-
1
-
-
0029032394
-
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
-
BELLUS, G.A., MACINTOSH, I , SMITH, E.A., KAITILA, I., HORTON, W.A., GREENHAW, G.A., HECHT, J.T. and FRANCOMANO, C.A. (1995). A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia. Nature Genet. 10: 357-359.
-
(1995)
Nature Genet.
, vol.10
, pp. 357-359
-
-
Bellus, G.A.1
Macintosh, I.2
Smith, E.A.3
Kaitila, I.4
Horton, W.A.5
Greenhaw, G.A.6
Hecht, J.T.7
Francomano, C.A.8
-
2
-
-
0028239789
-
Fibroblast growth factor receptor (FGFR) 3
-
CHELLAIAH, A.T., MCEWEN, D.G., WERNER, S., XU, J. and ORNITZ, D M. (1994). Fibroblast growth factor receptor (FGFR) 3. J. Biol. Chem. 269: 11620-11627.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 11620-11627
-
-
Chellaiah, A.T.1
Mcewen, D.G.2
Werner, S.3
Xu, J.4
Ornitz, D.M.5
-
3
-
-
0027344852
-
Structural and functional diversity in the FGF receptor multigene family
-
JOHNSON, D.E. and WILLIAMS, L.T. (1993). Structural and functional diversity in the FGF receptor multigene family. Adv. Cancer Res. 60: 1-41.
-
(1993)
Adv. Cancer Res.
, vol.60
, pp. 1-41
-
-
Johnson, D.E.1
Williams, L.T.2
-
4
-
-
0026020296
-
Isolation of an additional member of the fibroblast growth factor receptor family, FGFR3
-
KEEGAN, K., JOHNSON, D.E., WILLIAMS, L.T. and HAYMAN, M.J. (1991). Isolation of an additional member of the fibroblast growth factor receptor family, FGFR3. Proc. Natl. Acad. Sci. USA 88: 1095-1099.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 1095-1099
-
-
Keegan, K.1
Johnson, D.E.2
Williams, L.T.3
Hayman, M.J.4
-
5
-
-
0028793472
-
Fibroblast growth factor receptor 3 (FGRF3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans
-
MEYERS, G.A., ORLOW, S.J., MUNRO, I.R., PRZYLEPA, K.A. and JABS, E.W. (1995). Fibroblast growth factor receptor 3 (FGRF3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans. Nature Genet 11: 462-464.
-
(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
-
6
-
-
0027409017
-
Unique expression pattern of the FGF Receptor 3 gene during mouse organogenesis
-
PETERS, K., ORNITZ, D., WERNER, S. and WILLIAMS, L (1993) Unique expression pattern of the FGF Receptor 3 gene during mouse organogenesis. Dev. Biol. 155: 423-430.
-
(1993)
Dev. Biol.
, vol.155
, pp. 423-430
-
-
Peters, K.1
Ornitz, D.2
Werner, S.3
Williams, L.4
-
7
-
-
0025084732
-
Analysis of expression of cholecystokinin in dopamine cells in the ventral mesencephalon of several species and in humans with schizophrenia
-
SCHALLING M., FRIBERG, K., SEROOGY, K , RIEDERER, P., BIRD, E., SCHIFFMAN, S.N., MAILLEUX, P., VANDERHAEGHEN, J-J., KUGA, S., GOLDSTEIN, M., KITAHAMA, K., LUPPI, P.H., JOUVET, M. and HOEKFELT, T. (1990). Analysis of expression of cholecystokinin in dopamine cells in the ventral mesencephalon of several species and in humans with schizophrenia. Proc Natl. Acad. Sci. USA 87: 8427-8431.
-
(1990)
Proc Natl. Acad. Sci. USA
, vol.87
, pp. 8427-8431
-
-
Schalling, M.1
Friberg, K.2
Seroogy, K.3
Riederer, P.4
Bird, E.5
Schiffman, S.N.6
Mailleux, P.7
Vanderhaeghen, J.-J.8
Kuga, S.9
Goldstein, M.10
Kitahama, K.11
Luppi, P.H.12
Jouvet, M.13
Hoekfelt, T.14
-
8
-
-
0027964261
-
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
-
SHIANG, R., THOMPSON, L.M., ZHU, Y-Z, CHURCH, D.M., FIELDER, T.J., BOCIAN, M., WINOKUR, S.T and WASMUTH, J.J. (1994). Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia. Cell 78: 335-342.
-
(1994)
Cell
, vol.78
, pp. 335-342
-
-
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, P.L, SHIANG, R., THOMPSON, M., ZHU Y-Z., WILKIN, D J., LACHMAN, R.S , WILCOX, W.R., RIMOIN, D.L., COHN, D.C. and WASMUTH, J.J. (1995) Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3. Nature Genet. 9 321-328
-
(1995)
Nature Genet.
, vol.9
, pp. 321-328
-
-
Tavormina, P.L.1
Shiang, R.2
Thompson, M.3
Zhu, Y.-Z.4
Wilkin, D.J.5
Lachman, R.S.6
Wilcox, W.R.7
Rimoin, D.L.8
Cohn, D.C.9
Wasmuth, J.J.10
-
10
-
-
0029294653
-
Functions of fibroblast growth factors and their receptors
-
WILKIE, A.O.M., MORRISS-KAY, G.M., JONES, E.Y. and HEATH, J.K (1995) Functions of fibroblast growth factors and their receptors Curr. Biol. 5:500-507
-
(1995)
Curr. Biol.
, vol.5
, pp. 500-507
-
-
Wilkie, A.O.M.1
Morriss-Kay, G.M.2
Jones, E.Y.3
Heath, J.K.4
|