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Journal of the American Heart Association
|
May 22, 2016
Sphingosine-1-Phosphate Receptor 1 Regulates Cardiac Function by Modulating Ca2+ Sensitivity and Na+/H+ Exchange and Mediates Protection by Ischemic Preconditioning
Petra Keul, Marcel M G J van Borren, Alexander Ghanem, et al.
Immunity
|
December 3, 2020
The SPPL3-Defined Glycosphingolipid Repertoire Orchestrates HLA Class I-Mediated Immune Responses
Marlieke L M Jongsma, Antonius A de Waard, Matthijs Raaben, et al.
Cancer Discovery
|
September 25, 2025
Microbial Metabolic Pathways Guide Response to Immune Checkpoint Blockade Therapy
Iris L Mimpen, Thomas W Battaglia, Miguel Parra-Martinez, et al.
EMBO Molecular Medicine
|
November 19, 2016
TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT
Harsha D Devalla, Roselle Gélinas, Elhadi H Aburawi, et al.
Circulation Research
|
May 3, 2012
NPHP4 variants are associated with pleiotropic heart malformations
Vanessa M French, Ingrid M B H van de Laar, Marja W Wessels, et al.
The New England Journal of Medicine
|
October 4, 2013
PLS3 mutations in X-linked osteoporosis with fractures
Fleur S van Dijk, M Carola Zillikens, Dimitra Micha, et al.
The Journal of Investigative Dermatology
|
September 16, 2023
Disruption of TUFT1, a Desmosome-Associated Protein, Causes Skin Fragility, Woolly Hair, and Palmoplantar Keratoderma
Annemieke J M H Verkerk, Daniela Andrei, Mathilde C S C Vermeer, et al.
Plos One
|
June 5, 2026
Contemporary high resolution European forest structure assessed using tree-level National Forest Inventory data
Gert-Jan Nabuurs, Yasmin I Maximo, Ajdin Starcevic, et al.
Circulation
|
October 11, 2024
A Rare Noncoding Enhancer Variant in <i>SCN5A</i> Contributes to the High Prevalence of Brugada Syndrome in Thailand
Roddy Walsh, John Mauleekoonphairoj, Isabella Mengarelli, et al.
Nature Genetics
|
September 14, 2010
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14
Abbas M Solouki, Virginie J M Verhoeven, Cornelia M van Duijn, et al.
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of 78
Search research articles
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Showing results (761-770 of 778) with videos related to
Sort By:
Page
of 78
Journal of the American Heart Association
|
May 22, 2016
Sphingosine-1-Phosphate Receptor 1 Regulates Cardiac Function by Modulating Ca2+ Sensitivity and Na+/H+ Exchange and Mediates Protection by Ischemic Preconditioning
Petra Keul, Marcel M G J van Borren, Alexander Ghanem, et al.
Immunity
|
December 3, 2020
The SPPL3-Defined Glycosphingolipid Repertoire Orchestrates HLA Class I-Mediated Immune Responses
Marlieke L M Jongsma, Antonius A de Waard, Matthijs Raaben, et al.
Cancer Discovery
|
September 25, 2025
Microbial Metabolic Pathways Guide Response to Immune Checkpoint Blockade Therapy
Iris L Mimpen, Thomas W Battaglia, Miguel Parra-Martinez, et al.
EMBO Molecular Medicine
|
November 19, 2016
TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT
Harsha D Devalla, Roselle Gélinas, Elhadi H Aburawi, et al.
Circulation Research
|
May 3, 2012
NPHP4 variants are associated with pleiotropic heart malformations
Vanessa M French, Ingrid M B H van de Laar, Marja W Wessels, et al.
The New England Journal of Medicine
|
October 4, 2013
PLS3 mutations in X-linked osteoporosis with fractures
Fleur S van Dijk, M Carola Zillikens, Dimitra Micha, et al.
The Journal of Investigative Dermatology
|
September 16, 2023
Disruption of TUFT1, a Desmosome-Associated Protein, Causes Skin Fragility, Woolly Hair, and Palmoplantar Keratoderma
Annemieke J M H Verkerk, Daniela Andrei, Mathilde C S C Vermeer, et al.
Plos One
|
June 5, 2026
Contemporary high resolution European forest structure assessed using tree-level National Forest Inventory data
Gert-Jan Nabuurs, Yasmin I Maximo, Ajdin Starcevic, et al.
Circulation
|
October 11, 2024
A Rare Noncoding Enhancer Variant in <i>SCN5A</i> Contributes to the High Prevalence of Brugada Syndrome in Thailand
Roddy Walsh, John Mauleekoonphairoj, Isabella Mengarelli, et al.
Nature Genetics
|
September 14, 2010
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14
Abbas M Solouki, Virginie J M Verhoeven, Cornelia M van Duijn, et al.
Page
of 78