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Disease Models & Mechanisms|August 3, 2016
Dysfunction of intraflagellar transport-A causes hyperphagia-induced obesity and metabolic syndromeDamon T Jacobs, Luciane M Silva, Bailey A Allard, et al.The Journal of Clinical Investigation|November 4, 2009
Latent TGF-beta-binding protein 4 modifies muscular dystrophy in miceAhlke Heydemann, Ermelinda Ceco, Jackie E Lim, et al.Plos One|December 24, 2010
A transient transgenic RNAi strategy for rapid characterization of gene function during embryonic developmentBryan C Bjork, Yuko Fujiwara, Shannon W Davis, et al.NPJ Genomic Medicine|December 18, 2024
Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromesIftekhar A Showpnil, Maria E Hernandez Gonzalez, Swetha Ramadesikan, et al.Nature Genetics|January 31, 2002
Efficient generation and mapping of recessive developmental mutations using ENU mutagenesisBruce J Herron, Weining Lu, Cherie Rao, et al.Plos Genetics|August 26, 2025
A systems genetics approach identifies roles for proteasome factors in heart development and congenital heart defectsGist H Farr, Whitaker Reid, Eva H Hasegawa, et al.Development (Cambridge, England)|August 20, 2003
A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutationCherie Rao, Dorothee Foernzler, Stacie K Loftus, et al.Human Molecular Genetics|January 22, 2005
A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 miceBruce J Herron, Cherie Rao, Shanming Liu, et al.Journal of Muscle Research and Cell Motility|September 21, 2022
Mammalian organ regeneration in spiny miceDaryl M Okamura, Elizabeth D Nguyen, Sarah J Collins, et al.G3 (Bethesda, Md.)|June 23, 2022
The arginine methyltransferase Carm1 is necessary for heart developmentSophie Jamet, Seungshin Ha, Tzu-Hua Ho, et al.Pageof 15