sdhd gene
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scholarly journals SDHD Gene

2020 ◽  
Author(s):  
Keyword(s):  
Sdhd Gene

scholarly journals SDHD gene mutation in Mexican population with carotid body tumor

2019 ◽  
Vol 86 (1) ◽  
Author(s):  
María Elizabeth Enríquez-Vega ◽  
Jimena Gabriela Muñoz-Paredes ◽  
Alfonso Cossío-Zazueta ◽  
Yam Ontiveros-Carlos ◽  
Ernesto Pacheco-Pittaluga ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Carotid Body ◽  
Mexican Population ◽  
Carotid Body Tumor ◽  
Sdhd Gene

scholarly journals SDHD GENE MUTATIONS: LOOKING BEYOND HEAD AND NECK TUMORS

2018 ◽  
Vol 4 (3) ◽  
pp. e186-e190
Author(s):  
Sushma Kadiyala ◽  
Yasmin Khan ◽  
Valeria de Miguel ◽  
Megan N. Frone ◽  
Fiemu Nwariaku ◽  
...  
Keyword(s):  
Head And Neck ◽  
Gene Mutations ◽  
Head And Neck Tumors ◽  
Neck Tumors ◽  
Sdhd Gene

scholarly journals Sensitivity of hematopoietic stem cells to mitochondrial dysfunction by SdhD gene deletion

2016 ◽  
Vol 7 (12) ◽  
pp. e2516-e2516 ◽  
Author(s):  
José Antonio Bejarano-García ◽  
África Millán-Uclés ◽  
Iván V Rosado ◽  
Luís Ignacio Sánchez-Abarca ◽  
Teresa Caballero-Velázquez ◽  
...  
Keyword(s):  
Stem Cells ◽  
Hematopoietic Stem Cells ◽  
Mitochondrial Dysfunction ◽  
Gene Deletion ◽  
Hematopoietic Stem ◽  
Sdhd Gene

scholarly journals A Conditional Mouse Mutant in the Tumor Suppressor SdhD Gene Unveils a Link between p21WAF1/Cip1 Induction and Mitochondrial Dysfunction

PLoS ONE ◽  
2014 ◽  
Vol 9 (1) ◽  
pp. e85528 ◽  
Author(s):  
África Millán-Uclés ◽  
Blanca Díaz-Castro ◽  
Paula García-Flores ◽  
Alicia Báez ◽  
José Antonio Pérez-Simón ◽  
...  
Keyword(s):  
Tumor Suppressor ◽  
Mitochondrial Dysfunction ◽  
Mouse Mutant ◽  
Sdhd Gene

scholarly journals Over-representation of the G12S polymorphism of the SDHD gene in patients with MEN2A syndrome

Clinics ◽  
2012 ◽  
Vol 67 (S1) ◽  
pp. 85-89 ◽  
Author(s):  
N Lendvai ◽  
M Toth ◽  
Z Valkusz ◽  
G Beko ◽  
N Szucs ◽  
...  
Keyword(s):  
Sdhd Gene

Novel SDHD Gene Mutation (H102R) in a Patient With Metastatic Cervical Paraganglioma Effectively Treated by Peptide Receptor Radionuclide Therapy

2011 ◽  
Vol 29 (33) ◽  
pp. e812-e815 ◽  
Author(s):  
Thorsten D. Poeppel ◽  
Ali Yuece ◽  
Christian Boy ◽  
Klaus A. Metz ◽  
Elke Kaminsky ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Radionuclide Therapy ◽  
Peptide Receptor Radionuclide Therapy ◽  
Peptide Receptor ◽  
Sdhd Gene

Is the c.3G>C mutation in the succinate dehydrogenase subunit D (SDHD ) gene due to a founder effect in Chinese head and neck paraganglioma patients?

2011 ◽  
Vol 121 (8) ◽  
pp. 1760-1764 ◽  
Author(s):  
Yang Zha ◽  
Xing-ming Chen ◽  
Ching-wan Lam ◽  
Soo-chin Lee ◽  
Sui-fan Tong ◽  
...  
Keyword(s):  
Head And Neck ◽  
Succinate Dehydrogenase ◽  
Founder Effect ◽  
Sdhd Gene ◽  
Head And Neck Paraganglioma
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