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DHTKD1
Clinical Report of a Neonate Carrying a Large Deletion in the 10P15.3P13
Inherited Neuropathies
Crystal Structure and Interaction Studies of Human Iucrj DHTKD1 Provide Insight Into a Mitochondrial ISSN 2052-2525 Megacomplex in Lysine Catabolism Biologyjmedicine
Kif1b Rab7a Lmna
Synthetic Analogues of 2-Oxo Acids Discriminate Metabolic Contribution of the 2-Oxoglutarate and 2-Oxoadipate Dehydrogenases in Mammalian Cells and Tissues Artem V
Genetic and Functional Investigation of Inherited Neuropathies
A Case of a Boy with SOD and 7Q11.23 Microduplication Syndrome
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
DHTKD1 (Q-17): Sc-242577
DHTKD1 and OGDH Display in Vivo Substrate Overlap and Form a Hybrid Ketoacid
Clinical and Genetic Aspects of Charcot-Marie- Tooth Disease Subtypes
The Mitochondrial 2-Oxoadipate and 2-Oxoglutarate Dehydrogenase Complexes Share Their E2 and E3 Components for Their Function An
CMT2Q-Causing Mutation in the Dhtkd1 Gene Lead to Sensory
Dehydrogenase E1 and Transketolase Domain- Containing Protein 1 – DHTKD1 a Target Enabling Package (TEP)
Functional Analysis of Genomic Variation and Impact on Molecular and Higher Order Phenotypes Ashutosh Kumar Pandey University of Tennessee Health Science Center
From Novel Disease Genes to New Mouse Models - a Complementary Approach
Whole-Exome Sequencing Uncovers Oxidoreductases DHTKD1 and OGDHL As Linkers Between Mitochondrial Dysfunction and Eosinophilic Esophagitis
Peripheral Neuropathy in Mitochondrial Disorders
Top View
DHTKD1 Is Essential for Mitochondrial Biogenesis and Function Maintenance
2-Aminoadipic Acid Protects Against Obesity and Diabetes
The Expanded BXD Family of Mice: a Cohort for Experimental Systems
Crystal Structure and Interaction Studies of Human DHTKD1 Provide Insight Into a Mitochondrial Megacomplex in Lysine Catabolism
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
Mitochondrial Oxodicarboxylate Carrier Deficiency Is Associated with Mitochondrial DNA Depletion and Spinal Muscular Atrophy–Like Disease
A Chinese Pedigree with a Novel Mutation in GJB1 Gene and a Rare Variation in DHTKD1 Gene for Diverse Charcot‑Marie‑Tooth Diseases
An Integrative Transcriptomic and Methylation Approach for Identifying Differentially Expressed Circular Rnas Associated with DNA Methylation Change
Acute Lysine Administration to Raise 2-AAA Version 1.2 Protocol # 02-14-2017
Mouse Dhtkd1 Conditional Knockout Project (CRISPR/Cas9)
GM-CSF Driven Myeloid Cells in Adipose Tissue Link Weight Gain And
King's Research Portal