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American Journal of Medical Genetics. Part A
|
April 23, 2015
The third international meeting on genetic disorders in the RAS/MAPK pathway: towards a therapeutic approach
Bruce Korf, Reza Ahmadian, Judith Allanson, et al.
Scientific Reports
|
March 24, 2022
Glyoxylate protects against cyanide toxicity through metabolic modulation
Jason R Nielson, Anjali K Nath, Kim P Doane, 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.
Circulation Research
|
June 7, 2021
Targeting the Microtubule EB1-CLASP2 Complex Modulates Na<sub>V</sub>1.5 at Intercalated Discs
Gerard A Marchal, Mariam Jouni, David Y Chiang, et al.
Nature Medicine
|
April 3, 2012
RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing
Wei Guo, Sebastian Schafer, Marion L Greaser, et al.
Cell Reports. Medicine
|
May 22, 2024
Transcriptomic and spatial dissection of human ex vivo right atrial tissue reveals proinflammatory microvascular changes in ischemic heart disease
Suvi Linna-Kuosmanen, Eloi Schmauch, Kyriakitsa Galani, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 25, 2025
Mapping the Functional Landscape of <i>KCNQ1</i> to Define Ion Channel Mechanisms and Arrhythmia Risk
M Lorena Harvey, Ellen Osborn, Megan C Lancaster, et al.
Nature Genetics
|
December 4, 2023
Perturbational phenotyping of human blood cells reveals genetically determined latent traits associated with subsets of common diseases
Max Homilius, Wandi Zhu, Samuel S Eddy, et al.
European Heart Journal
|
January 15, 2009
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation
Stefan Kääb, Dawood Darbar, Charlotte van Noord, et al.
Cell
|
March 25, 2017
Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research
Teri A Manolio, Douglas M Fowler, Lea M Starita, et al.
Page
of 28
Search research articles
Search
Showing results (251-260 of 275) with videos related to
Sort By:
Page
of 28
American Journal of Medical Genetics. Part A
|
April 23, 2015
The third international meeting on genetic disorders in the RAS/MAPK pathway: towards a therapeutic approach
Bruce Korf, Reza Ahmadian, Judith Allanson, et al.
Scientific Reports
|
March 24, 2022
Glyoxylate protects against cyanide toxicity through metabolic modulation
Jason R Nielson, Anjali K Nath, Kim P Doane, 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.
Circulation Research
|
June 7, 2021
Targeting the Microtubule EB1-CLASP2 Complex Modulates Na<sub>V</sub>1.5 at Intercalated Discs
Gerard A Marchal, Mariam Jouni, David Y Chiang, et al.
Nature Medicine
|
April 3, 2012
RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing
Wei Guo, Sebastian Schafer, Marion L Greaser, et al.
Cell Reports. Medicine
|
May 22, 2024
Transcriptomic and spatial dissection of human ex vivo right atrial tissue reveals proinflammatory microvascular changes in ischemic heart disease
Suvi Linna-Kuosmanen, Eloi Schmauch, Kyriakitsa Galani, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 25, 2025
Mapping the Functional Landscape of <i>KCNQ1</i> to Define Ion Channel Mechanisms and Arrhythmia Risk
M Lorena Harvey, Ellen Osborn, Megan C Lancaster, et al.
Nature Genetics
|
December 4, 2023
Perturbational phenotyping of human blood cells reveals genetically determined latent traits associated with subsets of common diseases
Max Homilius, Wandi Zhu, Samuel S Eddy, et al.
European Heart Journal
|
January 15, 2009
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation
Stefan Kääb, Dawood Darbar, Charlotte van Noord, et al.
Cell
|
March 25, 2017
Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research
Teri A Manolio, Douglas M Fowler, Lea M Starita, et al.
Page
of 28