Defining the relationship between cathepsin B and esophageal adenocarcinoma: conjoint analysis of Mendelian randomization, transcriptome-wide association studies, and single-cell RNA sequencing data [PDF]
Background: Esophageal cancer poses a significant global health challenge, with the incidence of esophageal adenocarcinoma (EAC), a predominant subtype, increasing notably in Western countries. Cathepsins, a family of lysosomal proteolytic enzymes, have been implicated in the progression of various tumors.
arxiv
On Group bijections $φ$ with $φ(B)=A$ and $\forall a\in B, aφ(a) \notin A$ [PDF]
A {\em Wakeford pairing} from $S$ onto $T$ is a bijection $\phi : S \to T$ such that $x\phi(x)\notin T,$ for every $x\in S.$ The number of such pairings will be denoted by $\mu(S,T)$. Let $A$ and $ B$ be finite subsets of a group $G$ with $1\notin B$ and $|A|=|B|.$ Also assume that the order of every element of $B$ is $\ge |B|$. Extending results due
arxiv
Some examples of two-dimensional regular rings [PDF]
Let B be a ring and $A=B[X,Y]/(aX^2+bXY+cY^2-1)$ where $a,b,c\in B$. We study the smoothness of A over B, and the regularity of B when B is a ring of algebraic integers.
arxiv
A probable mechanism of inactivation by urea of goat spleen cathepsin B. Unfolding and refolding studies [PDF]
Sudhir K. Agarwal, M Y Khan
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Cathepsin B regulates the appearance and severity of mercury-induced inflammation and autoimmunity.
Susceptibility and resistance to systemic autoimmunity are genetically regulated. This is particularly true for murine mercury-induced autoimmunity (mHgIA) where DBA/2J mice are considered resistant to disease including polyclonal B cell activation ...
C. Toomey+4 more
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On Well-behaved Unbounded Representations of *-Algebras [PDF]
A general approach to the well-behaved unbounded *-representations of a *-algebra X is proposed. Let B be a normed *-algebra equipped with a left action |> of X on B such that (x |> a)^+ b=a^+(x^+ |> b) for a,b\in B and x\in X. Then the pair (X,B) is called a compatible pair.
arxiv
A comparison of four cathepsins (B, L, N and S) with collagenolytic activity from rabbit spleen [PDF]
Rose A. Maciewicz, David J. Etherington
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Sharp two parameter bounds for logarithmic and arithmetic-geometric means [PDF]
For fixed $s\geq 1$ and $t_{1},t_{2}\in(0,1/2)$ we prove that the inequalities $G^{s}(t_{1}a+(1-t_{1})b,t_{1}b+(1-t_{1})a)A^{1-s}(a,b)>AG(a,b)$ and $G^{s}(t_{2}a+(1-t_{2})b,t_{2}b+(1-t_{2})a)A^{1-s}(a,b)>L(a,b)$ hold for all $a,b>0$ with $a\neq b$ if and only if $t_{1}\geq 1/2-\sqrt{2s}/(4s)$ and $t_{2}\geq 1/2-\sqrt{6s}/(6s)$. Here $G(a,b)$, $L(a,b)$,
arxiv
Effect of proteinase inhibitors on intracellular processing of cathepsin B, H and L in rat macrophages [PDF]
Kenji Hara+2 more
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