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Molecular and Cellular Endocrinology|July 27, 2017
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencingPaul LaissueMolecular and Cellular Endocrinology|May 12, 2015
Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencingPaul LaissueMolecular Cancer|January 10, 2019
The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesisPaul LaissueCurrent Hypertension Reports|March 16, 2020
Exploring the Molecular Aetiology of Preeclampsia by Massive Parallel Sequencing of DNAPaul Laissue, Daniel VaimanReproductive Sciences (Thousand Oaks, Calif.)|March 19, 2019
Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing ApproachesPaula Quintero-Ronderos, Paul LaissueJournal of Molecular Medicine (Berlin, Germany)|July 1, 2018
The multisystemic functions of FOXD1 in development and diseasePaula Quintero-Ronderos, Paul LaissueReproductive Sciences (Thousand Oaks, Calif.)|May 21, 2020
Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing ApproachesPaula Quintero-Ronderos, Paul LaissueMammalian Genome : Official Journal of the International Mammalian Genome Society|August 4, 2014
A high resolution map of mammalian X chromosome fragile regions assessed by large-scale comparative genomicsCarlos Fernando Prada, Paul LaissueSystems Biology in Reproductive Medicine|March 18, 2017
A potential functional association between mutant BMPR2 and primary ovarian insufficiencyLiliana Catherine Patiño, Daniel Silgado, Paul LaissueMolecular and Cellular Endocrinology|January 1, 2008
Recent advances in the study of genes involved in non-syndromic premature ovarian failurePaul Laissue, Giovanna Vinci, Reiner A Veitia, et al.Pageof 7