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Genomics
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May 15, 1997
Genomic localization of the human gene for KCNA10, a cGMP-activated K channel
M Orias, P Bray-Ward, M E Curran, et al.
Cell
|
March 10, 1995
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
M 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 stenosis
M 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 sequences
M 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 channel
M C Sanguinetti, M E Curran, A Zou, et al.
Molecular Pharmacology
|
April 18, 2001
Direct activation of an inwardly rectifying potassium channel by arachidonic acid
Y Liu, D Liu, L Heath, et al.
Gut
|
January 13, 2001
Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease
J 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 11q12-13
D 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 osteoporosis
D 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 6p
J Hampe, S H Shaw, R Saiz, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Genomics
|
May 15, 1997
Genomic localization of the human gene for KCNA10, a cGMP-activated K channel
M Orias, P Bray-Ward, M E Curran, et al.
Cell
|
March 10, 1995
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
M 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 stenosis
M 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 sequences
M 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 channel
M C Sanguinetti, M E Curran, A Zou, et al.
Molecular Pharmacology
|
April 18, 2001
Direct activation of an inwardly rectifying potassium channel by arachidonic acid
Y Liu, D Liu, L Heath, et al.
Gut
|
January 13, 2001
Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease
J 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 11q12-13
D 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 osteoporosis
D 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 6p
J Hampe, S H Shaw, R Saiz, et al.
Page
of 3