-
2
-
-
0025343230
-
Signal transduction by receptors with tyrosine kinase activity
-
Ullrich A, Schlessinger J. Signal transduction by receptors with tyrosine kinase activity. Cell 1990; 61: 203-12.
-
(1990)
Cell
, vol.61
, pp. 203-212
-
-
Ullrich, A.1
Schlessinger, J.2
-
3
-
-
0028088073
-
The ins and outs of fibroblast growth factors
-
Mason IJ. The ins and outs of fibroblast growth factors. Cell 1994; 78: 547-52.
-
(1994)
Cell
, vol.78
, pp. 547-552
-
-
Mason, I.J.1
-
4
-
-
0026736833
-
The FGF family of growth factors and oncogenes
-
Basilico C, Moscatelli D. The FGF family of growth factors and oncogenes. Adv Cancer Res 1992; 59: 115-65.
-
(1992)
Adv Cancer Res
, vol.59
, pp. 115-165
-
-
Basilico, C.1
Moscatelli, D.2
-
5
-
-
0027409017
-
Unique expression pattern of the FGF receptor 3 gene during mouse organogenesis
-
Peters K, Ornitz DM, Werner S, Williams LT. Unique expression pattern of the FGF receptor 3 gene during mouse organogenesis. Dev Biol 1993; 155: 423-30.
-
(1993)
Dev Biol
, vol.155
, pp. 423-430
-
-
Peters, K.1
Ornitz, D.M.2
Werner, S.3
Williams, L.T.4
-
6
-
-
0028365599
-
A gene for achondroplasia-hypochondroplasia maps to chromosome 4p
-
Le Merrer M, Rousseau F, Legeai-Mallet L, Landais JC, Pelet A, Bonaventure I, Sanak M, Weissenbach J, Stoll C, Munnich A, Maroteaux P. A gene for achondroplasia-hypochondroplasia maps to chromosome 4p. Nature Genet 1994; 6: 318-21.
-
(1994)
Nature Genet
, vol.6
, pp. 318-321
-
-
Le Merrer, M.1
Rousseau, F.2
Legeai-Mallet, L.3
Landais, J.C.4
Pelet, A.5
Bonaventure, I.6
Sanak, M.7
Weissenbach, J.8
Stoll, C.9
Munnich, A.10
Maroteaux, P.11
-
7
-
-
0028093135
-
Mutations in the gene encoding fibroblast growth factor receptor 3 in achondroplasia
-
Rousseau F, Bonaventure J, Legeai-Mallet L, Pelet A, Rozet JM, Maroteaux P, Le Merrer M, Munnich A. Mutations in the gene encoding fibroblast growth factor receptor 3 in achondroplasia. Nature 1994; 371: 252-4.
-
(1994)
Nature
, vol.371
, pp. 252-254
-
-
Rousseau, F.1
Bonaventure, J.2
Legeai-Mallet, L.3
Pelet, A.4
Rozet, J.M.5
Maroteaux, P.6
Le Merrer, M.7
Munnich, A.8
-
8
-
-
0027964261
-
Mutations in the transmembrane domain of FGFR 3 cause the most common genetic form of dwarfism, achondroplasia
-
Shiang R, Thompson LM, Zhu YZ, Church DM, Fielder TJ, Bocian M, Winokur ST, Wasmuth JJ. Mutations in the transmembrane domain of FGFR 3 cause the most common genetic form of dwarfism, achondroplasia. Cell 1994; 78: 336-42.
-
(1994)
Cell
, vol.78
, pp. 336-342
-
-
Shiang, R.1
Thompson, L.M.2
Zhu, Y.Z.3
Church, D.M.4
Fielder, T.J.5
Bocian, M.6
Winokur, S.T.7
Wasmuth, J.J.8
-
9
-
-
0028872752
-
Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3
-
Tavormina PL, Shiang R, Thompson LM, Zhu YZ, Wilkin DJ, Lachman RS, Wilcox WR, Rimoin DL, Cohn DH, Wasmuth JJ. Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3. Nature Genet 1995; 9: 321-8.
-
(1995)
Nature Genet
, vol.9
, pp. 321-328
-
-
Tavormina, P.L.1
Shiang, R.2
Thompson, L.M.3
Zhu, Y.Z.4
Wilkin, D.J.5
Lachman, R.S.6
Wilcox, W.R.7
Rimoin, D.L.8
Cohn, D.H.9
Wasmuth, J.J.10
-
10
-
-
0029298121
-
Stop codon FGFR 3 mutations in thanatophoric dwarfism type I
-
Rousseau F, Saugier P, Le Merrer M, Munnich A, Delezoide AL, Maroteaux P, Bonaventure J, Narcy F, Sanak M. Stop codon FGFR 3 mutations in thanatophoric dwarfism type I. Nature Genet 1995; 10: 11-2.
-
(1995)
Nature Genet
, vol.10
, pp. 11-12
-
-
Rousseau, F.1
Saugier, P.2
Le Merrer, M.3
Munnich, A.4
Delezoide, A.L.5
Maroteaux, P.6
Bonaventure, J.7
Narcy, F.8
Sanak, M.9
-
11
-
-
0029937714
-
Missense FGFR 3 mutations create cysteine residues in thanatophoric dwarfism type I (TD I)
-
Rousseau F, El Ghouzzi V, Delezoide AL, Legeai-Mallet L, Le Merrer M, Munnich A, Bonaventure J. Missense FGFR 3 mutations create cysteine residues in thanatophoric dwarfism type I (TD I). Hum Mol Genet 1996; 5: 509-12.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 509-512
-
-
Rousseau, F.1
El Ghouzzi, V.2
Delezoide, A.L.3
Legeai-Mallet, L.4
Le Merrer, M.5
Munnich, A.6
Bonaventure, J.7
-
12
-
-
0027981524
-
Mutations in the fibroblast growth factor receptor 2 cause Crouzon syndrome
-
Reardon W, Winter RM, Rutland P, Pulleyn L, Jones BM, Malcolm S. Mutations in the fibroblast growth factor receptor 2 cause Crouzon syndrome. Nature Genet 1994; 8: 98-103.
