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Items: 12

1.

Distinct requirements of wls, wnt9a, wnt5b and gpc4 in regulating chondrocyte maturation and timing of endochondral ossification.

Ling IT, Rochard L, Liao EC.

Dev Biol. 2017 Jan 15;421(2):219-232. doi: 10.1016/j.ydbio.2016.11.016. Epub 2016 Nov 29.

2.

Roles of Wnt pathway genes wls, wnt9a, wnt5b, frzb and gpc4 in regulating convergent-extension during zebrafish palate morphogenesis.

Rochard L, Monica SD, Ling IT, Kong Y, Roberson S, Harland R, Halpern M, Liao EC.

Development. 2016 Jul 15;143(14):2541-7. doi: 10.1242/dev.137000. Epub 2016 Jun 10.

3.
4.

Abstract 69: analysis of the role of wls in craniofacial development.

Rochard LJ, Kong Y, Kawasaki KC, Grimaldi M, Hoyos T, Liao EC.

Plast Reconstr Surg. 2014 Mar;133(3 Suppl):81. doi: 10.1097/01.prs.0000445102.22341.4f. No abstract available.

PMID:
25942180
5.

Requirement for frzb and fzd7a in cranial neural crest convergence and extension mechanisms during zebrafish palate and jaw morphogenesis.

Kamel G, Hoyos T, Rochard L, Dougherty M, Kong Y, Tse W, Shubinets V, Grimaldi M, Liao EC.

Dev Biol. 2013 Sep 15;381(2):423-33. doi: 10.1016/j.ydbio.2013.06.012. Epub 2013 Jun 25.

6.

New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.

Mercier S, Dubourg C, Garcelon N, Campillo-Gimenez B, Gicquel I, Belleguic M, Ratié L, Pasquier L, Loget P, Bendavid C, Jaillard S, Rochard L, Quélin C, Dupé V, David V, Odent S.

J Med Genet. 2011 Nov;48(11):752-60. doi: 10.1136/jmedgenet-2011-100339. Epub 2011 Sep 22.

7.

Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.

Morcel K, Watrin T, Pasquier L, Rochard L, Le Caignec C, Dubourg C, Loget P, Paniel BJ, Odent S, David V, Pellerin I, Bendavid C, Guerrier D.

Orphanet J Rare Dis. 2011 Mar 15;6:9. doi: 10.1186/1750-1172-6-9.

8.

NOTCH, a new signaling pathway implicated in holoprosencephaly.

Dupé V, Rochard L, Mercier S, Le Pétillon Y, Gicquel I, Bendavid C, Bourrouillou G, Kini U, Thauvin-Robinet C, Bohan TP, Odent S, Dubourg C, David V.

Hum Mol Genet. 2011 Mar 15;20(6):1122-31. doi: 10.1093/hmg/ddq556. Epub 2010 Dec 31.

9.

Holoprosencephaly: An update on cytogenetic abnormalities.

Bendavid C, Dupé V, Rochard L, Gicquel I, Dubourg C, David V.

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):86-92. doi: 10.1002/ajmg.c.30250. Review.

10.

Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci.

Bendavid C, Rochard L, Dubourg C, Seguin J, Gicquel I, Pasquier L, Vigneron J, Laquerrière A, Marcorelles P, Jeanne-Pasquier C, Rouleau C, Jaillard S, Mosser J, Odent S, David V.

Hum Mutat. 2009 Aug;30(8):1175-82. doi: 10.1002/humu.21016.

11.

[Clinical update of global delusion of negation].

Le Roux A, Rochard L.

Ann Med Psychol (Paris). 1986 Nov;144(9):971-85. French.

PMID:
3579110
12.

[Contribution to the study of the relation between hysterical neurosis and schizophrenic psychosis].

Le Roux A, Rochard L.

Ann Med Psychol (Paris). 1984 Jul-Aug;142(7):975-88. French.

PMID:
6524805

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