Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas. - Test2 - elhamkhani - TriplyDB

Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas.

Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas.

http://www.wikidata.org/entity/Q34998940

about

Molecular markers of paragangliomas/pheochromocytomas Comprehensive 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 Tumours Whole Exome Sequencing Uncovers Germline Variants of Cancer-Related Genes in Sporadic Pheochromocytoma

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Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas.

http://www.wikidata.org/entity/Q34998940

description

2015 nî lūn-bûn

@nan

2015 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2015 թվականի հունվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Whole-exome sequencing identif ...... omocytomas and paragangliomas.

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Whole-exome sequencing identif ...... omocytomas and paragangliomas.

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Whole-exome sequencing identif ...... omocytomas and paragangliomas.

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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.

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Nature Communications

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Whole-exome sequencing identif ...... omocytomas and paragangliomas.

@en

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Bradley Wubbenhorst

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Daniel DeSloover

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Debbie L Cohen

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Douglas Fraker

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Kathleen Montone

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Kurt D'Andrea

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Lauren Fishbein

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Nam Woo Cho

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Robert Daber

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Roger A Greenberg

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P2860

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

ATRX-mediated chromatin association of histone variant macroH2A1 regulates α-globin expression

The death-associated protein DAXX is a novel histone chaperone involved in the replication-independent deposition of H3.3

A method and server for predicting damaging missense mutations

Distinct factors control histone variant H3.3 localization at specific genomic regions

DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors

Fast and accurate long-read alignment with Burrows-Wheeler transform

SIFT: Predicting amino acid changes that affect protein function

A framework for variation discovery and genotyping using next-generation DNA sequencing data

MutationTaster evaluates disease-causing potential of sequence alterations

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10.1038/NCOMMS7140

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6

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Katherine L Nathanson

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2015-01-21T00:00:00Z

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271538222

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1014909510

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25608029

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phaeochromocytoma

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4302757

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