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Showing results (81-90 of 93) with videos related to

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Journal of Neurosurgery. Pediatrics|April 22, 2014
Altered brain connectivity in sagittal craniosynostosisJoel S Beckett, Eric D Brooks, Cheryl Lacadie, et al.
Circulation. Arrhythmia and Electrophysiology|February 27, 2015
Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndromeTaisuke Ishikawa, Chuanchau J Jou, Akihiko Nogami, et al.
American Journal of Physiology. Heart and Circulatory Physiology|August 31, 2014
A near-infrared fluorescent voltage-sensitive dye allows for moderate-throughput electrophysiological analyses of human induced pluripotent stem cell-derived cardiomyocytesAngelica Lopez-Izquierdo, Mark Warren, Michael Riedel, et al.
Plos Biology|December 7, 2013
3-OST-7 regulates BMP-dependent cardiac contractionShiela C Samson, Tania Ferrer, Chuanchau J Jou, et al.
Journal of Cell Science|April 8, 2026
Biophysical and biochemical studies support PHD inhibitor development as a TPI deficiency therapyPresley Roberts, Joseph R Figura, Kaitlin McClure, et al.
Marine Pollution Bulletin|June 15, 2014
Capacitive deionization of seawater effected by nano Ag and Ag@C on grapheneP-F Cai, C-J Su, W-T Chang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 1, 1995
Extrauterine twin-twin transfusion syndrome after birth in conjoined twinsM K Shyu, J C Shih, C N Lee, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 14, 2017
A Functional Assay for Sick Sinus Syndrome Genetic VariantsChuanchau J Jou, Cammon B Arrington, Spencer Barnett, et al.
Genes|October 29, 2025
Newly Identified TPI Deficiency Treatments Function for Novel Disease-Causing Allele, <i>TPI1<sup>R5G</sup></i>Joseph R Figura, Presley Roberts, Riley Sawka, et al.
American Journal of Medical Genetics. Part A|August 19, 2015
Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locusNeil E Bowles, Chuanchau J Jou, Cammon B Arrington, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Journal of Neurosurgery. Pediatrics|April 22, 2014
Altered brain connectivity in sagittal craniosynostosisJoel S Beckett, Eric D Brooks, Cheryl Lacadie, et al.
Circulation. Arrhythmia and Electrophysiology|February 27, 2015
Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndromeTaisuke Ishikawa, Chuanchau J Jou, Akihiko Nogami, et al.
American Journal of Physiology. Heart and Circulatory Physiology|August 31, 2014
A near-infrared fluorescent voltage-sensitive dye allows for moderate-throughput electrophysiological analyses of human induced pluripotent stem cell-derived cardiomyocytesAngelica Lopez-Izquierdo, Mark Warren, Michael Riedel, et al.
Plos Biology|December 7, 2013
3-OST-7 regulates BMP-dependent cardiac contractionShiela C Samson, Tania Ferrer, Chuanchau J Jou, et al.
Journal of Cell Science|April 8, 2026
Biophysical and biochemical studies support PHD inhibitor development as a TPI deficiency therapyPresley Roberts, Joseph R Figura, Kaitlin McClure, et al.
Marine Pollution Bulletin|June 15, 2014
Capacitive deionization of seawater effected by nano Ag and Ag@C on grapheneP-F Cai, C-J Su, W-T Chang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 1, 1995
Extrauterine twin-twin transfusion syndrome after birth in conjoined twinsM K Shyu, J C Shih, C N Lee, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 14, 2017
A Functional Assay for Sick Sinus Syndrome Genetic VariantsChuanchau J Jou, Cammon B Arrington, Spencer Barnett, et al.
Genes|October 29, 2025
Newly Identified TPI Deficiency Treatments Function for Novel Disease-Causing Allele, <i>TPI1<sup>R5G</sup></i>Joseph R Figura, Presley Roberts, Riley Sawka, et al.
American Journal of Medical Genetics. Part A|August 19, 2015
Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locusNeil E Bowles, Chuanchau J Jou, Cammon B Arrington, et al.
Pageof 10