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English
Overview of RB gene mutations in patients with retinoblastoma. Implications for clinical genetic screening
scientific article published on 01 August 1998
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9709755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9709755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 December 2019
meta-analysis
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title
Overview of RB gene mutations in patients with retinoblastoma. Implications for clinical genetic screening
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9709755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9709755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 December 2019
author name string
Harbour JW
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9709755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9709755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 December 2019
publication date
1 August 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9709755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9709755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 December 2019
published in
Ophthalmology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9709755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9709755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 December 2019
volume
105
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9709755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9709755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 December 2019
issue
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9709755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9709755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 December 2019
page(s)
1442-1447
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9709755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9709755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 December 2019
cites work
Mortality from second tumors among long-term survivors of retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
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7 January 2021
based on heuristic
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The electroencephalogram (EEG) as a research tool in human behavior genetics: psychological examinations in healthy males with various inherited EEG variants. I. Rationale of the study. Material. Methods. Heritability of test parameters
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Unilateral retinoblastoma: new intraocular tumours after treatment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Predicting the risk of hereditary retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency of 13q abnormalities among 203 patients with retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The polymerase chain reaction (PCR) in the routine genetic characterization of retinoblastoma: a tool for the clinical laboratory
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regions of the retinoblastoma gene product required for its interaction with the E2F transcription factor are necessary for E2 promoter repression and pRb-mediated growth suppression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A single amino acid substitution results in a retinoblastoma protein defective in phosphorylation and oncoprotein binding
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the retinoblastoma gene and their expression in somatic and tumor cells of patients with hereditary retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spectrum of small length germline mutations in the RB1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mechanisms of oncogenesis in patients with familial retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline mutations in the RB1 gene in patients with hereditary retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rapid detection of BRCA1 mutations by the protein truncation test
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a growth suppression domain within the retinoblastoma gene product
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Integration of cell cycle control with transcriptional regulation by the retinoblastoma protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aberrations of p16Ink4 and retinoblastoma tumour-suppressor genes occur in distinct sub-sets of human cancer cell lines
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0161-6420%2898%2998025-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0161-6420(98)98025-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9709755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9709755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 December 2019
PubMed publication ID
9709755
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9709755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9709755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 December 2019
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