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COX10
COX10 (NM 001303) Human Untagged Clone Product Data
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Respiration-Deficient Astrocytes Survive As Glycolytic Cells in Vivo
Predict AID Targeting in Non-Ig Genes Multiple Transcription Factor
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
PRODUCT SPECIFICATION Product Datasheet
Functions of Cytochrome C Oxidase Assembly Factors
Genetic Testing for Neuromuscular Disorders
Hypoxia Promotes Mitochondrial Complex I Abundance Via HIF-1Α in Complex III and Complex IV Deficient Cells
Low Cytochrome Oxidase 4I1 Links Mitochondrial Dysfunction to Obesity and Type 2 Diabetes in Humans and Mice
COX10 (C-Term) Rabbit Polyclonal Antibody – AP51029PU-N | Origene
Review Charcot-Marie-Tooth Disease
Mutation Screening in Patients with Isolated Cytochrome C Oxidase Deficiency
Metabolic Requirements of NK Cell Responses to Viral Infection
COX10 Rabbit Pab
DNA Rearrangements on Both Homologues of Chromosome 17 In
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
Blueprint Genetics Charcot-Marie-Tooth Neuropathy
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Cytochrome C Oxidase Biogenesis in a Patient with a Mutation in COX10
SUPPLEMENTARY APPENDIX Transcriptional Activities of DUX4 Fusions in B-Cell Acute Lymphoblastic Leukemia
Identification of Candidate Genes Associated with Charcot-Marie- Tooth Disease by Network and Pathway Analysis
Defects in the Biosynthesis of Mitochondrial Heme C and Heme a in Yeast and Mammals
Retrospective, Multicentric Study of 180 Children with Cytochrome C Oxidase Deficiency
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Charcot-Marie-Tooth Disease
Parental Micronutrient Deficiency Distorts Liver DNA Methylation And
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
Genetic Features of Mitochondrial Respiratory Chain Disorders
Mutation Analysis of COX18 in 29 Patients with Isolated Cytochrome C Oxidase Deficiency
Hypoxia-Regulated Microrna-210 Modulates Mitochondrial Function and Decreases ISCU and COX10 Expression
COX10 Antibody (C-Term) Affinity Purified Rabbit Polyclonal Antibody (Pab) Catalog # Ap10714b
Clinical and Molecular Genetic Studies in Mitochondrial Disease
REVIEW ARTICLE Human Cytochrome Oxidase Deficiency
Genetics of Charcot-Marie-Tooth (CMT) Disease Within the Frame of the Human Genome Project Success
Mutations of the SCO1 Gene in Mitochondrial Cytochrome C
JCI Suppli Fig1 Revised Ver1のコピー
COX10 Polyclonal Antibody Catalog Number PA5-24207 Product Data Sheet
Cytochrome C Oxidase Deficiency Due to a Novel SCO2 Mutation Mimics Werdnig-Hoffmann Disease
Product Description SALSA® MLPA® Probemix P405-B1 CMT1 to Be Used with the MLPA General Protocol