Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Biorxiv : the Preprint Server for Biology|July 19, 2024
A Retinoic Acid:YAP1 signaling axis controls atrial lineage commitmentElizabeth Abraham, Brett Volmert, Thomas Roule, et al.
EMBO Reports|March 27, 2026
YAP1 and QSER1 are key modulators of embryonic signaling pathways in the mammalian epiblastElizabeth Abraham, Thomas Roule, Aidan Douglas, et al.
Cell Reports. Medicine|January 24, 2024
Targeted therapy improves cellular dysfunction, ataxia, and seizure susceptibility in a model of a progressive myoclonus epilepsyHuijie Feng, Jerome Clatot, Keisuke Kaneko, et al.
Biorxiv : the Preprint Server for Biology|July 16, 2025
YAP1 and QSER1 are Key Modulators of Embryonic Signaling Pathways in the Mammalian EpiblastElizabeth Abraham, Thomas Roule, Aidan Douglas, et al.
Cell Reports|May 9, 2025
A retinoic acid:YAP1 signaling axis controls atrial lineage commitmentElizabeth Abraham, Aleksandra Kostina, Brett Volmert, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
High density SNP array and reanalysis of genome sequencing uncovers CNVs associated with neurodevelopmental disorders in KOLF2.1J iPSCsCarolina Gracia-Diaz, Jonathan E Perdomo, Munir E Khan, et al.
American Journal of Human Genetics|March 5, 2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasiaNaiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, et al.
American Journal of Human Genetics|December 24, 2013
Mutations in CSPP1 lead to classical Joubert syndromeNaiara Akizu, Jennifer L Silhavy, Rasim Ozgur Rosti, et al.
Nature Genetics|May 26, 2015
Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndromeAlicia Guemez-Gamboa, Long N Nguyen, Hongbo Yang, et al.
Cell|August 6, 2013
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorderNaiara Akizu, Vincent Cantagrel, Jana Schroth, et al.
Pageof 4