043
[TBL] [Abstract][Full Text] [Related]
12. A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.
Kaunisto MA; Harno H; Vanmolkot KR; Gargus JJ; Sun G; Hämäläinen E; Liukkonen E; Kallela M; van den Maagdenberg AM; Frants RR; Färkkilä M; Palotie A; Wessman M
Neurogenetics; 2004 Jun; 5(2):141-6. PubMed ID: 15133718
[TBL] [Abstract][Full Text] [Related]
13. ATP1A2 mutations in 11 families with familial hemiplegic migraine.
Riant F; De Fusco M; Aridon P; Ducros A; Ploton C; Marchelli F; Maciazek J; Bousser MG; Casari G; Tournier-Lasserve E
Hum Mutat; 2005 Sep; 26(3):281. PubMed ID: 16088919
[TBL] [Abstract][Full Text] [Related]
14. A putative fourth Na+,K(+)-ATPase alpha-subunit gene is expressed in testis.
Shamraj OI; Lingrel JB
Proc Natl Acad Sci U S A; 1994 Dec; 91(26):12952-6. PubMed ID: 7809153
[TBL] [Abstract][Full Text] [Related]
15. Human gastric (H+ + K+)-ATPase gene. Similarity to (Na+ + K+)-ATPase genes in exon/intron organization but difference in control region.
Maeda M; Oshiman K; Tamura S; Futai M
J Biol Chem; 1990 Jun; 265(16):9027-32. PubMed ID: 2160952
[TBL] [Abstract][Full Text] [Related]
16. Genomic organization and tissue-specific expression of splice variants of mouse organic anion transporting polypeptide 2.
Ogura K; Choudhuri S; Klaassen CD
Biochem Biophys Res Commun; 2001 Feb; 281(2):431-9. PubMed ID: 11181066
[TBL] [Abstract][Full Text] [Related]
17. First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.
Vanmolkot KR; Stam AH; Raman A; Koenderink JB; de Vries B; van den Boogerd EH; van Vark J; van den Heuvel JJ; Bajaj N; Terwindt GM; Haan J; Frants RR; Ferrari MD; van den Maagdenberg AM
Eur J Hum Genet; 2007 Aug; 15(8):884-8. PubMed ID: 17473835
[TBL] [Abstract][Full Text] [Related]
18. Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2.
Kors EE; Vanmolkot KR; Haan J; Kheradmand Kia S; Stroink H; Laan LA; Gill DS; Pascual J; van den Maagdenberg AM; Frants RR; Ferrari MD
Neuropediatrics; 2004 Oct; 35(5):293-6. PubMed ID: 15534763
[TBL] [Abstract][Full Text] [Related]
19. Genomic organization and chromosomal localization of the Asna1 gene, a mouse homologue of a bacterial arsenic-translocating ATPase gene.
Bhattacharjee H; Ho YS; Rosen BP
Gene; 2001 Jul; 272(1-2):291-9. PubMed ID: 11470536
[TBL] [Abstract][Full Text] [Related]
20. Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Vanmolkot KR; Kors EE; Hottenga JJ; Terwindt GM; Haan J; Hoefnagels WA; Black DF; Sandkuijl LA; Frants RR; Ferrari MD; van den Maagdenberg AM
Ann Neurol; 2003 Sep; 54(3):360-6. PubMed ID: 12953268
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]