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Anne-Karin Arndt

Showing results (1-10 of 7) with videos related to

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Current Opinion in Cardiology|April 11, 2014
Genetic testing in cardiovascular diseasesAnne-Karin Arndt, Calum A MacRae
American Journal of Human Genetics|January 7, 2014
Reponse to De Leeuw and HougeAnne-Karin Arndt, Calum A Macrae, Sabine Klaassen
Kidney International|May 17, 2013
RAGE-mediated interstitial fibrosis in neonatal obstructive nephropathy is independent of NF-κB activationMojca Gasparitsch, Anne-Karin Arndt, Felix Pawlitschek, et al.
Science Translational Medicine|June 13, 2014
Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic cardiomyopathyAngeliki Asimaki, Sudhir Kapoor, Eva Plovie, et al.
American Journal of Human Genetics|June 18, 2013
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathyAnne-Karin Arndt, Sebastian Schafer, Jorg-Detlef Drenckhahn, et al.
American Journal of Human Genetics|September 2, 2017
Rare Variants in NR2F2 Cause Congenital Heart Defects in HumansSaeed Al Turki, Ashok K Manickaraj, Catherine L Mercer, et al.
American Journal of Human Genetics|April 8, 2014
Rare variants in NR2F2 cause congenital heart defects in humansSaeed Al Turki, Ashok K Manickaraj, Catherine L Mercer, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Current Opinion in Cardiology|April 11, 2014
Genetic testing in cardiovascular diseasesAnne-Karin Arndt, Calum A MacRae
American Journal of Human Genetics|January 7, 2014
Reponse to De Leeuw and HougeAnne-Karin Arndt, Calum A Macrae, Sabine Klaassen
Kidney International|May 17, 2013
RAGE-mediated interstitial fibrosis in neonatal obstructive nephropathy is independent of NF-κB activationMojca Gasparitsch, Anne-Karin Arndt, Felix Pawlitschek, et al.
Science Translational Medicine|June 13, 2014
Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic cardiomyopathyAngeliki Asimaki, Sudhir Kapoor, Eva Plovie, et al.
American Journal of Human Genetics|June 18, 2013
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathyAnne-Karin Arndt, Sebastian Schafer, Jorg-Detlef Drenckhahn, et al.
American Journal of Human Genetics|September 2, 2017
Rare Variants in NR2F2 Cause Congenital Heart Defects in HumansSaeed Al Turki, Ashok K Manickaraj, Catherine L Mercer, et al.
American Journal of Human Genetics|April 8, 2014
Rare variants in NR2F2 cause congenital heart defects in humansSaeed Al Turki, Ashok K Manickaraj, Catherine L Mercer, et al.
Pageof 1