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Showing results (71-80 of 96) with videos related to

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Journal of Molecular Biology|August 5, 2009
Structural and functional diversity of novel coronin 1C (CRN2) isoforms in muscleCharles-Peter Xavier, Raphael H Rastetter, Maria Stumpf, et al.
Pflugers Archiv : European Journal of Physiology|May 22, 2010
Enhanced eryptosis of erythrocytes from gene-targeted mice lacking annexin A7Elisabeth Lang, Philipp A Lang, Ekaterina Shumilina, et al.
FEBS Letters|June 28, 2005
Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathiesChristoph S Clemen, Dirk Fischer, Udo Roth, et al.
The Journal of Pathology|August 7, 2010
Primary effusion lymphoma: genomic profiling revealed amplification of SELPLG and CORO1C encoding for proteins important for cell migrationShi-Lu Luan, Emmanuelle Boulanger, Hongtao Ye, et al.
Cardiovascular Research|July 31, 2007
Enhanced heterogeneity of myocardial conduction and severe cardiac electrical instability in annexin A7-deficient miceJan W Schrickel, Klara Brixius, Claudia Herr, et al.
European Journal of Cell Biology|November 4, 2019
CRN2 binds to TIMP4 and MMP14 and promotes perivascular invasion of glioblastoma cellsRoxana Solga, Juliane Behrens, Anja Ziemann, et al.
Biochemical and Biophysical Research Communications|April 14, 2015
In vivo characterization of human myofibrillar myopathy genes in zebrafishJohn B Bührdel, Sofia Hirth, Mirjam Kessler, et al.
Scientific Reports|February 23, 2012
Phosphorylation of CRN2 by CK2 regulates F-actin and Arp2/3 interaction and inhibits cell migrationCharles-Peter Xavier, Raphael H Rastetter, Margit Blömacher, et al.
Plos One|March 4, 2020
Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in miceFlorian Stöckigt, Lars Eichhorn, Thomas Beiert, et al.
Human Molecular Genetics|March 7, 2003
On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondriaRolf Schröder, Bertrand Goudeau, Monique Casteras Simon, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
Journal of Molecular Biology|August 5, 2009
Structural and functional diversity of novel coronin 1C (CRN2) isoforms in muscleCharles-Peter Xavier, Raphael H Rastetter, Maria Stumpf, et al.
Pflugers Archiv : European Journal of Physiology|May 22, 2010
Enhanced eryptosis of erythrocytes from gene-targeted mice lacking annexin A7Elisabeth Lang, Philipp A Lang, Ekaterina Shumilina, et al.
FEBS Letters|June 28, 2005
Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathiesChristoph S Clemen, Dirk Fischer, Udo Roth, et al.
The Journal of Pathology|August 7, 2010
Primary effusion lymphoma: genomic profiling revealed amplification of SELPLG and CORO1C encoding for proteins important for cell migrationShi-Lu Luan, Emmanuelle Boulanger, Hongtao Ye, et al.
Cardiovascular Research|July 31, 2007
Enhanced heterogeneity of myocardial conduction and severe cardiac electrical instability in annexin A7-deficient miceJan W Schrickel, Klara Brixius, Claudia Herr, et al.
European Journal of Cell Biology|November 4, 2019
CRN2 binds to TIMP4 and MMP14 and promotes perivascular invasion of glioblastoma cellsRoxana Solga, Juliane Behrens, Anja Ziemann, et al.
Biochemical and Biophysical Research Communications|April 14, 2015
In vivo characterization of human myofibrillar myopathy genes in zebrafishJohn B Bührdel, Sofia Hirth, Mirjam Kessler, et al.
Scientific Reports|February 23, 2012
Phosphorylation of CRN2 by CK2 regulates F-actin and Arp2/3 interaction and inhibits cell migrationCharles-Peter Xavier, Raphael H Rastetter, Margit Blömacher, et al.
Plos One|March 4, 2020
Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in miceFlorian Stöckigt, Lars Eichhorn, Thomas Beiert, et al.
Human Molecular Genetics|March 7, 2003
On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondriaRolf Schröder, Bertrand Goudeau, Monique Casteras Simon, et al.
Pageof 10