(Q34206865)

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Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

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1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

2

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H Y Zoghbi

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

R C Allen

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

A B Moseley

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

H M Rosenblatt

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

J W Belmont

5

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

language of work or name

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publication date

1 December 1992

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

51

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1229-1239

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Agammaglobulinemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Mammalian X-chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Differential methylation of hypoxanthine phosphoribosyltransferase genes on active and inactive human X chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

The Primary Immunodeficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

X-chromosome inactivation and developmental patterns in mammals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Mechanisms of X-chromosome regulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Use of restriction fragment length polymorphisms to determine the clonal origin of human tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Characterization and expression of a cDNA encoding the human androgen receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Clonal analysis of human colorectal tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Demethylation of specific sites in the 5' region of the inactive X-linked human phosphoglycerate kinase gene correlates with the appearance of nuclease sensitivity and gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Differential methylation of the hypervariable locus DXS255 on active and inactive X chromosomes correlates with the expression of a human X-linked gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Localization of the X inactivation centre on the human X chromosome in Xq13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Clonality in myeloproliferative disorders: analysis by means of the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

A quantitative Hpall-PCR assay to measure methylation of DNA from a small number of cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682906

5 July 2018

Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/1281384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status

1 reference

https://pubmed.ncbi.nlm.nih.gov/1281384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of Staphylococcus aureus exotoxin A inhibition of Ig production by human B cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1281384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/1281384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clonal analysis using recombinant DNA probes from the X-chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1281384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1281384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1281384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection in typical and atypical X-linked agammaglobulinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1281384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of the gene defect in X-linked agammaglobulinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1281384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphism at the DXS178 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/1281384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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