Primary Site >> Pancreatic Cancer

Gene >> DAXX

  • 2012
  • 2013
  • 2014
  • 2015
  • 2016
  • 2017
  • 2018
Ref: Loss of ATRX or DAXX expression and concomitant acquisition of the alternative lengthening of telomeres phenotype are late events in a small subset of MEN-1 syndrome pancreatic neuroendocrine tumors.
PMID: 22575867
Ref: Altered PTEN, ATRX, CHGA, CHGB, and TP53 expression are associated with aggressive VHL-associated pancreatic neuroendocrine tumors.
PMID: 23361940
Ref: The genetics of neuroendocrine tumors.
PMID: 23391111
Ref: Current understanding of the molecular biology of pancreatic neuroendocrine tumors.
PMID: 23840053
Ref: Loss of DAXX and ATRX are associated with chromosome instability and reduced survival of patients with pancreatic neuroendocrine tumors.
PMID: 24148618
Ref: Neuroendocrine tumors of the pancreas: current concepts and controversies.
PMID: 24430597
Ref: Molecular genetics of pancreatic neoplasms and their morphologic correlates: an update on recent advances and potential diagnostic applications.
PMID: 24436263
Ref: Impact of the tumor microenvironment in predicting postoperative hepatic recurrence of pancreatic neuroendocrine tumors.
PMID: 25310565
Ref: Leiomyosarcoma with alternative lengthening of telomeres is associated with aggressive histologic features, loss of ATRX expression, and poor clinical outcome.
PMID: 25229770
Ref: Molecular pathogenesis and targeted therapy of sporadic pancreatic neuroendocrine tumors.
PMID: 25619712
Ref: Transcriptional Repressor DAXX Promotes Prostate Cancer Tumorigenicity via Suppression of Autophagy.
PMID: 25903140
Ref: Exome-level comparison of primary well-differentiated neuroendocrine tumors and their cell lines.
PMID: 26087898
Ref: Neuroendocrine Tumor of the Pancreas as a Manifestation of Cowden Syndrome: A Case Report.
PMID: 26678657
Ref: Molecular alterations in sporadic pancreatic neuroendocrine microadenomas.
PMID: 26905832
Ref: Study of clinicopathological features, hormone immunoexpression, and loss of ATRX and DAXX expression in pancreatic neuroendocrine tumors.
PMID: 27162024
Ref: A Practical Approach to the Classification of WHO Grade 3 (G3) Well-differentiated Neuroendocrine Tumor (WD-NET) and Poorly Differentiated Neuroendocrine Carcinoma (PD-NEC) of the Pancreas.
PMID: 27259015
Ref: New Genetics and Genomic Data on Pancreatic Neuroendocrine Tumors: Implications for Diagnosis, Treatment, and Targeted Therapies.
PMID: 27456058
Ref: Metastatic multiple endocrine neoplasia type 1: report of one case.
PMID: 28138639
Ref: Pancreatic Neuroendocrine Neoplasms: Basic Biology, Current Treatment Strategies and Prospects for the Future.
PMID: 28098761
Ref: Hypo-methylation mediates chromosomal instability in pancreatic NET.
PMID: 28115389
Ref: Detection of Somatic Mutations in Gastroenteropancreatic Neuroendocrine Tumors Using Targeted Deep Sequencing.
PMID: 28179320
Ref: Alternative lengthening of telomeres and ATRX/DAXX loss can be reliably detected in FNAs of pancreatic neuroendocrine tumors.
PMID: 28371511
Ref: Loss of Progesterone Receptor Expression Is an Early Tumorigenesis Event Associated with Tumor Progression and Shorter Survival in Pancreatic Neuroendocrine Tumor Patients.
PMID: 28597868
Ref: Assessment of pancreatic neuroendocrine tumor cytologic genotype diversity to guide personalized medicine using a custom gastroenteropancreatic next-generation sequencing panel.
PMID: 29212165
Ref: Molecular characterization of metastatic pancreatic neuroendocrine tumors (PNETs) using whole-genome and transcriptome sequencing.
PMID: 29092957
Ref: Genomic landscape of pancreatic neuroendocrine tumours: the International Cancer Genome Consortium.
PMID: 29321190
Ref: Site-Specific Genomic Alterations in a Well-Differentiated Pancreatic Neuroendocrine Tumor With High-Grade Progression.
PMID: 29521944
Ref: Pancreatic neuroendocrine carcinomas reveal a closer relationship to ductal adenocarcinomas than to neuroendocrine tumors G3.
PMID: 29596894
Ref: Glucagonoma With Necrolytic Migratory Erythema: Metabolic Profile and Detection of Biallelic Inactivation of DAXX Gene.
PMID: 29688432
Ref: Daxx Functions Are p53-Independent In Vivo.
PMID: 29903771
Ref: Hotspot DAXX, PTCH2 and CYFIP2 mutations in pancreatic neuroendocrine neoplasms.
PMID: 30021865