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Showing results (61-70 of 66) with videos related to

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American Journal of Human Genetics|March 26, 1999
Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmiasR Mohammad-Panah, S Demolombe, N Neyroud, et al.
American Journal of Physiology. Cell Physiology|February 24, 2001
Differential expression of KvLQT1 and its regulator IsK in mouse epitheliaS Demolombe, D Franco, P de Boer, et al.
Cardiovascular Research|September 15, 2001
Divergent expression of delayed rectifier K(+) channel subunits during mouse heart developmentD Franco, S Demolombe, S Kupershmidt, et al.
The Journal of Biological Chemistry|April 18, 1998
A dominant negative isoform of the long QT syndrome 1 gene productS Demolombe, I Baró, Y Péréon, et al.
Circulation|December 19, 2001
Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French familyF Kyndt, V Probst, F Potet, et al.
Cardiovascular Research|May 4, 2001
Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisationS Demolombe, G Lande, F Charpentier, et al.
Pageof 7

Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 66 results.
American Journal of Human Genetics|March 26, 1999
Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmiasR Mohammad-Panah, S Demolombe, N Neyroud, et al.
American Journal of Physiology. Cell Physiology|February 24, 2001
Differential expression of KvLQT1 and its regulator IsK in mouse epitheliaS Demolombe, D Franco, P de Boer, et al.
Cardiovascular Research|September 15, 2001
Divergent expression of delayed rectifier K(+) channel subunits during mouse heart developmentD Franco, S Demolombe, S Kupershmidt, et al.
The Journal of Biological Chemistry|April 18, 1998
A dominant negative isoform of the long QT syndrome 1 gene productS Demolombe, I Baró, Y Péréon, et al.
Circulation|December 19, 2001
Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French familyF Kyndt, V Probst, F Potet, et al.
Cardiovascular Research|May 4, 2001
Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisationS Demolombe, G Lande, F Charpentier, et al.
Pageof 7