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Genetics|October 10, 2006
De novo exon duplication in a new allele of mouse Glra1 (spasmodic)Katherine D Holland, Michelle T Fleming, Susannah Cheek, et al.
Disease Models & Mechanisms|May 19, 2019
Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defectsKrista A Geister, Alberto Jose Lopez-Jimenez, Scott Houghtaling, et al.
The Journal of Biological Chemistry|May 16, 2002
Impaired organic anion transport in kidney and choroid plexus of organic anion transporter 3 (Oat3 (Slc22a8)) knockout miceDouglas H Sweet, David S Miller, John B Pritchard, et al.
Developmental Biology|September 27, 2003
Cordon-bleu is a conserved gene involved in neural tube formationElizabeth A Carroll, Dianne Gerrelli, Stéphan Gasca, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 12, 2006
Description and genetic mapping of Polypodia: an X-linked dominant mouse mutant with ectopic caudal limbs and other malformationsJessica A Lehoczky, Wei-Wen Cai, Julie A Douglas, et al.
Development (Cambridge, England)|November 8, 2002
A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafishShanming Liu, Weining Lu, Tomoko Obara, et al.
The Journal of Comparative Neurology|July 24, 2012
Mutation of the BiP/GRP78 gene causes axon outgrowth and fasciculation defects in the thalamocortical connections of the mammalian forebrainCarlita B Favero, Rasha N Henshaw, Cynthia M Grimsley-Myers, et al.
The Journal of Biological Chemistry|May 12, 2011
Lipoxygenases mediate the effect of essential fatty acid in skin barrier formation: a proposed role in releasing omega-hydroxyceramide for construction of the corneocyte lipid envelopeYuxiang Zheng, Huiyong Yin, William E Boeglin, et al.
American Journal of Medical Genetics. Part A|October 8, 2022
PPP2R1A neurodevelopmental disorder is associated with congenital heart defectsElizabeth K Baker, Beulah Solivio, Ben Pode-Shakked, et al.
Plos One|December 11, 2012
A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosisJianning Tao, Maranke I Koster, Wilbur Harrison, et al.
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