‎the narumi-katayama index was the first topological index defined‎ ‎by the product of some graph theoretical quantities‎. ‎let $g$ be a ‎simple graph with vertex set $v = {v_1,ldots‎, ‎v_n }$ and $d(v)$ be‎ ‎the degree of vertex $v$ in the graph $g$‎. ‎the narumi-katayama ‎index is defined as $nk(g) = prod_{vin v}d(v)$‎. ‎in this paper,‎ ‎the narumi-katayama index is generalized using a $n$-ve...

a m i t r a z, a n i ns e c t i c i d e /a ca ri c i de of the f o r m a m i d i n e p e st i c i d e s group, is a ? 2 a d r e n e r g i c ag on i st a nd of t he a m i d i ne c h e m i ca l f a m il y generally us e d to c o n t r ol animal e c top a r a s i t e s. poisoning due to am i t r a z i s r a r e and characterized by c e nt r a l n e r v ous s y st e m a nd r e sp ir a to r y d e p ...

During B and T cell development, the RAG1/RAG2 protein complex cleaves DNA at conserved recombination signal sequences (RSS) to initiate V(D)J recombination. RAG1/2 has also been shown to catalyze transpositional strand transfer of RSS-containing substrates into target DNA to form branched DNA intermediates. We show that RAG1/2 can resolve these intermediates by two pathways. RAG1/2 catalyzes h...

The RAG-1 protein plays an essential role in V(D)j recombination, but its exact function has not yet been defined. Here we report that a particular mutation in RAG-1 affects recombination by altering the specificity of target sequence usage. Recombination mediated by wild-type RAG-1 is tolerant of a wide range of coding sequences adjacent to the recombination signal. With the mutant RAG-1, reco...

let g = (v, e) be a simple graph. hosoya polynomial of g isd(u,v)h(g, x) = {u,v}v(g)x , where, d(u ,v) denotes the distance between vertices uand v. as is the case with other graph polynomials, such as chromatic, independence anddomination polynomial, it is natural to study the roots of hosoya polynomial of a graph. inthis paper we study the roots of hosoya polynomials of some specific graphs.

Formation of double-strand breaks at recombination signal sequences is an early step in V(D)J recombination. Here we show that purified RAG1 and RAG2 proteins are sufficient to carry out this reaction. The cleavage reaction can be divided into two distinct steps. First, a nick is introduced at the 5' end of the signal sequence. The other strand is then broken, resulting in a hairpin structure a...

A m i t r a z, a n i ns e c t i c i d e /a ca ri c i de of the f o r m a m i d i n e p e st i c i d e s group, is a ? 2 a d r e n e r g i c ag on i st a nd of t he a m i d i ne c h e m i ca l f a m il y generally us e d to c o n t r ol animal e c top a r a s i t e s. Poisoning due to am i t r a z i s r a r e and character...

Let $D$ be a diameter and $d_G(v_i, v_j)$ be the distance between the vertices $v_i$ and $v_j$ of a connected graph $G$. The complementary distance signless Laplacian matrix of a graph $G$ is $CDL^+(G)=[c_{ij}]$ in which $c_{ij}=1+D-d_G(v_i, v_j)$ if $ineq j$ and $c_{ii}=sum_{j=1}^{n}(1+D-d_G(v_i, v_j))$. The complementary transmission $CT_G(v)$ of a vertex $v$ is defined as $CT_G(v)=sum_{u in ...