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Author/Creator Wehrens, Xander H. T.

1. Calcium‐calmodulin‐dependent protein kinase mediates the intracellular signalling pathways of cardiac apoptosis in mice with impaired glucose tolerance. (2nd March 2017)

Authors:
Federico, Marilen; Portiansky, Enrique L.; Sommese, Leandro; Alvarado, Francisco J.; Blanco, Paula G.; Zanuzzi, Carolina N.; Dedman, John; Kaetzel, Marcia; Wehrens, Xander H. T.; Mattiazzi, Alicia; Palomeque, Julieta
Journal:
Journal of physiology
Issue:
Volume 595:Number 12(2017)
Page Start:
4089
Record Type:
Journal Article
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3. Efficacy of RyR2 inhibitor EL20 in induced pluripotent stem cell‐derived cardiomyocytes from a patient with catecholaminergic polymorphic ventricular tachycardia. Issue 13 (10th June 2021)

Authors:
Word, Tarah A.; Quick, Ann P.; Miyake, Christina Y.; Shak, Mayra K.; Pan, Xiaolu; Kim, Jean J.; Allen, Hugh D.; Sibrian‐Vazquez, Martha; Strongin, Robert M.; Landstrom, Andrew P.; Wehrens, Xander H. T.
Journal:
Journal of cellular and molecular medicine
Issue:
Volume 25:Issue 13(2021)
Page Start:
6115
Record Type:
Journal Article
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4. In silico prediction of drug therapy in catecholaminergic polymorphic ventricular tachycardia. (30th December 2015)

Authors:
Yang, Pei‐Chi; Moreno, Jonathan D.; Miyake, Christina Y.; Vaughn‐Behrens, Steven B.; Jeng, Mao‐Tsuen; Grandi, Eleonora; Wehrens, Xander H. T.; Noskov, Sergei Y.; Clancy, Colleen E.
Journal:
Journal of physiology
Issue:
Volume 594:Number 3(2016:Feb.)
Page Start:
567
Record Type:
Journal Article
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8. TBX5‐encoded T‐box transcription factor 5 variant T223M is associated with long QT syndrome and pediatric sudden cardiac death. Issue 3 (23rd December 2020)

Authors:
Markunas, Alexandra M.; Manivannan, Perathu K. R.; Ezekian, Jordan E.; Agarwal, Agnim; Eisner, William; Alsina, Katherina; Allen, Hugh D.; Wray, Gregory A.; Kim, Jeffrey J.; Wehrens, Xander H. T.; Landstrom, Andrew P.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 3(2021)
Page Start:
923
Record Type:
Journal Article
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9. Wolff–Parkinson–White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation. Issue 6 (31st March 2020)

Authors:
Coban‐Akdemir, Zeynep H.; Charng, Wu‐Lin; Azamian, Mahshid; Paine, Ingrid S.; Punetha, Jaya; Grochowski, Christopher M.; Gambin, Tomasz; Valdes, Santiago O.; Cannon, Bryan; Zapata, Gladys; Hernandez, Patricia P.; Jhangiani, Shalini; Doddapaneni, Harsha; Hu, Jianhong; Boricha, Fatima; Muzny, Donna...
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 6(2020)
Page Start:
1387
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