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Journal of Molecular Evolution|January 1, 1987
The distribution of the dinucleotide CpG and cytosine methylation in the vitellogenin gene familyD N Cooper, S Gerber-Huber, D Nardelli, et al.Cytogenetic and Genome Research|February 3, 2007
Chromosomal speciation of humans and chimpanzees revisited: studies of DNA divergence within inverted regionsJ M Szamalek, D N Cooper, J Hoegel, et al.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.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.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.Human Genetics|September 1, 1991
The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqID S Millar, B Zoll, U Martinowitz, et al.Journal of Attention Disorders|March 14, 2023
Relationship Between Inhibitory Control and Arithmetic in Elementary School Children With ADHD: The Mediating Role of Working MemoryClara S C LeeBlood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 1, 1995
Polymorphic variation in the human protein C (PROC) gene promoter can influence transcriptional efficiency in vitroD Scopes, L P Berg, M Krawczak, et al.Prenatal Diagnosis|November 1, 1992
Prenatal exclusion of haemophilia A and carrier testing by direct detection of a disease lesionM Schwartz, D N Cooper, D S Millar, et al.Pageof 146