-
1
-
-
0027547331
-
Steel factor and c-kit receptor: From mutants to a growth factor system
-
Morrison-Graham K, Takahashi Y: Steel factor and c-kit receptor: From mutants to a growth factor system. Bioessays 1993;15:77-83.
-
(1993)
Bioessays
, vol.15
, pp. 77-83
-
-
Morrison-Graham, K.1
Takahashi, Y.2
-
2
-
-
0027218845
-
From white spots to stem cells: The role of the kit receptor in mammalian development
-
Fleischman RA. From white spots to stem cells: The role of the kit receptor in mammalian development. Trends Genet 1993;9:285-290.
-
(1993)
Trends Genet
, vol.9
, pp. 285-290
-
-
Fleischman, R.A.1
-
3
-
-
0006399935
-
Development of mast cells and basophils: Role of c-kit receptor tyrosine kinase for development, survival and neoplastic transformation of mast cells
-
Kitamura Y, Yamamoto S, Galli S, Greaves MW (eds): New York, Raven Press
-
Kitamura Y, Tsujimura T, Jippo T, Kasugai T, Kanakura Y: Development of mast cells and basophils: Role of c-kit receptor tyrosine kinase for development, survival and neoplastic transformation of mast cells; in Kitamura Y, Yamamoto S, Galli S, Greaves MW (eds): Biological and Molecular Aspects of Mast Cell and Basophil Differentiation and Function. New York, Raven Press, 1995, pp 91-103.
-
(1995)
Biological and Molecular Aspects of Mast Cell and Basophil Differentiation and Function
, pp. 91-103
-
-
Kitamura, Y.1
Tsujimura, T.2
Jippo, T.3
Kasugai, T.4
Kanakura, Y.5
-
4
-
-
0027996958
-
Molecular basis of human piebaldism
-
Spritz RA: Molecular basis of human piebaldism. J Invest Dermatol 1994;103(suppl):137S-140S.
-
(1994)
J Invest Dermatol
, vol.103
, Issue.SUPPL.
-
-
Spritz, R.A.1
-
5
-
-
0028856070
-
Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder
-
Nagata H, Worobec AS, Oh CK, Chowdhury BA, Tannenbaum S, Suzuki Y, Metcalfe DD: Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder. Proc Natl Acad Sci USA 1995;92:10560-10564.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 10560-10564
-
-
Nagata, H.1
Worobec, A.S.2
Oh, C.K.3
Chowdhury, B.A.4
Tannenbaum, S.5
Suzuki, Y.6
Metcalfe, D.D.7
-
6
-
-
0009013631
-
Somatic c-KIT activating mutation in urticaria pigmentosa and aggressive mastocytosis: Establishment of clonality in a human mast cell neoplasm
-
Longley BJ, Tyrrell L, Lu S, Ma Y, Langley K, Ding T, Duffy T, Jacobs P, Tang LH, Modlin I: Somatic c-KIT activating mutation in urticaria pigmentosa and aggressive mastocytosis: Establishment of clonality in a human mast cell neoplasm. Nat Genet 1996;12:312-314.
-
(1996)
Nat Genet
, vol.12
, pp. 312-314
-
-
Longley, B.J.1
Tyrrell, L.2
Lu, S.3
Ma, Y.4
Langley, K.5
Ding, T.6
Duffy, T.7
Jacobs, P.8
Tang, L.H.9
Modlin, I.10
-
7
-
-
0025921178
-
Classification and diagnosis of mastocytosis: Current status
-
Metcalfe DD: Classification and diagnosis of mastocytosis: Current status. J Invest Dermatol 1991; 96(suppl):2S-4S.
-
(1991)
J Invest Dermatol
, vol.96
, Issue.SUPPL.
-
-
Metcalfe, D.D.1
-
8
-
-
2742529418
-
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: Human proto-oncogene c-kit: A new cell surface receptor tyrosine kinase for an unidentified ligand. EMBO J 1987;6:3341-3351.
-
(1987)
EMBO J
, vol.6
, pp. 3341-3351
-
-
Yarden, Y.1
Kuang, W.J.2
Yang-Feng, T.3
Coussens, L.4
Munemitsu, S.5
Dull, T.J.6
Chen, E.7
Schlessinger, J.8
Francke, U.9
Ullrich, A.10
-
9
-
-
0026448961
-
Organization and nucleotide sequence of the human KIT (mast/stem cell growth factor receptor) proto-oncogene
-
Giebel LB, Strunk KM, Holmes SA, Spritz RA: Organization and nucleotide sequence of the human KIT (mast/stem cell growth factor receptor) proto-oncogene. Oncogene 1992;7:2207-2217.
-
(1992)
Oncogene
, vol.7
, pp. 2207-2217
-
-
Giebel, L.B.1
Strunk, K.M.2
Holmes, S.A.3
Spritz, R.A.4
-
10
-
-
0030297284
-
Immunodeficiency mutation databases - A new research tool
-
Smith CIE, Vihinen M: Immunodeficiency mutation databases - A new research tool. Immunol Today 1996; 17:485-496.
