285 related articles for article (PubMed ID: 1720553)
1. Deletion of the c-kit protooncogene in the human developmental defect piebald trait.
Fleischman RA; Saltman DL; Stastny V; Zneimer S
Proc Natl Acad Sci U S A; 1991 Dec; 88(23):10885-9. PubMed ID: 1720553
[TBL] [Abstract][Full Text] [Related]
2. Human piebald trait resulting from a dominant negative mutant allele of the c-kit membrane receptor gene.
Fleischman RA
J Clin Invest; 1992 Jun; 89(6):1713-7. PubMed ID: 1376329
[TBL] [Abstract][Full Text] [Related]
3. Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism.
Giebel LB; Spritz RA
Proc Natl Acad Sci U S A; 1991 Oct; 88(19):8696-9. PubMed ID: 1717985
[TBL] [Abstract][Full Text] [Related]
4. Deletion of the SLUG (SNAI2) gene results in human piebaldism.
Sánchez-Martín M; Pérez-Losada J; Rodríguez-García A; González-Sánchez B; Korf BR; Kuster W; Moss C; Spritz RA; Sánchez-García I
Am J Med Genet A; 2003 Oct; 122A(2):125-32. PubMed ID: 12955764
[TBL] [Abstract][Full Text] [Related]
5. Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism.
Spritz RA; Holmes SA; Ramesar R; Greenberg J; Curtis D; Beighton P
Am J Hum Genet; 1992 Nov; 51(5):1058-65. PubMed ID: 1384325
[TBL] [Abstract][Full Text] [Related]
6. Deletion of the KIT and PDGFRA genes in a patient with piebaldism.
Spritz RA; Droetto S; Fukushima Y
Am J Med Genet; 1992 Nov; 44(4):492-5. PubMed ID: 1279971
[TBL] [Abstract][Full Text] [Related]
7. Dominant negative and loss of function mutations of the c-kit (mast/stem cell growth factor receptor) proto-oncogene in human piebaldism.
Spritz RA; Giebel LB; Holmes SA
Am J Hum Genet; 1992 Feb; 50(2):261-9. PubMed ID: 1370874
[TBL] [Abstract][Full Text] [Related]
8. Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism.
Ezoe K; Holmes SA; Ho L; Bennett CP; Bolognia JL; Brueton L; Burn J; Falabella R; Gatto EM; Ishii N
Am J Hum Genet; 1995 Jan; 56(1):58-66. PubMed ID: 7529964
[TBL] [Abstract][Full Text] [Related]
9. Molecular basis of human piebaldism.
Spritz RA
J Invest Dermatol; 1994 Nov; 103(5 Suppl):137S-140S. PubMed ID: 7525736
[TBL] [Abstract][Full Text] [Related]
10. Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5.
Smith EA; Seldin MF; Martinez L; Watson ML; Choudhury GG; Lalley PA; Pierce J; Aaronson S; Barker J; Naylor SL
Proc Natl Acad Sci U S A; 1991 Jun; 88(11):4811-5. PubMed ID: 1647018
[TBL] [Abstract][Full Text] [Related]
11. The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus.
Chabot B; Stephenson DA; Chapman VM; Besmer P; Bernstein A
Nature; 1988 Sep; 335(6185):88-9. PubMed ID: 2457811
[TBL] [Abstract][Full Text] [Related]
12. Human proto-oncogene c-kit: a new cell surface receptor tyrosine kinase for an unidentified ligand.
Yarden Y; Kuang WJ; Yang-Feng T; Coussens L; Munemitsu S; Dull TJ; Chen E; Schlessinger J; Francke U; Ullrich A
EMBO J; 1987 Nov; 6(11):3341-51. PubMed ID: 2448137
[TBL] [Abstract][Full Text] [Related]
13. The human PDGF receptor alpha-subunit gene maps to chromosome 4 in close proximity to c-kit.
Gronwald RG; Adler DA; Kelly JD; Disteche CM; Bowen-Pope DF
Hum Genet; 1990 Aug; 85(3):383-5. PubMed ID: 1697560
[TBL] [Abstract][Full Text] [Related]
14. A recurrent deletion in the KIT (mast/stem cell growth factor receptor) proto-oncogene is a frequent cause of human piebaldism.
Spritz RA; Holmes SA; Berg SZ; Nordlund JJ; Fukai K
Hum Mol Genet; 1993 Sep; 2(9):1499-500. PubMed ID: 7694728
[No Abstract] [Full Text] [Related]
15. Platelet-derived growth factor receptor alpha-subunit gene (Pdgfra) is deleted in the mouse patch (Ph) mutation.
Stephenson DA; Mercola M; Anderson E; Wang CY; Stiles CD; Bowen-Pope DF; Chapman VM
Proc Natl Acad Sci U S A; 1991 Jan; 88(1):6-10. PubMed ID: 1846043
[TBL] [Abstract][Full Text] [Related]
16. Mice transgenic for Kit(V620A): recapitulation of piebaldism but not progressive depigmentation seen in humans with this mutation.
Tosaki H; Kunisada T; Motohashi T; Aoki H; Yoshida H; Kitajima Y
J Invest Dermatol; 2006 May; 126(5):1111-8. PubMed ID: 16456533
[TBL] [Abstract][Full Text] [Related]
17. Piebaldism in a mentally retarded girl with rare deletion of the long arm of chromosome 4.
Sijmons RH; Kristoffersson U; Tuerlings JH; Ljung R; Dijkhuis-Stoffelsma R; Breed AS
Pediatr Dermatol; 1993 Sep; 10(3):235-9. PubMed ID: 8415299
[TBL] [Abstract][Full Text] [Related]
18. The Wsh and Ph mutations affect the c-kit expression profile: c-kit misexpression in embryogenesis impairs melanogenesis in Wsh and Ph mutant mice.
Duttlinger R; Manova K; Berrozpe G; Chu TY; DeLeon V; Timokhina I; Chaganti RS; Zelenetz AD; Bachvarova RF; Besmer P
Proc Natl Acad Sci U S A; 1995 Apr; 92(9):3754-8. PubMed ID: 7537375
[TBL] [Abstract][Full Text] [Related]
19. The mouse W/c-kit locus.
Bernstein A; Chabot B; Dubreuil P; Reith A; Nocka K; Majumder S; Ray P; Besmer P
Ciba Found Symp; 1990; 148():158-66; discussion 166-72. PubMed ID: 1690623
[TBL] [Abstract][Full Text] [Related]
20. Primary structure of c-kit: relationship with the CSF-1/PDGF receptor kinase family--oncogenic activation of v-kit involves deletion of extracellular domain and C terminus.
Qiu FH; Ray P; Brown K; Barker PE; Jhanwar S; Ruddle FH; Besmer P
EMBO J; 1988 Apr; 7(4):1003-11. PubMed ID: 2456920
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]