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Nature Genetics|April 1, 1993
A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2pC Antignac, C H Arduy, J S Beckmann, et al.Neuropharmacology|December 21, 2023
Impacts of xylazine on fentanyl demand, body weight, and acute withdrawal in rats: A comparison to lofexidineSafiyah M Sadek, Shailesh N Khatri, Zachary Kipp, et al.Journal of Muscle Research and Cell Motility|December 26, 2002
Six and Eya expression during human somitogenesis and MyoD gene family activationFrançoise Fougerousse, Muriel Durand, Soledad Lopez, et al.American Journal of Human Genetics|March 4, 2014
A higher mutational burden in females supports a "female protective model" in neurodevelopmental disordersSébastien Jacquemont, Bradley P Coe, Micha Hersch, et al.Cancer Genetics and Cytogenetics|October 23, 2008
Automated four-color interphase fluorescence in situ hybridization approach for the simultaneous detection of specific aneuploidies of diagnostic and prognostic significance in high hyperdiploid acute lymphoblastic leukemiaAnna Talamo Blandin, Dominique Mühlematter, Sandrine Bougeon, et al.BMC Genomics|June 19, 2012
Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohortArmand Valsesia, Brian J Stevenson, Dawn Waterworth, et al.The American Journal of Pathology|October 20, 1998
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2AL V Anderson, K Davison, J A Moss, et al.Drug and Alcohol Dependence|October 7, 2011
A translational behavioral model of mood-based impulsivity: Implications for substance abuseCassandra D Gipson, Joshua S Beckmann, Zack W Adams, et al.Proceedings of the National Academy of Sciences of the United States of America|June 27, 2002
Stable expression of calpain 3 from a muscle transgene in vivo: immature muscle in transgenic mice suggests a role for calpain 3 in muscle maturationM J Spencer, J R Guyon, H Sorimachi, et al.American Journal of Human Genetics|November 22, 2000
A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16N Sylvius, F Tesson, C Gayet, et al.Pageof 38