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SDHA
Heme Oxygenase-1 Regulates Mitochondrial Quality Control in the Heart
Crystal Structure of Bacterial Succinate:Quinone Oxidoreductase Flavoprotein Sdha in Complex with Its Assembly Factor Sdhe
Updates on the Genetics of Neuroendocrine Tumors
The Microbiota-Produced N-Formyl Peptide Fmlf Promotes Obesity-Induced Glucose
Function and Structure of Complex Ii of The
First-Positive Surveillance Screening in an Asymptomatic SDHA Germline Mutation Carrier
(SDHA) Gene Mutation in Renal Cell Carcinoma: a New Subset of Hereditary Renal Cancer
Rapid Determination of Tricarboxylic Acid Cycle Enzyme Activities in Biological Samples
Inhibition of A-KG-Dependent Histone and DNA Demethylases by Fumarate and Succinate That Are Accumulated in Mutations of FH and SDH Tumor Suppressors
Genetic Testing Medical Policy – Genetics
SSIEM Classification of Inborn Errors of Metabolism 2011
Proteomic Analysis of Aged Microglia
Novel Mutations and Genetic Overlap with Hereditary Tumors
Spatial Sorting Enables Comprehensive Characterization of Liver Zonation
SDH) and Complex I Activity Is Necessary to Recapitulate the Metabolic Phenotype of SDH Mutant Tumors
Succinate Dehydrogenase and Human Diseases: New Insights Into a Well-Known Enzyme
Proteomic Anaysis of Aged Microglia: Shifts in Transcription, Bioenergetics, and Nutrient Response Antwoine Flowers1,2, Harris Bell-Temin3, Ahmad Jalloh1,2, Stanley M
S4.01 the Findings of Any Ancillary Studies, Where Performed, Must Be Recorded
Top View
Supplemental Figures 04 12 2017
Succinate Dehydrogenase and Fumarate Hydratase: Linking Mitochondrial Dysfunction and Cancer
Succinate Dehydrogenase-Deficient Renal Cell Carcinoma
Hypoxia Promotes Mitochondrial Complex I Abundance Via HIF-1Α in Complex III and Complex IV Deficient Cells
Good Survival Outcome of Metastatic SDH-Deficient Gastrointestinal Stromal Tumors Harboring SDHA Mutations
SDHA Clinical Guide
SDHA Gene Succinate Dehydrogenase Complex Flavoprotein Subunit A
High Molecular Weight Forms of Mammalian Respiratory Chain Complex II
AF1Q ALL1-Fused Gene from Chromosome 1Q PPP2CB Protein
1078-0432.CCR-17-1397.Full-Text.Pdf
Evidence Supporting Oxidative Stress in a Moderately Affected Area of The
The Genetic Nomenclature of Recessive Cerebellar Ataxias
PAX2 Promotes Epithelial Ovarian Cancer Progression Involving Fatty Acid Metabolic Reprogramming
SDHAF1, Encoding a LYR Complex-II Specific Assembly Factor, Is Mutated in SDH- Defective Infantile Leukoencephalopathy
Genomic Unity® Prenatal Analysis
(JCV) Large and Small Tumor Antigen Interacting Proteins
Efficacy of Immunohistochemistry for SDHB in the Screening Of
STO (%) % O (STO) Slices of 12Μm Thickness After Equilibration to -20 C
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Crystal Structure of Bacterial Succinate:Quinone Oxidoreductase Flavoprotein Sdha in Complex with Its Assembly Factor Sdhe
Succinate Dehydrogenase and Ribonucleic Acid Networks in Cancer and Other Diseases
Crystal Structure of Bacterial Succinate:Quinone Oxidoreductase Flavoprotein Sdha in Complex with Its Assembly Factor Sdhe
Dichloroacetate Prevents Cisplatin-Induced Nephrotoxicity Without Compromising Cisplatin Anticancer Properties
Potential Pitfalls of SDH Immunohistochemical Detection In
Comprehensive Diagnosis for Mitochondrial Disorders
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Responsive Nuclear Proteins in Collecting Duct Cells
NRF2, a Transcription Factor for Stress Response and Beyond
Proteo-Metabolomics Reveals Compensation Between Ischemic and Non-Injured Contralateral Kidneys After Reperfusion
Dysregulated Provision of Oxidisable Substrates to the Mitochondria in ME/CFS Lymphoblasts
STAT Autism and Intellectual Disability Panel
Loss of Expression of SDHA Predicts SDHA Mutations in Gastrointestinal
Assessing the Association of Mitochondrial Genetic Variation
Analysis of All Subunits, SDHA, SDHB, SDHC, SDHD, Of
The Citric Acid Cycle of Thiomicrospira Crunogena
Hereditary Paraganglioma-Pheochromocytoma (SDHA) Sequencing ARUP Test Code 2011461 Hereditary PGL/PCC (SDHA) Seq - Spcmn Whole Blood
Mitochondrial Oxodicarboxylate Carrier Deficiency Is Associated with Mitochondrial DNA Depletion and Spinal Muscular Atrophy–Like Disease
Label-Free Quantitative Proteomics of the Lysine Acetylome in Mitochondria Identifies Substrates of SIRT3 in Metabolic Pathways
About SDHA Gene Mutations
Whole-Genome Sequencing of the Snub-Nosed Monkey Provides Insights Into Folivory and Evolutionary History
Cisco Science: Using Omics to Answer a Range of Key Questions Hannah Lachance University of Vermont
Genomic Unity® Neurology Analysis
Specific Cyprinid HIF Isoforms Contribute to Cellular Mitochondrial
Mrna Changes in Nucleus Accumbens Related To