Structural and functional consequences of succinate dehydrogenase subunit B mutations
Published 2015 View Full Article
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Title
Structural and functional consequences of succinate dehydrogenase subunit B mutations
Authors
Keywords
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Journal
ENDOCRINE-RELATED CANCER
Volume 22, Issue 3, Pages 387-397
Publisher
Bioscientifica
Online
2015-05-14
DOI
10.1530/erc-15-0099
References
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Related references
Note: Only part of the references are listed.- The LYR Factors SDHAF1 and SDHAF3 Mediate Maturation of the Iron-Sulfur Subunit of Succinate Dehydrogenase
- (2014) Un Na et al. Cell Metabolism
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- (2014) Nunziata Maio et al. Cell Metabolism
- The Lure of a LYR: The Logistics of Iron Sulfur Cluster Delivery
- (2014) D.J.R. Lane et al. Cell Metabolism
- Current views on cell metabolism in SDHx-related pheochromocytoma and paraganglioma
- (2014) Ales Vicha et al. ENDOCRINE-RELATED CANCER
- Krebs Cycle Metabolite Profiling for Identification and Stratification of Pheochromocytomas/Paragangliomas due to Succinate Dehydrogenase Deficiency
- (2014) Susan Richter et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Pheochromocytoma and Paraganglioma: An Endocrine Society Clinical Practice Guideline
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- Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas
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- A New Specific Succinate-Glutamate Metabolomic Hallmark in Sdhx-Related Paragangliomas
- (2013) Alessio Imperiale et al. PLoS One
- Loss of SDHA Expression Identifies SDHA Mutations in Succinate Dehydrogenase–deficient Gastrointestinal Stromal Tumors
- (2012) Trisha Dwight et al. AMERICAN JOURNAL OF SURGICAL PATHOLOGY
- Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function
- (2012) Chunzhang Yang et al. FASEB JOURNAL
- An Update on the Genetics of Paraganglioma, Pheochromocytoma, and Associated Hereditary Syndromes
- (2012) A.-P. Gimenez-Roqueplo et al. HORMONE AND METABOLIC RESEARCH
- Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome
- (2012) E. Panizza et al. HUMAN MOLECULAR GENETICS
- Structural Basis for Malfunction in Complex II
- (2012) Tina M. Iverson et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Exploring biological electron transfer pathway dynamics with the Pathways Plugin for VMD
- (2012) Ilya A. Balabin et al. JOURNAL OF COMPUTATIONAL CHEMISTRY
- A novel EPAS1/HIF2A germline mutation in a congenital polycythemia with paraganglioma
- (2012) Felipe R. Lorenzo et al. JOURNAL OF MOLECULAR MEDICINE-JMM
- Renal Tumors Associated With Germline SDHB Mutation Show Distinctive Morphology
- (2011) Anthony J. Gill et al. AMERICAN JOURNAL OF SURGICAL PATHOLOGY
- LOVD v.2.0: the next generation in gene variant databases
- (2011) Ivo F. A. C. Fokkema et al. HUMAN MUTATION
- A method and server for predicting damaging missense mutations
- (2010) Ivan A Adzhubei et al. NATURE METHODS
- Functional study in a yeast model of a novel succinate dehydrogenase subunit B gene germline missense mutation (C191Y) diagnosed in a patient affected by a glomus tumor
- (2009) P. Goffrini et al. HUMAN MOLECULAR GENETICS
- Clinical manifestations of familial paraganglioma and phaeochromocytomas insuccinate dehydrogenase B(SDH-B) gene mutation carriers
- (2008) Umasuthan Srirangalingam et al. CLINICAL ENDOCRINOLOGY
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