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OXA1L
New Approaches to Functional Process Discovery in HPV 16-Associated Cervical Cancer Cells by Gene Ontology
Screening of a Clinically and Biochemically Diagnosed SOD Patient Using Exome Sequencing: a Case Report with a Mutations/Variations Analysis Approach
A Genome-Wide Association Study of Asthma Symptoms in Latin American Children Gustavo N
Noelia Díaz Blanco
(12) United States Patent (10) Patent No.: US 7.873,482 B2 Stefanon Et Al
Identification of Recurrent Non-Coding Mutations in B-Cell Lymphoma Using Capture Hi-C
Screening of a Clinically and Biochemically Diagnosed SOD Patient Using Exome Sequencing: a Case Report with a Mutations/Variations Analysis Approach
Characterization of Five Transmembrane Proteins: with Focus on the Tweety, Sideroflexin, and YIP1 Domain Families
The Role of Human Sco1, Sco2, Surf1 and Oxa1l in the Biogenesis of the Oxidative Phosphorylation System
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
A Network Inference Approach to Understanding Musculoskeletal
Functions of Cytochrome C Oxidase Assembly Factors
Coexpression Networks Based on Natural Variation in Human Gene Expression at Baseline and Under Stress
Rabbit Anti-MRPL48/FITC Conjugated Antibody-SL17801R-FITC
The Green Alga Chlamydomonas Reinhardtii: a New Model System To
Genome-Wide Association Study and Pathway Analysis for Female Fertility Traits in Iranian Holstein Cattle
Comparison Between Timelines of Transcriptional Regulation in Mammals, Birds, and Teleost Fish Somitogenesis
Anti-OXA1L Antibody (ARG40528)
Top View
A Computational Screen for Regulators of Oxidative Phosphorylation Implicates SLIRP in Mitochondrial RNA Homeostasis
Convergent Evolution of Genes Controlling Mitonuclear Balance in Annual Fishes
OXA1L Mutations Cause Mitochondrial Encephalopathy and a Combined Oxidative Phosphorylation Defect
OXA1L Mutations Cause Mitochondrial Encephalopathy and a Combined Oxidative Phosphorylation Defect
Modifiers of Beta-Amyloid Metabolism and Deposition in Mouse Models of Alzheimer’S Disease
Exonic Trinucleotide Microsatellites: Applying Genomic and Bioinformatic Techniques to Wildlife Forensic Science
A Genome-Wide Screen for ER Autophagy Highlights Key Roles of Mitochondrial Metabolism and ER
Polymorphisms in the DAD1 and OXA1L Genes Are Associated with Asthma and Atopy in a South American Population T
Polymorphisms in the DAD1 and OXA1L Genes Are Associated with Asthma and Atopy in a South American Population T
The Role of MRPL45 and OXA1L in Human Mitochondrial Protein Synthesis
Evidence for RPGRIP1 Gene As Risk Factor for Primary Open Angle Glaucoma
Inbreeding and Inbreeding Depression in Linebred Beef Cattle (PDF)
Linkage Analysis Identifies an Isolated Strabismus Locus at 14Q12 Overlapping with FOXG1 Syndrome Region
Nuclear RNA-Seq of Single Neurons Reveals Molecular Signatures of Activation