‎let us consider the set of non-abelian finite simple groups which‎ ‎admit non-trivial irreducible projective representations of degree $le 7$ over‎ ‎an algebraically closed field $f$ of characteristic $pgeq 0$‎. ‎we survey some recent results which‎ ‎lead to the complete list of the groups in this set which are‎ ‎$(2‎, ‎3‎, ‎7)$-generated and of those which are $(2,3)$-generated‎.

‎let us consider the set of non-abelian finite simple groups which‎ ‎admit non-trivial irreducible projective representations of degree $le 7$ over‎ ‎an algebraically closed field $mathbb{f}$ of characteristic $pgeq 0$‎. ‎we survey some recent results which‎ ‎lead to the complete list of the groups in this set which are‎ ‎$(2,3,7)$-generated and of those which are $(2,3)$-generated‎.

Experimental evidence suggests that the hippocampal theta rhythm plays a critical role in learning. Previous studies have shown long-term potentiation (LTP) to be preferentially induced with stimulation on the peak of local theta rhythm in region CA1 in anesthetized rats and with stimulation of the perforant path at the peak of theta in both anesthetized and behaving animals. We set out to dete...

The alpha-like globin gene cluster in rabbits contains embryonic zeta-globin genes, an adult alpha-globin gene, and theta-globin genes of undetermined function. The basic arrangement of genes, deduced from analysis of cloned DNA fragments, is 5'-zeta 0-zeta 1-alpha 1-theta 1-zeta 2-zeta 3-theta 2-3'. However, the pattern of restriction fragments containing zeta- and theta-globin genes varies am...

Accumulating evidence suggests that top-down processes, reflected by frontal-midline theta-band (4-8 Hz) electroencephalogram (EEG) oscillations, strengthen the activation of a memory set during short-term memory (STM) retention. In addition, the amplitude of posterior alpha-band (8-13 Hz) oscillations during STM retention is thought to reflect a mechanism that protects fragile STM activations ...

For two normed algebras $A$ and $B$ with the character space   $bigtriangleup(B)neq emptyset$  and a left $B-$module $X,$  a certain class of bounded linear maps from $A$ into $X$ is introduced. We set $CMH_B(A, X)$  as the set of all non-zero $B-$character module homomorphisms from $A$ into $X$. In the case where $bigtriangleup(B)=lbrace varphirbrace$ then $CMH_B(A, X)bigcup lbrace 0rbrace$ is...

OBJECTIVE We compared EEG coherence in children with and without AD/HD, and sought to relate observed anomalies to AD/HD symptoms. METHODS Forty children with AD/HD and 40 age- and sex-matched controls had eyes-closed resting EEG coherence calculated for eight interhemispheric electrode pairs and eight intrahemispheric pairs (four within each hemisphere) in the delta, theta, alpha, beta and "...