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Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 7, 2002
Confirmation and high resolution mapping of an atherosclerosis susceptibility gene in mice on Chromosome 1Shelley A Phelan, David R Beier, David C Higgins, et al.
Journal of Cell Science|June 24, 2025
Inhibition of Hedgehog signaling does not mitigate polycystic kidney disease severity in a Pkd1 mutant mouse modelSean K Gombart, Scott Houghtaling, Tzu-Hua Ho, et al.
G3 (Bethesda, Md.)|June 5, 2016
Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in MiceSeungshin Ha, Anna M Lindsay, Andrew E Timms, et al.
Development (Cambridge, England)|February 15, 2023
Successful therapeutic intervention in new mouse models of frizzled 2-associated congenital malformationsRyan P Liegel, Megan N Michalski, Sanika Vaidya, et al.
Current Topics in Developmental Biology|April 24, 2022
Wound healing and regeneration in spiny mice (Acomys cahirinus)Daryl M Okamura, Elizabeth D Nguyen, David R Beier, et al.
G3 (Bethesda, Md.)|March 14, 2012
Production of a natural antibody to the mouse polyoma virus is a multigenic traitErik Andrews, Palanivel Velupillai, Chang Kyoo Sung, et al.
Cytoskeleton (Hoboken, N.J.)|February 20, 2010
Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary ciliaDai Shiba, Danielle K Manning, Hisashi Koga, et al.
Human Molecular Genetics|October 17, 2017
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephalyAndrew DiStasio, Ashley Driver, Kristen Sund, et al.
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