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Cancer Research|October 16, 1999
Solid tissues removed from ATM homozygous deficient mice do not exhibit a mutator phenotype for second-step autosomal mutationsM S Turker, B M Gage, J A Rose, et al.Oncogene|October 1, 2013
Tumor resident mesenchymal stromal cells endow naïve stromal cells with tumor-promoting propertiesG Ren, Y Liu, X Zhao, et al.Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.Molecular Genetics and Metabolism|September 10, 1999
Combined adenine phosphoribosyltransferase and N-acetylgalactosamine-6-sulfate sulfatase deficiencyL Wang, X Ou, I Sebesta, et al.Cancer Research|March 15, 1997
High frequency in vivo loss of heterozygosity is primarily a consequence of mitotic recombinationP K Gupta, A Sahota, S A Boyadjiev, et al.Cancer Research|March 1, 1996
Three secretory phospholipase A(2) genes that map to human chromosome 1P35-36 are not mutated in individuals with attenuated adenomatous polyposis coliL N Spirio, W Kutchera, M V Winstead, et al.Proceedings of the National Academy of Sciences of the United States of America|May 28, 1996
Adenine phosphoribosyltransferase-deficient mice develop 2,8-dihydroxyadenine nephrolithiasisS J Engle, M G Stockelman, J Chen, et al.Molecular Psychiatry|September 13, 2017
The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex familyN Sun, C Nasello, L Deng, et al.Proceedings of the National Academy of Sciences of the United States of America|August 5, 1998
Single-nucleotide polymorphism in the human mu opioid receptor gene alters beta-endorphin binding and activity: possible implications for opiate addictionC Bond, K S LaForge, M Tian, et al.Kidney International|September 5, 2001
Sequential analysis of kidney stone formation in the Aprt knockout mouseA P Evan, S B Bledsoe, B A Connors, et al.Pageof 9