Ranjana Arya

New Delhi, DL 110067, India

Last Updated: 09/26/2026

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Found 23 publications

Hydroxyethylamine & phthalimide analogs restoring defects due to GNE dysfunction: rare disease therapeutic significance.

Hydroxyethylamine & phthalimide analogs restoring defects due to GNE dysfunction: rare disease therapeutic significance.

Journal: Molecular medicine (Cambridge, Mass.)

Published: July 10, 2025

Calcium level and autophagy defect in GNE mutants of rare neuromuscular disorder.

Calcium level and autophagy defect in GNE mutants of rare neuromuscular disorder.

Journal: Cell biology international

Published: June 12, 2024

Altered autophagic flux in GNE mutant cells of Indian origin: Potential drug target for GNE myopathy.

Altered autophagic flux in GNE mutant cells of Indian origin: Potential drug target for GNE myopathy.

Journal: Experimental cell research

Published: March 26, 2024

Understanding pathophysiology of GNE myopathy and current progress towards drug development.

Understanding pathophysiology of GNE myopathy and current progress towards drug development.

Journal: Journal of biosciences

Published: February 22, 2024

Potential small effector molecules restoring cellular defects due to sialic acid biosynthetic enzyme deficiency: Pathological relevance to GNE myopathy.

Potential small effector molecules restoring cellular defects due to sialic acid biosynthetic enzyme deficiency: Pathological relevance to GNE myopathy.

Journal: Biochemical pharmacology

Published: October 29, 2023

Bases immediate upstream of the TATAAT box of the sigma 70 promoter of Escherichia coli significantly influence the activity of a model promoter by altering the bending angle of DNA.

Bases immediate upstream of the TATAAT box of the sigma 70 promoter of Escherichia coli significantly influence the activity of a model promoter by altering the bending angle of DNA.

Journal: Gene

Published: June 06, 2022

Role of HSP70 chaperone in protein aggregate phenomenon of GNE mutant cells: Therapeutic lead for GNE Myopathy.

Role of HSP70 chaperone in protein aggregate phenomenon of GNE mutant cells: Therapeutic lead for GNE Myopathy.

Journal: The international journal of biochemistry & cell biology

Published: March 22, 2022

Optimizing Chaperone Removal Strategy from Overexpressed Recombinant Proteins : GNE, a Case Study.

Optimizing Chaperone Removal Strategy from Overexpressed Recombinant Proteins : GNE, a Case Study.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: January 28, 2022

Functional characterization of GNE mutations prevalent in Asian subjects with GNE myopathy, an ultra-rare neuromuscular disorder.

Functional characterization of GNE mutations prevalent in Asian subjects with GNE myopathy, an ultra-rare neuromuscular disorder.

Journal: Biochimie

Published: September 08, 2021

Effect of GNE Mutations on Cytoskeletal Network Proteins: Potential Gateway to Understand Pathomechanism of GNEM.

Effect of GNE Mutations on Cytoskeletal Network Proteins: Potential Gateway to Understand Pathomechanism of GNEM.

Journal: Neuromolecular medicine

Published: July 15, 2021

Elucidation of ER stress and UPR pathway in sialic acid-deficient cells: Pathological relevance to GNEM.

Elucidation of ER stress and UPR pathway in sialic acid-deficient cells: Pathological relevance to GNEM.

Journal: Journal of cellular biochemistry

Published: June 07, 2021

Generation and Characterization of a Skeletal Muscle Cell-Based Model Carrying One Single Gne Allele: Implications in Actin Dynamics.

Generation and Characterization of a Skeletal Muscle Cell-Based Model Carrying One Single Gne Allele: Implications in Actin Dynamics.

Journal: Molecular neurobiology

Published: March 01, 2021

Showing 1-12 of 23

Last Updated: 09/26/2026