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Mutations in <i>SDHD</i> , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma

2000· article· en· 1,639 citations· W2126511952 on OpenAlex· 10.1126/science.287.5454.848

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Opus teacher head0.015
GPT teacher head0.265
Teacher spread
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Validation status
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Abstract

Hereditary paraganglioma (PGL) is characterized by the development of benign, vascularized tumors in the head and neck. The most common tumor site is the carotid body (CB), a chemoreceptive organ that senses oxygen levels in the blood. Analysis of families carrying the PGL1 gene, described here, revealed germ line mutations in the SDHD gene on chromosome 11q23. SDHD encodes a mitochondrial respiratory chain protein-the small subunit of cytochrome b in succinate-ubiquinone oxidoreductase (cybS). In contrast to expectations based on the inheritance pattern of PGL, the SDHD gene showed no evidence of imprinting. These findings indicate that mitochondria play an important role in the pathogenesis of certain tumors and that cybS plays a role in normal CB physiology.

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The record

Venue
Science
Topic
Mitochondrial Function and Pathology
Field
Biochemistry, Genetics and Molecular Biology
Canadian institutions
Women's Health Research Institute
Funders
National Institute of Mental Health
Keywords
SDHDParagangliomaBiologyGeneticsMitochondrial respiratory chainGeneMitochondrial DNARespiratory chainMitochondrionPheochromocytomaMutationGermline mutationEndocrinologyPathologyMedicine
Has abstract in OpenAlex
yes