Author pages are created from data sourced from our academic publisher partnerships and public sources.
Chemistry, Metabolism, and Toxicology of Cannabis: Clinical Implications
Cannabis is one of the most widely abused substances throughout the world. The primary psychoactive constituent of cannabis, delta 9-tetrahydrocannabinol (▵9_THC), produces a myriad of… Expand
Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India.
BACKGROUND There are relatively few studies, which focus on peripheral neuropathy in large cohorts of genetically characterized patients with mitochondrial disorders. This study sought to analyze the… Expand
Post-Translational Oxidative Modifications of Mitochondrial Complex I (NADH: Ubiquinone Oxidoreductase): Implications for Pathogenesis and Therapeutics in Human Diseases.
- M. M. S. Bharath
Mitochondrial complex I (NADH: ubiquinone oxidoreductase; CI) is central to the electron transport chain (ETC), oxidative phosphorylation, and ATP production in eukaryotes. CI is a multi-subunit… Expand
Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1
Huppke -Brendel syndrome is a new addition to the evolving spectrum of copper metabolism defects. It is an autosomal recessive disorder characterized by congenital cataract, impaired hearing, and… Expand
Analysis of calpain-3 protein in muscle biopsies of different muscular dystrophies from India
- R. Renjini, N. Gayathri, A. Nalini, M. M. S. Bharath
- The Indian journal of medical research
- 1 June 2012
Background & objectives: Calpain-3, a Ca2+-dependent protease has been implicated in the pathology of neuromuscular disorders (NMDs). The current study aimed to analyze calpain-3 expression in cases… Expand
Disulfiram in a 'traditional' medicine sold to patients with alcohol dependence in India.
Human muscle pathology is associated with altered phosphoprotein profile of mitochondrial proteins in the skeletal muscle.
- B. Sunitha, M. Kumar, +9 authors M. M. S. Bharath
- Chemistry, Medicine
- Journal of proteomics
- 16 January 2020
Analysis of human muscle diseases highlights the role of mitochondrial dysfunction in the skeletal muscle. Our previous work revealed that diverse upstream events correlated with altered… Expand
LGMD2I: Immunohistochemical and immunoblot technique assisted identification of 51 cases with both duchenne and becker phenotype
Magnetic resonance imaging findings in immunohistochemically confirmed sarcoglycanopathies