Profiling genomic copy number changes in retinoblastoma beyond loss of RB1 (Q28273606)

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English	Profiling genomic copy number changes in retinoblastoma beyond loss of RB1	scientific article

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instance of

scholarly article

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title

Profiling genomic copy number changes in retinoblastoma beyond loss of RB1 (English)

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main subject

retinoblastoma

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based on heuristic

inferred from title

author

Timothy W. Corson

object named as

Timothy W Corson

series ordinal

2

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Brenda L. Gallie

object named as

Brenda L Gallie

series ordinal

7

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Paul Bo-San Lai

object named as

Paul B-S Lai

series ordinal

6

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Jeremy A. Squire

object named as

Jeremy A Squire

series ordinal

4

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author name string

Ella Bowles

series ordinal

1

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Jane Bayani

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3

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Nathalie Wong

series ordinal

5

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language of work or name

English

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publication date

February 2007

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published in

Genes, Chromosomes and Cancer

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volume

46

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issue

2

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page(s)

118-29

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cites work

Loss of retinoblastoma gene and amplification of N-myc gene in retinoblastoma

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Retinoma: spontaneous regression of retinoblastoma or benign manifestation of the mutation?

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SCOMP is superior to degenerated oligonucleotide primed-polymerase chain reaction for global amplification of minute amounts of DNA from microdissected archival tissue samples

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Minimal regions of chromosomal imbalance in retinoblastoma detected by comparative genomic hybridization

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Clinical implications of promoter hypermethylation in RASSF1A and MGMT in retinoblastoma

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Microsatellite instability and MLH1 promoter methylation in human retinoblastoma

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KIF14 mRNA expression is a predictor of grade and outcome in breast cancer

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KIF14 is a candidate oncogene in the 1q minimal region of genomic gain in multiple cancers

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Altered expression and activation of the nerve growth factor receptors TrkA and p75 provide the first evidence of tumor progression to effusion in breast carcinoma

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Loss of p75 neurotrophin receptor expression accompanies malignant progression to human and murine retinoblastoma

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N-MYC amplification, loss of heterozygosity on the short arm of chromosome 1 and DNA ploidy in retinoblastoma

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Hyperdiploidy Plus NonamplifiedMYCNConfers a Favorable Prognosis in Children 12 to 18 Months Old With Disseminated Neuroblastoma: A Pediatric Oncology Group Study

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Overexpression of a DEAD box protein (DDX1) in neuroblastoma and retinoblastoma cell lines

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Gains and overexpression identify DEK and E2F3 as targets of chromosome 6p gains in retinoblastoma.

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Genomic gains on chromosome 1q in retinoblastoma: consequences on gene expression and association with clinical manifestation

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Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridization

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Mutation and cancer: statistical study of retinoblastoma

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Expression and amplification of the N-myc gene in primary retinoblastoma

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7 January 2021

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High level amplification of N-MYC is not associated with adverse histology or outcome in primary retinoblastoma tumours

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Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome.

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7 January 2021

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inferred from DOI database lookup

Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FGCC.20383

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7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome evolution in retinoblastoma

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FGCC.20383

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7 January 2021

based on heuristic

inferred from DOI database lookup

Expression analysis of 6p22 genomic gain in retinoblastoma

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FGCC.20383

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Diagnostic utility of p75 neurotrophin receptor (p75NTR) as a marker of breast myoepithelial cells

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20383

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7 January 2021

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Chromosomal abnormalities in human retinoblastoma. A review

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Crossref

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7 January 2021

based on heuristic

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Distribution and significance of nerve growth factor receptor (NGFR/p75NTR) in normal, benign and malignant breast tissue

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Crossref

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7 January 2021

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Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma

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stated in

Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20383

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7 January 2021

based on heuristic

inferred from DOI database lookup

Increase in copy number of N-myc in retinoblastomas in comparison with chromosome abnormality

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stated in

Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20383

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7 January 2021

based on heuristic

inferred from DOI database lookup

MYCN in neuronal tumours

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stated in

Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20383

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7 January 2021

based on heuristic

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A detailed analysis of chromosomal changes in heritable and non-heritable retinoblastoma.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FGCC.20383

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7 January 2021

based on heuristic

inferred from DOI database lookup

Tumour induction by the retinoblastoma mutation is independent of N-myc expression.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FGCC.20383

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Comparative genomic hybridisation divides retinoblastomas into a high and a low level chromosomal instability group

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FGCC.20383

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Relationship between MYCN copy number and expression in rhabdomyosarcomas and correlation with adverse prognosis in the alveolar subtype

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FGCC.20383

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7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FGCC.20383

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1002/GCC.20383

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1924132

OpenCitations bibliographic resource ID

1924132

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1924132

PubMed publication ID

17099872

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1924132

 

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