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FOXRED1
High-Throughput, Pooled Sequencing Identifies Mutations in NUBPL And
FOXRED1 (D-4): Sc-377010
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Ykt6 Membrane-To-Cytosol Cycling Regulates Exosomal Wnt Secretion
Biogenesis of NDUFS3-Less Complex I Indicates TMEM126A/OPA7 As an Assembly Factor of the ND4-Module
Leigh Syndrome
Produktinformation
Genomic Landscape of Paediatric Adrenocortical Tumours
Respiratory Chain Complex I Deficiency Caused by Mitochondrial DNA
Supernumerary Subunits NDUFA3, NDUFA5 and NDUFA12
Maternally Inherited Mitochondrial DNA Disease in Consanguineous Families
Transcriptomic and Proteomic Landscape of Mitochondrial
Supplementary Figure S1 Fluorescent Substrate Digestion in the Droplet
Proteomic Analysis of the Increased Proteins in Peroxiredoxin 0
FOXRED1, Encoding a FAD-Dependent Oxidoreductase Complex-I Specific Molecular Chaperone, Is Mutated in Infantile-Onset Mitochondrial Encephalopathy
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
The Mitochondrial Calcium Uniporter Compensates for Complex I Dysfunction Enrique Balderas
Biallelic P4HTM Variants Associated with HIDEA Syndrome and Mitochondrial Respiratory Chain Complex I Deficiency ✉ Eleanor Hay 1, Louise C
Top View
Analysis of Human Mutations in the Supernumerary Subunits of Complex I
Leigh Syndrome
Assembly Factors for the Membrane Arm of Human Complex I
Mitochondrial DNA (Mtdna) Test Requisition
Genes and Variants Underlying Human Congenital Lactic Acidosis—From Genetics to Personalized Treatment
Rabbit Anti-FOXRED1/FITC Conjugated Antibody
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
EGL Test Description
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
Mitochondrial Complex I Deficiency
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
Comprehensive Diagnosis for Mitochondrial Disorders
Severe Multisystem Pathology, Metabolic Acidosis, Mitochondrial Dysfunction, and Early Death Associated with an X-Linked AIFM1 Variant
FOXRED1 Silencing in Mice: a Possible Animal Model for Leigh Syndrome
NDUFA10 Mutations Cause Complex I Deficiency in a Patient with Leigh Disease
Leigh Syndrome: One Disorder, More Than 75 Monogenic Causes
Molecular Basis of Leigh Syndrome: a Current Look Manuela Schubert Baldo* and Laura Vilarinho
Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies
Identification and Characterization of New Variants in FOXRED1 Gene
Product Name: FOXRED1 Polyclonal Antibody, ALEXA FLUOR® 594 Conjugated Catalog No
S1- Alphabetical List of Aging-Related Genes