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N Cooper

Showing results (541-550 of 1,439) with videos related to

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Depression and Anxiety|August 27, 2020
Consumption of energy drinks is associated with depression, anxiety, and stress in young adult males: Evidence from a longitudinal cohort studySimrat Kaur, Hayley Christian, Matthew N Cooper, et al.
Human Mutation|July 19, 2012
Assessment of the potential pathogenicity of missense mutations identified in the GTPase-activating protein (GAP)-related domain of the neurofibromatosis type-1 (NF1) geneLaura Thomas, Mark Richards, Matthew Mort, et al.
Surgical Forum|January 1, 1974
Effects of temperature, time, and perfusion pressure on coronary flow during ventricular fibrillationJ Brazier, D McConnell, N Cooper, et al.
The Journal of Investigative Dermatology|August 25, 2005
Gonosomal mosaicism for a nonsense mutation (R1947X) in the NF1 gene in segmental neurofibromatosis type 1Claudia Consoli, Celia Moss, Stuart Green, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|January 15, 2013
Evaluating risks of insertional mutagenesis by DNA transposons in gene therapyPerry B Hackett, David A Largaespada, Kirsten C Switzer, et al.
Cell and Tissue Research|May 16, 2002
Contractile properties, structure and fiber phenotype of intact and regenerating slow-twitch muscles of mice treated with cyclosporin AAndrey Irintchev, Margit Zweyer, Racquel N Cooper, et al.
Blood 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.
Journal of Biomedical Nanotechnology|August 8, 2019
Gold Nanoparticles Enhance Radiation Therapy at Low Concentrations, and Remain in Tumors for DaysBindeshwar Sah, Samana Shrestha, Jing Wu, 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.
Human Mutation|June 25, 2005
Complex gene rearrangements caused by serial replication slippageJian-Min Chen, Nadia Chuzhanova, Peter D Stenson, et al.
Pageof 144

Showing results (541-550 of 1,439) with videos related to

Sort By:
Pageof 144
Depression and Anxiety|August 27, 2020
Consumption of energy drinks is associated with depression, anxiety, and stress in young adult males: Evidence from a longitudinal cohort studySimrat Kaur, Hayley Christian, Matthew N Cooper, et al.
Human Mutation|July 19, 2012
Assessment of the potential pathogenicity of missense mutations identified in the GTPase-activating protein (GAP)-related domain of the neurofibromatosis type-1 (NF1) geneLaura Thomas, Mark Richards, Matthew Mort, et al.
Surgical Forum|January 1, 1974
Effects of temperature, time, and perfusion pressure on coronary flow during ventricular fibrillationJ Brazier, D McConnell, N Cooper, et al.
The Journal of Investigative Dermatology|August 25, 2005
Gonosomal mosaicism for a nonsense mutation (R1947X) in the NF1 gene in segmental neurofibromatosis type 1Claudia Consoli, Celia Moss, Stuart Green, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|January 15, 2013
Evaluating risks of insertional mutagenesis by DNA transposons in gene therapyPerry B Hackett, David A Largaespada, Kirsten C Switzer, et al.
Cell and Tissue Research|May 16, 2002
Contractile properties, structure and fiber phenotype of intact and regenerating slow-twitch muscles of mice treated with cyclosporin AAndrey Irintchev, Margit Zweyer, Racquel N Cooper, et al.
Blood 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.
Journal of Biomedical Nanotechnology|August 8, 2019
Gold Nanoparticles Enhance Radiation Therapy at Low Concentrations, and Remain in Tumors for DaysBindeshwar Sah, Samana Shrestha, Jing Wu, 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.
Human Mutation|June 25, 2005
Complex gene rearrangements caused by serial replication slippageJian-Min Chen, Nadia Chuzhanova, Peter D Stenson, et al.
Pageof 144