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J S Beckmann

Showing results (81-90 of 165) with videos related to

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TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 21, 2013
Physical mapping of plastid DNA variation among eleven Nicotiana speciesY Salts, R G Herrmann, N Peleg, et al.
Nucleic Acids Research|March 11, 1990
Large restriction fragments containing poly-TG are highly polymorphic in a variety of vertebratesY Kashi, Y Tikochinsky, E Genislav, et al.
Genomics|January 15, 1994
Targeted development of microsatellite markers from inter-Alu amplification of YAC clonesA P de Souza, V Allamand, I Richard, et al.
American Journal of Physiology. Cell Physiology|May 15, 2001
Calpain 3 mRNA expression in mice after denervation and during muscle regenerationD Stockholm, M Herasse, S Marchand, et al.
Biophysical Journal|May 24, 2001
Mutations in calpain 3 associated with limb girdle muscular dystrophy: analysis by molecular modeling and by mutation in m-calpainZ Jia, V Petrounevitch, A Wong, et al.
Neuromuscular Disorders : NMD|May 1, 1996
Prenatal diagnosis of limb-girdle muscular dystrophy type 2AG Restagno, N Romero, I Richard, et al.
Human Molecular Genetics|November 1, 1995
Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosisA Fuchshuber, G Jean, O Gribouval, et al.
Journal of Medical Genetics|November 1, 1993
Estimating locus heterogeneity in autosomal dominant polycystic kidney disease (ADPKD) in the Spanish populationB Peral, J L San Millán, C Hernández, et al.
The Journal of Biological Chemistry|June 27, 1998
Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2AY Ono, H Shimada, H Sorimachi, et al.
Human Molecular Genetics|February 9, 1999
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21M Mustapha, D Weil, S Chardenoux, et al.
Pageof 17

Showing results (81-90 of 165) with videos related to

Sort By:
Pageof 17
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|November 21, 2013
Physical mapping of plastid DNA variation among eleven Nicotiana speciesY Salts, R G Herrmann, N Peleg, et al.
Nucleic Acids Research|March 11, 1990
Large restriction fragments containing poly-TG are highly polymorphic in a variety of vertebratesY Kashi, Y Tikochinsky, E Genislav, et al.
Genomics|January 15, 1994
Targeted development of microsatellite markers from inter-Alu amplification of YAC clonesA P de Souza, V Allamand, I Richard, et al.
American Journal of Physiology. Cell Physiology|May 15, 2001
Calpain 3 mRNA expression in mice after denervation and during muscle regenerationD Stockholm, M Herasse, S Marchand, et al.
Biophysical Journal|May 24, 2001
Mutations in calpain 3 associated with limb girdle muscular dystrophy: analysis by molecular modeling and by mutation in m-calpainZ Jia, V Petrounevitch, A Wong, et al.
Neuromuscular Disorders : NMD|May 1, 1996
Prenatal diagnosis of limb-girdle muscular dystrophy type 2AG Restagno, N Romero, I Richard, et al.
Human Molecular Genetics|November 1, 1995
Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosisA Fuchshuber, G Jean, O Gribouval, et al.
Journal of Medical Genetics|November 1, 1993
Estimating locus heterogeneity in autosomal dominant polycystic kidney disease (ADPKD) in the Spanish populationB Peral, J L San Millán, C Hernández, et al.
The Journal of Biological Chemistry|June 27, 1998
Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2AY Ono, H Shimada, H Sorimachi, et al.
Human Molecular Genetics|February 9, 1999
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21M Mustapha, D Weil, S Chardenoux, et al.
Pageof 17