-
(1994)
Nature Genet
, vol.8
, pp. 98-103
-
-
Reardon, W.1
Winter, R.M.2
Rutland, P.3
Pulleyn, L.4
Jones, B.M.5
Malcolm, S.6
-
13
-
-
0028046606
-
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome
-
Muenke M, Schell U, Hehr A, Robin NH, Losken W, Schinzel A, Pulleyn LJ, Rutland P, Reardon W, Malcolm S, Winter RM. A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome. Nature Genet 1994; 8: 269-74.
-
(1994)
Nature Genet
, vol.8
, pp. 269-274
-
-
Muenke, M.1
Schell, U.2
Hehr, A.3
Robin, N.H.4
Losken, W.5
Schinzel, A.6
Pulleyn, L.J.7
Rutland, P.8
Reardon, W.9
Malcolm, S.10
Winter, R.M.11
-
14
-
-
0029242747
-
FGFR 2 mutations in Pfeiffer syndrome
-
Lajeunie E, Ma HW, Bonaventure J, Munnich A, Le Merrer M, Rénier D. FGFR 2 mutations in Pfeiffer syndrome. Nature Genet 1995; 9: 108.
-
(1995)
Nature Genet
, vol.9
, pp. 108
-
-
Lajeunie, E.1
Ma, H.W.2
Bonaventure, J.3
Munnich, A.4
Le Merrer, M.5
Rénier, D.6
-
15
-
-
0028793472
-
Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans
-
Meyers GA, Orlow SJ, Munro IR, Przylepa KA, Jabs EW. Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans. Nature Genet 1995; 11: 462-4.
-
(1995)
Nature Genet
, vol.11
, pp. 462-464
-
-
Meyers, G.A.1
Orlow, S.J.2
Munro, I.R.3
Przylepa, K.A.4
Jabs, E.W.5
-
16
-
-
0028608075
-
Heparin-inducea oligomerizauon of FGF molecules is responsible for FGF receptor dimerization, activation and cell proliferation
-
Spivak-Kroizman T, Lemmon MA, Dikic I, Ladbury JE, Pinchasi D, Huang J, Jaye M, Crumley G, Schlessinger J, Lax I. Heparin-inducea oligomerizauon of FGF molecules is responsible for FGF receptor dimerization, activation and cell proliferation. Cell 1994; 79: 1015-24.
-
(1994)
Cell
, vol.79
, pp. 1015-1024
-
-
Spivak-Kroizman, T.1
Lemmon, M.A.2
Dikic, I.3
Ladbury, J.E.4
Pinchasi, D.5
Huang, J.6
Jaye, M.7
Crumley, G.8
Schlessinger, J.9
Lax, I.10
-
17
-
-
13344278032
-
Chondrodysplasia and neurological abnormalities in ATF-2 deficient mice
-
Reimold AM, Grusby MJ, Kosaras B, Fries JWU, Mori R, Maniwa S, Clauss IM, Collins T, Sidman RL, Glimcher MJ, Glimcher LH. Chondrodysplasia and neurological abnormalities in ATF-2 deficient mice. Nature 1996; 379: 262-5.
-
(1996)
Nature
, vol.379
, pp. 262-265
-
-
Reimold, A.M.1
Grusby, M.J.2
Kosaras, B.3
Fries, J.W.U.4
Mori, R.5
Maniwa, S.6
Clauss, I.M.7
Collins, T.8
Sidman, R.L.9
Glimcher, M.J.10
Glimcher, L.H.11
-
18
-
-
0030064347
-
Constitutive activation of fibroblast growth factor receptor 3 by the transmembrane domain point mutation found in achondroplasia
-
Webster MK, Donoghue DJ. Constitutive activation of fibroblast growth factor receptor 3 by the transmembrane domain point mutation found in achondroplasia. EMBO J 1996; 15: 520-7.
-
(1996)
EMBO J
, vol.15
, pp. 520-527
-
-
Webster, M.K.1
Donoghue, D.J.2
-
19
-
-
0028846512
-
Constitutive activation of fibroblast growth factor receptor 2 by a point mutation associated with Crouzon syndrome
-
Nielson KM, Friesel RE. Constitutive activation of fibroblast growth factor receptor 2 by a point mutation associated with Crouzon syndrome. J Biol Chem 1995; 270: 26037-40.
-
(1995)
J Biol Chem
, vol.270
, pp. 26037-26040
-
-
Nielson, K.M.1
Friesel, R.E.2
-
20
-
-
0029917507
-
Fibroblast growth factor receptor 3 is a negative regulator of bone growth
-
Deng C, Wynshaw-Boris A, Zhou F, Kuo A, Leder P. Fibroblast growth factor receptor 3 is a negative regulator of bone growth. Cell 1996; 84: 911-21.
-
(1996)
Cell
, vol.84
, pp. 911-921
-
-
Deng, C.1
Wynshaw-Boris, A.2
Zhou, F.3
Kuo, A.4
Leder, P.5
|