Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas.
about
Molecular markers of paragangliomas/pheochromocytomasComprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma.Oncogenic features of the bone morphogenic protein 7 (BMP7) in pheochromocytoma.HRAS mutation prevalence and associated expression patterns in pheochromocytoma.Recurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and Paragangliomas.A patient-derived-xenograft platform to study BRCA-deficient ovarian cancers.Paclitaxel is necessary for improved survival in epithelial ovarian cancers with homologous recombination gene mutations.Global DNA Methylation Analysis Identifies Two Discrete clusters of Pheochromocytoma with Distinct Genomic and Genetic Alterations.Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes.Rethinking pheochromocytomas and paragangliomas from a genomic perspective.Next-generation sequencing for endocrine cancers: Recent advances and challenges.PheoSeq: A Targeted Next-Generation Sequencing Assay for Pheochromocytoma and Paraganglioma Diagnostics.Precision medicine in pheochromocytoma and paraganglioma: current and future concepts.Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas.BRCA locus-specific loss of heterozygosity in germline BRCA1 and BRCA2 carriers.Extent of surgery for phaeochromocytomas in the genomic era.Loss of Myosin Vb in colorectal cancer is a strong prognostic factor for disease recurrence.Retinal interneuron survival requires non-cell-autonomous Atrx activity.New Perspectives on Pheochromocytoma and Paraganglioma: Toward a Molecular Classification.Activating FGFR1 Mutations in Sporadic Pheochromocytomas.Metabologenomics of Phaeochromocytoma and Paraganglioma: An Integrated Approach for Personalised Biochemical and Genetic Testing.Metabolic implications of hypoxia and pseudohypoxia in pheochromocytoma and paraganglioma.Comprehensive screening of alternative lengthening of telomeres phenotype and loss of ATRX expression in sarcomas.Differential nuclear ATRX expression in sarcomas.Treatment for Patients With Malignant Pheochromocytomas and Paragangliomas: A Perspective From the Hallmarks of Cancer.Molecular Genetics of Gastroenteropancreatic Neuroendocrine TumoursWhole Exome Sequencing Uncovers Germline Variants of Cancer-Related Genes in Sporadic Pheochromocytoma
P2860
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P2860
Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas.
description
2015 nî lūn-bûn
@nan
2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Whole-exome sequencing identif ...... omocytomas and paragangliomas.
@ast
Whole-exome sequencing identif ...... omocytomas and paragangliomas.
@en
Whole-exome sequencing identif ...... omocytomas and paragangliomas.
@nl
type
label
Whole-exome sequencing identif ...... omocytomas and paragangliomas.
@ast
Whole-exome sequencing identif ...... omocytomas and paragangliomas.
@en
Whole-exome sequencing identif ...... omocytomas and paragangliomas.
@nl
prefLabel
Whole-exome sequencing identif ...... omocytomas and paragangliomas.
@ast
Whole-exome sequencing identif ...... omocytomas and paragangliomas.
@en
Whole-exome sequencing identif ...... omocytomas and paragangliomas.
@nl
P2093
P2860
P356
P1476
Whole-exome sequencing identif ...... omocytomas and paragangliomas.
@en
P2093
Bradley Wubbenhorst
Daniel DeSloover
Debbie L Cohen
Douglas Fraker
Kathleen Montone
Kurt D'Andrea
Lauren Fishbein
Nam Woo Cho
Robert Daber
Roger A Greenberg
P2860
P2888
P356
10.1038/NCOMMS7140
P407
P577
2015-01-21T00:00:00Z
P5875
P6179
1014909510