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C Kubisch

Showing results (11-20 of 34) with videos related to

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FEBS Letters|November 29, 1993
Immediate-early gene induction by repetitive mechanical but not electrical activity in adult rat cardiomyocytesC Kubisch, B Wollnik, A Maass, et al.
Thyroid : Official Journal of the American Thyroid Association|December 16, 1998
The extracellular thyrotropin receptor domain is not a major candidate for mutations in toxic thyroid nodulesD Führer, C Kubisch, U Scheibler, et al.
European Heart Journal|May 1, 1995
Hormonal induction of an immediate-early gene response in myogenic cell lines--a paradigm for heart growthA Maass, C Grohé, C Kubisch, et al.
Neurology|May 5, 1999
Phenotypic variability in rippling muscle diseaseM Vorgerd, H Bolz, T Patzold, et al.
Human Molecular Genetics|September 16, 1998
ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependenceC Kubisch, T Schmidt-Rose, B Fontaine, et al.
Clinical Hemorheology and Microcirculation|February 6, 2010
B-flow and color Doppler sonography findings in iatrogenic carotid-jugular arteriovenous fistulaD-A Clevert, C Kubisch, S Weckbach, et al.
Genomics|March 15, 2001
Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene familyS Waldegger, I Moschen, A Ramirez, et al.
Human Molecular Genetics|September 25, 1997
Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmiasB Wollnik, B C Schroeder, C Kubisch, et al.
Neurology|November 15, 2006
Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with auraU Todt, J Freudenberg, I Goebel, et al.
Science (New York, N.Y.)|February 7, 1998
A potassium channel mutation in neonatal human epilepsyC Biervert, B C Schroeder, C Kubisch, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
FEBS Letters|November 29, 1993
Immediate-early gene induction by repetitive mechanical but not electrical activity in adult rat cardiomyocytesC Kubisch, B Wollnik, A Maass, et al.
Thyroid : Official Journal of the American Thyroid Association|December 16, 1998
The extracellular thyrotropin receptor domain is not a major candidate for mutations in toxic thyroid nodulesD Führer, C Kubisch, U Scheibler, et al.
European Heart Journal|May 1, 1995
Hormonal induction of an immediate-early gene response in myogenic cell lines--a paradigm for heart growthA Maass, C Grohé, C Kubisch, et al.
Neurology|May 5, 1999
Phenotypic variability in rippling muscle diseaseM Vorgerd, H Bolz, T Patzold, et al.
Human Molecular Genetics|September 16, 1998
ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependenceC Kubisch, T Schmidt-Rose, B Fontaine, et al.
Clinical Hemorheology and Microcirculation|February 6, 2010
B-flow and color Doppler sonography findings in iatrogenic carotid-jugular arteriovenous fistulaD-A Clevert, C Kubisch, S Weckbach, et al.
Genomics|March 15, 2001
Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene familyS Waldegger, I Moschen, A Ramirez, et al.
Human Molecular Genetics|September 25, 1997
Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmiasB Wollnik, B C Schroeder, C Kubisch, et al.
Neurology|November 15, 2006
Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with auraU Todt, J Freudenberg, I Goebel, et al.
Science (New York, N.Y.)|February 7, 1998
A potassium channel mutation in neonatal human epilepsyC Biervert, B C Schroeder, C Kubisch, et al.
Pageof 4