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Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|January 22, 2010
Interspecific resources: a major tool for quantitative trait locus cloning and speciation researchDavid L'Hôte, Paul Laissue, Catherine Serres, et al.
Scientific Reports|September 29, 2025
MIEN1 promoter deletion leads to impaired migration and invasion potential via actin cytoskeleton rearrangement in colorectal cancerPayal Ranade, Rucha Trivedi, Diana Carolina Sierra-Díaz, et al.
Pharmacogenomics and Personalized Medicine|March 10, 2021
Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the PhenotypeDora Janeth Fonseca, Adrien Morel, Kevin Llinás-Caballero, et al.
Experimental Dermatology|March 9, 2018
Transcriptomic analysis of FUCA1 knock-down in keratinocytes reveals new insights into the pathogenesis of fucosidosis skin lesionsDanyela Valero-Rubio, Karen Marcela Jiménez, Dora Janeth Fonseca, et al.
Human Genetics|June 7, 2020
DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformationMaëva Elzaiat, Delphine Flatters, Diana Carolina Sierra-Díaz, et al.
Genetics|May 8, 2007
Centimorgan-range one-step mapping of fertility traits using interspecific recombinant congenic miceDavid L'Hôte, Catherine Serres, Paul Laissue, et al.
Human Mutation|October 11, 2018
Functional evidence implicating NOTCH2 missense mutations in primary ovarian insufficiency etiologyLiliana C Patiño, Isabelle Beau, Adrien Morel, et al.
Human Molecular Genetics|May 26, 2017
A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiencyCarolina Carlosama, Maëva Elzaiat, Liliana C Patiño, et al.
The Journal of Clinical Endocrinology and Metabolism|November 27, 2019
BMPR1A and BMPR1B Missense Mutations Cause Primary Ovarian InsufficiencyLucie Renault, Liliana C Patiño, Françoise Magnin, et al.
Plos One|October 22, 2014
Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosisLiliana Catherine Patiño, Rajani Battu, Oscar Ortega-Recalde, et al.
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