Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ankit Verma

Showing results (141-150 of 153) with videos related to

Pageof 16
Sort By:
Genome Announcements|January 10, 2015
Draft Genome Sequence of the Extremely Halophilic Bacterium Halomonas salina Strain CIFRI1, Isolated from the East Coast of IndiaBijay Kumar Behera, Priyanka Das, Jitendra Maharana, et al.
Mitochondrion|January 18, 2024
Whole genome sequencing followed by functional analysis of genomic deletion encompassing ERCC8 and NDUFAF2 genes in a non-consanguineous Indian family reveals dysfunctional mitochondrial bioenergetics leading to infant mortalityAnkit Sabharwal, Vishu Gupta, Shamsudheen Kv, et al.
Human Genomics|August 5, 2022
1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variantsAnjali Bajaj, Vigneshwar Senthivel, Rahul Bhoyar, et al.
Clinical Epigenetics|December 13, 2019
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotypeAngela Sparago, Ankit Verma, Maria Grazia Patricelli, et al.
Pharmacogenomics|December 15, 2017
Pharmacogenetic landscape of DPYD variants in south Asian populations by integration of genome-scale dataJudith M Hariprakash, Shamsudheen K Vellarikkal, Pavithran Keechilat, et al.
Journal of Family Medicine and Primary Care|March 8, 2021
Characteristics and outcomes of 231 COVID-19 cases admitted at a tertiary facility in India: An observational cohort studyRohit Kumar, Bisakh Bhattacharya, Ved Prakash Meena, et al.
Plos One|September 28, 2018
Large scale changes in the transcriptome of Eisenia fetida during regenerationAksheev Bhambri, Neeraj Dhaunta, Surendra Singh Patel, et al.
Molecular Cell|June 14, 2025
CRAMP1 drives linker histone expression to enable Polycomb repressionRachael E Matthews, Joshua Miguel C Danac, Emily L Naden, et al.
Nature Materials|January 29, 2021
Linking void and interphase evolution to electrochemistry in solid-state batteries using operando X-ray tomographyJohn A Lewis, Francisco Javier Quintero Cortes, Yuhgene Liu, et al.
Clinical Epigenetics|June 1, 2022
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbancesLaura Pignata, Francesco Cecere, Ankit Verma, et al.
Pageof 16

Showing results (141-150 of 153) with videos related to

Sort By:
Pageof 16
Genome Announcements|January 10, 2015
Draft Genome Sequence of the Extremely Halophilic Bacterium Halomonas salina Strain CIFRI1, Isolated from the East Coast of IndiaBijay Kumar Behera, Priyanka Das, Jitendra Maharana, et al.
Mitochondrion|January 18, 2024
Whole genome sequencing followed by functional analysis of genomic deletion encompassing ERCC8 and NDUFAF2 genes in a non-consanguineous Indian family reveals dysfunctional mitochondrial bioenergetics leading to infant mortalityAnkit Sabharwal, Vishu Gupta, Shamsudheen Kv, et al.
Human Genomics|August 5, 2022
1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variantsAnjali Bajaj, Vigneshwar Senthivel, Rahul Bhoyar, et al.
Clinical Epigenetics|December 13, 2019
The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotypeAngela Sparago, Ankit Verma, Maria Grazia Patricelli, et al.
Pharmacogenomics|December 15, 2017
Pharmacogenetic landscape of DPYD variants in south Asian populations by integration of genome-scale dataJudith M Hariprakash, Shamsudheen K Vellarikkal, Pavithran Keechilat, et al.
Journal of Family Medicine and Primary Care|March 8, 2021
Characteristics and outcomes of 231 COVID-19 cases admitted at a tertiary facility in India: An observational cohort studyRohit Kumar, Bisakh Bhattacharya, Ved Prakash Meena, et al.
Plos One|September 28, 2018
Large scale changes in the transcriptome of Eisenia fetida during regenerationAksheev Bhambri, Neeraj Dhaunta, Surendra Singh Patel, et al.
Molecular Cell|June 14, 2025
CRAMP1 drives linker histone expression to enable Polycomb repressionRachael E Matthews, Joshua Miguel C Danac, Emily L Naden, et al.
Nature Materials|January 29, 2021
Linking void and interphase evolution to electrochemistry in solid-state batteries using operando X-ray tomographyJohn A Lewis, Francisco Javier Quintero Cortes, Yuhgene Liu, et al.
Clinical Epigenetics|June 1, 2022
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbancesLaura Pignata, Francesco Cecere, Ankit Verma, et al.
Pageof 16