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Cerebral Cortex (New York, N.Y. : 1991)|December 3, 2014
Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron GenerationElizabeth M Paronett, Daniel W Meechan, Beverly A Karpinski, et al.
Human Molecular Genetics|October 19, 2012
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early developmentThomas M Maynard, Deepak Gopalakrishna, Daniel W Meechan, et al.
Biorxiv : the Preprint Server for Biology|December 19, 2025
Distinct cellular and transcriptional mechanisms mediate an antioxidant therapeutic response in 22q11-deleted upper layer cortical projection neuronsShah Rukh, Daniel W Meechan, Abra Roberts, et al.
Disease Models & Mechanisms|June 19, 2026
An antioxidant therapy elicits distinct transcriptome responses in 22q11-deleted upper layer cortical projection neuronsShah Rukh, Daniel W Meechan, Abra Roberts, et al.
Mechanisms of Development|January 24, 2002
RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial inductionThomas M Maynard, Gloria T Haskell, Naina Bhasin, et al.
Progress in Neurobiology|April 14, 2015
Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit developmentDaniel W Meechan, Thomas M Maynard, Eric S Tucker, et al.
Disease Models & Mechanisms|December 21, 2013
Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndromeBeverly A Karpinski, Thomas M Maynard, Matthew S Fralish, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 10, 2006
No evidence for parental imprinting of mouse 22q11 gene orthologsThomas M Maynard, Daniel W Meechan, Clifford C Heindel, et al.
Human Molecular Genetics|February 15, 2023
Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndromeElizabeth M Paronett, Corey A Bryan, Megan E Maynard, et al.
Disease Models & Mechanisms|March 16, 2021
Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndromeBeverly A Karpinski, Thomas M Maynard, Corey A Bryan, et al.
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