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N Cooper

Showing results (521-530 of 1,439) with videos related to

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Genome Research|November 18, 2011
Interlocus gene conversion events introduce deleterious mutations into at least 1% of human genes associated with inherited diseaseClaudio Casola, Ugne Zekonyte, Andrew D Phillips, et al.
Biochemical Society Transactions|February 1, 1993
Analysis of a gene cluster from S. longisporoflavus potentially involved in tetronasin biosynthesisH N Cooper, J Cortes, D J Bevitt, 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.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 5, 2008
Beckwith Weidemann syndrome: a behavioral phenotype-genotype studyLindsey Kent, Sarah Bowdin, Gail A Kirby, et al.
Annals of Translational Medicine|February 22, 2019
Trochanteric pressure ulcers: preoperative management and reconstructive considerationsGiulia Daneshgaran, Michael N Cooper, Jaeyon Park, et al.
Lancet (London, England)|May 30, 1992
Prenatal exclusion of severe factor VII deficiency by DNA sequencingD S Millar, D N Cooper, V V Kakkar, 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.
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.
Pageof 144

Showing results (521-530 of 1,439) with videos related to

Sort By:
Pageof 144
Genome Research|November 18, 2011
Interlocus gene conversion events introduce deleterious mutations into at least 1% of human genes associated with inherited diseaseClaudio Casola, Ugne Zekonyte, Andrew D Phillips, et al.
Biochemical Society Transactions|February 1, 1993
Analysis of a gene cluster from S. longisporoflavus potentially involved in tetronasin biosynthesisH N Cooper, J Cortes, D J Bevitt, 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.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 5, 2008
Beckwith Weidemann syndrome: a behavioral phenotype-genotype studyLindsey Kent, Sarah Bowdin, Gail A Kirby, et al.
Annals of Translational Medicine|February 22, 2019
Trochanteric pressure ulcers: preoperative management and reconstructive considerationsGiulia Daneshgaran, Michael N Cooper, Jaeyon Park, et al.
Lancet (London, England)|May 30, 1992
Prenatal exclusion of severe factor VII deficiency by DNA sequencingD S Millar, D N Cooper, V V Kakkar, 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.
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.
Pageof 144