Behcet's disease (ED) is a chronic multisystemic inflammatory disorder characterized mainly by recurrent oral and genital aphthous ulcerations and uveitis. Etiology and pathogenesis of ED remain unknown. T cell receptor (TCR) V alpha/N beta gene product expression as well as J beta gene segment expression in peripheral blood of BD patients were analysed to investigate the possible role of T lymphocytes in the etiopathogenesis of BD. Flow cytometry with 12 TCR V-specific MoAbs was used for TCRV analyses. J beta gene segment usage by T cell populations expressing certain V beta s was determined by polymerase chain reaction (PCR) technique with V beta- and C beta-specific primers, Southern blotting of PCR products, and subsequent hybridization...
Background: Behcet's disease (BD), first described in 1937 as a triadic complex of symptoms (oral ap...
Th1/Th17-type T-cell responses are upregulated in Behcet’s disease (BD). However, signaling pathways...
Wegener's granulomatosis (WG) and polyarteritis nodosa (PAN) are systemic necrotizing vasculitides o...
Behcet's disease (BD) is a chronic multisystemic inflammatory disorder characterized mainly by recur...
Behcet's disease (BD) is a multisystem disorder with oral and genital ulcers, mucocutaneous, ocular,...
Behçet's disease (BD) is a multisystem disorder with oral and genital ulcers, mucocutaneous, ocular,...
T Iymphocytes use the T cell receptor (TCR) to specifically recognize antigens. According to the typ...
T lymphocytes use the T cell receptor (TCR) to specifically recognize antigens. According to the typ...
PURPOSE: To investigate the frequency and phenotypic and functional characteristics of S-antigen (S-...
Objective. Increased numbers of spontaneous Ig secreting B cells and elevated immunoglobulin levels ...
The association of the cytokine gene polymorphisms with the development of Behcet's Disease (BD) was...
Behçet disease (BD) is a chronic inflammatory multisystem disease characterized by oral and genital ...
Background: Behcets disease represents a polysymptomatic, recurrent vasculitis' with a chronic cours...
Behcet's disease (BD) is an immuno-mediated vasculitis in which knowledge of its etiology and geneti...
Behcet’s disease (BD) is characterized by recurrent attacks of uveitis, oral aphtha, genital ulcers ...
Background: Behcet's disease (BD), first described in 1937 as a triadic complex of symptoms (oral ap...
Th1/Th17-type T-cell responses are upregulated in Behcet’s disease (BD). However, signaling pathways...
Wegener's granulomatosis (WG) and polyarteritis nodosa (PAN) are systemic necrotizing vasculitides o...
Behcet's disease (BD) is a chronic multisystemic inflammatory disorder characterized mainly by recur...
Behcet's disease (BD) is a multisystem disorder with oral and genital ulcers, mucocutaneous, ocular,...
Behçet's disease (BD) is a multisystem disorder with oral and genital ulcers, mucocutaneous, ocular,...
T Iymphocytes use the T cell receptor (TCR) to specifically recognize antigens. According to the typ...
T lymphocytes use the T cell receptor (TCR) to specifically recognize antigens. According to the typ...
PURPOSE: To investigate the frequency and phenotypic and functional characteristics of S-antigen (S-...
Objective. Increased numbers of spontaneous Ig secreting B cells and elevated immunoglobulin levels ...
The association of the cytokine gene polymorphisms with the development of Behcet's Disease (BD) was...
Behçet disease (BD) is a chronic inflammatory multisystem disease characterized by oral and genital ...
Background: Behcets disease represents a polysymptomatic, recurrent vasculitis' with a chronic cours...
Behcet's disease (BD) is an immuno-mediated vasculitis in which knowledge of its etiology and geneti...
Behcet’s disease (BD) is characterized by recurrent attacks of uveitis, oral aphtha, genital ulcers ...
Background: Behcet's disease (BD), first described in 1937 as a triadic complex of symptoms (oral ap...
Th1/Th17-type T-cell responses are upregulated in Behcet’s disease (BD). However, signaling pathways...
Wegener's granulomatosis (WG) and polyarteritis nodosa (PAN) are systemic necrotizing vasculitides o...