Title of article :
A novel mutation in FOXN1 resulting in SCID: A case report and literature review
Author/Authors :
Chou، نويسنده , , Janet and Massaad، نويسنده , , Michel J. and Wakim، نويسنده , , Rima Hanna and Bainter، نويسنده , , Wayne and Dbaibo، نويسنده , , Ghassan and Geha، نويسنده , , Raif S.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2014
Pages :
3
From page :
30
To page :
32
Abstract :
The current treatments of systemic lupus erythematosus (SLE) have been based on the use of immunosuppressive drugs which are linked to serious side effects. The more effective therapeutic approaches with minimal or no side effects for SLE patients are hard to develop, mainly due to the complexity of the disease. The discovery of pharmacoepigenetics provides a new way to solve this problem. Epigenetic modifications can influence drug efficacy by altering gene expression via changing chromatin structure. Although still in early development, epigenetic studies in SLE are expected to reveal novel therapeutic targets and disease biomarkers in autoimmunity. For example, miRNAs, which have been identified to govern many genes including drug targets, are altered in disease development and after drug administration. This review aims to present an overview of current epigenetic mechanisms involved in the pathogenesis of SLE, and discuss their potential roles in clinical and pharmacological applications.
Keywords :
Foxn1 , whole exome sequencing , Severe combined immunodeficiency
Journal title :
Clinical Immunology
Serial Year :
2014
Journal title :
Clinical Immunology
Record number :
1857062
Link To Document :
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