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Journal of Cell Science
|
April 8, 2017
Multiple roles of integrin-α3 at the neuromuscular junction
Jacob A Ross, Richard G Webster, Tanguy Lechertier, et al.
Biochemical and Biophysical Research Communications
|
February 8, 2005
Hypertrophic effects of urocortin homologous peptides are mediated via activation of the Akt pathway
Anastasios Chanalaris, Kevin M Lawrence, Paul A Townsend, et al.
Scientific Reports
|
June 23, 2019
Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy
Edward G Jones, Neda Mazaheri, Reza Maroofian, et al.
Circulation
|
February 28, 2002
Peroxisome proliferator--activated receptor alpha gene regulates left ventricular growth in response to exercise and hypertension
Yalda Jamshidi, Hugh E Montgomery, Hans-Werner Hense, et al.
Circulation
|
March 27, 2002
Peroxisome proliferator-activated receptor alpha gene variants influence progression of coronary atherosclerosis and risk of coronary artery disease
David M Flavell, Yalda Jamshidi, Emma Hawe, et al.
International Journal of Cardiology
|
October 10, 2018
The narrow-sense and common single nucleotide polymorphism heritability of early repolarization
Rachel Bastiaenen, Ilja M Nolte, Patricia B Munroe, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 8, 2020
Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3
Daniel Peter Sayer Osborn, Leila Emrahi, Joshua Clayton, et al.
Annals of Clinical and Translational Neurology
|
September 26, 2025
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
Gregorio A Nolasco, Mònica Roldán, Yalda Jamshidi, et al.
Journal of the American College of Cardiology
|
June 12, 2012
Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia
Yalda Jamshidi, Ilja M Nolte, Chrysoula Dalageorgou, et al.
Clinical Genetics
|
July 30, 2022
HIDEA syndrome is caused by biallelic, pathogenic, rare or founder P4HTM variants impacting the active site or the overall stability of the P4H-TM protein
Minna Kraatari-Tiri, Leila Soikkonen, Matti Myllykoski, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 75) with videos related to
Sort By:
Page
of 8
Journal of Cell Science
|
April 8, 2017
Multiple roles of integrin-α3 at the neuromuscular junction
Jacob A Ross, Richard G Webster, Tanguy Lechertier, et al.
Biochemical and Biophysical Research Communications
|
February 8, 2005
Hypertrophic effects of urocortin homologous peptides are mediated via activation of the Akt pathway
Anastasios Chanalaris, Kevin M Lawrence, Paul A Townsend, et al.
Scientific Reports
|
June 23, 2019
Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy
Edward G Jones, Neda Mazaheri, Reza Maroofian, et al.
Circulation
|
February 28, 2002
Peroxisome proliferator--activated receptor alpha gene regulates left ventricular growth in response to exercise and hypertension
Yalda Jamshidi, Hugh E Montgomery, Hans-Werner Hense, et al.
Circulation
|
March 27, 2002
Peroxisome proliferator-activated receptor alpha gene variants influence progression of coronary atherosclerosis and risk of coronary artery disease
David M Flavell, Yalda Jamshidi, Emma Hawe, et al.
International Journal of Cardiology
|
October 10, 2018
The narrow-sense and common single nucleotide polymorphism heritability of early repolarization
Rachel Bastiaenen, Ilja M Nolte, Patricia B Munroe, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 8, 2020
Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3
Daniel Peter Sayer Osborn, Leila Emrahi, Joshua Clayton, et al.
Annals of Clinical and Translational Neurology
|
September 26, 2025
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
Gregorio A Nolasco, Mònica Roldán, Yalda Jamshidi, et al.
Journal of the American College of Cardiology
|
June 12, 2012
Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia
Yalda Jamshidi, Ilja M Nolte, Chrysoula Dalageorgou, et al.
Clinical Genetics
|
July 30, 2022
HIDEA syndrome is caused by biallelic, pathogenic, rare or founder P4HTM variants impacting the active site or the overall stability of the P4H-TM protein
Minna Kraatari-Tiri, Leila Soikkonen, Matti Myllykoski, et al.
Page
of 8