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J Vuust

Showing results (51-60 of 69) with videos related to

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The EMBO Journal|March 1, 1985
The human ubiquitin multigene family: some genes contain multiple directly repeated ubiquitin coding sequencesO Wiborg, M S Pedersen, A Wind, et al.
Clinical Genetics|November 24, 1999
Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 geneP S Andersen, O Havndrup, H Bundgaard, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1983
Molecular cloning of human gastrin cDNA: evidence for evolution of gastrin by gene duplicationE Boel, J Vuust, F Norris, et al.
The American Journal of Cardiology|May 30, 2001
The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young ageO Havndrup, H Bundgaard, P S Andersen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 25, 1999
A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndromeL A Larsen, P S Andersen, J K Kanters, et al.
Scandinavian Cardiovascular Journal : SCJ|February 24, 2001
A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathyO Havndrup, H Bundgaard, P S Andersen, et al.
Human Mutation|October 23, 2001
Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresisL A Larsen, M Johnson, C Brown, et al.
Journal of Cardiovascular Electrophysiology|July 8, 1998
Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndromeJ K Kanters, L A Larsen, M Orholm, et al.
Infection and Immunity|January 10, 1998
The glutamate-rich protein (GLURP) of Plasmodium falciparum is a target for antibody-dependent monocyte-mediated inhibition of parasite growth in vitroM Theisen, S Soe, C Oeuvray, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 geneL A Larsen, I Fosdal, P S Andersen, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
The EMBO Journal|March 1, 1985
The human ubiquitin multigene family: some genes contain multiple directly repeated ubiquitin coding sequencesO Wiborg, M S Pedersen, A Wind, et al.
Clinical Genetics|November 24, 1999
Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 geneP S Andersen, O Havndrup, H Bundgaard, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1983
Molecular cloning of human gastrin cDNA: evidence for evolution of gastrin by gene duplicationE Boel, J Vuust, F Norris, et al.
The American Journal of Cardiology|May 30, 2001
The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young ageO Havndrup, H Bundgaard, P S Andersen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 25, 1999
A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndromeL A Larsen, P S Andersen, J K Kanters, et al.
Scandinavian Cardiovascular Journal : SCJ|February 24, 2001
A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathyO Havndrup, H Bundgaard, P S Andersen, et al.
Human Mutation|October 23, 2001
Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresisL A Larsen, M Johnson, C Brown, et al.
Journal of Cardiovascular Electrophysiology|July 8, 1998
Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndromeJ K Kanters, L A Larsen, M Orholm, et al.
Infection and Immunity|January 10, 1998
The glutamate-rich protein (GLURP) of Plasmodium falciparum is a target for antibody-dependent monocyte-mediated inhibition of parasite growth in vitroM Theisen, S Soe, C Oeuvray, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 geneL A Larsen, I Fosdal, P S Andersen, et al.
Pageof 7