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B Wieringa

Showing results (141-150 of 173) with videos related to

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American Journal of Human Genetics|June 1, 1990
The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophyA E MacKenzie, R G Korneluk, F Zorzato, et al.
Atherosclerosis|November 1, 1995
Variability in cholesterol content in serum and aortic tissue in apolipoprotein E-deficient mice is comparable in inbred (129/Sv) and outbred (mixed 129/Sv and C57BL/6) miceJ H van Ree, W J van den Broek, V E Dahlmans, et al.
Genomics|May 1, 1995
The mouse gene Ptprf encoding the leukocyte common antigen-related molecule LAR: cloning, characterization, and chromosomal localizationR Q Schaapveld, A M van den Maagdenberg, J T Schepens, et al.
Human Genetics|November 1, 1990
Cloning of the breakpoints of a deletion associated with choroidermiaF P Cremers, F Brunsmann, W Berger, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35 --> q36.1 and identification of an intragenic genetic markerA M van den Maagdenberg, D Olde Weghuis, J Rijss, et al.
Human Genetics|November 1, 1986
Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophyM H Hofker, A A Bergen, M I Skraastad, et al.
Genomics|May 1, 1989
Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosomeM N Patterson, M V Bell, J Bloomfield, et al.
Cytogenetics and Cell Genetics|July 7, 1999
Assignment1 of the PTP-SL/PTPBR7 gene (Ptprr/PTPRR) to mouse chromosome region 8A2 by in situ hybridizationA M van den Maagdenberg, J T Schepens, M T Schepens, et al.
The EMBO Journal|December 2, 2000
Adenylate kinase 1 gene deletion disrupts muscle energetic economy despite metabolic rearrangementE Janssen, P P Dzeja, F Oerlemans, et al.
Human Genetics|March 1, 1989
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)H G Brunner, R G Korneluk, M Coerwinkel-Driessen, et al.
Pageof 18

Showing results (141-150 of 173) with videos related to

Sort By:
Pageof 18
American Journal of Human Genetics|June 1, 1990
The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophyA E MacKenzie, R G Korneluk, F Zorzato, et al.
Atherosclerosis|November 1, 1995
Variability in cholesterol content in serum and aortic tissue in apolipoprotein E-deficient mice is comparable in inbred (129/Sv) and outbred (mixed 129/Sv and C57BL/6) miceJ H van Ree, W J van den Broek, V E Dahlmans, et al.
Genomics|May 1, 1995
The mouse gene Ptprf encoding the leukocyte common antigen-related molecule LAR: cloning, characterization, and chromosomal localizationR Q Schaapveld, A M van den Maagdenberg, J T Schepens, et al.
Human Genetics|November 1, 1990
Cloning of the breakpoints of a deletion associated with choroidermiaF P Cremers, F Brunsmann, W Berger, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35 --> q36.1 and identification of an intragenic genetic markerA M van den Maagdenberg, D Olde Weghuis, J Rijss, et al.
Human Genetics|November 1, 1986
Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophyM H Hofker, A A Bergen, M I Skraastad, et al.
Genomics|May 1, 1989
Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosomeM N Patterson, M V Bell, J Bloomfield, et al.
Cytogenetics and Cell Genetics|July 7, 1999
Assignment1 of the PTP-SL/PTPBR7 gene (Ptprr/PTPRR) to mouse chromosome region 8A2 by in situ hybridizationA M van den Maagdenberg, J T Schepens, M T Schepens, et al.
The EMBO Journal|December 2, 2000
Adenylate kinase 1 gene deletion disrupts muscle energetic economy despite metabolic rearrangementE Janssen, P P Dzeja, F Oerlemans, et al.
Human Genetics|March 1, 1989
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)H G Brunner, R G Korneluk, M Coerwinkel-Driessen, et al.
Pageof 18