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Peter Pytel

Showing results (81-90 of 138) with videos related to

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The American Journal of Surgical Pathology|June 25, 2025
Renal Tumorigenesis via RAS/RAF/MAPK Pathway Alterations Beyond Papillary Renal Neoplasm With Reverse PolarityJung Woo Kwon, Peng Wang, Pankhuri Wanjari, et al.
Science Translational Medicine|July 6, 2018
<i>BCL3</i> expression promotes resistance to alkylating chemotherapy in gliomasLongtao Wu, Giovanna M Bernal, Kirk E Cahill, et al.
Muscle & Nerve|May 26, 2021
Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutationsRicardo A Maselli, David T Wei, Trent S Hodgson, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculationLisa M Dellefave, Peter Pytel, Stephanie Mewborn, et al.
Biorxiv : the Preprint Server for Biology|September 11, 2023
Pervasive nuclear envelope ruptures precede ECM signaling and disease onset without activating cGAS-STING in Lamin-cardiomyopathy miceAtsuki En, Hanumakumar Bogireddi, Briana Thomas, et al.
Molecular Genetics & Genomic Medicine|February 15, 2018
Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3ARicardo A Maselli, Jessica Vázquez, Leah Schrumpf, et al.
Matters|February 27, 2018
BIN1 localization is distinct from Tau tangles in Alzheimer's diseasePierre De Rossi, Virginie Buggia-Prevot, Robert J Andrew, et al.
The Journal of Biological Chemistry|May 27, 2008
The endocytic recycling protein EHD2 interacts with myoferlin to regulate myoblast fusionKatherine R Doherty, Alexis R Demonbreun, Gregory Q Wallace, et al.
Cell Reports|May 30, 2024
Pervasive nuclear envelope ruptures precede ECM signaling and disease onset without activating cGAS-STING in Lamin-cardiomyopathy miceAtsuki En, Hanumakumar Bogireddi, Briana Thomas, et al.
Circulation. Cardiovascular Genetics|September 3, 2014
Targeted analysis of whole genome sequence data to diagnose genetic cardiomyopathyJessica R Golbus, Megan J Puckelwartz, Lisa Dellefave-Castillo, et al.
Pageof 14

Showing results (81-90 of 138) with videos related to

Sort By:
Pageof 14
The American Journal of Surgical Pathology|June 25, 2025
Renal Tumorigenesis via RAS/RAF/MAPK Pathway Alterations Beyond Papillary Renal Neoplasm With Reverse PolarityJung Woo Kwon, Peng Wang, Pankhuri Wanjari, et al.
Science Translational Medicine|July 6, 2018
<i>BCL3</i> expression promotes resistance to alkylating chemotherapy in gliomasLongtao Wu, Giovanna M Bernal, Kirk E Cahill, et al.
Muscle & Nerve|May 26, 2021
Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutationsRicardo A Maselli, David T Wei, Trent S Hodgson, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculationLisa M Dellefave, Peter Pytel, Stephanie Mewborn, et al.
Biorxiv : the Preprint Server for Biology|September 11, 2023
Pervasive nuclear envelope ruptures precede ECM signaling and disease onset without activating cGAS-STING in Lamin-cardiomyopathy miceAtsuki En, Hanumakumar Bogireddi, Briana Thomas, et al.
Molecular Genetics & Genomic Medicine|February 15, 2018
Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3ARicardo A Maselli, Jessica Vázquez, Leah Schrumpf, et al.
Matters|February 27, 2018
BIN1 localization is distinct from Tau tangles in Alzheimer's diseasePierre De Rossi, Virginie Buggia-Prevot, Robert J Andrew, et al.
The Journal of Biological Chemistry|May 27, 2008
The endocytic recycling protein EHD2 interacts with myoferlin to regulate myoblast fusionKatherine R Doherty, Alexis R Demonbreun, Gregory Q Wallace, et al.
Cell Reports|May 30, 2024
Pervasive nuclear envelope ruptures precede ECM signaling and disease onset without activating cGAS-STING in Lamin-cardiomyopathy miceAtsuki En, Hanumakumar Bogireddi, Briana Thomas, et al.
Circulation. Cardiovascular Genetics|September 3, 2014
Targeted analysis of whole genome sequence data to diagnose genetic cardiomyopathyJessica R Golbus, Megan J Puckelwartz, Lisa Dellefave-Castillo, et al.
Pageof 14