Background: Autoimmune thyroid diseases (AITD), including Graves' disease and Hashimoto's thyroiditis, arise due to complex interactions between environmental and …
Y Tomer, A Huber - Journal of autoimmunity, 2009 - Elsevier
Autoimmune thyroid diseases (AITDs), including Graves' disease (GD) and Hashimoto's thyroiditis (HT) are prevalent autoimmune diseases, affecting up to 5% of the general …
K Zaletel, S Gaberscek - Current genomics, 2011 - ingentaconnect.com
Hashimoto's thyroiditis (HT) is the most prevalent autoimmune thyroid disorder. Intrathyroidal lymphocytic infiltration is followed by a gradual destruction of the thyroid gland which may …
A Huber, F Menconi, S Corathers… - Endocrine …, 2008 - academic.oup.com
Abstract Type 1 diabetes (T1D) and autoimmune thyroid diseases (AITD) frequently occur together within families and in the same individual. The co-occurrence of T1D and AITD in …
TF Davies, T Ando, RY Lin, Y Tomer… - The Journal of clinical …, 2005 - Am Soc Clin Investig
The thyroid-stimulating hormone receptor (TSHR) is a G protein–linked, 7–transmembrane domain (7-TMD) receptor that undergoes complex posttranslational processing unique to …
EM Jacobson, Y Tomer - Journal of autoimmunity, 2007 - Elsevier
Autoimmune thyroid diseases (AITD) are common autoimmune diseases, affecting up to 5% of the general population. Thyroid-directed autoimmunity is manifested in two classical …
▪ Abstract Psoriasis is an inflammatory/autoimmune disease and, as with many autoimmune diseases, is associated with alleles from the major histocompatibility complex (MHC). With …
EM Jacobson, Y Tomer - Thyroid, 2007 - liebertpub.com
Autoimmune thyroid diseases (AITDs), including Graves' disease (GD) and Hashimoto's thyroiditis (HT), are prevalent autoimmune diseases, affecting up to 5% of the general …
Y Ban, T Tozaki, T Tobe, Y Ban, EM Jacobson… - Journal of …, 2007 - Elsevier
FOXP3 is a key gene in the development of regulatory T cells (Treg). FOXP3 expression commits naïve T cells to become Treg cells. Indeed, mutations in the FOXP3 gene cause …