A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3 - Wikidata - wikimedia - TriplyDB

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

http://www.wikidata.org/entity/Q24563121

about

Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family Analyses of apoptotic regulators CASP9 and DFFA at 1P36.2, reveal rare allele variants in human neuroblastoma tumours An 85-kb tandem triplication in the slow Wallerian degeneration (Wlds) mouse cDNA array-CGH profiling identifies genomic alterations specific to stage and MYCN-amplification in neuroblastoma A cluster of genes located in 1p36 are down-regulated in neuroblastomas with poor prognosis, but not due to CpG island methylation Neuroblastoma: oncogenic mechanisms and therapeutic exploitation of necroptosis Role of CHD5 in human cancers: 10 years later Panobinostat synergistically enhances the cytotoxic effects of cisplatin, doxorubicin or etoposide on high-risk neuroblastoma cells Expression of GITR Enhances Multiple Myeloma Cell Sensitivity to Bortezomib 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.Array comparative genomic hybridisation-based identification of two imbalances of chromosome 1p in a 9-year-old girl with a monosomy 1p36 related phenotype and a family history of learning difficulties: a case report.Specific gene expression profiles and chromosomal abnormalities are associated with infant disseminated neuroblastoma.PHOX2B-mediated regulation of ALK expression: in vitro identification of a functional relationship between two genes involved in neuroblastoma.Targeted expression of MYCN causes neuroblastoma in transgenic mice.Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome.Identification and characterization of a 500-kb homozygously deleted region at 1p36.2-p36.3 in a neuroblastoma cell line.Refinement of 1p36 alterations not involving PRDM16 in myeloid and lymphoid malignancies Genetics of prostate cancer: too many loci, too few genes Current status of linkage studies in hereditary prostate cancer.Screening for gene mutations in a 500 kb neuroblastoma tumor suppressor candidate region in chromosome 1p; mutation and stage-specific expression in UBE4B/UFD2.Clinical categories of neuroblastoma are associated with different patterns of loss of heterozygosity on chromosome arm 1p.Autoinhibitory regulation of p73 by Delta Np73 to modulate cell survival and death through a p73-specific target element within the Delta Np73 promoter Analysis of genomic imprinting at 1p35-36 in neuroblastoma.Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36.Neuroblastoma tumour genetics: clinical and biological aspects.Novel tumor suppressor function of glucocorticoid-induced TNF receptor GITR in multiple myeloma.Primary adenocarcinomas of lower esophagus, esophagogastric junction and gastric cardia: in special reference to China Lack of homozygously inactivated p73 in single-copy MYCN primary neuroblastomas and neuroblastoma cell lines.The tumour suppressor CHD5 forms a NuRD-type chromatin remodelling complex.Mechanisms of CHD5 Inactivation in neuroblastomas.Expression of mRNA for the neurotrophin receptor trkC in neuroblastomas with favourable tumour stage and good prognosis.Loss of heterozygosity on chromosome 1 in sporadic colorectal carcinoma.Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival.CHD5, a tumor suppressor gene deleted from 1p36.31 in neuroblastomas.The MYCN oncogene is a direct target of miR-34a.DNA hypermethylation profiles in squamous cell carcinoma of the vulva.Role of microRNAs in epigenetic silencing of the CHD5 tumor suppressor gene in neuroblastomas.The quest for the 1p36 tumor suppressor.Presence of 1q gain and absence of 7p gain are new predictors of local or metastatic relapse in localized resectable neuroblastoma.A novel 1p36.2 located gene, APITD1, with tumour-suppressive properties and a putative p53-binding domain, shows low expression in neuroblastoma tumours.

P2860

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P2860

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

http://www.wikidata.org/entity/Q24563121

description

1995 nî lūn-bûn

@nan

1995 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

1995 թվականի հունիսին հրատարակված գիտական հոդված

@hy

1995年の論文

@ja

1995年学术文章

@wuu

1995年学术文章

@zh-cn

1995年学术文章

@zh-hans

1995年学术文章

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1995年学术文章

@zh-sg

1995年學術文章

@yue

name

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

@ast

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

@en

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

@nl

type

label

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

@ast

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

@en

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

@nl

prefLabel

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

@ast

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

@en

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

@nl

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PNAS.92.12.5520

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

@en

P2093

A T Look

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

B A Kaufman

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C Allen

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C Beltinger

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C Hilliard

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E Sulman

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G M Brodeur

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H Enomoto

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H N Marshall

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J A Biegel

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P2860

Mutually exclusive expression of a helix-loop-helix gene and N-myc in human neuroblastomas and in normal development

The retinoblastoma protein binds to a family of E2F transcription factors

The gene for PAX7, a member of the paired-box-containing genes, is localized on human chromosome arm 1p36

Antioncogenes and human cancer.

Alterations in the PITSLRE protein kinase gene complex on chromosome 1p36 in childhood neuroblastoma

Cloning and chromosomal localization of the human TRK-B tyrosine kinase receptor gene (NTRK2)

Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification.

Neuroblastoma consensus deletion maps to 1p36.1-2.

Constitutional 1p36 deletion in a child with neuroblastoma.

Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE.

P304

5520-4

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scholarly article

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10.1073/PNAS.92.12.5520

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P407

P433

12

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P478

92

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P577

1995-06-06T00:00:00Z

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P5875

15420737

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7777541

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41727

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