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M E Curran

Showing results (11-20 of 24) with videos related to

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Genomics|May 15, 1997
Genomic localization of the human gene for KCNA10, a cGMP-activated K channelM Orias, P Bray-Ward, M E Curran, et al.
Cell|March 10, 1995
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeM E Curran, I Splawski, K W Timothy, et al.
Cell|April 9, 1993
The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosisM E Curran, D L Atkinson, A K Ewart, et al.
Nucleic Acids Research|October 25, 1988
Sequence of a transcribed Physarum genomic DNA fragment containing a cluster of different U-RNA sequencesM E Curran, D S Sullivan, E A Arn, et al.
Nature|November 7, 1996
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channelM C Sanguinetti, M E Curran, A Zou, et al.
Molecular Pharmacology|April 18, 2001
Direct activation of an inwardly rectifying potassium channel by arachidonic acidY Liu, D Liu, L Heath, et al.
Gut|January 13, 2001
Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel diseaseJ Hampe, N J Lynch, S Daniels, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 9, 1998
Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13D L Koller, L A Rodriguez, J C Christian, et al.
The Journal of Clinical Endocrinology and Metabolism|September 22, 2000
Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosisD L Koller, M J Econs, P A Morin, et al.
American Journal of Human Genetics|December 1, 1999
Linkage of inflammatory bowel disease to human chromosome 6pJ Hampe, S H Shaw, R Saiz, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Genomics|May 15, 1997
Genomic localization of the human gene for KCNA10, a cGMP-activated K channelM Orias, P Bray-Ward, M E Curran, et al.
Cell|March 10, 1995
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeM E Curran, I Splawski, K W Timothy, et al.
Cell|April 9, 1993
The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosisM E Curran, D L Atkinson, A K Ewart, et al.
Nucleic Acids Research|October 25, 1988
Sequence of a transcribed Physarum genomic DNA fragment containing a cluster of different U-RNA sequencesM E Curran, D S Sullivan, E A Arn, et al.
Nature|November 7, 1996
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channelM C Sanguinetti, M E Curran, A Zou, et al.
Molecular Pharmacology|April 18, 2001
Direct activation of an inwardly rectifying potassium channel by arachidonic acidY Liu, D Liu, L Heath, et al.
Gut|January 13, 2001
Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel diseaseJ Hampe, N J Lynch, S Daniels, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 9, 1998
Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13D L Koller, L A Rodriguez, J C Christian, et al.
The Journal of Clinical Endocrinology and Metabolism|September 22, 2000
Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosisD L Koller, M J Econs, P A Morin, et al.
American Journal of Human Genetics|December 1, 1999
Linkage of inflammatory bowel disease to human chromosome 6pJ Hampe, S H Shaw, R Saiz, et al.
Pageof 3