SCOPUS 정보 검색 플랫폼

Volumn 57, Issue 3, 1996, Pages 151-152

Achondroplasy associated with mutation of the transmembrane domain of fibroblastic growth factor receptor 3 (FGFR3);Association de l'achondroplasie a une mutation dnas le domaine transmembranaire du recepteur 3 des facteurs de croissance fibroblastiques (FGFR3)

(4) Rousseau, F a Bonaventure, J a Le Merrer, M a Munnich, A a

a HÔPITAL NECKER ENFANTS MALADES (France)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR;

ACHONDROPLASIA; HUMAN; MUTATION; SHORT SURVEY;

ACHONDROPLASIA; HUMANS; MEMBRANE PROTEINS; MUTATION; PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 3; RECEPTORS, FIBROBLAST GROWTH FACTOR;

EID: 0029744648 PISSN: 00034266 EISSN: None Source Type: Journal
DOI: None Document Type: Short Survey

Times cited : (4)

References (6)

1
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- Fibroblast growth factor receptor (FGFR3)
- CHELLAIAH AT, MCEWEN DG, WERNER S, XU J, ORNITZ DM. Fibroblast growth factor receptor (FGFR3). J Biol Chem 1994 ; 269 : 11620-27.
- (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

2
- 0026020296
- Isolation of an additional member of the fibroblast growth factor receptor family, FGFR-3
- KEEGAN K, JOHNSON DE, WILLIMAS LT, HAYMAN MJ. Isolation of an additional member of the fibroblast growth factor receptor family, FGFR-3. Proc Natl Acad Sci USA 1991 ; 88 : 1095-99.
- (1991) Proc Natl Acad Sci USA , vol.88 , pp. 1095-1099
- Keegan, K.¹ Johnson, D.E.² Willimas, L.T.³ Hayman, M.J.⁴

3
- 0028329818
- Un gène de l'achondroplasie/hypochondroplasie est localisé sur l'extrémité du bras court du chromosome 4
- LE MERRER M, ROUSSEAU F, MUNNICH A, MAROTEAUX P. Un gène de l'achondroplasie/hypochondroplasie est localisé sur l'extrémité du bras court du chromosome 4 Médecine/Sciences 1994 ; 10 : 486.
- (1994) Médecine/Sciences , vol.10 , pp. 486
- Le Merrer, M.¹ Rousseau, F.² Munnich, A.³ Maroteaux, P.⁴

4
- 0028093135
- Mutations of the fibroblast growth factor receptor 3 gene in achondroplasia
- ROUSSEAU F, BONAVENTURE J, LEGEAI-MALLET L, PELET A, ROZET JM, MAROTEAUX P, LE MERRER M, MUNNICH A. Mutations of the fibroblast growth factor receptor 3 gene in achondroplasia. Nature 1994 ; 371 : 252-54.
- (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

5
- 0027964261
- Mutations in the transmembrane domain of FGFR3 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 FGFR3 cause the most common genetic form of dwarfism, achondroplasia. Cell 1994 ; 78 : 335-42.
- (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

6
- 0026345681
- A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4
- THOMPSON LM, PLUMMER S, SCHALLING M, ALTHERR MR, GUSELLA JF, HOUSMAN DE, WASMUTH JJ. A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4. Genomics 1991 ; 11 . 1133-42.
- (1991) Genomics , vol.11 , pp. 1133-1142
- Thompson, L.M.¹ Plummer, S.² Schalling, M.³ Altherr, M.R.⁴ Gusella, J.F.⁵ Housman, D.E.⁶ Wasmuth, J.J.⁷

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.