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UQCRQ
Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ
Molecular Characterization of Acute Myeloid Leukemia by Next Generation Sequencing: Identification of Novel Biomarkers and Targets of Personalized Therapies
Genetic Loci on Chromosome 5 Are Associated with Circulating Levels Of
Mouse Uqcrq Knockout Project (CRISPR/Cas9)
THE FUNCTIONAL SIGNIFICANCE of MITOCHONDRIAL SUPERCOMPLEXES in C. ELEGANS by WICHIT SUTHAMMARAK Submitted in Partial Fulfillment
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Single Cell Transcriptomics in Schizophrenia Postmortem Brain: Moving Beyond Bulk Lysate
Electron Transport Chain Activity Is a Predictor and Target for Venetoclax Sensitivity in Multiple Myeloma
Anti-UQCRQ Antibody (ARG54995)
Genetic Loci on Chromosome 5 Are Associated with Circulating
Thesis Reference
Identification of Four Novel Associations for B-Cell Acute
Mutations in CYC1, Encoding Cytochrome C1 Subunit Of
Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions
Online Appendix 3. Supplemental Information Methods the Complete Methods Used in These Studies Are Described Below. Subjects. Le
UQCRC2 Polyclonal Antibody
The Biological Age of a Bloodstain Donor Author(S): Jack Ballantyne, Ph.D
Inflammatory and Adipogenic Stromal Subpopulations in Visceral Adipose Tissue Of
Top View
RPKM Data from Gtex TPM Data Normalization for Age, Gender And
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
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Mitochondrial Markers 1
Graphene Oxide Down-Regulates Genes of the Oxidative
Organization of the Respiratory Supercomplexes in Cells with Defective Complex III: Structural Features and Metabolic Consequences
Mitochondrial Complex III Deficiency
Complex III Mitochondrial Leukoencephalopathy Masquerading Acute Demyelinating Syndrome Due to a Novel Variant in CYC1
Tryptophan Oxidation in the UQCRC1 Subunit of Mitochondrial Complex
A Japanese Case of Cerebellar Ataxia, Spastic Paraparesis and Deep Sensory Impairment Associated with a Novel Homozygous TTC19 Mutation
Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function
Navigating the Complexities of the Human Oncoproteome with the Signet Knowledgebank
Mackenzie's Mission Gene & Condition List
Responsive Nuclear Proteins in Collecting Duct Cells
Innate Immune Activity Is Detected Prior to Seroconversion in Children
CYC1 Predicts Poor Prognosis in Patients with Breast Cancer
Individual Genome Sequence Gene List (By Disease)
Supplementary File 1
Genome-Wide Crispri Screening Identifies OCIAD1 As a Prohibitin
Targeted PI3K/AKT-Hyperactivation Induces Cell Death in Chronic Lymphocytic Leukemia