Benoist-Lasselin C - Search Results

1

ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome.

Dagoneau N, Benoist-Lasselin C, Huber C, Faivre L, Mégarbané A, Alswaid A, Dollfus H, Alembik Y, Munnich A, Legeai-Mallet L, Cormier-Daire V. Dagoneau N, et al. Am J Hum Genet. 2004 Nov;75(5):801-6. doi: 10.1086/425231. Epub 2004 Sep 13. Am J Hum Genet. 2004. PMID: 15368195 Free PMC article.

2

An activating Fgfr3 mutation affects trabecular bone formation via a paracrine mechanism during growth.

Mugniery E, Dacquin R, Marty C, Benoist-Lasselin C, de Vernejoul MC, Jurdic P, Munnich A, Geoffroy V, Legeai-Mallet L. Mugniery E, et al. Among authors: benoist lasselin c. Hum Mol Genet. 2012 Jun 1;21(11):2503-13. doi: 10.1093/hmg/dds065. Epub 2012 Feb 24. Hum Mol Genet. 2012. PMID: 22367969

3

FGFR3 mutation causes abnormal membranous ossification in achondroplasia.

Di Rocco F, Biosse Duplan M, Heuzé Y, Kaci N, Komla-Ebri D, Munnich A, Mugniery E, Benoist-Lasselin C, Legeai-Mallet L. Di Rocco F, et al. Among authors: benoist lasselin c. Hum Mol Genet. 2014 Jun 1;23(11):2914-25. doi: 10.1093/hmg/ddu004. Epub 2014 Jan 12. Hum Mol Genet. 2014. PMID: 24419316

4

Human immortalized chondrocytes carrying heterozygous FGFR3 mutations: an in vitro model to study chondrodysplasias.

Benoist-Lasselin C, Gibbs L, Heuertz S, Odent T, Munnich A, Legeai-Mallet L. Benoist-Lasselin C, et al. FEBS Lett. 2007 Jun 12;581(14):2593-8. doi: 10.1016/j.febslet.2007.04.079. Epub 2007 May 8. FEBS Lett. 2007. PMID: 17507011 Free article.

5

A novel tyrosine kinase inhibitor restores chondrocyte differentiation and promotes bone growth in a gain-of-function Fgfr3 mouse model.

Jonquoy A, Mugniery E, Benoist-Lasselin C, Kaci N, Le Corre L, Barbault F, Girard AL, Le Merrer Y, Busca P, Schibler L, Munnich A, Legeai-Mallet L. Jonquoy A, et al. Among authors: benoist lasselin c. Hum Mol Genet. 2012 Feb 15;21(4):841-51. doi: 10.1093/hmg/ddr514. Epub 2011 Nov 9. Hum Mol Genet. 2012. PMID: 22072392

6

Defective chondrocyte proliferation and differentiation in osteochondromas of MHE patients.

Benoist-Lasselin C, de Margerie E, Gibbs L, Cormier S, Silve C, Nicolas G, LeMerrer M, Mallet JF, Munnich A, Bonaventure J, Zylberberg L, Legeai-Mallet L. Benoist-Lasselin C, et al. Bone. 2006 Jul;39(1):17-26. doi: 10.1016/j.bone.2005.12.003. Epub 2006 Feb 13. Bone. 2006. PMID: 16476576

7

Constitutively-active FGFR3 disrupts primary cilium length and IFT20 trafficking in various chondrocyte models of achondroplasia.

Martin L, Kaci N, Estibals V, Goudin N, Garfa-Traore M, Benoist-Lasselin C, Dambroise E, Legeai-Mallet L. Martin L, et al. Among authors: benoist lasselin c. Hum Mol Genet. 2018 Jan 1;27(1):1-13. doi: 10.1093/hmg/ddx374. Hum Mol Genet. 2018. PMID: 29040558

8

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.

9

EXT 1 gene mutation induces chondrocyte cytoskeletal abnormalities and defective collagen expression in the exostoses.

Legeai-Mallet L, Rossi A, Benoist-Lasselin C, Piazza R, Mallet JF, Delezoide AL, Munnich A, Bonaventure J, Zylberberg L. Legeai-Mallet L, et al. J Bone Miner Res. 2000 Aug;15(8):1489-500. doi: 10.1359/jbmr.2000.15.8.1489. J Bone Miner Res. 2000. PMID: 10934647 Free article.

10

Mutations in the basic domain and the loop-helix II junction of TWIST abolish DNA binding in Saethre-Chotzen syndrome.

El Ghouzzi V, Legeai-Mallet L, Benoist-Lasselin C, Lajeunie E, Renier D, Munnich A, Bonaventure J. El Ghouzzi V, et al. FEBS Lett. 2001 Mar 9;492(1-2):112-8. doi: 10.1016/s0014-5793(01)02238-4. FEBS Lett. 2001. PMID: 11248247 Free article.

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