(Q34439696)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16075461%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

title

Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH (English)

1 reference

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5 January 2020

1 reference

5

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5 January 2020

author name string

Rebecca R Selzer

1

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5 January 2020

Todd A Richmond

2

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5 January 2020

Nathan J Pofahl

3

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5 January 2020

Roland D Green

4

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5 January 2020

Prakash Nair

6

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5 January 2020

Arthur R Brothman

7

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5 January 2020

Raymond L Stallings

8

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5 January 2020

publication date

1 November 2005

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Genes, Chromosomes and Cancer

5 January 2020

published in

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5 January 2020

volume

44

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5 January 2020

page(s)

305-319

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5 January 2020

issue

3

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The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

5 January 2020

cites work

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7 January 2021

Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA.

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7 January 2021

Coordinate deletion of chromosome 3p and 11q in neuroblastoma detected by comparative genomic hybridization

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7 January 2021

High-resolution global profiling of genomic alterations with long oligonucleotide microarray

1 reference

7 January 2021

Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome

1 reference

7 January 2021

Cytogenetic and molecular study of two human neuroblastoma cell lines.

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7 January 2021

1 reference

7 January 2021

Bioconductor: open software development for computational biology and bioinformatics

1 reference

7 January 2021

Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas

1 reference

7 January 2021

Detection of large-scale variation in the human genome

1 reference

7 January 2021

A tiling resolution DNA microarray with complete coverage of the human genome

1 reference

7 January 2021

Molecular analysis of chromosome arm 17q gain in neuroblastoma

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7 January 2021

Chromosomal aberrations in neuroblastoma cell lines identified by cross species color banding and chromosome painting

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7 January 2021

Promiscuous translocations of chromosome arm 17q in human neuroblastomas

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7 January 2021

Breakpoint position on 17q identifies the most aggressive neuroblastoma tumors

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7 January 2021

Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

1 reference

7 January 2021

Oligonucleotide microarray analysis of gene expression in neuroblastoma displaying loss of chromosome 11q.

1 reference

7 January 2021

Detection of MYCN amplification in three neuroblastoma cell lines by non-radioactive chromosomal in situ hybridization

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7 January 2021

Gene expression analysis using oligonucleotide arrays produced by maskless photolithography

1 reference

7 January 2021

Circular binary segmentation for the analysis of array-based DNA copy number data

1 reference

7 January 2021

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

1 reference

7 January 2021

Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11q deletion in tumors lackingMYCN amplification

1 reference

7 January 2021

Genome-wide analysis of DNA copy-number changes using cDNA microarrays

1 reference

7 January 2021

Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors

1 reference

7 January 2021

Spatial proximity of translocation-prone gene loci in human lymphomas

1 reference

7 January 2021

A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation

1 reference

7 January 2021

Large-scale copy number polymorphism in the human genome

1 reference

7 January 2021

Molecular mechanisms for constitutional chromosomal rearrangements in humans

1 reference

7 January 2021

Maskless fabrication of light-directed oligonucleotide microarrays using a digital micromirror array

1 reference

7 January 2021

Are gains of chromosomal regions 7q and 11p important abnormalities in neuroblastoma?

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7 January 2021

Molecular cytogenetic analysis of recurrent unbalanced t(11;17) in neuroblastoma

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7 January 2021

Chromosome transfer induced aneuploidy results in complex dysregulation of the cellular transcriptome in immortalized and cancer cells

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7 January 2021

Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization.

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7 January 2021

Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines.

1 reference

7 January 2021

Association of epigenetic inactivation of RASSF1A with poor outcome in human neuroblastoma.

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.20243

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16075461%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

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