Autoimmune polyendocrinopathy syndrome type 1 (APS1) results from homozygous Aire mutations that cripple thymic deletion of organ-specific T cells. The clinical course in man and mouse is characterized by high variability both in the latent period befor
The mechanism underlying the generation of T and B autoreactive clones in autoimmune diseases is sti...
Loss of function mutations in the autoimmune regulator (Aire) gene in autoimmune polyendocrinopathy-...
Mutations in the autoimmune regulator (AIRE) gene lead to autoimmune polyendocrinopathy syndrome typ...
Autoimmune polyendocrinopathy syndrome type 1 (APS1) results from homozygous Aire mutations that cri...
Autoimmune polyendocrine syndrome type 1 (APS-1) is a rare but severe monogenetic autoimmune endocri...
Autoimmune polyendocrine syndrome type 1 (APS-1) is a rare but severe monogenetic autoimmune endocri...
The T and B lymphocytes of the adaptive immune system face the challenge of correctly recognizing an...
Inactivation of the autoimmune regulator (Aire) gene causes a rare recessive disorder, autoimmune po...
Inactivation of the autoimmune regulator (Aire) gene causes a rare recessive disorder, autoimmune po...
Multiple immune tolerance checkpoints ensure that T cells carrying self-reactive T cell receptors (T...
Autoimmune polyendocrinopathy syndrome type I is a recessive Mendelian disorder resulting from mutat...
Autoimmune diseases such as diabetes mellitus and multiple sclerosis are increasing today, but the m...
The maintenance of immune tolerance is an essential process to prevent autoimmunity. A critical prot...
Mutations in the autoimmune regulator (AIRE) gene lead to autoimmune polyendocrinopathy syndrome typ...
Next generation sequencing of T and B cell receptors is emerging as a valuable and effective method ...
The mechanism underlying the generation of T and B autoreactive clones in autoimmune diseases is sti...
Loss of function mutations in the autoimmune regulator (Aire) gene in autoimmune polyendocrinopathy-...
Mutations in the autoimmune regulator (AIRE) gene lead to autoimmune polyendocrinopathy syndrome typ...
Autoimmune polyendocrinopathy syndrome type 1 (APS1) results from homozygous Aire mutations that cri...
Autoimmune polyendocrine syndrome type 1 (APS-1) is a rare but severe monogenetic autoimmune endocri...
Autoimmune polyendocrine syndrome type 1 (APS-1) is a rare but severe monogenetic autoimmune endocri...
The T and B lymphocytes of the adaptive immune system face the challenge of correctly recognizing an...
Inactivation of the autoimmune regulator (Aire) gene causes a rare recessive disorder, autoimmune po...
Inactivation of the autoimmune regulator (Aire) gene causes a rare recessive disorder, autoimmune po...
Multiple immune tolerance checkpoints ensure that T cells carrying self-reactive T cell receptors (T...
Autoimmune polyendocrinopathy syndrome type I is a recessive Mendelian disorder resulting from mutat...
Autoimmune diseases such as diabetes mellitus and multiple sclerosis are increasing today, but the m...
The maintenance of immune tolerance is an essential process to prevent autoimmunity. A critical prot...
Mutations in the autoimmune regulator (AIRE) gene lead to autoimmune polyendocrinopathy syndrome typ...
Next generation sequencing of T and B cell receptors is emerging as a valuable and effective method ...
The mechanism underlying the generation of T and B autoreactive clones in autoimmune diseases is sti...
Loss of function mutations in the autoimmune regulator (Aire) gene in autoimmune polyendocrinopathy-...
Mutations in the autoimmune regulator (AIRE) gene lead to autoimmune polyendocrinopathy syndrome typ...