相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。SDH Mutations Establish a Hypermethylator Phenotype in Paraganglioma
Eric Letouze et al.
CANCER CELL (2013)
Oncometabolites: linking altered metabolism with cancer
Ming Yang et al.
JOURNAL OF CLINICAL INVESTIGATION (2013)
MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
Nelly Burnichon et al.
CLINICAL CANCER RESEARCH (2012)
Inhibition of α-KG-dependent histone and DNA demethylases by fumarate and succinate that are accumulated in mutations of FH and SDH tumor suppressors
Mengtao Xiao et al.
GENES & DEVELOPMENT (2012)
An Update on the Genetics of Paraganglioma, Pheochromocytoma, and Associated Hereditary Syndromes
A. -P. Gimenez-Roqueplo et al.
HORMONE AND METABOLIC RESEARCH (2012)
Epithelial to Mesenchymal Transition Is Activated in Metastatic Pheochromocytomas and Paragangliomas Caused by SDHB Gene Mutations
Celine Loriot et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)
TMEM127 Screening in a Large Cohort of Patients with Pheochromocytoma and/or Paraganglioma
Nassera Abermil et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)
Frequent Mutation of Isocitrate Dehydrogenase (IDH)1 and IDH2 in Cholangiocarcinoma Identified Through Broad-Based Tumor Genotyping
Darrell R. Borger et al.
ONCOLOGIST (2012)
Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma
Nelly Burnichon et al.
HUMAN MOLECULAR GENETICS (2011)
Aberrant succination of proteins in fumarate hydratase-deficient mice and HLRCC patients is a robust biomarker of mutation status
Chiara Bardella et al.
JOURNAL OF PATHOLOGY (2011)
IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours
M. Fernanda Amary et al.
JOURNAL OF PATHOLOGY (2011)
Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations
Katherine A. Janeway et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Revisiting the TCA cycle: signaling to tumor formation
Nuno Raimundo et al.
TRENDS IN MOLECULAR MEDICINE (2011)
Pheochromocytomas: The (pseudo)-hypoxia hypothesis
Judith Favier et al.
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM (2010)
Research Resource: Transcriptional Profiling Reveals Different Pseudohypoxic Signatures in SDHB and VHL-Related Pheochromocytomas
Elena Lopez-Jimenez et al.
MOLECULAR ENDOCRINOLOGY (2010)
Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome
Elaine R. Mardis et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency
Jean-Pierre Bayley et al.
BMC MEDICAL GENETICS (2008)
Germline SDHB mutations and familial renal cell carcinoma
Christopher Ricketts et al.
JOURNAL OF THE NATIONAL CANCER INSTITUTE (2008)
An integrated genomic analysis of human glioblastoma Multiforme
D. Williams Parsons et al.
SCIENCE (2008)
Succination of protein thiols during adipocyte maturation - A biomarker of mitochondrial stress
Ryoji Nagai et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas
Laurence Amar et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2007)
S-(2-succinyl)cysteine:: A novel chemical modification of tissue proteins by a Krebs cycle intermediate
Nathan L. Alderson et al.
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS (2006)
Mitochondrial succinate is instrumental for HIF1α nuclear translocation in SDHA-mutant fibroblasts under normoxic conditions
JJ Brière et al.
HUMAN MOLECULAR GENETICS (2005)
A HIF1α regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas
PLM Dahia et al.
PLOS GENETICS (2005)
Year of diagnosis, features at presentation, and risk of recurrence in patients with pheochromocytoma or secreting paraganglioma
L Amar et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2005)
Succinate links TCA cycle dysfunction to oncogenesis by inhibiting HIF-alpha prolyl hydroxylase
MA Selak et al.
CANCER CELL (2005)
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer
IPM Tomlinson et al.
NATURE GENETICS (2002)
分享论文
