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SDHB protein, human

Known as: Ip, SDHB, Ip protein, human 
Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial (280 aa, ~32 kDa) is encoded by the human SDHB gene. This protein plays a… 
National Institutes of Health

Related topics

Related topics

13 relations
Alzheimer's Disease Pathway KEGGCell RespirationCitrate Cycle (TCA Cycle) PathwayElectron Transport Pathway

Broader (1)

Succinate Dehydrogenase

Papers overview

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2016
2016
SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery.
BACKGROUND Mutations in the Fe-S cluster-containing SDHB subunit of succinate dehydrogenase cause familial cancer syndromes… 
2016
2016
Disease-Causing SDHAF 1 Mutations Impair Transfer of FeS Clusters to SDHB Graphical Abstract Highlights
2016
2016
LASS5 Interacts with SDHB and Synergistically Represses p53 and p21 Activity.
Longevity Assurance 5 (LASS5), a member of the LASS/Ceramide Synthases family, synthesizes C16-ceramide and is implicated in… 
2014
2014
Phenotype of SDHB mutation carriers in the Netherlands
SDHB mutation carriers are predisposed to developing paragangliomas (PGLs). The objective of this study was to assess genotype… 
2014
2014
Association of cancer metabolism-related proteins with oral carcinogenesis – indications for chemoprevention and metabolic sensitizing of oral squamous cell carcinoma?
Tumor metabolism is a crucial factor for the carcinogenesis of oral squamous cell carcinoma (OSCC). Expression of IGF-R1… 
2012
2012
Use of SDHB immunohistochemistry to identify germline mutations of SDH genes
2011
2011
[SDHB expression in Warthin's tumour].
2011
2011
[SDHB expression in Warthin's tumour].
2010
2010
Paraganglioma in a 13-year-old girl: a novel SDHB gene mutation in the family?
Review
2009
Review
2009
SDHB-associated renal oncocytoma suggests a broadening of the renal phenotype in hereditary paragangliomatosis
Mutations in SDHB are one of the causes of hereditary paraganglioma syndrome. Germline mutations in SDHB predispose to the… 
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