Pavithra S. Iyer
Zurich, ZH 8093, Switzerland
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
Pharmacological inhibition of Lin28 promotes ketogenesis and restores lipid homeostasis in models of non-alcoholic fatty liver disease.
Journal: Nature communications
Published: July 15, 2021
Rheological properties of skeletal muscles in a Duchenne muscular dystrophy murine model before and after autologous cell therapy.
Journal: Journal of biomechanics
Published: February 04, 2021
Repurposing of glycine transport inhibitors for the treatment of erythropoietic protoporphyria.
Journal: Cell chemical biology
Published: November 18, 2020
Delivery of oligonucleotides to bone marrow to modulate ferrochelatase splicing in a mouse model of erythropoietic protoporphyria.
Journal: Nucleic acids research
Published: February 14, 2020
Characterization of mesoangioblast cell fate and improved promyogenic potential of a satellite cell-like subpopulation upon transplantation in dystrophic murine muscles.
Journal: Stem cell research
Published: June 28, 2019
Delta-aminolevulinic acid synthase 2 expression in combination with iron as modifiers of disease severity in erythropoietic protoporphyria.
Journal: Molecular genetics and metabolism
Published: October 17, 2018
Autologous Cell Therapy Approach for Duchenne Muscular Dystrophy using PiggyBac Transposons and Mesoangioblasts.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: June 21, 2017
A PiggyBac-mediated approach for muscle gene transfer or cell therapy.
Journal: Stem cell research
Published: May 02, 2014
Showing 1-9 of 9
Last Updated: 09/26/2026