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Molecular Genetics & Genomic Medicine|January 29, 2015
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindredsJie Yang, Shih-Kai Wang, Murim Choi, et al.
Scientific Reports|August 3, 2019
Genome-wide screening of mouse knockouts reveals novel genes required for normal integumentary and oculocutaneous structure and functionBret A Moore, Ann M Flenniken, Dave Clary, et al.
Investigative Ophthalmology & Visual Science|May 31, 2018
A Population Study of Common Ocular Abnormalities in C57BL/6N rd8 MiceBret A Moore, Michel J Roux, Lionel Sebbag, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 20, 2024
The mutant mouse resource and research center (MMRRC) consortium: the US-based public mouse repository systemYuksel Agca, James Amos-Landgraf, Renee Araiza, et al.
Science (New York, N.Y.)|January 14, 2017
Deficiency of microRNA miR-34a expands cell fate potential in pluripotent stem cellsYong Jin Choi, Chao-Po Lin, Davide Risso, et al.
Developmental Biology|October 22, 2019
Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 miceYoung Sam Kwon, Addy Tham, Antonio Jacobo Lopez, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|December 17, 2013
The influence of Shc proteins on life span in miceJon J Ramsey, Dianna Tran, Marco Giorgio, et al.
Experimental Eye Research|March 26, 2026
Zfp503 haploinsufficiency causes optic nerve coloboma in miceJenna Wong-Fortunato, Benjamin Yang, Louise Lanoue, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 27, 2024
The mouse metabolic phenotyping center (MMPC) live consortium: an NIH resource for in vivo characterization of mouse models of diabetes and obesityMaren Laughlin, Richard McIndoe, Sean H Adams, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2022
A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorderSuma P Shankar, Kristin Grimsrud, Louise Lanoue, et al.
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