DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» UQCRB
UQCRB
Establishing the Pathogenicity of Novel Mitochondrial DNA Sequence Variations: a Cell and Molecular Biology Approach
Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ
Mir-4435 Is an UQCRB-Related Circulating Mirna in Human
Low Abundance of the Matrix Arm of Complex I in Mitochondria Predicts Longevity in Mice
In This Table Protein Name, Uniprot Code, Gene Name P-Value
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
UQCRB Antibody Cat
Carrier Screening Panel
Thesis Reference
Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions
Nuclear Gene Mutations As the Cause of Mitochondrial Complex III Deficiency
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Co-Expression Network Analysis Reveals Key Genes Related To
Discovery Protein Names Uniprot Gene Names Average Log2 L/H
Impaired Mitochondrial Biogenesis in Adipose Tissue in Acquired Obesity
Mitochondrial Markers 1
Mitochondrial and Metabolic Gene Expression in the Aged Rat Heart
Supplementary Figure (Legends in the Main Text): S1
Top View
Mitochondrial Lipid Homeostasis at the Crossroads of Liver and Heart Diseases
Mitochondrial UQCRB As a New Molecular Prognostic Biomarker of Human Colorectal Cancer
Mitochondrial Complex III Deficiency
Complex III Mitochondrial Leukoencephalopathy Masquerading Acute Demyelinating Syndrome Due to a Novel Variant in CYC1
Mitochondria in Epithelial Ovarian Carcinoma Exhibit Abnormal Phenotypes and Blunted Associations with Biobehavioral Factors Snehal Bindra1, Marlon A
Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
The Genetic Evidence of Burn-Induced Cardiac Mitochondrial Metabolism Dysfunction
Mitochondria and Disease: Mutation and Expression Landscape of Mitochondri-Associated Genes in Different Disease Types
Altered Skeletal Muscle Mitochondrial Proteome As the Basis of Disruption of Mitochondrial Function in Diabetic Mice Piotr Zabie
UQCRB Antibody Order 021-34695924
[email protected]
Support 400-6123-828 50Ul
[email protected]
100 Ul √ √ Web
Preconception Genetic Carrier Screen
Genetic Features of Mitochondrial Respiratory Chain Disorders
Membrane Disruption, but Not Metabolic Rewiring, Is the Key Mechanism of Anticancer‑Action of FASN‑Inhibitors: a Multi‑Omics Analysis in Ovarian Cancer Thomas W
Metabolske Sykdommer V02
Common Variants in Mendelian Kidney Disorder Genes and Their Association with Renal Function And
Downregulation of Mitochondrial UQCRB Inhibits Cancer Stem Cell-Like Properties in Glioblastoma
Mass-Spectrometry Based Proteomics Reveals Mitochondrial
Polymorphisms in the Mitochondrial Oxidative Phosphorylation Chain
Responsive Nuclear Proteins in Collecting Duct Cells
Supplementary File 2B Revised
Anti-UQCRB Antibody (ARG54994)
Supplementary Table 1
Positive Control Is Provided for Testing of a Specific Variant Identified at Another Laboratory
Electronic Supplementary Material (ESI) for Food & Function. This Journal Is © the Royal Society of Chemistry 2020
Mitochondrial Respiratory Chain Protein Co-Regulation in the Human Brain
Tackling Dysfunction of Mitochondrial Bioenergetics in the Brain by Omics Technologies
List of Nephropathy Genes
Recessive Gene List V2.0
Ovarian Tumor Mitochondria Exhibit Abnormal Phenotypes and Blunted Associations with Biobehavioral Factors
Impaired Mitochondrial Biogenesis in Adipose Tissue in Acquired Obesity Running Title: Impaired Mitochondrial Function in Obesity