DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» PET100
PET100
Mackenzie's Mission Gene & Condition List
Rcf2 Revealed in Cryo-EM Structures of Hypoxic Isoforms of Mature Mitochondrial III-IV Supercomplexes
Directional TOPO® Expression Kits
Regulation of COX Assembly and Function by Twin CX9C Proteins—Implications for Human Disease
Role of Cytochrome C Oxidase Nuclear-Encoded Subunits in Health and Disease
Pet Directional TOPO® Expression Kits
Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions
High-Resolution, Genome-Wide Mapping of Positive Supercoiling in Chromosomes Monica S Guo1†*, Ryo Kawamura2, Megan L Littlehale1, John F Marko2,3, Michael T Laub1,4*
Underexpression of HOXA11 Is Associated with Treatment Resistance and Poor Prognosis in Glioblastoma
Cytochrome C Oxidase Deficiency
Functions of Cytochrome C Oxidase Assembly Factors
Clinical and Genetic Studies in Paediatric Mitochondrial Disease
HIGD-Driven Regulation of Cytochrome C Oxidase Biogenesis and Function
Cloning, Expression, and Sequence Analysis of Camelysin, a Zinc Metalloprotease from Bacillus Anthracis and B
Leigh Syndrome
Sequence Properties of Certain GC Rich Avian Genes
The Genome-Wide Expression Response to Telomerase Deletion in Saccharomyces Cerevisiae
HIM-8 Binds to the X Chromosome Pairing Center and Mediates Chromosome-Specific Meiotic Synapsis
Top View
COX6B2 Drives Metabolic Reprogramming Toward Oxidative
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
PET100 (NM 001171155) Human Tagged ORF Clone Product Data
Iterative Orthology Prediction Uncovers New
Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
Syndromic Inherited Retinal Diseases: Genetic, Clinical and Diagnostic Aspects
Identification of Mitochondrial Electron Transport Chain Mutations That Effect Ageing
Table S4. Genes That Partition Or Associate to Mitochondrion Gene
Mutated PET117 Causes Complex IV Deficiency and Is Associated With
A Truncating PET100 Variant Causing Fatal Infantile Lactic Acidosis and Isolated Cytochrome C Oxidase Deficiency
A Novel Variant in COX16 Causes Cytochrome C Oxidase Deficiency, Severe Fatal Neonatal Lactic Acidosis, Encephalopathy, Cardiomyopathy, and Liver Dysfunction