Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases
dc.citation.epage | 8 | en_US |
dc.citation.issueNumber | 4 | en_US |
dc.citation.spage | 1 | en_US |
dc.citation.volumeNumber | 11 | en_US |
dc.contributor.author | Chabchoub, G. | en_US |
dc.contributor.author | Uz, E. | en_US |
dc.contributor.author | Maalej, A. | en_US |
dc.contributor.author | Mustafa, C. A. | en_US |
dc.contributor.author | Rebai, A. | en_US |
dc.contributor.author | Mnif, M. | en_US |
dc.contributor.author | Bahloul, Z. | en_US |
dc.contributor.author | Farid, N. R. | en_US |
dc.contributor.author | Ozcelik, T. | en_US |
dc.contributor.author | Ayadi, H. | en_US |
dc.date.accessioned | 2016-02-08T10:03:34Z | |
dc.date.available | 2016-02-08T10:03:34Z | |
dc.date.issued | 2009 | en_US |
dc.department | Department of Molecular Biology and Genetics | en_US |
dc.department | Nanotechnology Research Center (NANOTAM) | en_US |
dc.description.abstract | Introduction The majority of autoimmune diseases such as rheumatoid arthritis (RA) and autoimmune thyroid diseases (AITDs) are characterized by a striking female predominance superimposed on a predisposing genetic background. The role of extremely skewed X-chromosome inactivation (XCI) has been questioned in the pathogenesis of several autoimmune diseases. | en_US |
dc.description.provenance | Made available in DSpace on 2016-02-08T10:03:34Z (GMT). No. of bitstreams: 1 bilkent-research-paper.pdf: 70227 bytes, checksum: 26e812c6f5156f83f0e77b261a471b5a (MD5) Previous issue date: 2009 | en |
dc.identifier.doi | 10.1186/ar2759 | en_US |
dc.identifier.issn | 1478-6362 | |
dc.identifier.uri | http://hdl.handle.net/11693/22696 | |
dc.language.iso | English | en_US |
dc.publisher | BioMed Central | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1186/ar2759 | en_US |
dc.source.title | Arthritis Research and Therapy | en_US |
dc.subject | Androgen receptor | en_US |
dc.subject | Cyclic citrullinated peptide antibody | en_US |
dc.subject | Hydroxychloroquine | en_US |
dc.subject | Methotrexate | en_US |
dc.subject | Penicillamine | en_US |
dc.subject | Rheumatoid factor | en_US |
dc.subject | Autoantibody | en_US |
dc.subject | Allele | en_US |
dc.subject | Autoimmune thyroiditis | en_US |
dc.subject | Chromosome analysis | en_US |
dc.subject | Controlled study | en_US |
dc.subject | Female | en_US |
dc.subject | Genetic association | en_US |
dc.subject | Genetic predisposition | en_US |
dc.subject | Human | en_US |
dc.subject | Immunosuppressive treatment | en_US |
dc.subject | Major clinical study | en_US |
dc.subject | Phenotype | en_US |
dc.subject | Polymerase chain reaction | en_US |
dc.subject | X chromosome inactivation | en_US |
dc.subject | Autoimmune disease | en_US |
dc.subject | Blood | en_US |
dc.subject | Enzyme linked immunosorbent assay | en_US |
dc.subject | Genetics | en_US |
dc.subject | Middle aged | en_US |
dc.subject | Rheumatoid arthritis | en_US |
dc.subject | Thyroid disease | en_US |
dc.subject | X chromosome | en_US |
dc.subject | Adult | en_US |
dc.subject | Arthritis, Rheumatoid | en_US |
dc.subject | Autoantibodies | en_US |
dc.subject | Autoimmune Diseases | en_US |
dc.subject | Chromosomes, Human, X | en_US |
dc.subject | Enzyme-Linked Immunosorbent Assay | en_US |
dc.subject | Fluorescent Antibody Technique | en_US |
dc.subject | Genetic Predisposition to Disease | en_US |
dc.subject | Humans | en_US |
dc.subject | Polymerase Chain Reaction | en_US |
dc.subject | Thyroid Diseases | en_US |
dc.subject | Tunisia | en_US |
dc.title | Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases | en_US |
dc.type | Article | en_US |
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