Zobrazeno 1 - 10 of 14 pro vyhledávání: '"Lucie Rochard"'
1
Distinct requirements of wls, wnt9a, wnt5b and gpc4 in regulating chondrocyte maturation and timing of endochondral ossification
Autor: Eric C. Liao, Lucie Rochard, Irving T.C. Ling
Formation of the mandible requires progressive morphologic change, proliferation, differentiation and organization of chondrocytes preceding osteogenesis. The Wnt signaling pathway is involved in regulating bone development and maintenance. Chondrocy
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e3df854bf245f6e9fc30469e0afa6c6
https://eprints.gla.ac.uk/132714/1/132714.pdf
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2
Requirement for frzb and fzd7a in cranial neural crest convergence and extension mechanisms during zebrafish palate and jaw morphogenesis
Autor: Tatiana Hoyos, Michael Grimaldi, Eric C. Liao, Valeriy Shubinets, William Ka Fai Tse, George N. Kamel, Max L. Dougherty, Lucie Rochard, Yawei Kong
Publikováno v: Developmental Biology. 381:423-433
Regulation of convergence and extension by wnt-frizzled signaling is a common theme in embryogenesis. This study examines the functional requirements of frzb and fzd7a in convergence and extension mechanisms during craniofacial development. Using a m
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::186dc3af398f6077164f258903f16307
https://doi.org/10.1016/j.ydbio.2013.06.012
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3
Roles of Wnt pathway genes wls, wnt9a, wnt5b, frzb and gpc4 in regulating convergent-extension during palate morphogenesis
Autor: Sara Roberson, Lucie Rochard, Marnie E. Halpern, Richard M. Harland, Eric C. Liao, Stefanie D. Monica, Yawei Kong, Irving T.C. Ling
Publikováno v: Development.
The Wnt signaling pathway is crucial for tissue morphogenesis, participating in cellular behavior changes, notably during the process of convergent-extension. Interactions between Wnt-secreting and receiving cells during convergent-extension remain e
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e689a9c457b5da91f7fb74c3adbd4248
https://doi.org/10.1242/dev.137000
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4
Holoprosencephaly: An update on cytogenetic abnormalities
Autor: Valérie Dupé, Claude Bendavid, Isabelle Gicquel, Véronique David, Christèle Dubourg, Lucie Rochard
Publikováno v: American Journal of Medical Genetics Part C: Seminars in Medical Genetics. :86-92
Holoprosencephaly (HPE), the most common developmental defect of the forebrain and midface, is caused by a failure of midline cleavage early in gestation. Isolated HPE, which is highly genetically heterogeneous, can be due to major chromosomal abnorm
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f9f9fe40e5b5c41020aea0a559dc73e
https://doi.org/10.1002/ajmg.c.30250
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5
Visualization of Chondrocyte Intercalation and Directional Proliferation via Zebrabow Clonal Cell Analysis in the Embryonic Meckel’s Cartilage
Autor: Irving T.C. Ling, Yawei Kong, Eric C. Liao, Lucie Rochard
Publikováno v: Journal of Visualized Experiments.
Development of the vertebrate craniofacial structures requires precise coordination of cell migration, proliferation, adhesion and differentiation. Patterning of the Meckel's cartilage, a first pharyngeal arch derivative, involves the migration of cr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::519cca334d7a01a137eff8463f4cd781
https://doi.org/10.3791/52935-v
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7
New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases
Autor: Laurent Pasquier, Chloé Quélin, Véronique David, Sylvie Jaillard, Isabelle Gicquel, Marion Belleguic, Philippe Loget, Sandra Mercier, Christèle Dubourg, Sylvie Odent, Valérie Dupé, Nicolas Garcelon, Lucie Rochard, Claude Bendavid, Boris Campillo-Gimenez, Leslie Ratié
Publikováno v: Journal of Medical Genetics
Journal of Medical Genetics, 2011, 48 (11), pp.752-60. ⟨10.1136/jmedgenet-2011-100339⟩
Journal of Medical Genetics, BMJ Publishing Group, 2011, 48 (11), pp.752-60. ⟨10.1136/jmedgenet-2011-100339⟩
International audience; BACKGROUND: Holoprosencephaly (HPE) is the most common forebrain defect in humans. It results from incomplete midline cleavage of the prosencephalon. METHODS: A large European series of 645 HPE probands (and 699 relatives), co
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0795f8110528966f9170b0bc4ba0bdec
https://www.hal.inserm.fr/inserm-00626407/document
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8
NOTCH, a new signaling pathway implicated in holoprosencephaly
Autor: Valérie Dupé, Véronique David, Isabelle Gicquel, Christèle Dubourg, Yann Le Pétillon, Claude Bendavid, Timothy P. Bohan, Sandra Mercier, Usha Kini, Georges Bourrouillou, Sylvie Odent, Christel Thauvin-Robinet, Lucie Rochard
Publikováno v: Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (6), pp.1122-31. ⟨10.1093/hmg/ddq556⟩
Human Molecular Genetics, 2011, 20 (6), pp.1122-31. ⟨10.1093/hmg/ddq556⟩
International audience; Genetics of Holoprosencephaly (HPE), a congenital malformation of the developing human forebrain, is due to multiple genetic defects. Most genes that have been implicated in HPE belong to the sonic hedgehog signaling pathway.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0416e0669b3c99a84b9b35241338d90f
https://www.hal.inserm.fr/inserm-00554387/file/Dupe-2010-hum_mol_genet.pdf
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9
Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci
Autor: Karine Morcel, Tanguy Watrin, Véronique David, Cédric Le Caignec, Lucie Rochard, Claude Bendavid, Bernard-Jean Paniel, Isabelle Pellerin, Christèle Dubourg, Daniel Guerrier, Sylvie Odent, Laurent Pasquier, Philippe Loget
Publikováno v: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.9. ⟨10.1186/1750-1172-6-9⟩
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 9 (2011)
Orphanet Journal of Rare Diseases, BioMed Central, 2011, 6 (1), pp.9. ⟨10.1186/1750-1172-6-9⟩
Background Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype. Th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f3e4b03d229dd671ce518f065a24c89
https://www.hal.inserm.fr/inserm-00582863/file/1750-1172-6-9.pdf
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10
Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci
Autor: Jaqueline Vigneron, Isabelle Gicquel, Jonathan Seguin, Caroline Rouleau, Annie Laquerrière, Véronique David, Claude Bendavid, Jean Mosser, Sylvie Jaillard, Christèle Dubourg, Sylvie Odent, Corinne Jeanne-Pasquier, Pascale Marcorelles, Lucie Rochard, Laurent Pasquier
Publikováno v: Human Mutation
Human Mutation, Wiley, 2009, 30 (8), pp.1175-82. ⟨10.1002/humu.21016⟩
Human Mutation, 2009, 30 (8), pp.1175-82. ⟨10.1002/humu.21016⟩
International audience; Holoprosencephaly (HPE) is the most frequent malformation of the brain. To date, 12 different HPE loci and 8 HPE genes have been identified from recurrent chromosomal rearrangements or from the sequencing of genes from Nodal a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c36cebe9e5efffdefbfe4305f4454ec8
https://www.hal.inserm.fr/inserm-00404487
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