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Rohit Budhraja

Showing results (21-30 of 30) with videos related to

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Cell Reports|March 2, 2024
Neural and metabolic dysregulation in PMM2-deficient human in vitro neural modelsSilvia Radenkovic, Rohit Budhraja, Teun Klein-Gunnewiek, et al.
Journal of Proteome Research|June 2, 2021
Mass Spectrometric Analysis of Urine from COVID-19 Patients for Detection of SARS-CoV-2 Viral Antigen and to Study Host ResponseSandip Chavan, Kiran K Mangalaparthi, Smrita Singh, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
PGM1 deficiency disrupts sarcomere and mitochondrial function in a stem-cell cardiomyocyte modelSilvia Radenkovic, Graeme Preston, Rohit Budhraja, et al.
Journal of Translational Medicine|February 21, 2026
PGM1 deficiency is linked to sarcomeric and mitochondrial dysfunction in patient-derived iPSC-cardiomyocytesSilvia Radenkovic, Graeme Preston, Rohit Budhraja, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2025
ALG13 loss-of-function alters glycosylation, impairs neuronal maturation, and drives network hypoactivity in a cortical organoid model of CDGRameen Shah, Rohit Budhraja, Silvia Radenkovic, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Novel mouse model reveals neurodevelopmental origin of PMM2-CDG brain pathologyAndrew C Edmondson, Rohit Budhraja, Zijie Xia, et al.
Communications Biology|July 19, 2024
Diversity of post-translational modifications and cell signaling revealed by single cell and single organelle mass spectrometryDong-Gi Mun, Firdous A Bhat, Neha Joshi, et al.
JCI Insight|April 8, 2024
A complement C4-derived glycopeptide is a biomarker for PMM2-CDGKishore Garapati, Rohit Budhraja, Mayank Saraswat, et al.
Biorxiv : the Preprint Server for Biology|September 2, 2025
Mono-allelic p.R37H Dehydrodolichyl Diphosphate Synthase variants lead to protein glycosylation defects, aberrant lipid profiles and interneuron scarcity in a novel mouse model of progressive epileptic encephalopathyAfitz Da Silva, Samuel Boris Tene Tadoum, Irena J J Muffels, et al.
Hepatology (Baltimore, Md.)|September 29, 2025
Multiomics combined with machine learning defines unique molecular subtypes of cholangiocarcinoma and identifies TNK1 as a therapeutic targetDong-Gi Mun, Erik Jessen, Jennifer L Tomlinson, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Cell Reports|March 2, 2024
Neural and metabolic dysregulation in PMM2-deficient human in vitro neural modelsSilvia Radenkovic, Rohit Budhraja, Teun Klein-Gunnewiek, et al.
Journal of Proteome Research|June 2, 2021
Mass Spectrometric Analysis of Urine from COVID-19 Patients for Detection of SARS-CoV-2 Viral Antigen and to Study Host ResponseSandip Chavan, Kiran K Mangalaparthi, Smrita Singh, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
PGM1 deficiency disrupts sarcomere and mitochondrial function in a stem-cell cardiomyocyte modelSilvia Radenkovic, Graeme Preston, Rohit Budhraja, et al.
Journal of Translational Medicine|February 21, 2026
PGM1 deficiency is linked to sarcomeric and mitochondrial dysfunction in patient-derived iPSC-cardiomyocytesSilvia Radenkovic, Graeme Preston, Rohit Budhraja, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2025
ALG13 loss-of-function alters glycosylation, impairs neuronal maturation, and drives network hypoactivity in a cortical organoid model of CDGRameen Shah, Rohit Budhraja, Silvia Radenkovic, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Novel mouse model reveals neurodevelopmental origin of PMM2-CDG brain pathologyAndrew C Edmondson, Rohit Budhraja, Zijie Xia, et al.
Communications Biology|July 19, 2024
Diversity of post-translational modifications and cell signaling revealed by single cell and single organelle mass spectrometryDong-Gi Mun, Firdous A Bhat, Neha Joshi, et al.
JCI Insight|April 8, 2024
A complement C4-derived glycopeptide is a biomarker for PMM2-CDGKishore Garapati, Rohit Budhraja, Mayank Saraswat, et al.
Biorxiv : the Preprint Server for Biology|September 2, 2025
Mono-allelic p.R37H Dehydrodolichyl Diphosphate Synthase variants lead to protein glycosylation defects, aberrant lipid profiles and interneuron scarcity in a novel mouse model of progressive epileptic encephalopathyAfitz Da Silva, Samuel Boris Tene Tadoum, Irena J J Muffels, et al.
Hepatology (Baltimore, Md.)|September 29, 2025
Multiomics combined with machine learning defines unique molecular subtypes of cholangiocarcinoma and identifies TNK1 as a therapeutic targetDong-Gi Mun, Erik Jessen, Jennifer L Tomlinson, et al.
Pageof 3