B10.Q mice are normally susceptible to the induction of collagen-induced arthritis. We noted that one subline of B10.Q mice, B10.Q/J, was completely resistant to disease induction when immunized with collagen in CFA. B10.Q/J mice have a global defect in the generation of Th1 responses, and Ag-specific T cells derived from this strain failed to produce IFN-gamma. Because T cells from these mice ...

We evaluated the role of gamma interferon (IFN-gamma) in protecting neurons from virus-induced injury following central nervous system infection. IFN-gamma(-/-) and IFN-gamma(+/+) mice of the resistant major histocompatibility complex (MHC) H-2(b) haplotype and intracerebrally infected with Theiler's murine encephalomyelitis virus (TMEV) cleared virus infection from anterior horn cell neurons. ...

In this paper, we study the existence and non-existence of normalized solutions to lower critical Choquard equation with a local perturbation $ \begin{equation*} \begin{cases} -\Delta u+\lambda u = \gamma (I_{\alpha}\ast|u|^{\frac{N+\alpha}{N}})|u|^{\frac{N+\alpha}{N}-2}u+\mu |u|^{q-2}u, \quad {\rm{in}}\ \mathbb{R}^N, \\ \int_{\mathbb{R}^N}|u|^2dx c^2, \end{cases} \end{equation*} where \gamma, ...

Given an integer $q\ge 2$ and a real number $c\in [0,1)$, consider the generalized Thue-Morse sequence $(t_n^{(q;c)})_{n\ge 0}$ defined by $t_n^{(q;c)} = e^{2\pi i c S_q(n)}$, where $S_q(n)$ is sum of digits $q$-expansion $n$. We prove that $L^\infty$-norm trigonometric polynomials $\sigma_{N}^{(q;c)} (x) := \sum_{n=0}^{N-1} t_n^{(q;c)} n x}$, behaves like $N^{\gamma(q;c)}$, $\gamma(q;c)$ equal...

Fc gamma RIIa is widely expressed on hematopoietic cells. There are two known allelic polymorphic forms of Fc gamma RIIa, Fc gamma RIIa-R131 and Fc gamma RIIa-H131, which differ in the amino acid at position 131 in the second lg-like domain. In contrast to Fc gamma RIIa-R131, Fc gamma RIIa-H131 binds hlgG2 but not mIgG1, and this differential binding has clinical implications for host defense, ...

The inactivation of charge movement components by small (-100 to -70 mV) shifts in holding potential was examined in voltage-clamped intact amphibian muscle fibers in low [Ca2+], Mg(2+)-containing solutions. The pulse protocols used both large voltage excursions and smaller potential steps that elicited prolonged (q gamma) transients. Charge species were distinguished through the pharmacologica...

We study the $L^{2}$-boundedness of $3$-dimensional (Heisenberg) Riesz transform on intrinsic Lipschitz graphs in first Heisenberg group $\mathbb{H}$. Inspired by notion vertical perimeter, recently defined and studied Lafforgue, Naor, Young, we introduce new scale translation invariant coefficients $\operatorname{osc}_{\Omega}(B(q,r))$. These quantify oscillation a domain $\Omega \subset \math...