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Environmental Science & Technology|August 2, 2011
Zebrafish eleutheroembryos provide a suitable vertebrate model for screening chemicals that impair thyroid hormone synthesisBenedicte Thienpont, Angèle Tingaud-Sequeira, Eva Prats, et al.
BMC Genomics|September 17, 2009
New insights into molecular pathways associated with flatfish ovarian development and atresia revealed by transcriptional analysisAngèle Tingaud-Sequeira, François Chauvigné, Juanjo Lozano, et al.
BMC Evolutionary Biology|February 13, 2010
The zebrafish genome encodes the largest vertebrate repertoire of functional aquaporins with dual paralogy and substrate specificities similar to mammalsAngèle Tingaud-Sequeira, Magdalena Calusinska, Roderick N Finn, et al.
General and Comparative Endocrinology|April 15, 2014
Endocrinology: advances through omics and related technologiesNatàlia Garcia-Reyero, Angèle Tingaud-Sequeira, Mengxi Cao, et al.
General and Comparative Endocrinology|October 13, 2010
Molecular and functional characterization of catfish (Heteropneustes fossilis) aquaporin-1b: changes in expression during ovarian development and hormone-induced follicular maturationRadha Chaube, François Chauvigné, Angèle Tingaud-Sequeira, et al.
Plos One|June 7, 2013
A rapid transcriptome response is associated with desiccation resistance in aerially-exposed killifish embryosAngèle Tingaud-Sequeira, Juan-José Lozano, Cinta Zapater, et al.
Biology of Reproduction|March 5, 2010
Functional and evolutionary analysis of flatfish gonadotropin receptors reveals cladal- and lineage-level divergence of the teleost glycoprotein receptor familyFrançois Chauvigné, Angèle Tingaud-Sequeira, María J Agulleiro, et al.
Clinical Genetics|July 9, 2020
Description of a family with X-linked oculo-auriculo-vertebral spectrum associated with polyalanine tract expansion in ZIC3Aurélien Trimouille, Angèle Tingaud-Sequeira, Didier Lacombe, et al.
Molecular Genetics & Genomic Medicine|August 2, 2020
Functional and genetic analyses of ZYG11B provide evidences for its involvement in OAVSAngèle Tingaud-Sequeira, Aurélien Trimouille, Sandrine Marlin, et al.
European Journal of Human Genetics : EJHG|October 31, 2018
Deletion in 2q35 excluding the IHH gene leads to fetal severe limb anomalies and suggests a disruption of chromatin architectureAurélien Trimouille, Angèle Tingaud-Sequeira, Perrine Pennamen, et al.
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