Tissue Specific Distribution of Pyrimidine Deoxynucleoside Salvage Enzymes Shed Light on the Mechanism of Mitochondrial DNA Depletion
Author:
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/15257771003741042
Reference6 articles.
1. Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
2. mtDNA depletion myopathy: elucidation of the tissue specificity in the mitochondrial thymidine kinase (TK2) deficiency
3. Kinetic Properties of Mutant Human Thymidine Kinase 2 Suggest a Mechanism for Mitochondrial DNA Depletion Myopathy
4. Human thymidine kinase 2: molecular cloning and characterisation of the enzyme activity with antiviral and cytostatic nucleoside substrates
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1. Differential expression of enzymes in thymidylate biosynthesis in zebrafish at different developmental stages: implications for dtymk mutation-caused neurodegenerative disorders;BMC Neuroscience;2022-03-27
2. Biochemical Characterizations of Human TMPK Mutations Identified in Patients with Severe Microcephaly: Single Amino Acid Substitutions Impair Dimerization and Abolish Their Catalytic Activity;ACS Omega;2021-12-06
3. Purine and Pyrimidine Metabolism;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2021
4. Basic biochemical characterization of cytosolic enzymes in thymidine nucleotide synthesis in adult rat tissues: implications for tissue specific mitochondrial DNA depletion and deoxynucleoside-based therapy for TK2-deficiency;BMC Molecular and Cell Biology;2020-04-28
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