305 related articles for article (PubMed ID: 8490646)
21. Molecular basis of the brindled mouse mutant (Mo(br)): a murine model of Menkes disease.
Grimes A; Hearn CJ; Lockhart P; Newgreen DF; Mercer JF
Hum Mol Genet; 1997 Jul; 6(7):1037-42. PubMed ID: 9215672
[TBL] [Abstract][Full Text] [Related]
22. Genomic organization of the mottled gene, the mouse homologue of the human Menkes disease gene.
Cecchi C; Avner P
Genomics; 1996 Oct; 37(1):96-104. PubMed ID: 8921375
[TBL] [Abstract][Full Text] [Related]
23. Screening of 383 unrelated patients affected with Menkes disease and finding of 57 gross deletions in ATP7A.
Tümer Z; Birk Møller L; Horn N
Hum Mutat; 2003 Dec; 22(6):457-64. PubMed ID: 14635105
[TBL] [Abstract][Full Text] [Related]
24. Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
Goodyer ID; Jones EE; Monaco AP; Francis MJ
Hum Mol Genet; 1999 Aug; 8(8):1473-8. PubMed ID: 10400994
[TBL] [Abstract][Full Text] [Related]
25. X-linked recessive Menkes disease: identification of partial gene deletions in affected males.
Poulsen L; Horn N; Heilstrup H; Lund C; Tümer Z; Møller LB
Clin Genet; 2002 Dec; 62(6):449-57. PubMed ID: 12485192
[TBL] [Abstract][Full Text] [Related]
26. Prenatal diagnosis of Menkes disease.
Kaler SG; Tümer Z
Prenat Diagn; 1998 Mar; 18(3):287-9. PubMed ID: 9556046
[No Abstract] [Full Text] [Related]
27. [The proposed role of the ceruloplasmin receptor and Cu2+-transferring Menkes ATPase in copper metabolism in mammals].
Puchkova LV; Sasina LK; Tsymbalenko NV; Voronina OV; Platonova NA; Mokshina SV; Skvortsova NN; Vlasov GP; Egorov TsA; Gaĭtskhoki VS
Mol Biol (Mosk); 1999; 33(2):287-90. PubMed ID: 10377576
[No Abstract] [Full Text] [Related]
28. Investigation of the copper binding sites in the Menkes disease protein, ATP7A. SSIEM Award. Society of the Study of Inborn Errors of Metabolism.
Jensen PY; Bonander N; Karlsson BG; Horn N; Tümer Z; Farver O
J Inherit Metab Dis; 1998 Jun; 21(3):195-8. PubMed ID: 9686355
[No Abstract] [Full Text] [Related]
29. The cell biology of the Menkes disease protein.
Petris MJ; Mercer JF; Camakaris J
Adv Exp Med Biol; 1999; 448():53-66. PubMed ID: 10079815
[No Abstract] [Full Text] [Related]
30. Novel bacterial P-type ATPases with histidine-rich heavy-metal-associated sequences.
Trenor C; Lin W; Andrews NC
Biochem Biophys Res Commun; 1994 Dec; 205(3):1644-50. PubMed ID: 7811248
[TBL] [Abstract][Full Text] [Related]
31. Copper efflux from murine microvascular cells requires expression of the menkes disease Cu-ATPase.
Qian Y; Tiffany-Castiglioni E; Welsh J; Harris ED
J Nutr; 1998 Aug; 128(8):1276-82. PubMed ID: 9687544
[TBL] [Abstract][Full Text] [Related]
32. Successful early copper therapy in Menkes disease associated with a mutant transcript containing a small In-frame deletion.
Kaler SG; Das S; Levinson B; Goldstein DS; Holmes CS; Patronas NJ; Packman S; Gahl WA
Biochem Mol Med; 1996 Feb; 57(1):37-46. PubMed ID: 8812725
[TBL] [Abstract][Full Text] [Related]
33. Identification of three novel mutations in the MNK gene in three unrelated Japanese patients with classical Menkes disease.
Ogawa A; Yamamoto S; Takayanagi M; Kogo T; Kanazawa M; Kohno Y
J Hum Genet; 1999; 44(3):206-9. PubMed ID: 10319589
[TBL] [Abstract][Full Text] [Related]
34. Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus.
Kaler SG; Gallo LK; Proud VK; Percy AK; Mark Y; Segal NA; Goldstein DS; Holmes CS; Gahl WA
Nat Genet; 1994 Oct; 8(2):195-202. PubMed ID: 7842019
[TBL] [Abstract][Full Text] [Related]
35. Gene symbol: ATP7A. Disease: Menkes disease.
Tumer Z; Horn N; Tonnesen T; Christodoulou J; Clarke JT; Sarkar B
Hum Genet; 2004 May; 114(6):606. PubMed ID: 15176369
[No Abstract] [Full Text] [Related]
36. Translocation t(X;21)(q13.3; p11.1) in a girl with Menkes disease.
Sugio Y; Sugio Y; Kuwano A; Miyoshi O; Yamada K; Niikawa N; Tsukahara M
Am J Med Genet; 1998 Sep; 79(3):191-4. PubMed ID: 9788559
[TBL] [Abstract][Full Text] [Related]
37. [Menkes' disease and brain dysfunction].
Aoki T; Yamaguchi Y; Omura I; Watanabe A; Shimizu N
No To Shinkei; 2001 May; 53(5):427-35. PubMed ID: 11424353
[No Abstract] [Full Text] [Related]
38. Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes disease.
Murata Y; Kodama H; Abe T; Ishida N; Nishimura M; Levinson B; Gitschier J; Packman S
Pediatr Res; 1997 Oct; 42(4):436-42. PubMed ID: 9380433
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice.
Mercer JF; Grimes A; Ambrosini L; Lockhart P; Paynter JA; Dierick H; Glover TW
Nat Genet; 1994 Apr; 6(4):374-8. PubMed ID: 8054977
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
