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R F Hrstka

Showing results (1-10 of 9) with videos related to

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Human Molecular Genetics|June 22, 2000
Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia miceE V Semina, J C Murray, R Reiter, et al.
Molecular and Cellular Biology|February 12, 2000
Sarcospan-deficient mice maintain normal muscle functionC S Lebakken, D P Venzke, R F Hrstka, et al.
Science (New York, N.Y.)|July 17, 1998
Requirement for the leukocyte-specific adapter protein SLP-76 for normal T cell developmentJ L Clements, B Yang, S E Ross-Barta, et al.
Molecular Cell|March 11, 2000
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2EM Durbeej, R D Cohn, R F Hrstka, et al.
Human Molecular Genetics|June 1, 1997
Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null miceR A Williamson, M D Henry, K J Daniels, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 17, 1999
Disruption of the beta subunit of the epithelial Na+ channel in mice: hyperkalemia and neonatal death associated with a pseudohypoaldosteronism phenotypeF J McDonald, B Yang, R F Hrstka, et al.
Cell|September 11, 1999
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophyR Coral-Vazquez, R D Cohn, S A Moore, et al.
Nature|November 9, 2000
The mammalian sodium channel BNC1 is required for normal touch sensationM P Price, G R Lewin, S L McIlwrath, et al.
The Journal of Cell Biology|September 23, 1998
Progressive muscular dystrophy in alpha-sarcoglycan-deficient miceF Duclos, V Straub, S A Moore, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|June 22, 2000
Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia miceE V Semina, J C Murray, R Reiter, et al.
Molecular and Cellular Biology|February 12, 2000
Sarcospan-deficient mice maintain normal muscle functionC S Lebakken, D P Venzke, R F Hrstka, et al.
Science (New York, N.Y.)|July 17, 1998
Requirement for the leukocyte-specific adapter protein SLP-76 for normal T cell developmentJ L Clements, B Yang, S E Ross-Barta, et al.
Molecular Cell|March 11, 2000
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2EM Durbeej, R D Cohn, R F Hrstka, et al.
Human Molecular Genetics|June 1, 1997
Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null miceR A Williamson, M D Henry, K J Daniels, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 17, 1999
Disruption of the beta subunit of the epithelial Na+ channel in mice: hyperkalemia and neonatal death associated with a pseudohypoaldosteronism phenotypeF J McDonald, B Yang, R F Hrstka, et al.
Cell|September 11, 1999
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophyR Coral-Vazquez, R D Cohn, S A Moore, et al.
Nature|November 9, 2000
The mammalian sodium channel BNC1 is required for normal touch sensationM P Price, G R Lewin, S L McIlwrath, et al.
The Journal of Cell Biology|September 23, 1998
Progressive muscular dystrophy in alpha-sarcoglycan-deficient miceF Duclos, V Straub, S A Moore, et al.
Pageof 1