-
(1996)
Immunol Today
, vol.17
, pp. 485-496
-
-
Smith, C.I.E.1
Vihinen, M.2
-
11
-
-
1842411828
-
Human severe combined immunodeficiency (SCID): Genetic, phenotypic and functional diversity in 108 infants
-
in press
-
Buckley RH, Schiff SE, Schiff RI: Human severe combined immunodeficiency (SCID): Genetic, phenotypic and functional diversity in 108 infants. J Pediatr, in press.
-
J Pediatr
-
-
Buckley, R.H.1
Schiff, S.E.2
Schiff, R.I.3
-
12
-
-
0030296468
-
IL2RG base: A database of γc-chain defects causing human X-SCID
-
Puck JM: IL2RG base: A database of γc-chain defects causing human X-SCID. Immunol Today 1996;17: 507-510.
-
(1996)
Immunol Today
, vol.17
, pp. 507-510
-
-
Puck, J.M.1
-
13
-
-
0030297003
-
CD40Lbase: A database of CD40L gene mutations causing X-linked hyper-IgM syndrome
-
Notarangelo LD, Peitsch M: CD40Lbase: A database of CD40L gene mutations causing X-linked hyper-IgM syndrome. Immunol Today 1996;17:511-516.
-
(1996)
Immunol Today
, vol.17
, pp. 511-516
-
-
Notarangelo, L.D.1
Peitsch, M.2
-
14
-
-
0030279618
-
BTKbase: XLA-mutation registry
-
Vihinen M: BTKbase: XLA-mutation registry. Immunol Today 1996; 17:502-506.
-
(1996)
Immunol Today
, vol.17
, pp. 502-506
-
-
Vihinen, M.1
-
15
-
-
10344239867
-
Mutations in the mu heavy-chain gene in patients with agammaglobulinemia
-
Yel L, Minegishi Y, Coustan-Smith E, Buckley R, Trubel H, Pochman L, Kitchingman G: Mutations in the mu heavy-chain gene in patients with agammaglobulinemia. N Engl J Med 1996;335:1486-1493.
-
(1996)
N Engl J Med
, vol.335
, pp. 1486-1493
-
-
Yel, L.1
Minegishi, Y.2
Coustan-Smith, E.3
Buckley, R.4
Trubel, H.5
Pochman, L.6
Kitchingman, G.7
-
16
-
-
20244379555
-
WASPbase: A database of WAS- and XLT-causing mutations
-
Schwarz K: WASPbase: A database of WAS- and XLT-causing mutations. Immunol Today 1996; 17: 496-502.
-
(1996)
Immunol Today
, vol.17
, pp. 496-502
-
-
Schwarz, K.1
-
17
-
-
0028292001
-
Human severe combined immunodeficiency due to a defect in ZAP70, a T cell tyrosine kinase
-
Elder M, Lin D, Clever J, Chan A, Hope T, Weiss A, Parslow T: Human severe combined immunodeficiency due to a defect in ZAP70, a T cell tyrosine kinase. Science 1994; 264:1596-1599.
-
(1994)
Science
, vol.264
, pp. 1596-1599
-
-
Elder, M.1
Lin, D.2
Clever, J.3
Chan, A.4
Hope, T.5
Weiss, A.6
Parslow, T.7
-
18
-
-
0029151944
-
Activating and inhibitory mutations in adjacent tyrosines in the kinase domain of ZAP-70
-
Wange RL, Guitian R, Isakov N, Watts JD, Aebersold R, Samelson LE. Activating and inhibitory mutations in adjacent tyrosines in the kinase domain of ZAP-70. J Biol Chem 1995;270:18730-18733.
-
(1995)
J Biol Chem
, vol.270
, pp. 18730-18733
-
-
Wange, R.L.1
Guitian, R.2
Isakov, N.3
Watts, J.D.4
Aebersold, R.5
Samelson, L.E.6
-
19
-
-
0027346976
-
Molecular biology of cystic fibrosis
-
Drumm ML, Collins FS: Molecular biology of cystic fibrosis. Mol Genet Med 1993;3:33-68.
-
(1993)
Mol Genet Med
, vol.3
, pp. 33-68
-
-
Drumm, M.L.1
Collins, F.S.2
-
20
-
-
0027550821
-
The cystic fibrosis gene and its product CFTR
-
Harris A, Argent BE: The cystic fibrosis gene and its product CFTR. Semin Cell Biol 1993;4:37-44.
-
(1993)
Semin Cell Biol
, vol.4
, pp. 37-44
-
-
Harris, A.1
Argent, B.E.2
-
21
-
-
0028220333
-
Heterogeneity in the severity of cystic fibrosis and the role of CFTR gene mutations
-
Dean M, Santis G: Heterogeneity in the severity of cystic fibrosis and the role of CFTR gene mutations. Hum Genet 1994;93:364-368.
-
(1994)
Hum Genet
, vol.93
, pp. 364-368
-
-
Dean, M.1
Santis, G.2
-
22
-
-
0023989811
-
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 F, Ray P, Brown K, Baker PE, Jhanwar S, Ruddle FH, Besmer P: 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. EMBO J 1988,7:1003-1011.
-
(1988)
EMBO J
, vol.7
, pp. 1003-1011
-
-
Qiu, F.1
Ray, P.2
Brown, K.3
Baker, P.E.4
Jhanwar, S.5
Ruddle, F.H.6
Besmer, P.7
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