Cytogenetically balanced translocations are associated with focal copy number alterations (Q38465671)

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scientific article published on 19 October 2006

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English	Cytogenetically balanced translocations are associated with focal copy number alterations	scientific article published on 19 October 2006

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scholarly article

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Europe PubMed Central

PubMed publication ID

17051368

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3 September 2017

title

Cytogenetically balanced translocations are associated with focal copy number alterations (English)

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Europe PubMed Central

PubMed publication ID

17051368

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3 September 2017

author

Jeremy A. Squire

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Jeremy A Squire

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4

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author name string

Spencer K Watson

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1

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Europe PubMed Central

PubMed publication ID

17051368

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3 September 2017

Ronald J deLeeuw

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2

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stated in

Europe PubMed Central

PubMed publication ID

17051368

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3 September 2017

Doug E Horsman

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3

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Europe PubMed Central

PubMed publication ID

17051368

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3 September 2017

Wan L Lam

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5

1 reference

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Europe PubMed Central

PubMed publication ID

17051368

retrieved

3 September 2017

language of work or name

English

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publication date

19 October 2006

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Europe PubMed Central

PubMed publication ID

17051368

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3 September 2017

published in

Human Genetics

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Europe PubMed Central

PubMed publication ID

17051368

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3 September 2017

volume

120

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Europe PubMed Central

PubMed publication ID

17051368

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3 September 2017

issue

6

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Europe PubMed Central

PubMed publication ID

17051368

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3 September 2017

page(s)

795-805

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Europe PubMed Central

PubMed publication ID

17051368

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3 September 2017

cites work

Loss of a small region around the PTEN locus is a major chromosome 10 alteration in prostate cancer xenografts and cell lines

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

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Multiple microalterations detected at high frequency in oral cancer

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

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Primary cell cultures as models of prostate cancer development

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

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inferred from PubMed ID database lookup

Use of whole genome amplification and comparative genomic hybridisation to detect chromosomal copy number alterations in cell line material and tumour tissue.

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

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inferred from PubMed ID database lookup

Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution cDNA microarray CGH mapping of genomic imbalances in osteosarcoma using formalin-fixed paraffin-embedded tissue

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of chromosomal instability in prostate cancer determined by spectral karyotyping (SKY) and interphase fish analysis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

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Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

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Reciprocal translocations: a trap for cytogenetists?

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

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SeeGH--a software tool for visualization of whole genome array comparative genomic hybridization data

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rearrangement of the long arm of chromosome 10 in the prostate adenocarcinoma cell line LNCaP.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methods for high throughput validation of amplified fragment pools of BAC DNA for constructing high resolution CGH arrays

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined spectral karyotyping, multicolor banding, and microarray comparative genomic hybridization analysis provides a detailed characterization of complex structural chromosomal rearrangements associated with gene amplification in the osteosarcoma

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interphase FISH analysis of PTEN in histologic sections shows genomic deletions in 68% of primary prostate cancer and 23% of high-grade prostatic intra-epithelial neoplasias

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a high frequency of chromosomal rearrangements in the centromeric regions of prostate cancer cell lines by sequential Giemsa banding and spectral karyotyping

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide screening for complete genetic loss in prostate cancer by comparative hybridization onto cDNA microarrays

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic alterations in doxorubicin-resistant hepatocellular carcinoma cells: a combined study of spectral karyotyping, positional expression profiling and candidate genes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of multicolor fluorescence technologies in the characterization of prostate carcinoma cell lines: a comparison of multiplex fluorescence in situ hybridization and spectral karyotyping data

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlating breakage-fusion-bridge events with the overall chromosomal instability and in vitro karyotype evolution in prostate cancer

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide characterization of gene expression variations and DNA copy number changes in prostate cancer cell lines

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analysis in mantle cell lymphoma: a review of 214 cases

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A set of BAC clones spanning the human genome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

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Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

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HOX11, a homeobox-containing T-cell oncogene on human chromosome 10q24

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution analysis of gene copy number alterations in human prostate cancer using CGH on cDNA microarrays: impact of copy number on gene expression

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Resolution of genotypic heterogeneity in prostate tumors using polymerase chain reaction and comparative genomic hybridization on microdissected carcinoma and prostatic intraepithelial neoplasia foci

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

APC/CTNNB1 (?-catenin) pathway alterations in human prostate cancers

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17051368

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00439-006-0251-9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17051368

retrieved

3 September 2017

Dimensions Publication ID

1032968805

0 references

PubMed publication ID

17051368

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17051368

retrieved

3 September 2017

 

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