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Genomics|February 16, 2000
Cloning, characterization, and chromosomal localization of Pnck, a Ca(2+)/calmodulin-dependent protein kinaseH P Gardner, J V Rajan, S I Ha, et al.Cytokine|August 6, 1999
Characterization of the cDNA and gene for mouse tumour necrosis factor alpha converting enzyme (TACE/ADAM17) and its location to mouse chromosome 12 and human chromosome 2p25D P Cerretti, K Poindexter, B J Castner, et al.Genomics|July 20, 1995
Murine chromosomal location of five bHLH-Zip transcription factor genesE Steingrímsson, M Sawadogo, D J Gilbert, et al.Genetics|August 1, 1990
A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcrossM J Justice, L D Siracusa, D J Gilbert, et al.Human Genetics|February 26, 2003
Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinicsClare L Scott, Mark A Jenkins, Melissa C Southey, et al.The American Journal of Cardiology|August 27, 2013
Predictors of regional variations in hospitalizations following emergency department visits for atrial fibrillationTyler W Barrett, Wesley H Self, Cathy A Jenkins, et al.Molecular and Cellular Biology|April 11, 2000
Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast linesG Piras, A El Kharroubi, S Kozlov, et al.Journal of Virology|September 5, 2001
Retroviral integration at the Epi1 locus cooperates with Nf1 gene loss in the progression to acute myeloid leukemiaS M Blaydes, S C Kogan, B T Truong, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 14, 2001
Evidence for a common binding cavity for three general anesthetics within the GABAA receptorA Jenkins, E P Greenblatt, H J Faulkner, et al.Human Mutation|October 8, 2005
Molecular characterization and cancer risk associated with BRCA1 and BRCA2 splice site variants identified in multiple-case breast cancer familiesA A Tesoriero, E M Wong, M A Jenkins, et al.Pageof 284