X chromosome inactivation and female predisposition to autoimmunity (Q37039682)

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scientific article published on June 2008

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English	X chromosome inactivation and female predisposition to autoimmunity	scientific article published on June 2008

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18097773

retrieved

17 August 2017

review article

1 reference

stated in

Europe PubMed Central

title

X chromosome inactivation and female predisposition to autoimmunity (English)

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stated in

Europe PubMed Central

PubMed publication ID

18097773

retrieved

17 August 2017

author name string

Tayfun Ozcelik

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18097773

retrieved

17 August 2017

publication date

1 June 2008

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18097773

retrieved

17 August 2017

published in

Clinical Reviews in Allergy & Immunology

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stated in

Europe PubMed Central

PubMed publication ID

18097773

retrieved

17 August 2017

volume

34

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18097773

retrieved

17 August 2017

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18097773

retrieved

17 August 2017

page(s)

348-351

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Europe PubMed Central

PubMed publication ID

18097773

retrieved

17 August 2017

cites work

X chromosome monosomy: a common mechanism for autoimmune diseases.

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS12016-007-8051-0

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21 January 2018

Association between familial autoimmune diseases and recurrent spontaneous abortions

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Crossref

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https://api.crossref.org/works/10.1007%2FS12016-007-8051-0

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21 January 2018

X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autoimmune response directed against conserved determinants of nuclear envelope proteins in a patient with linear scleroderma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uncovering the complex mysteries of mosaicism

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localized scleroderma is an autoimmune disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localized forms of scleroderma, including morphea, linear scleroderma, and eosinophilic fasciitis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Turner's syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The X chromosome and systemic sclerosis

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaicism in human skin. Understanding the patterns and mechanisms

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The lines of Blaschko: a review and reconsideration: Observations of the cause of certain unusual linear conditions of the skin

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extremely skewed X-chromosome inactivation is increased in pre-eclampsia

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene profiling of scleroderma skin reveals robust signatures of disease that are imperfectly reflected in the transcript profiles of explanted fibroblasts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High Frequency of Skewed X-Chromosome Inactivation in Females with Autoimmune Thyroid Disease: A Possible Explanation for the Female Predisposition to Thyroid Autoimmunity

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary biliary cirrhosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genes and translocations involved in POF.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of X inactivation and cellular mosaicism in women's health and sex-specific diseases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex differences in autoimmune disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lyonization and the lines of Blaschko

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic significance of skewed X-chromosome inactivation in premature ovarian failure

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frontoparietal scleroderma (en coup de sabre) following Blaschko's lines

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cancer/testis genes: review, standardization, and commentary.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X chromosome-inactivation patterns of 1,005 phenotypically unaffected females

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Signatures of differentially regulated interferon gene expression and vasculotrophism in the peripheral blood cells of systemic sclerosis patients

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The DNA sequence of the human X chromosome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The female X-inactivation mosaic in systemic lupus erythematosus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosome inactivation: role in skin disease expression

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of X-chromosome inactivation in female predisposition to autoimmunity

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predominance of autoimmune and rheumatic diseases in females

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skewed X chromosome inactivation in blood cells of women with scleroderma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18097773

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S12016-007-8051-0

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18097773

retrieved

17 August 2017

PubMed publication ID

18097773

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18097773

retrieved

17 August 2017

 

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