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Pradeep Reddy

Showing results (111-120 of 138) with videos related to

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Imaging Neuroscience (Cambridge, Mass.)|August 13, 2025
Creating diverse and inclusive scientific practices for research datasets and disseminationJulia W Y Kam, AmanPreet Badhwar, Valentina Borghesani, et al.
Plant Biotechnology Journal|September 17, 2018
Zinc finger nuclease-mediated targeting of multiple transgenes to an endogenous soybean genomic locus via non-homologous end joiningNicholas D Bonawitz, W Michael Ainley, Asuka Itaya, et al.
Journal of Neurology|January 9, 2026
Clinical trajectories and genetic profiles of SOD1-related amyotrophic lateral sclerosis: insights from a single-center cohort in IndiaMuddasu Suhasini Keerthipriya, Ananthapadmanabha Kotambail, Madhusudhan Deekshitha, et al.
Frontiers in Cell and Developmental Biology|March 21, 2022
Myc Supports Self-Renewal of Basal Cells in the Esophageal EpitheliumTomoaki Hishida, Eric Vazquez-Ferrer, Yuriko Hishida-Nozaki, et al.
Frontiers in Neuroscience|December 31, 2020
Cortical Thickness Estimation in Individuals With Cerebral Small Vessel Disease, Focal Atrophy, and Chronic Stroke LesionsMiracle Ozzoude, Joel Ramirez, Pradeep Reddy Raamana, et al.
Cell|December 17, 2016
In Vivo Amelioration of Age-Associated Hallmarks by Partial ReprogrammingAlejandro Ocampo, Pradeep Reddy, Paloma Martinez-Redondo, et al.
Protein & Cell|May 2, 2019
Mutations in foregut SOX2<sup>+</sup> cells induce efficient proliferation via CXCR2 pathwayTomoaki Hishida, Eric Vazquez-Ferrer, Yuriko Hishida-Nozaki, et al.
Nature Communications|February 23, 2016
Establishment of human iPSC-based models for the study and targeting of glioma initiating cellsIgnacio Sancho-Martinez, Emmanuel Nivet, Yun Xia, et al.
Cell|April 25, 2015
Selective elimination of mitochondrial mutations in the germline by genome editingPradeep Reddy, Alejandro Ocampo, Keiichiro Suzuki, et al.
Journal of Neurology|July 1, 2026
Genome-wide spectrum of coding DNA variations in Indian patients with amyotrophic lateral sclerosisAnanthapadmanabha Kotambail, Gautham Arunachal, Muddasu Suhasini Keerthipriya, et al.
Pageof 14

Showing results (111-120 of 138) with videos related to

Sort By:
Pageof 14
Imaging Neuroscience (Cambridge, Mass.)|August 13, 2025
Creating diverse and inclusive scientific practices for research datasets and disseminationJulia W Y Kam, AmanPreet Badhwar, Valentina Borghesani, et al.
Plant Biotechnology Journal|September 17, 2018
Zinc finger nuclease-mediated targeting of multiple transgenes to an endogenous soybean genomic locus via non-homologous end joiningNicholas D Bonawitz, W Michael Ainley, Asuka Itaya, et al.
Journal of Neurology|January 9, 2026
Clinical trajectories and genetic profiles of SOD1-related amyotrophic lateral sclerosis: insights from a single-center cohort in IndiaMuddasu Suhasini Keerthipriya, Ananthapadmanabha Kotambail, Madhusudhan Deekshitha, et al.
Frontiers in Cell and Developmental Biology|March 21, 2022
Myc Supports Self-Renewal of Basal Cells in the Esophageal EpitheliumTomoaki Hishida, Eric Vazquez-Ferrer, Yuriko Hishida-Nozaki, et al.
Frontiers in Neuroscience|December 31, 2020
Cortical Thickness Estimation in Individuals With Cerebral Small Vessel Disease, Focal Atrophy, and Chronic Stroke LesionsMiracle Ozzoude, Joel Ramirez, Pradeep Reddy Raamana, et al.
Cell|December 17, 2016
In Vivo Amelioration of Age-Associated Hallmarks by Partial ReprogrammingAlejandro Ocampo, Pradeep Reddy, Paloma Martinez-Redondo, et al.
Protein & Cell|May 2, 2019
Mutations in foregut SOX2<sup>+</sup> cells induce efficient proliferation via CXCR2 pathwayTomoaki Hishida, Eric Vazquez-Ferrer, Yuriko Hishida-Nozaki, et al.
Nature Communications|February 23, 2016
Establishment of human iPSC-based models for the study and targeting of glioma initiating cellsIgnacio Sancho-Martinez, Emmanuel Nivet, Yun Xia, et al.
Cell|April 25, 2015
Selective elimination of mitochondrial mutations in the germline by genome editingPradeep Reddy, Alejandro Ocampo, Keiichiro Suzuki, et al.
Journal of Neurology|July 1, 2026
Genome-wide spectrum of coding DNA variations in Indian patients with amyotrophic lateral sclerosisAnanthapadmanabha Kotambail, Gautham Arunachal, Muddasu Suhasini Keerthipriya, et al.
Pageof 14