Kishore Garapati

International Technology Park
Bengaluru, KA, India

Last Updated: 09/26/2026

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Found 30 publications

DHDDS-related juvenile parkinsonism is caused by impaired lipid metabolism, glycosylation, and mitochondrial dysfunction, which can be rescued by NAD⁺ treatment.

DHDDS-related juvenile parkinsonism is caused by impaired lipid metabolism, glycosylation, and mitochondrial dysfunction, which can be rescued by NAD⁺ treatment.

Journal: medRxiv : the preprint server for health sciences

Published: June 12, 2026

Hemoglobin alpha-like subunit mu is expressed during ontogeny and is elevated in alpha thalassemia.

Hemoglobin alpha-like subunit mu is expressed during ontogeny and is elevated in alpha thalassemia.

Journal: Blood. Red cells & iron

Published: April 20, 2026

Stress-induced secretory pathway disruption causes atypical metalloproteinase transport in PMM2-CDG.

Stress-induced secretory pathway disruption causes atypical metalloproteinase transport in PMM2-CDG.

Journal: iScience

Published: April 01, 2026

Proteomic alterations in patient bone-derived stromal cells and their secretomes in osteogenesis imperfecta.

Proteomic alterations in patient bone-derived stromal cells and their secretomes in osteogenesis imperfecta.

Journal: Molecular genetics and metabolism reports

Published: February 03, 2026

N-Glycosylation of AXL Receptor Tyrosine Kinase Regulates Its Stability, Phosphorylation, and Oncogenic Function.

N-Glycosylation of AXL Receptor Tyrosine Kinase Regulates Its Stability, Phosphorylation, and Oncogenic Function.

Journal: Molecular & cellular proteomics : MCP

Published: December 05, 2025

Extensive Hypoglycosylation of Serum N-Glycoproteins in SRD5A3 Deficiency.

Extensive Hypoglycosylation of Serum N-Glycoproteins in SRD5A3 Deficiency.

Journal: Journal of inherited metabolic disease

Published: November 17, 2025

Albumin as a glycoprotein biomarker in congenital disorders of glycosylation.

Albumin as a glycoprotein biomarker in congenital disorders of glycosylation.

Journal: Molecular genetics and metabolism

Published: October 20, 2025

Defining the proteome of bone marrow plasma in multiple myeloma and monoclonal gammopathy of undetermined significance.

Defining the proteome of bone marrow plasma in multiple myeloma and monoclonal gammopathy of undetermined significance.

Journal: Blood cancer journal

Published: July 18, 2025

Advances in mucopolysaccharidosis research: the impact of mass spectrometry-based approaches.

Advances in mucopolysaccharidosis research: the impact of mass spectrometry-based approaches.

Journal: Clinical proteomics

Published: January 15, 2025

Alterations in Hurler-Scheie Syndrome Revealed by Mass Spectrometry-Based Proteomics and Phosphoproteomics Analysis.

Alterations in Hurler-Scheie Syndrome Revealed by Mass Spectrometry-Based Proteomics and Phosphoproteomics Analysis.

Journal: Omics : a journal of integrative biology

Published: October 29, 2024

Further delineation of defects in MRPS2 causing human OXPHOS deficiency and early developmental abnormalities in zebrafish.

Further delineation of defects in MRPS2 causing human OXPHOS deficiency and early developmental abnormalities in zebrafish.

Journal: European journal of human genetics : EJHG

Published: August 30, 2024

N-glycoproteomic and proteomic alterations in SRD5A3-deficient fibroblasts.

N-glycoproteomic and proteomic alterations in SRD5A3-deficient fibroblasts.

Journal: Glycobiology

Published: July 15, 2024

Showing 1-12 of 30

Last Updated: 09/26/2026