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J S Beckmann

Showing results (121-130 of 165) with videos related to

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American Journal of Human Genetics|November 22, 2000
A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16N Sylvius, F Tesson, C Gayet, et al.
Science (New York, N.Y.)|September 5, 1997
Dynamic molecular combing: stretching the whole human genome for high-resolution studiesX Michalet, R Ekong, F Fougerousse, et al.
Nature Genetics|April 1, 1993
Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive ratsC Dubay, M Vincent, N J Samani, et al.
Molecular and Cellular Biology|May 18, 1999
Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional eventsM Herasse, Y Ono, F Fougerousse, et al.
Neurology|April 11, 2001
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate geneH Haravuori, A Vihola, V Straub, et al.
Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.
Human Molecular Genetics|December 1, 1994
Adhalin gene polymorphismV Allamand, F Leturcq, F Piccolo, et al.
Oncogene|May 8, 2009
The Wnt receptor FZD1 mediates chemoresistance in neuroblastoma through activation of the Wnt/beta-catenin pathwayM Flahaut, R Meier, A Coulon, et al.
Human Molecular Genetics|December 23, 1999
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genesF Fougerousse, P Bullen, M Herasse, et al.
Journal of Medical Genetics|May 12, 2000
A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 familiesP Dinçer, Z Akçören, E Demir, et al.
Pageof 17

Showing results (121-130 of 165) with videos related to

Sort By:
Pageof 17
American Journal of Human Genetics|November 22, 2000
A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16N Sylvius, F Tesson, C Gayet, et al.
Science (New York, N.Y.)|September 5, 1997
Dynamic molecular combing: stretching the whole human genome for high-resolution studiesX Michalet, R Ekong, F Fougerousse, et al.
Nature Genetics|April 1, 1993
Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive ratsC Dubay, M Vincent, N J Samani, et al.
Molecular and Cellular Biology|May 18, 1999
Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional eventsM Herasse, Y Ono, F Fougerousse, et al.
Neurology|April 11, 2001
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate geneH Haravuori, A Vihola, V Straub, et al.
Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.
Human Molecular Genetics|December 1, 1994
Adhalin gene polymorphismV Allamand, F Leturcq, F Piccolo, et al.
Oncogene|May 8, 2009
The Wnt receptor FZD1 mediates chemoresistance in neuroblastoma through activation of the Wnt/beta-catenin pathwayM Flahaut, R Meier, A Coulon, et al.
Human Molecular Genetics|December 23, 1999
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genesF Fougerousse, P Bullen, M Herasse, et al.
Journal of Medical Genetics|May 12, 2000
A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 familiesP Dinçer, Z Akçören, E Demir, et al.
Pageof 17