Legeai-Mallet L - Search Results

1

Parathyroid hormone receptor type 1/Indian hedgehog expression is preserved in the growth plate of human fetuses affected with fibroblast growth factor receptor type 3 activating mutations.

Cormier S, Delezoide AL, Benoist-Lasselin C, Legeai-Mallet L, Bonaventure J, Silve C. Cormier S, et al. Am J Pathol. 2002 Oct;161(4):1325-35. doi: 10.1016/S0002-9440(10)64409-4. Am J Pathol. 2002. PMID: 12368206 Free PMC article.

2

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. Rousseau F, et al. Nature. 1994 Sep 15;371(6494):252-4. doi: 10.1038/371252a0. Nature. 1994. PMID: 8078586

3

Common mutations in the fibroblast growth factor receptor 3 (FGFR 3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfism.

Bonaventure J, Rousseau F, Legeai-Mallet L, Le Merrer M, Munnich A, Maroteaux P. Bonaventure J, et al. Am J Med Genet. 1996 May 3;63(1):148-54. doi: 10.1002/(SICI)1096-8628(19960503)63:1<148::AID-AJMG26>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8723101

4

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. Rousseau F, et al. Horm Res. 1996;45(1-2):108-10. doi: 10.1159/000184768. Horm Res. 1996. PMID: 8742128 Review.

5

Missense FGFR3 mutations create cysteine residues in thanatophoric dwarfism type I (TD1).

Rousseau F, el Ghouzzi V, Delezoide AL, Legeai-Mallet L, Le Merrer M, Munnich A, Bonaventure J. Rousseau F, et al. Hum Mol Genet. 1996 Apr;5(4):509-12. doi: 10.1093/hmg/5.4.509. Hum Mol Genet. 1996. PMID: 8845844

6

Clinical and genetic heterogeneity of hypochondroplasia.

Rousseau F, Bonaventure J, Legeai-Mallet L, Schmidt H, Weissenbach J, Maroteaux P, Munnich A, Le Merrer M. Rousseau F, et al. J Med Genet. 1996 Sep;33(9):749-52. doi: 10.1136/jmg.33.9.749. J Med Genet. 1996. PMID: 8880574 Free PMC article.

7

Common mutations in the gene encoding fibroblast growth factor receptor 3 account for achondroplasia, hypochondroplasia and thanatophoric dysplasia.

Bonaventure J, Rousseau F, Legeai-Mallet L, Le Merrer M, Munnich A, Maroteaux P. Bonaventure J, et al. Acta Paediatr Suppl. 1996 Oct;417:33-8. doi: 10.1111/j.1651-2227.1996.tb14291.x. Acta Paediatr Suppl. 1996. PMID: 9055906

8

[Fibroblast growth factor receptors and hereditary abnormalities of bone growth].

Bonaventure J, Rousseau F, Legeai-Mallet L, Benoist-Lasselin C, Le Merrer M, Munnich A. Bonaventure J, et al. Arch Pediatr. 1997;4(2 Suppl 2):112s-117s. doi: 10.1016/s0929-693x(97)86475-5. Arch Pediatr. 1997. PMID: 9246316 French. No abstract available.

9

Abnormal FGFR 3 expression in cartilage of thanatophoric dysplasia fetuses.

Delezoide AL, Lasselin-Benoist C, Legeai-Mallet L, Brice P, Senée V, Yayon A, Munnich A, Vekemans M, Bonaventure J. Delezoide AL, et al. Hum Mol Genet. 1997 Oct;6(11):1899-906. doi: 10.1093/hmg/6.11.1899. Hum Mol Genet. 1997. PMID: 9302269

10

Fibroblast growth factor receptor 3 mutations promote apoptosis but do not alter chondrocyte proliferation in thanatophoric dysplasia.

Legeai-Mallet L, Benoist-Lasselin C, Delezoide AL, Munnich A, Bonaventure J. Legeai-Mallet L, et al. J Biol Chem. 1998 May 22;273(21):13007-14. doi: 10.1074/jbc.273.21.13007. J Biol Chem. 1998. PMID: 9582336 Free article.

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