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NDUFAF3
Molecular Mechanism of ACAD9 in Mitochondrial Respiratory Complex 1 Assembly
High-Throughput, Pooled Sequencing Identifies Mutations in NUBPL And
Assembly Factors for the Membrane Arm of Human Complex I
Biogenesis of NDUFS3-Less Complex I Indicates TMEM126A/OPA7 As an Assembly Factor of the ND4-Module
NDUFAF3 (Q-15): Sc-99317
Electron Transport Chain Activity Is a Predictor and Target for Venetoclax Sensitivity in Multiple Myeloma
Instability in NAD Metabolism Leads to Impaired Cardiac Mitochondrial
Mitochondrial Disease Associated with Complex I (NADH-Coq Oxidoreductase) Deficiency
NDUF3 (NDUFAF3) (NM 199069) Human Recombinant Protein Product Data
Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions
Understanding Mitochondrial Complex I Assembly in Health and Disease☆
Accessory Subunits Are Integral for Assembly and Function of Human Mitochondrial Complex I
Supplementary Material Complex I Deficiency: Clinical Features
Analysis of Human Mutations in the Supernumerary Subunits of Complex I
Comparing Divergence Landscapes from Reduced-Representation and Whole-Genome Re-Sequencing in The
Assembly Factors for the Membrane Arm of Human Complex I
Mitochondrial DNA (Mtdna) Test Requisition
Mitochondrial Functionality in Male Fertility: from Spermatogenesis to Fertilization
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Metabolism Leads to Impaired Cardiac Mitochondrial Function and Communication
NDUFAF4 Variants Are Associated with Leigh Syndrome and Cause a Specific Mitochondrial Complex I Assembly Defect
NDUFAF3 CRISPR/Cas9 KO Plasmid (M): Sc-426157
Genepanel Mitochondrial Diseases Genepanel Paediatric Cardiomyopathy AARS2 AARS2 ABAT ABCC6 ACAD9 ABCC9 ACO2 ACAD8 AFG3L2 ACAD9
TMEM70 Is an Assembly Factor of Mitochondrial Complexes I and V
A Salvage Pathway Maintains Highly Functional Respiratory Complex I
Mitochondrial Complex I Deficiency
ATM Regulates ATP Levels Through NRF1)
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
Comprehensive Diagnosis for Mitochondrial Disorders
Mass-Spectrometry Based Proteomics Reveals Mitochondrial
NDUFA10 Mutations Cause Complex I Deficiency in a Patient with Leigh Disease
Leigh Syndrome and Mitochondrial Encephalopathy Precision Panel
The Long Non-Coding RNA Cerox1 Is a Post Transcriptional Regulator Of
Effect of Experimental Complex III Deficiency on Respiratory Chain Assembly and Function