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

Debasish Kumar Ghosh

Showing results (31-40 of 42) with videos related to

Pageof 5
Sort By:
Neuropathology and Applied Neurobiology|January 30, 2026
Truncating GAS6 Variant Disrupts Neuroglial Homeostasis in a Childhood-Onset Demyelinating DisorderDiksha, Abhishek Kumar, Vishal Gaurav, et al.
Protein Science : a Publication of the Protein Society|July 9, 2026
NEPRO forms fibrous scaffolds in the nucleolus to maintain nucleolar integrity and orchestrate ribosome biogenesisAbhishek Kumar, Shailesh Kumar Gupta, Yogendra Pratap Mathuria, et al.
Chembiochem : a European Journal of Chemical Biology|February 7, 2026
Structure-Guided Synthetic Peptide Targeting Nucleolus and Neural Progenitor Protein Nuclear Import Impairs Ribosome Biogenesis and Cancer Cell ProliferationAbhishek Kumar, Suvam Saha, Yogendra Pratap Mathuria, et al.
Journal of Human Genetics|October 15, 2025
NOL10 variant disrupts ribosome biogenesis and underlies hippocampal sclerosisAbhishek Kumar, Vishal Gaurav, Yogendra Pratap Mathuria, et al.
Current Genomics|May 21, 2026
Analysis of Endoplasmic Reticulum Stress-Associated Proteins As Prognostic Markers In Breast CancerSmriti Shreya, Shweta Pandey, Debasish Kumar Ghosh, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|December 16, 2022
Mutant MESD links cellular stress to type I collagen aggregation in osteogenesis imperfecta type XXDebasish Kumar Ghosh, Prajna Udupa, Akshaykumar Nanaji Shrikondawar, et al.
Biochemical and Biophysical Research Communications|November 22, 2025
Non-invasive and rapid diagnosis of Niemann-Pick disease type C1 by immunocytochemical detection of leaky lysosomes in squamous epithelial cellsDiksha, Vishal Gaurav, Dharmendra Kamla, et al.
ACS Chemical Neuroscience|January 21, 2026
Structural Destabilization of FRMD3 by a FERM Domain Mutation Causes Hypomyelinating Disease via Oligodendrocyte DysfunctionDiksha, Abhishek Kumar, Smita Saha, et al.
Journal of Human Genetics|December 16, 2022
Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosisPrajna Udupa, Debasish Kumar Ghosh, Neethukrishna Kausthubham, et al.
NPJ Genomic Medicine|February 20, 2026
Variants in MTNAP1 underlie a neurodegenerative disorder by impairing mitochondrial stabilityAbhishek Kumar, Smita Saha, Nazim Nasir, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Neuropathology and Applied Neurobiology|January 30, 2026
Truncating GAS6 Variant Disrupts Neuroglial Homeostasis in a Childhood-Onset Demyelinating DisorderDiksha, Abhishek Kumar, Vishal Gaurav, et al.
Protein Science : a Publication of the Protein Society|July 9, 2026
NEPRO forms fibrous scaffolds in the nucleolus to maintain nucleolar integrity and orchestrate ribosome biogenesisAbhishek Kumar, Shailesh Kumar Gupta, Yogendra Pratap Mathuria, et al.
Chembiochem : a European Journal of Chemical Biology|February 7, 2026
Structure-Guided Synthetic Peptide Targeting Nucleolus and Neural Progenitor Protein Nuclear Import Impairs Ribosome Biogenesis and Cancer Cell ProliferationAbhishek Kumar, Suvam Saha, Yogendra Pratap Mathuria, et al.
Journal of Human Genetics|October 15, 2025
NOL10 variant disrupts ribosome biogenesis and underlies hippocampal sclerosisAbhishek Kumar, Vishal Gaurav, Yogendra Pratap Mathuria, et al.
Current Genomics|May 21, 2026
Analysis of Endoplasmic Reticulum Stress-Associated Proteins As Prognostic Markers In Breast CancerSmriti Shreya, Shweta Pandey, Debasish Kumar Ghosh, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|December 16, 2022
Mutant MESD links cellular stress to type I collagen aggregation in osteogenesis imperfecta type XXDebasish Kumar Ghosh, Prajna Udupa, Akshaykumar Nanaji Shrikondawar, et al.
Biochemical and Biophysical Research Communications|November 22, 2025
Non-invasive and rapid diagnosis of Niemann-Pick disease type C1 by immunocytochemical detection of leaky lysosomes in squamous epithelial cellsDiksha, Vishal Gaurav, Dharmendra Kamla, et al.
ACS Chemical Neuroscience|January 21, 2026
Structural Destabilization of FRMD3 by a FERM Domain Mutation Causes Hypomyelinating Disease via Oligodendrocyte DysfunctionDiksha, Abhishek Kumar, Smita Saha, et al.
Journal of Human Genetics|December 16, 2022
Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosisPrajna Udupa, Debasish Kumar Ghosh, Neethukrishna Kausthubham, et al.
NPJ Genomic Medicine|February 20, 2026
Variants in MTNAP1 underlie a neurodegenerative disorder by impairing mitochondrial stabilityAbhishek Kumar, Smita Saha, Nazim Nasir, et al.
Pageof 5