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English
Germline mutation screening of the STK11/LKB1 gene in familial breast cancer with LOH on 19p
scientific article published on 01 May 2000
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
title
Germline mutation screening of the STK11/LKB1 gene in familial breast cancer with LOH on 19p
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
author
Annika Lindblom
series ordinal
2
object named as
A Lindblom
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
author name string
J Chen
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
publication date
1 May 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
volume
57
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
page(s)
394-397
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
cites work
Tumor suppressor genes and breast cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genotyping shows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exclusion of a major role for the PTEN tumour-suppressor gene in breast carcinomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peutz-Jeghers syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peutz-Jeghers syndrome: clinical and roentgenographic features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Screening for TP53 mutations in patients and tumours from 109 Swedish breast cancer families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
BRCA2 germline mutations in Swedish breast cancer families.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MSH2 genomic deletions are a frequent cause of HNPCC
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Somatic mutations in the Peutz-Jeghers (LKB1/STKII) gene in sporadic malignant melanomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LKB1 somatic mutations in sporadic tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.570511.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1034/J.1399-0004.2000.570511.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
PubMed publication ID
10852375
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10852375
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10852375%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
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