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Plos Genetics|October 12, 2012
A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouseYoko Nakano, Israt Jahan, Gregory Bonde, et al.
Journal of Cardiovascular Pharmacology|July 29, 2022
Hypersensitivity of Zebrafish htr2b Mutant Embryos to Sertraline Indicates a Role for Serotonin Signaling in Cardiac DevelopmentMitchell E Kent, Bo Hu, Timothy M Eggleston, et al.
Development (Cambridge, England)|December 8, 2023
TFAP2 paralogs regulate midfacial development in part through a conserved ALX genetic pathwayTimothy T Nguyen, Jennyfer M Mitchell, Michaela D Kiel, et al.
Cell Reports|October 23, 2015
New Functional Signatures for Understanding Melanoma Biology from Tumor Cell Lineage-Specific AnalysisFlorian Rambow, Bastien Job, Valérie Petit, et al.
Annals of Clinical and Translational Neurology|March 9, 2019
Drug repositioning in epilepsy reveals novel antiseizure candidatesLeo Brueggeman, Morgan L Sturgeon, Russell M Martin, et al.
Plos Genetics|March 2, 2017
TFAP2 paralogs regulate melanocyte differentiation in parallel with MITFHannah E Seberg, Eric Van Otterloo, Stacie K Loftus, et al.
Genetics|November 23, 2017
Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in HumansLisa A Lansdon, Benjamin W Darbro, Aline L Petrin, et al.
International Journal of Oral Science|March 1, 2026
Soluble Notch agonist enables human ameloblast maturation and enamel-like tissue formation for tooth regenerationAnjali P Patni, Rubul Mout, Ammar Alghadeer, et al.
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