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。SDHA is a tumor suppressor gene causing paraganglioma
Nelly Burnichon et al.
HUMAN MOLECULAR GENETICS (2010)
Mutations of the Metabolic Genes IDH1, IDH2, and SDHAF2 Are Not Major Determinants of the Pseudohypoxic Phenotype of Sporadic Pheochromocytomas and Paragangliomas
Li Yao et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2010)
Isocitrate Dehydrogenase Mutations Are Rare in Pheochromocytomas and Paragangliomas
Jose Gaal et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2010)
SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma
Jean-Pierre Bayley et al.
LANCET ONCOLOGY (2010)
Monoclonal Antibody DOG1.1 Shows Higher Sensitivity Than KIT in the Diagnosis of Gastrointestinal Stromal Tumors, Including Unusual Subtypes
Bernadette Liegl et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2009)
The Succinate Dehydrogenase Genetic Testing in a Large Prospective Series of Patients with Paragangliomas
Nelly Burnichon et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis
Francien H. van Nederveen et al.
LANCET ONCOLOGY (2009)
Sunitinib Treatment in Pediatric Patients With Advanced GIST Following Failure of Imatinib
Katherine A. Janeway et al.
PEDIATRIC BLOOD & CANCER (2009)
SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma
Huai-Xiang Hao et al.
SCIENCE (2009)
Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes
Ying Ni et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Molecular characterization of pediatric gastrointestinal stromal tumors
Narasimhan P. Agaram et al.
CLINICAL CANCER RESEARCH (2008)
Correlation of Kinase Genotype and Clinical Outcome in the North American Intergroup Phase III Trial of Imatinib Mesylate for Treatment of Advanced Gastrointestinal Stromal Tumor: CALGB 150105 Study by Cancer and Leukemia Group B and Southwest Oncology Group
Michael C. Heinrich et al.
JOURNAL OF CLINICAL ONCOLOGY (2008)
Primary and Secondary Kinase Genotypes Correlate With the Biological and Clinical Activity of Sunitinib in Imatinib-Resistant Gastrointestinal Stromal Tumor
Michael C. Heinrich et al.
JOURNAL OF CLINICAL ONCOLOGY (2008)
Heterogeneity of kinase inhibitor resistance mechanisms in GIST
B. Liegl et al.
JOURNAL OF PATHOLOGY (2008)
Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD
Barbara Pasini et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
Pediatric KIT-wild-type and platelet-derived growth factor receptor α-wild-type gastrointestinal stromal tumors share KIT activation but not mechanisms of genetic progression with adult gastrointestinal stromal tumors
Katherine A. Janeway et al.
CANCER RESEARCH (2007)
Familial gastrointestinal stromal tumors and germ-line mutations
Sarah R. McWhinney et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
Outcome of metastatic GIST in the era before tyrosine kinase inhibitors
Jason S. Gold et al.
ANNALS OF SURGICAL ONCOLOGY (2007)
Three spectrophotometric assays for the measurement of the five respiratory chain complexes in minuscule biological samples
Paule Benit et al.
CLINICA CHIMICA ACTA (2006)
Efficacy and safety of sunitinib in patients with advanced gastrointestinal stromal tumour after failure of imatinib: a randomised controlled trial
George D. Demetri et al.
LANCET (2006)
Review:: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?
Camilo Jimenez et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)
Genetic testing in pheochromocytoma or functional paraganglioma
L Amar et al.
JOURNAL OF CLINICAL ONCOLOGY (2005)
The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency
JP Bayley et al.
BMC MEDICAL GENETICS (2005)
Mitochondrial tumour suppressors: A genetic and biochemical update
E Gottlieb et al.
NATURE REVIEWS CANCER (2005)
Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene
F Schiavi et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2005)
Gastrointestinal stromal tumors of the stomach in children and young adults - A clinicopathologic, immunohistochemical, and molecular genetic study of 44 cases with long-term follow-up and review of the literature
M Miettinen et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2005)
A HIF1α regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas
PLM Dahia et al.
PLOS GENETICS (2005)
Biology of gastrointestinal stromal tumors
CL Corless et al.
JOURNAL OF CLINICAL ONCOLOGY (2004)
Mechanisms of oncogenic KIT signal transduction in primary gastrointestinal stromal tumors (GISTs)
A Duensing et al.
ONCOGENE (2004)
PDGFRA activating mutations in gastrointestinal stromal tumors
MC Heinrich et al.
SCIENCE (2003)
SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation
A. Cascon et al.
JOURNAL OF MEDICAL GENETICS (2002)
Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma
AP Gimenez-Roqueplo et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2002)
Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors
GD Demetri et al.
NEW ENGLAND JOURNAL OF MEDICINE (2002)
Familial paraganglioma and gastric stromal sarcoma: A new syndrome distinct from the Carney triad
JA Carney et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway
AP Gimenez-Roqueplo et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene
PEM Taschner et al.
GENES CHROMOSOMES & CANCER (2001)
Mutations in SDHC cause autosomal dominant paraganglioma, type 3
S Niemann et al.
NATURE GENETICS (2000)