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Developmental Biology|March 19, 2016
A cellular and molecular mosaic establishes growth and differentiation states for cranial sensory neuronsBeverly A Karpinski, Corey A Bryan, Elizabeth M Paronett, et al.
Genetics|April 15, 2016
Functional Divergence of the Nuclear Receptor NR2C1 as a Modulator of Pluripotentiality During Hominid EvolutionJennifer L Baker, Katherine A Dunn, Joseph Mingrone, et al.
Genesis (New York, N.Y. : 2000)|March 20, 2017
Foxd4 is essential for establishing neural cell fate and for neuronal differentiationJonathan H Sherman, Beverly A Karpinski, Matthew S Fralish, et al.
Birth Defects Research|May 21, 2020
Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndromeGelila Yitsege, Bethany A Stokes, Julia A Sabatino, et al.
Human Molecular Genetics|February 13, 2020
Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndromeThomas M Maynard, Anelia Horvath, James P Bernot, et al.
Experimental Eye Research|December 20, 2022
Molecular mechanisms regulating wound repair: Evidence for paracrine signaling from corneal epithelial cells to fibroblasts and immune cells following transient epithelial cell treatment with Mitomycin CSonali Pal-Ghosh, Beverly A Karpinski, Himani Datta Majumdar, et al.
Neuron|May 14, 2019
Mitochondrial Dysfunction Leads to Cortical Under-Connectivity and Cognitive ImpairmentAlejandra Fernandez, Daniel W Meechan, Beverly A Karpinski, et al.
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