(Q40501792)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15495191%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

title

Homozygous deletions of CDKN2A caused by alternative mechanisms in various human cancer cell lines (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15495191%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

4

1 reference

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4 January 2020

Thomas Efferth

3

1 reference

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4 January 2020

author name string

Sascha Raschke

1

1 reference

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4 January 2020

Vera Balz

2

1 reference

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4 January 2020

Andrea R Florl

5

1 reference

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4 January 2020

publication date

1 January 2005

1 reference

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Genes, Chromosomes and Cancer

4 January 2020

published in

1 reference

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4 January 2020

volume

42

1 reference

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4 January 2020

page(s)

58-67

1 reference

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4 January 2020

issue

1

1 reference

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Double-strand breaks and tumorigenesis

4 January 2020

cites work

1 reference

Breakpoint junctions of chromosome 9p deletions in two human glioma cell lines

21 January 2018

1 reference

Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells

21 January 2018

1 reference

7 January 2021

p16 Mutation Frequency and Clinical Correlation in Head and Neck Cancer

1 reference

7 January 2021

The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome

1 reference

7 January 2021

DNA methylation and the mechanisms of CDKN2A inactivation in transitional cell carcinoma of the urinary bladder

1 reference

7 January 2021

Peculiar structure and location of 9p21 homozygous deletion breakpoints in human cancer cells

1 reference

7 January 2021

1 reference

7 January 2021

Inactivation of tumor suppressor genes and deregulation of the c-myc gene in urothelial cancer cell lines

1 reference

7 January 2021

Reliable detection of p53 aberrations in squamous cell carcinomas of the head and neck requires transcript analysis of the entire coding region

1 reference

7 January 2021

Prevalent involvement of illegitimate V(D)J recombination in chromosome 9p21 deletions in lymphoid leukemia

1 reference

7 January 2021

Hypermethylation and transcriptional downregulation of the carboxyl-terminal modulator protein gene in glioblastomas

1 reference

7 January 2021

The genetics of transitional cell carcinoma: progress and potential clinical application

1 reference

7 January 2021

Cancer-specific chromosome alterations in the constitutive fragile region FRA3B.

1 reference

7 January 2021

Expression of G1-->S transition regulatory molecules in human urothelial cancer.

1 reference

7 January 2021

Mechanisms of DNA double-strand break repair and their potential to induce chromosomal aberrations

1 reference

7 January 2021

Molecular processes of chromosome 9p21 deletions in human cancers

1 reference

7 January 2021

Cytosine methylation and the ecology of intragenomic parasites

1 reference

7 January 2021

DNA studies underestimate the major role of CDKN2A inactivation in oral and oropharyngeal squamous cell carcinomas

1 reference

7 January 2021