Chronic renal failure in a mouse model of human adenine phosphoribosyltransferase deficiency
Michael Stockelman(Indiana University – Purdue University Indianapolis), Peter J. Stambrook(Indiana University School of Medicine), Amrik Sahota(Indiana University School of Medicine), John N. Lorenz(University of Cincinnati Medical Center), F. N. L. Smith(University of Cincinnati Medical Center), Gregory P. Boivin(University of Cincinnati Medical Center), Jay A. Tischfield(Rutgers, The State University of New Jersey)
Cited by 60
Related Papers
Single-nucleotide polymorphism in the human mu opioid receptor gene alters β-endorphin binding and activity: Possible implications for opiate addiction
|Proceedings of the National Academy of Sciences|1998|1.1k
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
|Cell|1995|998
Transforming growth factor–β3 is required for secondary palate fusion
|Nature Genetics|1995|904
Genome-wide search for genes affecting the risk for alcohol dependence
|American Journal of Medical Genetics|1998|739
Variants in Nicotinic Receptors and Risk for Nicotine Dependence
|American Journal of Psychiatry|2008|641