(Q53222152)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25787918%20AND%20SRC:MED&resulttype=core&format=json

3 March 2020

title

A child with Li-Fraumeni syndrome: Modes to inactivate the second allele of TP53 in three different malignancies (English)

1 reference

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3 March 2020

1 reference

8

1 reference

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3 March 2020

Nataliya Di Donato

9

1 reference

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3 March 2020

10

Meinolf Suttorp

1 reference

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3 March 2020

6

Gudrun Göhring

1 reference

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3 March 2020

author name string

Brigitte Schlegelberger

1

1 reference

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3 March 2020

Hans Kreipe

2

1 reference

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3 March 2020

Ulrich Lehmann

3

1 reference

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3 March 2020

Doris Steinemann

4

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3 March 2020

Tim Ripperger

5

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3 March 2020

Kathrin Thomay

7

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3 March 2020

publication date

18 March 2015

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3 March 2020

published in

Pediatric Blood & Cancer

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3 March 2020

volume

62

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3 March 2020

issue

8

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3 March 2020

page(s)

1481-1484

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Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

3 March 2020

cites work

1 reference

Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome

21 January 2018

1 reference

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

21 January 2018

1 reference

Cancer. p53, guardian of the genome

21 January 2018

1 reference

Mutant p53 in cancer: new functions and therapeutic opportunities

21 January 2018

1 reference

TP53 mutations in myelodysplastic syndrome are strongly correlated with aberrations of chromosome 5, and correlate with adverse prognosis.

21 January 2018

1 reference

Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations

21 January 2018

1 reference

Prediction of pathogenic mutations in patients with early-onset breast cancer by family history

21 January 2018

1 reference

Gain of function of mutant p53 by coaggregation with multiple tumor suppressors

21 January 2018

1 reference

TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PBC.25486

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25787918%20AND%20SRC:MED&resulttype=core&format=json

3 March 2020

1 reference