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Human Genetics|August 1, 1992
Two different missense mutations at Arg 178 of the protein C (PROC) gene causing recurrent venous thrombosisC B Grundy, S Schulman, L Tengborn, et al.Genome Research|July 14, 2011
Loss of exon identity is a common mechanism of human inherited diseaseTimothy Sterne-Weiler, Jonathan Howard, Matthew Mort, et al.International Journal of Oncology|January 26, 1999
Induction of differentiation and apoptosis in the prostate cancer cell line LNCaP by sodium butyrate and galectin-1J Ellerhorst, T Nguyen, D N Cooper, et al.Human Mutation|August 26, 2003
Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifsShaun S Abeysinghe, Nadia Chuzhanova, Michael Krawczak, et al.Plos One|August 17, 2013
A conservative assessment of the major genetic causes of idiopathic chronic pancreatitis: data from a comprehensive analysis of PRSS1, SPINK1, CTRC and CFTR genes in 253 young French patientsEmmanuelle Masson, Jian-Min Chen, Marie-Pierre Audrézet, et al.Medical Physics|June 7, 2000
An edge spread technique for measurement of the scatter-to-primary ratio in mammographyV N Cooper, J M Boone, J A Seibert, et al.Journal of Cell Science|January 1, 1994
Selective modulation of the interaction of alpha 7 beta 1 integrin with fibronectin and laminin by L-14 lectin during skeletal muscle differentiationM Gu, W Wang, W K Song, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancyD S Millar, J Allgrove, C Rodeck, et al.The Journal of Experimental Biology|January 26, 2013
Regulation of succinate-fuelled mitochondrial respiration in liver and skeletal muscle of hibernating thirteen-lined ground squirrelsJason C L Brown, Dillon J Chung, Alex N Cooper, et al.Human Genetics|July 4, 2013
Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited diseaseDavid N Cooper, Michael Krawczak, Constantin Polychronakos, et al.Pageof 123