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X-linked tumor suppressors: perplexing inheritance, a unique therapeutic opportunity.
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2901104
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1 February 2020
title
X-linked tumor suppressors: perplexing inheritance, a unique therapeutic opportunity
(English)
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2901104
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1 February 2020
author
Yang Liu
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1
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2901104
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1 February 2020
Pan Zheng
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3
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2901104
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1 February 2020
author name string
Lizhong Wang
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2
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1 February 2020
publication date
29 April 2010
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1 February 2020
published in
Trends in Genetics
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2901104
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1 February 2020
volume
26
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Europe PubMed Central
PMC publication ID
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20434787%20AND%20SRC:MED&resulttype=core&format=json
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1 February 2020
issue
6
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2901104
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1 February 2020
page(s)
260-265
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1 February 2020
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An X chromosome gene, WTX, is commonly inactivated in Wilms tumor
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X chromosomal abnormalities in basal-like human breast cancer
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Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse
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The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
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X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
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5 July 2018
JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome
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Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP)
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5 July 2018
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
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5 July 2018
Evidence of an X-linked or recessive genetic component to prostate cancer risk
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5 July 2018
Mutation and cancer: statistical study of retinoblastoma
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5 July 2018
Familial testicular cancer: a report of the UK family register, estimation of risk and an HLA class 1 sib-pair analysis
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5 July 2018
Documentation of Burkitt lymphoma with t(8;14) (q24;q32) in X-linked lymphoproliferative disease
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5 July 2018
Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21.
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5 July 2018
WTX inactivation is a frequent, but late event in Wilms tumors without apparent clinical impact
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
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29 October 2018
FOXP3 expression and overall survival in breast cancer.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
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29 October 2018
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
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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
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
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29 October 2018
An investigation of the familial aspects of carcinoma of the prostate
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
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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
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901104
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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
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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
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