Narayanappa Gayathri

Bengaluru, KA, India

Last Updated: 09/26/2026

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Found 68 publications

Neuroanatomical zones of human traumatic brain injury reveal significant differences in protein profile and protein oxidation: Implications for secondary injury events.

Neuroanatomical zones of human traumatic brain injury reveal significant differences in protein profile and protein oxidation: Implications for secondary injury events.

Journal: Journal of neurochemistry

Published: June 03, 2023

A detailed review on advanced oxidation process in treatment of wastewater: Mechanism, challenges and future outlook.

A detailed review on advanced oxidation process in treatment of wastewater: Mechanism, challenges and future outlook.

Journal: Chemosphere

Published: July 06, 2022

Hereditary neuropathies: Genetics and utility of nerve biopsy.

Hereditary neuropathies: Genetics and utility of nerve biopsy.

Journal: Indian journal of pathology & microbiology

Published: May 13, 2022

Whole exome sequencing reveals a homozygous C1QBP deletion as the cause of progressive external ophthalmoplegia and multiple mtDNA deletions.

Whole exome sequencing reveals a homozygous C1QBP deletion as the cause of progressive external ophthalmoplegia and multiple mtDNA deletions.

Journal: Neuromuscular disorders : NMD

Published: February 17, 2021

Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters the mitochondrial function in human skeletal muscle proteome.

Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters the mitochondrial function in human skeletal muscle proteome.

Journal: Mitochondrion

Published: September 22, 2020

Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.

Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.

Journal: Journal of neurology

Published: July 31, 2020

Whole-exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations.

Whole-exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations.

Journal: European journal of neurology

Published: July 09, 2020

Exposure to the neurotoxin 3-nitropropionic acid in neuronal cells induces unique histone acetylation pattern: Implications for neurodegeneration.

Exposure to the neurotoxin 3-nitropropionic acid in neuronal cells induces unique histone acetylation pattern: Implications for neurodegeneration.

Journal: Neurochemistry international

Published: May 25, 2020

Child Neurology: Ethylmalonic encephalopathy.

Child Neurology: Ethylmalonic encephalopathy.

Journal: Neurology

Published: March 01, 2020

Inhibition of mitochondrial complex II in neuronal cells triggers unique pathways culminating in autophagy with implications for neurodegeneration.

Inhibition of mitochondrial complex II in neuronal cells triggers unique pathways culminating in autophagy with implications for neurodegeneration.

Journal: Scientific reports

Published: October 07, 2019

Human muscle pathology is associated with altered phosphoprotein profile of mitochondrial proteins in the skeletal muscle.

Human muscle pathology is associated with altered phosphoprotein profile of mitochondrial proteins in the skeletal muscle.

Journal: Journal of proteomics

Published: April 29, 2019

Author Response: Penetrance of the LHON Mutation m.11778G>A May Depend on Factors Other Than Haplotype or Heteroplasmy Rate.

Author Response: Penetrance of the LHON Mutation m.11778G>A May Depend on Factors Other Than Haplotype or Heteroplasmy Rate.

Journal: Investigative ophthalmology & visual science

Published: January 19, 2018

Showing 1-12 of 68

Last Updated: 09/26/2026