Succinate dehydrogenase (SDH) and mitochondrial driven neoplasia

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Gastric Stromal Tumors in Carney Triad Are Different Clinically, Pathologically, and Behaviorally From Sporadic Gastric Gastrointestinal Stromal Tumors: Findings in 104 Cases

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Immunohistochemistry for SDHB Divides Gastrointestinal Stromal Tumors (GISTs) into 2 Distinct Types

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Metastatic Pheochromocytoma/Paraganglioma Related to Primary Tumor Development in Childhood or Adolescence: Significant Link to SDHB Mutations

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Renal Tumors Associated With Germline SDHB Mutation Show Distinctive Morphology

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Succinate Dehydrogenase (SDH) D Subunit (SDHD) Inactivation in a Growth-Hormone-Producing Pituitary Tumor: A New Association for SDH?

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Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma

Bayley, J., van Minderhout, I. J. H. M., Weiss, M. M., Jansen, J. C., Oomen, P. H. N., Menko, F. H., Pasini, B., Ferrando, B., Wong, N., Alpert, L., et al. (2006) · BMC Medical Genetics · doi:10.1186/1471-2350-7-1 · Cited by 158 · see citing works

SDHA Loss-of-Function Mutations in KIT-PDGFRA Wild-Type Gastrointestinal Stromal Tumors Identified by Massively Parallel Sequencing

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A germline mutation of the KIF1Bβ gene on 1p36 in a family with neural and nonneural tumors

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Immunohistochemistry for PMS2 and MSH6 alone can replace a four antibody panel for mismatch repair deficiency screening in colorectal adenocarcinoma

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Renal Tumors and Hereditary Pheochromocytoma-Paraganglioma Syndrome Type 4

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“Pediatric-type” Gastrointestinal Stromal Tumors in Adults

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Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma

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Paraganglioma, neuroblastoma, and a SDHB mutation: Resolution of a 30‐year‐old mystery

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Mutation of SDHB is a Cause of Hypoxia-Related High-Altitude Paraganglioma

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SomaticSDHBMutation in an Extraadrenal Pheochromocytoma

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Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3

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“Pediatric-Type” Gastrointestinal Stromal Tumors Are SDHB Negative (“Type 2”) GISTs

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Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma

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Succinate Dehydrogenase Subunit B (SDHB) Is Expressed in Neurofibromatosis 1-Associated Gastrointestinal Stromal Tumors (Gists): Implications for the SDHB Expression Based Classification of Gists

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A Distinct Pediatric-type Gastrointestinal Stromal Tumor in Adults

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Genetic Analyses of Apparently Sporadic Pheochromocytomas

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There Is No Evidence That the SDHB Gene Is Involved in Neuroblastoma Development

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Adenomatoid tumour of the adrenal gland in a patient with germline SDHD mutation: a case report and review of the literature

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Screening for ovarian cancer is not effective

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The International Society of Urological Pathology (ISUP) Vancouver Classification of Renal Neoplasia

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SIRT5-mediated lysine desuccinylation impacts diverse metabolic pathways

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Succinate Dehydrogenase (SDH)-deficient Renal Carcinoma

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Gastrointestinal Stromal Tumors

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Mitochondrial complex ii: At the crossroads

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New developments in existing WHO entities and evolving molecular concepts: The Genitourinary Pathology Society (GUPS) update on renal neoplasia

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Succinate dehydrogenase (SDH)‐deficient neoplasia

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Recurrent epimutation of SDHC in gastrointestinal stromal tumors

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Dysfunctional oxidative phosphorylation makes malignant melanoma cells addicted to glycolysis driven by the V600EBRAF oncogene

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Succinate dehydrogenase deficient gastrointestinal stromal tumors (GISTs) – A review

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Renal Cell Tumors: Understanding Their Molecular Pathological Epidemiology and the 2016 WHO Classification

Inamura, K. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18102195 · Cited by 160 · see citing works

Pathology and genetics of phaeochromocytoma and paraganglioma

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Non-pheochromocytoma (PCC)/paraganglioma (PGL) tumors in patients with succinate dehydrogenase-related PCC–PGL syndromes: a clinicopathological and molecular analysis

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Fumarate Hydratase–deficient Uterine Leiomyomas Occur in Both the Syndromic and Sporadic Settings

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New and emerging renal entities: a perspective post‐ WHO 2016 classification

Trpkov, K., & Hes, O. (2018) · Histopathology · doi:10.1111/his.13727 · Cited by 147 · see citing works

Loss of expression of SDHA predicts SDHA mutations in gastrointestinal stromal tumors

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The role of complex II in disease

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Molecular subtypes of gastrointestinal stromal tumors and their prognostic and therapeutic implications

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Re‐evaluation of 33 ‘unclassified’ eosinophilic renal cell carcinomas in young patients

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IDH1/2 mutations target a key hallmark of cancer by deregulating cellular metabolism in glioma

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Genomic classifications of renal cell carcinoma: a critical step towards the future application of personalized kidney cancer care with pan‐omics precision

Hsieh, J. J.-D., Le, V., Cao, D., Cheng, E. H. Y., & Creighton, C. J. (2017) · The Journal of Pathology · doi:10.1002/path.5022 · Cited by 126 · see citing works

SDHB-Deficient Cancers: The Role of Mutations That Impair Iron Sulfur Cluster Delivery

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Loss of SDHA Expression Identifies SDHA Mutations in Succinate Dehydrogenase–deficient Gastrointestinal Stromal Tumors

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Iron: An Essential Element of Cancer Metabolism

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Succinate in the cancer–immune cycle

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Report From the International Society of Urological Pathology (ISUP) Consultation Conference on Molecular Pathology of Urogenital Cancers

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Fumarase-deficient Uterine Leiomyomas

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Metabolic alterations in renal cell carcinoma

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Ginsenoside Rb1 and mitochondria: A short review of the literature

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Succinate Dehydrogenase Deficiency Is Rare in Pituitary Adenomas

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