Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q33980087)
Watch
English
X-linked tumor suppressors: perplexing inheritance, a unique therapeutic opportunity.
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
title
X-linked tumor suppressors: perplexing inheritance, a unique therapeutic opportunity
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
author
Yang Liu
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
Pan Zheng
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
author name string
Lizhong Wang
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
publication date
29 April 2010
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
published in
Trends in Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
volume
26
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
issue
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
page(s)
260-265
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
cites work
Somatic single hits inactivate the X-linked tumor suppressor FOXP3 in the prostate
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Causes and consequences of microRNA dysregulation in cancer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Up-regulation of Foxp3 inhibits cell proliferation, migration and invasion in epithelial ovarian cancer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Activating transcription factor 2 and c-Jun-mediated induction of FoxP3 for experimental therapy of mammary tumor in the mouse.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
FOXP3 up-regulates p21 expression by site-specific inhibition of histone deacetylase 2/histone deacetylase 4 association to the locus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Wnt signalling and its impact on development and cancer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Functional inactivation of the WTX gene is not a frequent event in Wilms' tumors
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
A haplotype at chromosome Xq27.2 confers susceptibility to prostate cancer.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Multiple newly identified loci associated with prostate cancer susceptibility
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Dosage compensation in the mouse balances up-regulation and silencing of X-linked genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
FOXP3 is a novel transcriptional repressor for the breast cancer oncogene SKP2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
FOXP3 is an X-linked breast cancer suppressor gene and an important repressor of the HER-2/ErbB2 oncogene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Wilms tumor suppressor WTX negatively regulates WNT/beta-catenin signaling
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Restoration of p53 function leads to tumour regression in vivo
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
An X chromosome gene, WTX, is commonly inactivated in Wilms tumor
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
X chromosomal abnormalities in basal-like human breast cancer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
X-inactivation profile reveals extensive variability in X-linked gene expression in females
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
X-linked inheritance of Fanconi anemia complementation group B
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
X-chromosome genetics and human cancer
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Hereditary prostate cancer in African American families: linkage analysis using markers that map to five candidate susceptibility loci
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Gene action in the X-chromosome of the mouse (Mus musculus L.)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
X-chromosome inactivation analysis in a female carrier of FOXP3 mutation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Familial testicular cancer in Norway and southern Sweden
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Evidence of an X-linked or recessive genetic component to prostate cancer risk
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Mutation and cancer: statistical study of retinoblastoma
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Familial testicular cancer: a report of the UK family register, estimation of risk and an HLA class 1 sib-pair analysis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Documentation of Burkitt lymphoma with t(8;14) (q24;q32) in X-linked lymphoproliferative disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
5 July 2018
WTX inactivation is a frequent, but late event in Wilms tumors without apparent clinical impact
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
29 October 2018
FOXP3 expression and overall survival in breast cancer.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
29 October 2018
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
29 October 2018
A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
29 October 2018
An investigation of the familial aspects of carcinoma of the prostate
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
29 October 2018
A genetic epidemiological study of hereditary prostate cancer (HPC) in Finland: frequent HPCX linkage in families with late-onset disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
29 October 2018
Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
29 October 2018
Linkage analysis of 153 prostate cancer families over a 30-cM region containing the putative susceptibility locus HPCX.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
29 October 2018
Familial bladder cancer in the National Swedish Family Cancer Database
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
29 October 2018
Evidence for a prostate cancer susceptibility locus on the X chromosome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
retrieved
29 October 2018
Confirmation of the prostate cancer susceptibility locus HPCX in a set of 104 German prostate cancer families
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20434787
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The impact of family history on early detection of prostate cancer
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20434787
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Xist-deficient mice are defective in dosage compensation but not spermatogenesis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20434787
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Evaluation of breast tumour sex chromatin (Barr body) as an index of survival and response to pituitary ablation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20434787
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.TIG.2010.03.004
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
PMC publication ID
2901104
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
PubMed publication ID
20434787
1 reference
stated in
Europe PubMed Central
PMC publication ID
2901104
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
ResearchGate publication ID
43533815
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit