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Human Molecular Genetics|October 1, 2005
Mitochondrial succinate is instrumental for HIF1alpha nuclear translocation in SDHA-mutant fibroblasts under normoxic conditionsJean-Jacques Brière, Judith Favier, Paule Bénit, et al.
Plos One|November 8, 2019
Evolutionarily conserved susceptibility of the mitochondrial respiratory chain to SDHI pesticides and its consequence on the impact of SDHIs on human cultured cellsPaule Bénit, Agathe Kahn, Dominique Chretien, et al.
Cancers|August 30, 2020
Usefulness of FDG-PET/CT-Based Radiomics for the Characterization and Genetic Orientation of Pheochromocytomas Before SurgeryCatherine Ansquer, Delphine Drui, Eric Mirallié, et al.
The Journal of Clinical Endocrinology and Metabolism|November 17, 2009
Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomasJosé Gaal, Nelly Burnichon, Esther Korpershoek, et al.
The Journal of Clinical Endocrinology and Metabolism|July 27, 2007
Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomasLaurence Amar, Eric Baudin, Nelly Burnichon, et al.
Cancer Research|September 23, 2003
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomasAnne-Paule Gimenez-Roqueplo, Judith Favier, Pierre Rustin, et al.
European Journal of Human Genetics : EJHG|January 8, 2026
Insights from 2057 germline genetic tests in renal cell carcinoma patients support revisiting testing criteriaRoseline Vibert, Yahya El Baroudi, Maude Vecten, et al.
Clinical Endocrinology|October 28, 2016
Pheochromocytomas are diagnosed incidentally and at older age in neurofibromatosis type 1Jessica Moramarco, Nada El Ghorayeb, Nadine Dumas, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|September 17, 2021
Low-grade oncocytic renal tumor (LOT): mutations in mTOR pathway genes and low expression of FOXI1Aurélien Morini, Tom Drossart, Marc-Olivier Timsit, et al.
British Journal of Haematology|January 10, 2024
EPAS1-mutated paragangliomas associated with haemoglobin disordersMaxence Mancini, Alexandre Buffet, Baptiste Porte, et al.
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