Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy. - Wikidata - awgldk - TriplyDB

Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy.

Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy.

http://www.wikidata.org/entity/Q37981893

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The Role of ATRX in the Alternative Lengthening of Telomeres (ALT) Phenotype Prognostic relevance of UCH-L1 and α-internexin in pancreatic neuroendocrine tumors.Predictive value of preoperative peripheral blood neutrophil/lymphocyte ratio for lymph node metastasis in patients of resectable pancreatic neuroendocrine tumors: a nomogram-based study PHLDA3 is a novel tumor suppressor of pancreatic neuroendocrine tumors.Update on pancreatic neuroendocrine tumors.Pancreatic Neuroendocrine Tumors: an Update.von Hippel-Lindau disease-associated solid microcystic serous adenomas masquerading as pancreatic neuroendocrine neoplasms.Endoscopic ultrasound-guided ethanol ablation of pancreatic neuroendocrine tumours: A case study and literature review.Pharmacotherapy of Zollinger-Ellison syndrome.Altered PTEN, ATRX, CHGA, CHGB, and TP53 expression are associated with aggressive VHL-associated pancreatic neuroendocrine tumors.Comparison of WHO Classifications (2004, 2010), the Hochwald grading system, and AJCC and ENETS staging systems in predicting prognosis in locoregional well-differentiated pancreatic neuroendocrine tumors.ENETS Consensus Guidelines Update for the Management of Patients with Functional Pancreatic Neuroendocrine Tumors and Non-Functional Pancreatic Neuroendocrine Tumors.A Cross-Species Analysis in Pancreatic Neuroendocrine Tumors Reveals Molecular Subtypes with Distinctive Clinical, Metastatic, Developmental, and Metabolic Characteristics Therapy of metastatic pancreatic neuroendocrine tumors (pNETs): recent insights and advances RSUME is implicated in tumorigenesis and metastasis of pancreatic neuroendocrine tumors.Pancreatic Neuroendocrine Neoplasms: Basic Biology, Current Treatment Strategies and Prospects for the Future.Everolimus for the treatment of pancreatic neuroendocrine tumors.Current understanding of the molecular biology of pancreatic neuroendocrine tumors.Advancements in pancreatic neuroendocrine tumors.Translational research in endocrine surgery.Molecular biology of neuroendocrine tumors: from pathways to biomarkers and targets.The genetic classification of pancreatic neoplasia.Molecular pathogenesis and targeted therapy of sporadic pancreatic neuroendocrine tumors.Role of Locoregional and Systemic Approaches for the Treatment of Patients with Metastatic Neuroendocrine Tumors.Spatial intratumoral heterogeneity of proliferation in immunohistochemical images of solid tumors.Translational research in neuroendocrine tumors: pitfalls and opportunities.Duodenal and Ampullary Carcinoid Tumors: Size Predicts Necessity for Lymphadenectomy.DAXX/ATRX and MEN1 genes are strong prognostic markers in pancreatic neuroendocrine tumors.Sunitinib is effective and tolerable in Chinese patients with advanced pancreatic neuroendocrine tumors: a multicenter retrospective study in China.

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P2860

Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy.

http://www.wikidata.org/entity/Q37981893

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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artikel ilmiah

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name

Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy.

@en

Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy.

@nl

type

label

Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy.

@en

Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy.

@nl

prefLabel

Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy.

@en

Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy.

@nl

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NRGASTRO.2012.9

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Nature Reviews Gastroenterology & Hepatology

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Well-differentiated pancreatic neuroendocrine tumors: from genetics to therapy.

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Anirban Maitra

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Barish H Edil

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Roeland F de Wilde

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P2860

Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription

Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres

Menin associates with a trithorax family histone methyltransferase complex and with the hoxc8 locus

Primary peptic ulcerations of the jejunum associated with islet cell tumors of the pancreas

Core signaling pathways in human pancreatic cancers revealed by global genomic analyses

Antiangiogenic therapy elicits malignant progression of tumors to increased local invasion and distant metastasis

Inherited pancreatic endocrine tumor syndromes: advances in molecular pathogenesis, diagnosis, management, and controversies

Benefits of targeting both pericytes and endothelial cells in the tumor vasculature with kinase inhibitors

Classification and pathology of gastroenteropancreatic neuroendocrine neoplasms

High frequency of mutations of the PIK3CA gene in human cancers

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nrgastro.2012.9

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199-208

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scholarly article

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10.1038/NRGASTRO.2012.9

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4

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9

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Ralph H. Hruban

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2012-02-07T00:00:00Z

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22310917

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3544293

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