Comprehensive SNP array study of frequently used neuroblastoma cell lines; copy neutral loss of heterozygosity is common in the cell lines but uncommon in primary tumors - Wikidata - wikimedia - TriplyDB

Comprehensive SNP array study of frequently used neuroblastoma cell lines; copy neutral loss of heterozygosity is common in the cell lines but uncommon in primary tumors

Comprehensive SNP array study of frequently used neuroblastoma cell lines; copy neutral loss of heterozygosity is common in the cell lines but uncommon in primary tumors

http://www.wikidata.org/entity/Q31030415

about

Acquired genetic alterations in tumor cells dictate the development of high-risk neuroblastoma and clinical outcomes Ultra-High Density SNParray in Neuroblastoma Molecular Diagnostics Autocrine prostaglandin E2 signaling promotes tumor cell survival and proliferation in childhood neuroblastoma.Neuroblastoma after childhood: prognostic relevance of segmental chromosome aberrations, ATRX protein status, and immune cell infiltration Neuroblastoma patient-derived orthotopic xenografts retain metastatic patterns and geno- and phenotypes of patient tumours.Germline DNA copy number aberrations identified as potential prognostic factors for breast cancer recurrence.High-resolution array CGH profiling identifies Na/K transporting ATPase interacting 2 (NKAIN2) as a predisposing candidate gene in neuroblastoma COX/mPGES-1/PGE2 pathway depicts an inflammatory-dependent high-risk neuroblastoma subset.Planar cell polarity gene expression correlates with tumor cell viability and prognostic outcome in neuroblastoma Generation of KCL040 clinical grade human embryonic stem cell line.The Molecular Karyotype of 25 Clinical-Grade Human Embryonic Stem Cell Lines.The RASSF gene family members RASSF5, RASSF6 and RASSF7 show frequent DNA methylation in neuroblastoma.The genetic tumor background is an important determinant for heterogeneous MYCN-amplified neuroblastoma.New prognostic markers in neuroblastoma.Recent insights into the biology of neuroblastoma.Orexin a phosphorylates the γ-Aminobutyric acid type A receptor β2 subunit on a serine residue and changes the surface expression of the receptor in SH-SY5Y cells exposed to propofol.Comprehensive cytogenomic profile of the in vitro neuronal model SH-SY5Y.Aggressive neuroblastomas have high p110alpha but low p110delta and p55alpha/p50alpha protein levels compared to low stage neuroblastomas.Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development.Inhibition of Microsomal Prostaglandin E Synthase-1 in Cancer-Associated Fibroblasts Suppresses Neuroblastoma Tumor Growth.

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P2860

Comprehensive SNP array study of frequently used neuroblastoma cell lines; copy neutral loss of heterozygosity is common in the cell lines but uncommon in primary tumors

http://www.wikidata.org/entity/Q31030415

description

2011 nî lūn-bûn

@nan

2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Comprehensive SNP array study ...... but uncommon in primary tumors

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Comprehensive SNP array study ...... but uncommon in primary tumors

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type

label

Comprehensive SNP array study ...... but uncommon in primary tumors

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Comprehensive SNP array study ...... but uncommon in primary tumors

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prefLabel

Comprehensive SNP array study ...... but uncommon in primary tumors

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Comprehensive SNP array study ...... but uncommon in primary tumors

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Comprehensive SNP array study ...... but uncommon in primary tumors

@en

P2093

Hanna Kryh

http://www.w3.org/2001/XMLSchema#string

Jennie Erichsen

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Rose-Marie Sjöberg

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P2860

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

Combined subtractive cDNA cloning and array CGH: an efficient approach for identification of overexpressed genes in DNA amplicons

Mechanisms leading to uniparental disomy and their clinical consequences

A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera

Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis

A gain-of-function mutation of JAK2 in myeloproliferative disorders

Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

Genome-wide analysis of neuroblastomas using high-density single nucleotide polymorphism arrays.

High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: four cases of homozygous deletions of the CDKN2A gene.

High-risk neuroblastoma tumors with 11q-deletion display a poor prognostic, chromosome instability phenotype with later onset.

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1471-2164-12-443

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scholarly article

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10.1186/1471-2164-12-443

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12

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Tommy Martinsson

Jonas Abrahamsson

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51619910

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21899760

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3178547

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