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SDHC wt Allele

Known as: Cytochrome B Large Subunit of Complex II Gene, CYBL, CYB560 
Human SDHC wild-type allele is located in the vicinity of 1q23.3 and is approximately 50 kb in length. This allele, which encodes succinate… 
National Institutes of Health

Related topics

Related topics

13 relations
1q23.3Alzheimer's Disease Pathway KEGGCell RespirationCitrate Cycle (TCA Cycle) Pathway

Narrower (1)

PARAGANGLIOMAS 3

Broader (1)

SDHC gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Purification, structural elucidation and in vivo immunity-enhancing activity of polysaccharides from quinoa (Chenopodium quinoa Willd.) seeds
ABSTRACT Quinoa crude polysaccharides (QPS) were extracted from Chenopodium quinoa Willd. The soluble non-starch polysaccharide… 
2015
2015
Quinazoline‐4‐piperidine sulfamides are specific inhibitors of human NPP1 and prevent pathological mineralization of valve interstitial cells
Ectonucleotide pyrophosphatase/PDE1 (NPP1) is an ectoenzyme, which plays a role in several disorders including calcific aortic… 
Highly Cited
2014
Highly Cited
2014
Marine mammals trace anthropogenic structures at sea
Review
2014
Review
2014
The clinical phenotype of SDHC-associated hereditary paraganglioma syndrome (PGL3).
CONTEXT Mutations in the genes encoding subunits of the succinate dehydrogenase complex cause hereditary paraganglioma syndromes… 
Highly Cited
2010
Highly Cited
2010
Mutations in the Saccharomyces cerevisiae succinate dehydrogenase result in distinct metabolic phenotypes revealed through (1)H NMR-based metabolic footprinting.
Metabolomics is a powerful method of examining the intricate connections between mutations, metabolism, and disease. Metabolic… 
2009
2009
Characterization of New PPARγ Agonists: Benzimidazole Derivatives – the Importance of Position 2
Probing SAR: The 1‐(biphenyl‐4‐ylmethyl)‐1H‐benzo[d]imidazole moiety is known to be an essential structural component of… 
2008
2008
Maternal transmission of symptomatic disease with SDHD mutation: fact or fiction?
Paraganglioma syndrome (PGL) has been known as an inherited disorder for decades. However, it was not until the year 2000, when… 
Review
2004
Review
2004
An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma
Hereditary paraganglioma (PGL) is characterised by slow growing, vascular tumours that can develop in any component of the… 
Highly Cited
1994
Highly Cited
1994
Structure and regulation of SDH3, the yeast gene encoding the cytochrome b560 subunit of respiratory complex II.
1990
1990
Rat serine dehydratase gene codes for two species of mRNA of which only one is translated into serine dehydratase.
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