260 related articles for article (PubMed ID: 7951327)
21. Wilson disease.
Harada M
Med Electron Microsc; 2002 Jun; 35(2):61-6. PubMed ID: 12181646
[TBL] [Abstract][Full Text] [Related]
22. Functional characterization of new mutations in Wilson disease gene (ATP7B) using the yeast model.
Papur OS; Terzioglu O; Koc A
J Trace Elem Med Biol; 2015; 31():33-6. PubMed ID: 26004889
[TBL] [Abstract][Full Text] [Related]
23. Disturbed copper transport in humans. Part 2: mutations of the ATP7B gene lead to Wilson disease (WD).
Seidel J; Caca K; Schwab SG; Berr F; Wildenauer DB; Mentzel HJ; Horn N; Kauf E
Cell Mol Biol (Noisy-le-grand); 2001; 47 Online Pub():OL149-57. PubMed ID: 11936861
[TBL] [Abstract][Full Text] [Related]
24. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene.
Bull PC; Thomas GR; Rommens JM; Forbes JR; Cox DW
Nat Genet; 1993 Dec; 5(4):327-37. PubMed ID: 8298639
[TBL] [Abstract][Full Text] [Related]
25. 24 bp deletion and Ala1278 to Val mutation of the ATP7B gene in a Sardinian family with Wilson disease.
OrrĂ¹ S; Thomas G; Loizedda A; Cox DW; Contu L
Hum Mutat; 1997; 10(1):84-5. PubMed ID: 9222767
[No Abstract] [Full Text] [Related]
26. Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16.
van de Sluis BJ; Breen M; Nanji M; van Wolferen M; de Jong P; Binns MM; Pearson PL; Kuipers J; Rothuizen J; Cox DW; Wijmenga C; van Oost BA
Hum Mol Genet; 1999 Mar; 8(3):501-7. PubMed ID: 9949209
[TBL] [Abstract][Full Text] [Related]
27. Biliary excretion of copper in LEC rat after introduction of copper transporting P-type ATPase, ATP7B.
Terada K; Aiba N; Yang XL; Iida M; Nakai M; Miura N; Sugiyama T
FEBS Lett; 1999 Apr; 448(1):53-6. PubMed ID: 10217409
[TBL] [Abstract][Full Text] [Related]
28. Animal models of Wilson disease.
Medici V; Huster D
Handb Clin Neurol; 2017; 142():57-70. PubMed ID: 28433110
[TBL] [Abstract][Full Text] [Related]
29. Spectrum of mutations in the Wilson disease gene (ATP7B) in the Bulgarian population.
Todorov T; Savov A; Jelev H; Panteleeva E; Konstantinova D; Krustev Z; Mihaylova V; Tournev I; Tankova L; Tzolova N; Kremensky I
Clin Genet; 2005 Nov; 68(5):474-6. PubMed ID: 16207219
[No Abstract] [Full Text] [Related]
30. Increased mutant frequency and altered mutation spectrum of the lacI transgene in Wilson disease rats with hepatitis.
Sone H; Li YJ; Ishizuka M; Aoki Y; Nagao M
Cancer Res; 2000 Sep; 60(18):5080-6. PubMed ID: 11016632
[TBL] [Abstract][Full Text] [Related]
31. Genetic variation in the promoter and 5' UTR of the copper transporter, ATP7B, in patients with Wilson disease.
Cullen LM; Prat L; Cox DW
Clin Genet; 2003 Nov; 64(5):429-32. PubMed ID: 14616767
[TBL] [Abstract][Full Text] [Related]
32. A structural model of the copper ATPase ATP7B to facilitate analysis of Wilson disease-causing mutations and studies of the transport mechanism.
Schushan M; Bhattacharjee A; Ben-Tal N; Lutsenko S
Metallomics; 2012 Jul; 4(7):669-78. PubMed ID: 22692182
[TBL] [Abstract][Full Text] [Related]
33. [Biological regulation of copper and selective removal of copper: therapy for Wilson disease and its molecular mechanism].
Suzuki KT; Ogura Y
Yakugaku Zasshi; 2000 Oct; 120(10):899-908. PubMed ID: 11082702
[TBL] [Abstract][Full Text] [Related]
34. Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.
Buiakova OI; Xu J; Lutsenko S; Zeitlin S; Das K; Das S; Ross BM; Mekios C; Scheinberg IH; Gilliam TC
Hum Mol Genet; 1999 Sep; 8(9):1665-71. PubMed ID: 10441329
[TBL] [Abstract][Full Text] [Related]
35. Gene symbol: ATP7B. Disease: Wilson disease.
Santhosh S; Eapen CE; Shaji RV; Kurian G; Chandy GM
Hum Genet; 2006 Apr; 119(3):362. PubMed ID: 17230654
[No Abstract] [Full Text] [Related]
36. Gene symbol: ATP7B. Disease: Wilson disease.
Santosh S; Eapen CE; Shaji RV; Kurian G; Chandy GM
Hum Genet; 2006 Apr; 119(3):362. PubMed ID: 17230652
[No Abstract] [Full Text] [Related]
37. Copper-dependent trafficking of Wilson disease mutant ATP7B proteins.
Forbes JR; Cox DW
Hum Mol Genet; 2000 Aug; 9(13):1927-35. PubMed ID: 10942420
[TBL] [Abstract][Full Text] [Related]
38. A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease.
Majumdar R; Al Jumah M; Al Rajeh S; Fraser M; Al Zaben A; Awada A; Al Traif I; Paterson M
J Neurol Sci; 2000 Oct; 179(S 1-2):140-3. PubMed ID: 11054498
[TBL] [Abstract][Full Text] [Related]
39. Copper binding to the N-terminal metal-binding sites or the CPC motif is not essential for copper-induced trafficking of the human Wilson protein (ATP7B).
Cater MA; La Fontaine S; Mercer JF
Biochem J; 2007 Jan; 401(1):143-53. PubMed ID: 16939419
[TBL] [Abstract][Full Text] [Related]
40. Gene symbol: ATP7B. Disease: Wilson disease.
Santhosh S; Eapen CE; Shaji RV; Kurian G; Chandy GM
Hum Genet; 2006 Apr; 119(3):361. PubMed ID: 17230650
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]