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Ankit Verma

Showing results (121-130 of 153) with videos related to

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International Journal of Rheumatic Diseases|February 18, 2017
Egyptian tale from India: application of whole-exome sequencing in diagnosis of atypical familial Mediterranean feverPulukool Sandhya, Shamsudheen Karuthedath Vellarikkal, Aswin Nair, et al.
Scientific Reports|March 16, 2025
Insights into the enhanced photocatalytic degradation of congo red using advanced BaDy<sub>x</sub>Fe<sub>12-x</sub>O<sub>19</sub> catalytic hexamaterialsHimanshi, Jayanti Makasana, Subbulakshmi Ganesan, et al.
Environmental Research|November 19, 2023
Photo/electro catalytic green hydrogen production promoted by Ga modified Co<sub>0.6</sub>Cu<sub>0.4</sub>Fe<sub>2</sub>O<sub>4</sub> nano catalystsPinki Kotwal, Rohit Jasrotia, Anant Vidya Nidhi, et al.
European Journal of Pharmacology|October 30, 2016
Synergistic effect of piperine and paclitaxel on cell fate via cyt-c, Bax/Bcl-2-caspase-3 pathway in ovarian adenocarcinomas SKOV-3 cellsManish Kumar Pal, Shyama Pyari Jaiswar, Ajeet Kumar Srivastav, et al.
F1000Research|October 31, 2017
Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in <i>RAG1</i> associated with B- T- NK+ severe combined immunodeficiencyGeeta Madathil Govindaraj, Shamsudheen Karuthedath Vellarikkal, Rijith Jayarajan, et al.
Clinical Epigenetics|September 15, 2020
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbanceMaria Vittoria Cubellis, Laura Pignata, Ankit Verma, et al.
Purinergic Signalling|June 2, 2019
Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathyAmitabh Biswas, Ali Raza, Soumi Das, et al.
Genome Medicine|December 19, 2019
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisationHannah Demond, Zahra Anvar, Bahia Namavar Jahromi, et al.
Molecules (Basel, Switzerland)|July 14, 2023
Catalytic Acceptorless Dehydrogenation (CAD) of Secondary Benzylic Alcohols into Value-Added Ketones Using Pd(II)-NHC ComplexesAbeer Nasser Al-Romaizan, Manoj Kumar Gangwar, Ankit Verma, et al.
Acta Dermato-Venereologica|July 3, 2018
Genotype-Phenotype Correlations of Dystrophic Epidermolysis Bullosa in India: Experience from a Tertiary Care CentreVamsi K Yenamandra, Shamsudheen K Vellarikkal, Madhumita R Chowdhury, et al.
Pageof 16

Showing results (121-130 of 153) with videos related to

Sort By:
Pageof 16
International Journal of Rheumatic Diseases|February 18, 2017
Egyptian tale from India: application of whole-exome sequencing in diagnosis of atypical familial Mediterranean feverPulukool Sandhya, Shamsudheen Karuthedath Vellarikkal, Aswin Nair, et al.
Scientific Reports|March 16, 2025
Insights into the enhanced photocatalytic degradation of congo red using advanced BaDy<sub>x</sub>Fe<sub>12-x</sub>O<sub>19</sub> catalytic hexamaterialsHimanshi, Jayanti Makasana, Subbulakshmi Ganesan, et al.
Environmental Research|November 19, 2023
Photo/electro catalytic green hydrogen production promoted by Ga modified Co<sub>0.6</sub>Cu<sub>0.4</sub>Fe<sub>2</sub>O<sub>4</sub> nano catalystsPinki Kotwal, Rohit Jasrotia, Anant Vidya Nidhi, et al.
European Journal of Pharmacology|October 30, 2016
Synergistic effect of piperine and paclitaxel on cell fate via cyt-c, Bax/Bcl-2-caspase-3 pathway in ovarian adenocarcinomas SKOV-3 cellsManish Kumar Pal, Shyama Pyari Jaiswar, Ajeet Kumar Srivastav, et al.
F1000Research|October 31, 2017
Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in <i>RAG1</i> associated with B- T- NK+ severe combined immunodeficiencyGeeta Madathil Govindaraj, Shamsudheen Karuthedath Vellarikkal, Rijith Jayarajan, et al.
Clinical Epigenetics|September 15, 2020
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbanceMaria Vittoria Cubellis, Laura Pignata, Ankit Verma, et al.
Purinergic Signalling|June 2, 2019
Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathyAmitabh Biswas, Ali Raza, Soumi Das, et al.
Genome Medicine|December 19, 2019
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisationHannah Demond, Zahra Anvar, Bahia Namavar Jahromi, et al.
Molecules (Basel, Switzerland)|July 14, 2023
Catalytic Acceptorless Dehydrogenation (CAD) of Secondary Benzylic Alcohols into Value-Added Ketones Using Pd(II)-NHC ComplexesAbeer Nasser Al-Romaizan, Manoj Kumar Gangwar, Ankit Verma, et al.
Acta Dermato-Venereologica|July 3, 2018
Genotype-Phenotype Correlations of Dystrophic Epidermolysis Bullosa in India: Experience from a Tertiary Care CentreVamsi K Yenamandra, Shamsudheen K Vellarikkal, Madhumita R Chowdhury, et al.
Pageof 16