Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Succinate dehydrogenase complex"'
Autor:
Maike Pohlers, Selina Gies, Tanja Taenzer, Russalina Stroeder, Laura Theobald, Nicole Ludwig, Yoo‐Jin Kim, Rainer Maria Bohle, Erich Franz Solomayer, Eckart Meese, Martin Hart, Barbara Walch‐Rückheim
Publikováno v:
Molecular Oncology, Vol 18, Iss 9, Pp 2157-2178 (2024)
During cervical carcinogenesis, T‐helper (Th)‐17 cells accumulate in the peripheral blood and tumor tissues of cancer patients. We previously demonstrated that Th17 cells are associated with therapy resistance as well as cervical cancer metastase
Externí odkaz:
https://doaj.org/article/f428a7b9ddb34a2188fd9525ee1f3e6c
Publikováno v:
Clinical Case Reports, Vol 12, Iss 10, Pp n/a-n/a (2024)
Key Clinical Message Pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries, paragangliomas, and syringomyelia are uncommon diseases. Furthermore, in the absence of any genetic link and with less than five repor
Externí odkaz:
https://doaj.org/article/4d64c180f9d347a58e89f872f2a4735a
Autor:
Francesco Fabozzi, Rosalba Carrozzo, Mariachiara Lodi, Angela Di Giannatale, Selene Cipri, Chiara Rosignoli, Isabella Giovannoni, Alessandra Stracuzzi, Teresa Rizza, Claudio Montante, Emanuele Agolini, Michela Di Nottia, Federica Galaverna, Giada Del Baldo, Francesco Del Bufalo, Angela Mastronuzzi, Maria Antonietta De Ioris
Publikováno v:
Frontiers in Oncology, Vol 13 (2024)
The increased availability of genetic technologies has significantly improved the detection of novel germline variants conferring a predisposition to tumor development in patients with malignant disease. The identification of variants of uncertain si
Externí odkaz:
https://doaj.org/article/9a9082b1342045729d45a563947a18ad
Akademický článek
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Publikováno v:
AACE Clinical Case Reports, Vol 7, Iss 3, Pp 174-176 (2021)
Objective: Familial paraganglioma syndrome type 4 is associated with mutations in the succinate dehydrogenase complex subunit B (SDHB) gene. We report the case of a patient with familial paraganglioma syndrome type 4 with the mutation c.600G>T; p.Trp
Externí odkaz:
https://doaj.org/article/9cbf99315d8645a4873e3d7763cc1e2e
Autor:
Yifei Xie, Jing Zhang, Bingbing Lu, Zhuo Bao, Jimin Zhao, Xianyu Lu, Yaxing Wei, Ke Yao, Yanan Jiang, Qiang Yuan, Xiaofan Zhang, Bo Li, Xinhuan Chen, Zigang Dong, Kangdong Liu
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Esophageal squamous cell carcinoma (ESCC) has a worldwide impact on human health, due to its high incidence and mortality. Therefore, identifying compounds to increase patients' survival rate is urgently needed. Mefloquine (MQ) is an FDA-approved ant
Externí odkaz:
https://doaj.org/article/4a587e54387c462ba7fdb3ba028f19d5
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Cassandra L.A. Hawco, Robyn L. Houlden
Publikováno v:
AACE Clinical Case Reports, Vol 7, Iss 3, Pp 174-176 (2021)
AACE Clinical Case Reports
AACE Clinical Case Reports
Objective Familial paraganglioma syndrome type 4 is associated with mutations in the succinate dehydrogenase complex subunit B (SDHB) gene. We report the case of a patient with familial paraganglioma syndrome type 4 with the mutation c.600G>T; p.Trp2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5980fc8cb3cceebe58c4fae89dd4edb5
http://www.sciencedirect.com/science/article/pii/S2376060521000055
http://www.sciencedirect.com/science/article/pii/S2376060521000055
Publikováno v:
Genes. 14:646
Loss of function of the succinate dehydrogenase complex characterizes 20–40% of all KIT/PDGFRA-negative GIST. Approximately half of SDH-deficient GIST patients lack SDHx mutations and are caused by a hypermethylation of the SDHC promoter, which cau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ed3b4acaa97a8f4c7c65b93587d20c8
https://doi.org/10.3390/genes14030646
https://doi.org/10.3390/genes14030646
Akademický článek
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