X chromosome inactivation and female predisposition to autoimmunity
dc.citation.epage | 351 | en_US |
dc.citation.issueNumber | 3 | en_US |
dc.citation.spage | 348 | en_US |
dc.citation.volumeNumber | 34 | en_US |
dc.contributor.author | Ozcelik, T. | en_US |
dc.date.accessioned | 2018-04-12T13:44:45Z | |
dc.date.available | 2018-04-12T13:44:45Z | |
dc.date.issued | 2008 | en_US |
dc.department | Institute of Materials Science and Nanotechnology (UNAM) | en_US |
dc.department | Department of Molecular Biology and Genetics | en_US |
dc.description.abstract | [No abstract available] | en_US |
dc.description.provenance | Made available in DSpace on 2018-04-12T13:44:45Z (GMT). No. of bitstreams: 1 bilkent-research-paper.pdf: 179475 bytes, checksum: ea0bedeb05ac9ccfb983c327e155f0c2 (MD5) Previous issue date: 2008 | en |
dc.identifier.doi | 10.1007/s12016-007-8051-0 | en_US |
dc.identifier.issn | 1559-0267 | |
dc.identifier.uri | http://hdl.handle.net/11693/38115 | |
dc.language.iso | English | en_US |
dc.publisher | Springer New York | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1007/s12016-007-8051-0 | en_US |
dc.source.title | Clinical Reviews in Allergy and Immunology | en_US |
dc.subject | Autoimmune diseases | en_US |
dc.subject | Female predisposition | en_US |
dc.subject | Mosaicism | en_US |
dc.subject | X chromosome inactivation | en_US |
dc.subject | Androgen receptor | en_US |
dc.subject | Melanoma antigen | en_US |
dc.subject | Chromosome translocation | en_US |
dc.subject | Clinical feature | en_US |
dc.subject | Disease association | en_US |
dc.subject | Disease course | en_US |
dc.subject | Disease predisposition | en_US |
dc.subject | Duchenne muscular dystrophy | en_US |
dc.subject | Fragile X syndrome | en_US |
dc.subject | Gene expression | en_US |
dc.subject | Gene locus | en_US |
dc.subject | Gene mutation | en_US |
dc.subject | Genetic linkage | en_US |
dc.subject | Genetic trait | en_US |
dc.subject | Genetic variability | en_US |
dc.subject | Hematopoietic stem cell | en_US |
dc.subject | Heterozygosity | en_US |
dc.subject | Human | en_US |
dc.subject | Immunological tolerance | en_US |
dc.subject | Review | en_US |
dc.subject | Scleroderma | en_US |
dc.subject | Wiskott Aldrich syndrome | en_US |
dc.subject | X chromosome inactivation | en_US |
dc.subject | X chromosome linked disorder | en_US |
dc.subject | X linked agammaglobulinemia | en_US |
dc.subject | X linked mental retardation | en_US |
dc.subject | Autoimmunity | en_US |
dc.subject | Female | en_US |
dc.subject | Genetic Predisposition to Disease | en_US |
dc.subject | Humans | en_US |
dc.subject | Male | en_US |
dc.subject | Mutation | en_US |
dc.subject | Scleroderma, Systemic | en_US |
dc.subject | Sex Characteristics | en_US |
dc.subject | X Chromosome Inactivation | en_US |
dc.title | X chromosome inactivation and female predisposition to autoimmunity | en_US |
dc.type | Article | en_US |
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