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UQCR11
Gene Expression Profiling Analysis of Lung Adenocarcinoma
A High-Throughput Approach to Uncover Novel Roles of APOBEC2, a Functional Orphan of the AID/APOBEC Family
Lncrna SNHG8 Is Identified As a Key Regulator of Acute Myocardial
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Electron Transport Chain Activity Is a Predictor and Target for Venetoclax Sensitivity in Multiple Myeloma
Primepcr™Assay Validation Report
Downloaded Per Proteome Cohort Via the Web- Site Links of Table 1, Also Providing Information on the Deposited Spectral Datasets
Molecular Architecture Underlying Fluid Absorption by the Developing Inner
Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions
UQCR11 (NM 006830) Human Tagged ORF Clone – RC201360
UQCRC2 Polyclonal Antibody
Mouse Uqcr11 Conditional Knockout Project (CRISPR/Cas9)
Nuclear Gene Mutations As the Cause of Mitochondrial Complex III Deficiency
The Transcriptional Regulator CBX2 and Ovarian Function
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
An Integrative Genomic Analysis of the Longshanks Selection Experiment for Longer Limbs in Mice
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Graphene Oxide Down-Regulates Genes of the Oxidative
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INTRODUCING a NOVEL METHOD for GENETIC ANALYSIS of AUTISM SPECTRUM DISORDER Sepideh Nouri
Single-Cell RNA-Seq of Mouse Dopaminergic Neurons Informs Candidate Gene Selection For
Degs) with an Enrichment Score >2.5
Identification and Mechanistic Investigation of Recurrent Functional Genomic and Transcriptional Alterations in Advanced Prostat
Wasin Vol. 9 N. 4 2558.Pmd
Product Data Sheet
Leveraging Tissue Specific Gene Expression Regulation to Identify Genes Associated with Complex Diseases
Complex III Mitochondrial Leukoencephalopathy Masquerading Acute Demyelinating Syndrome Due to a Novel Variant in CYC1
Supplementary Information
HBV DNA Integration and Clonal Hepatocyte Expansion in Chronic Hepatitis B Patients Considered Immune Tolerant
Tryptophan Oxidation in the UQCRC1 Subunit of Mitochondrial Complex
Primepcr™Assay Validation Report
SUPPORTING INFORMATION APPENDIX Mitochondrial Genomes
Regulation of Mitochondrial Gene Expression in Multiple
A Japanese Case of Cerebellar Ataxia, Spastic Paraparesis and Deep Sensory Impairment Associated with a Novel Homozygous TTC19 Mutation
S41467-021-25259-2.Pdf
Mitochondria and Disease: Mutation and Expression Landscape of Mitochondri-Associated Genes in Different Disease Types
Genetic Diversity, Molecular Phylogeny, and Selection Evidence of Jinchuan Yak Revealed by Whole-Genome Resequencing