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J S Beckmann

Showing results (111-120 of 165) with videos related to

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Human Molecular Genetics|September 1, 1993
Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12K Azibi, L Bachner, J S Beckmann, et al.
Molecular Psychiatry|September 29, 2005
The trace amine receptor 4 gene is not associated with schizophrenia in a sample linked to chromosome 6q23D Amann, N Avidan, K Kanyas, et al.
Nature|October 10, 1991
Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive ratsP Hilbert, K Lindpaintner, J S Beckmann, et al.
Investigative Ophthalmology & Visual Science|November 30, 2000
Influence of specific regions in Lp82 calpain on protein stability, activity, and localization within lensH Ma, M Shih, C Fukiage, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 11, 1991
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkageJ S Beckmann, I Richard, D Hillaire, et al.
Neuropediatrics|August 1, 1997
Calpain-3 deficiency causes a mild muscular dystrophy in childhoodH Topaloğlu, P Dinçer, I Richard, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 15C Joyce, L Fanning, S Malcolm, et al.
Nature Genetics|April 1, 1993
A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2pC Antignac, C H Arduy, J S Beckmann, et al.
The American Journal of Pathology|October 20, 1998
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2AL V Anderson, K Davison, J A Moss, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2002
Stable expression of calpain 3 from a muscle transgene in vivo: immature muscle in transgenic mice suggests a role for calpain 3 in muscle maturationM J Spencer, J R Guyon, H Sorimachi, et al.
Pageof 17

Showing results (111-120 of 165) with videos related to

Sort By:
Pageof 17
Human Molecular Genetics|September 1, 1993
Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12K Azibi, L Bachner, J S Beckmann, et al.
Molecular Psychiatry|September 29, 2005
The trace amine receptor 4 gene is not associated with schizophrenia in a sample linked to chromosome 6q23D Amann, N Avidan, K Kanyas, et al.
Nature|October 10, 1991
Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive ratsP Hilbert, K Lindpaintner, J S Beckmann, et al.
Investigative Ophthalmology & Visual Science|November 30, 2000
Influence of specific regions in Lp82 calpain on protein stability, activity, and localization within lensH Ma, M Shih, C Fukiage, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 11, 1991
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkageJ S Beckmann, I Richard, D Hillaire, et al.
Neuropediatrics|August 1, 1997
Calpain-3 deficiency causes a mild muscular dystrophy in childhoodH Topaloğlu, P Dinçer, I Richard, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 15C Joyce, L Fanning, S Malcolm, et al.
Nature Genetics|April 1, 1993
A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2pC Antignac, C H Arduy, J S Beckmann, et al.
The American Journal of Pathology|October 20, 1998
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2AL V Anderson, K Davison, J A Moss, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2002
Stable expression of calpain 3 from a muscle transgene in vivo: immature muscle in transgenic mice suggests a role for calpain 3 in muscle maturationM J Spencer, J R Guyon, H Sorimachi, et al.
Pageof 17