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The Journal of Comparative Neurology|July 24, 2010
Inherited neuroaxonal dystrophy in dogs causing lethal, fetal-onset motor system dysfunction and cerebellar hypoplasiaJohn C Fyfe, Raba' A Al-Tamimi, Rudy J Castellani, et al.
Toxicologic Pathology|August 18, 2005
Brainstem axonal degeneration in mice with deletion of selenoprotein pWilliam M Valentine, Kristina E Hill, Lori M Austin, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 28, 2005
A deletion causing spontaneous fracture identified from a candidate region of mouse Chromosome 14Yan Jiao, Xinmin Li, Wesley G Beamer, et al.
Brain, Behavior, and Immunity|July 31, 2017
Systemic inflammation combined with neonatal cerebellar haemorrhage aggravates long-term structural and functional outcomes in a mouse modelSophie Tremblay, Alex Pai, Lindsay Richter, et al.
Seminars in Pediatric Neurology|May 18, 2011
Fetal alcohol spectrum disorders: gene-environment interactions, predictive biomarkers, and the relationship between structural alterations in the brain and functional outcomesJames N Reynolds, Joanne Weinberg, Sterling Clarren, et al.
JCI Insight|December 10, 2020
STOX1 deficiency is associated with renin-mediated gestational hypertension and placental defectsJacqueline G Parchem, Keizo Kanasaki, Soo Bong Lee, et al.
Visual Neuroscience|December 8, 2005
The Tennessee Mouse Genome Consortium: identification of ocular mutantsMonica M Jablonski, Xiaofei Wang, Lu Lu, et al.
Journal of the American Society of Nephrology : JASN|October 17, 2009
Stem cell therapies benefit Alport syndromeValerie LeBleu, Hikaru Sugimoto, Thomas M Mundel, et al.
Kidney International|September 19, 2008
A rat model of chronic kidney disease-mineral bone disorderSharon M Moe, Neal X Chen, Mark F Seifert, et al.
Genes, Brain, and Behavior|August 9, 2023
Developmental coordination disorder: What can we learn from RI mice using motor learning tasks and QTL analysisKamaldeep Gill, Jeffy Rajan Soundara Rajan, Eric Chow, et al.
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