Search research articles
Contact Us
Filters
Showing results (1-10 of 7) with videos related to
Page
of 1
Sort By:
Current Opinion in Cardiology
|
April 11, 2014
Genetic testing in cardiovascular diseases
Anne-Karin Arndt, Calum A MacRae
American Journal of Human Genetics
|
January 7, 2014
Reponse to De Leeuw and Houge
Anne-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 activation
Mojca 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 cardiomyopathy
Angeliki 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 cardiomyopathy
Anne-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 Humans
Saeed 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 humans
Saeed Al Turki, Ashok K Manickaraj, Catherine L Mercer, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Current Opinion in Cardiology
|
April 11, 2014
Genetic testing in cardiovascular diseases
Anne-Karin Arndt, Calum A MacRae
American Journal of Human Genetics
|
January 7, 2014
Reponse to De Leeuw and Houge
Anne-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 activation
Mojca 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 cardiomyopathy
Angeliki 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 cardiomyopathy
Anne-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 Humans
Saeed 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 humans
Saeed Al Turki, Ashok K Manickaraj, Catherine L Mercer, et al.
Page
of 1