Last Posted: Feb 29, 2016
- High sodium chloride consumption enhances the effects of smoking but does not interact with SGK1 polymorphisms in the development of ACPA-positive status in patients with RA.
Jiang Xia, et al. Annals of the rheumatic diseases 2016 2
- Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS.
Schrewe L, et al. Journal of neuroinflammation 2015 0 (1) 234
- New candidates for CD4 T cell pathogenicity in experimental neuroinflammation and multiple sclerosis.
Hoppmann Nicola, et al. Brain : a journal of neurology 2015 4 (Pt 4) 902-17
- RGMA and IL21R show association with experimental inflammation and multiple sclerosis.
Nohra R, et al. Genes and immunity 2010 6 (4) 279-93
- Genetic variants of CC chemokine genes in experimental autoimmune encephalomyelitis, multiple sclerosis and rheumatoid arthritis.
Ockinger J, et al. Genes and immunity 2010 3 (2) 142-54
- ABC-transporter gene-polymorphisms are potential pharmacogenetic markers for mitoxantrone response in multiple sclerosis.
Cotte S, et al. Brain : a journal of neurology 2009 9 (Pt 9) 2517-30
- Multiple sclerosis and polymorphisms of innate pattern recognition receptors TLR1-10, NOD1-2, DDX58, and IFIH1.
Enevold Christian, et al. Journal of neuroimmunology 2009 7 (1-2) 125-31
- Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.
Caillier Stacy J, et al. Journal of immunology (Baltimore, Md. : 1950) 2008 10 (8) 5473-80
- CD24 is a genetic modifier for risk and progression of multiple sclerosis.
Zhou Qunmin, et al. Proceedings of the National Academy of Sciences of the United States of America 2003 12 (25) 15041-6
- Osteopontin gene and clinical severity of multiple sclerosis.
Hensiek A E, et al. Journal of neurology 2003 8 (8) 943-7
- Genetic variation in the transforming growth factor beta1 gene in multiple sclerosis.
Weinshenker B G, et al. Journal of neuroimmunology 2001 11 (1-2) 138-45
- The T cell regulator gene SH2D2A contributes to the genetic susceptibility of multiple sclerosis.
Dai K Z, et al. Genes and immunity 2001 8 (5) 263-8
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Graves Disease
- Huntington Disease
- Myasthenia Gravis
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.