(Q74298014)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

title

Novel p53 splice site mutations in three families with Li-Fraumeni syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

Verselis SJ

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Rheinwald JG

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Fraumeni JF Jr

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Li FP

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

language of work or name

English

0 references

publication date

1 August 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

37

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

4230-4235

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10980596%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.onc.1203758

10 November 2019

exact match

0 references

cites work

Codon 72 polymorphism of the TP53 gene

1 reference

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7 January 2021

Exon recognition in vertebrate splicing

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7 January 2021

p53 gene mutation: software and database

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7 January 2021

Crystal structure of a p53 tumor suppressor-DNA complex: understanding tumorigenic mutations

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7 January 2021

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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7 January 2021

Cycloheximide facilitates the identification of aberrant transcripts resulting from a novel splice-site mutation in COL17A1 in a patient with generalized atrophic benign epidermolysis bullosa

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7 January 2021

Human keratinocytes that express hTERT and also bypass a p16(INK4a)-enforced mechanism that limits life span become immortal yet retain normal growth and differentiation characteristics

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7 January 2021

A simple p53 functional assay for screening cell lines, blood, and tumors

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7 January 2021

Database of p53 gene somatic mutations in human tumors and cell lines: updated compilation and future prospects

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7 January 2021

Interrelationships of the pathways of mRNA decay and translation in eukaryotic cells

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Primary structure polymorphism at amino acid residue 72 of human p53.

1 reference

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7 January 2021

Splicing of messenger RNA precursors

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7 January 2021

A database of germline p53 mutations in cancer-prone families

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7 January 2021

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

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7 January 2021

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

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7 January 2021

Genetic and functional studies of a germline TP53 splicing mutation in a Li-Fraumeni-like family

1 reference

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7 January 2021

Li-Fraumeni syndrome--a molecular and clinical review

1 reference

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7 January 2021

A novel TP53 splicing mutation in a Li-Fraumeni syndrome family: a patient with Wilms' tumour is not a mutation carrier

1 reference

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7 January 2021

Functionally null mutations in patients with the cblG-variant form of methionine synthase deficiency

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7 January 2021