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ATPAF2
Multivariate Analysis Reveals Genetic Associations of the Resting Default
ATPAF2 CRISPR/Cas9 KO Plasmid (M): Sc-434234
Anti-ATPAF2 (Aa 159-289) Polyclonal Antibody (DPABH-12101) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Characterizing Genomic Duplication in Autism Spectrum Disorder by Edward James Higginbotham a Thesis Submitted in Conformity
Mark Adam Scott Mitochondrial Survival Without Oxygen
Downloaded Per Proteome Cohort Via the Web- Site Links of Table 1, Also Providing Information on the Deposited Spectral Datasets
Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease Alison M
Genomic Approach in Idiopathic Intellectual Disability Maria De Fátima E Costa Torres
Mitochondrial Complex V Deficiency
Transcriptomic and Proteomic Landscape of Mitochondrial
Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease Alison M
Quantitative Trait Loci Mapping of Macrophage Atherogenic Phenotypes
Nuclear Genetic Defects of Mitochondrial ATP Synthase
Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions
ATPAF2 (H-76): Sc-366968
Phenotype Informatics
Gnomad Lof Supplement
Identification of Novel Regulatory Genes in Acetaminophen
Top View
Atpaf2 (NM 145427) Mouse Tagged ORF Clone – MR203936 | Origene
Mitochondrial Dysfunction and Its Role in Tissue-Specific Cellular Stress
Population-Level Genetics Human Gene-Muscle-Bone Associations
Detection of Classical 17P11.2 Deletions, an Atypical Deletion and RAI1 Alterations in Patients with Features Suggestive of Smith–Magenis Syndrome
The ATP Synthase Deficiency in Human Diseases
THE USE of WHOLE EXOME SEQUENCING to DETECT NOVEL GENETIC DISORDERS: TWO CASES and an ASSESSMENT of the TECHNOLOGY by Lauren
(12) Patent Application Publication (10) Pub. No.: US 2011/0098188 A1 Niculescu Et Al
Identification of Human Haploinsufficient Genes and Their Genomic Proximity to Segmental Duplications
ATM Regulates ATP Levels Through NRF1)
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
Investigation of Mutations in Nuclear Genes That Affect the Atp Synthase Russell Dsouza Wayne State University
ATPAF2 Human Sirna Oligo Duplex (Locus ID 91647) Product Data
Recent Advances in Understanding the Molecular Genetic Basis of Mitochondrial Disease
PRICKLE3 Linked to Atpase Biogenesis Manifested Leber's Hereditary Optic Neuropathy
List for Testing Done out of Québec LABORATOIRE CLINIQUES CUSM MUHC CLINICAL LABS
Analysis of Expression Profiles of Genes Involved in Fof1-ATP Synthase Biogenesis During Perinatal Development in Rat Liver and Skeletal Muscle
WO 2014/100434 Al 26 June 2014 (26.06.2014) W P O P C T
Limiting Factors in ATP Synthesis