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SDHAF1
The Orphan Disease Networks
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Mutations in SDHD Lead to Autosomal Recessive Encephalomyopathy And
Crystal Structure of Bacterial Succinate:Quinone Oxidoreductase Flavoprotein Sdha in Complex with Its Assembly Factor Sdhe
Mitofusins Regulate Lipid Metabolism to Mediate the Development of Lung Fibrosis
Succinate Dehydrogenase Inhibition Leads to Epithelial-Mesenchymal Transition and Reprogrammed Carbon Metabolism." Cancer & Metabolism
Systems Genetics Analysis of the LXS Recombinant Inbred Mouse Strains:Genetic and Molecular Insights Into Acute Ethanol Tolerance
SDHAF1 Antibody (Center) Affinity Purified Rabbit Polyclonal Antibody (Pab) Catalog # AP5392C
Gnomad Lof Supplement
Supplementary Table S1. Relative Change in Proteins Associated with Heme Biosynthesis and Degradation
The Role of Immunohistochemistry and Molecular Analysis of Succinate Dehydrogenase in the Diagnosis of Endocrine and Non-Endocrine Tumors and Related Syndromes
Leukoencephalopathy with Accumulated Succinate Is Indicative
SDHAF1 Antibody Cat
1078-0432.CCR-17-1397.Full-Text.Pdf
Leigh Syndrome
Analysis of SDHAF3 in Familial and Sporadic Pheochromocytoma and Paraganglioma Trisha Dwight1,2* ,Unna3,4, Edward Kim1,2, Ying Zhu5, Anne Louise Richardson1, Bruce G
Immunohistochemistry and Mutation Analysis of Sdhx Genes in Carotid Paragangliomas
Heme Biosynthesis Depends on Previously Unrecognized Acquisition of Iron-Sulfur Cofactors in Human Amino-Levulinic Acid Dehydratase
Top View
Sdhaf1 (NM 001033140) Mouse Tagged ORF Clone Product Data
Genetic Testing of Leukodystrophies Unraveling Extensive Heterogeneity
Mitochondrial Respiratory Chain Complexes: Apoptosis Sensors Mutated in Cancer
Recessive Germline SDHA and SDHB Mutations Causing Leukodystrophy
Toward an Improved Definition of the Genetic and Tumor Spectrum Associated with SDH Germ-Line Mutations
SDHAF1, Encoding a LYR Complex-II Specific Assembly Factor, Is Mutated in SDH- Defective Infantile Leukoencephalopathy
Mitochondrial Disorders
Iron Regulatory Protein Deficiency Compromises Mitochondrial Function in Murine Embryonic Fibroblasts
Succinate Dehydrogenase and Ribonucleic Acid Networks in Cancer and Other Diseases
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
Mitochondria and Disease: Mutation and Expression Landscape of Mitochondri-Associated Genes in Different Disease Types
Crystal Structure of Bacterial Succinate:Quinone Oxidoreductase Flavoprotein Sdha in Complex with Its Assembly Factor Sdhe
Potential Pitfalls of SDH Immunohistochemical Detection In
Analytical Performance of NGS-Based Molecular Genetic Tests Used in the Diagnostic Workflow of Pheochromocytoma/Paraganglioma
Biochemical, Molecular, and Clinical Characterization of Succinate Dehydrogenase Subunit a Variants of Unknown Significance Amber E
Mitochondrial Syndromes with Leukoencephalopathies
Leigh Syndrome: One Disorder, More Than 75 Monogenic Causes
Molecular Basis of Leigh Syndrome: a Current Look Manuela Schubert Baldo* and Laura Vilarinho