We classify irreducible representations of finite W-algebra for the queer Lie superalgebra Q(n) associated with principal nilpotent coadjoint orbits. use this classification and our previous results to obtain a finite-dimensional super Yangian YQ(1).

Finally the paper deals with the solution of the following problem: Let signals y1(iT), ..., yq(iT) (elements of output vector y(iT)) be responses of MIMO discretetime system to the input signals u1(iT),..,uq(iT) (elements of input vector u(iT)). Determine discrete-time excitations uA1,......,uAq (elements of vector uA) scaling the system responses to the required forms y1(iA-1T),...,yq(iA-1T),...

background: infertility is a health problem which affects about 10-20% of married couples. male factor infertility is involved approximately 50% of infertile couples. most of male infertility is regarding to deletions in the male-specific region of the y chromosome. objective: in this study, the occurrence of deletions in the azf region and association between infertility and paternal age were ...

Turner syndrome is thought to result from the haploinsufficiency of genes on the sex chromosomes, but these genes have not been identified yet. We describe two males with deleted ring Y chromosomes, one (TS) with full Turner syndrome and one (DM) without. TS has short stature, skeletal anomalies, lymphogenic obstruction, cardiovascular abnormalities, and miscellaneous features including pigment...

In numerical algebraic geometry, algebraic sets are represented by witness sets. This paper presents an algorithm, based on the regeneration technique, that solves the following problem: given a witness set for a pure-dimensional algebraic set Z, along with a system of polynomial equations f : Z Ñ C, compute a numerical irreducible decomposition of V Z X Vpfq. An important special case is when ...

About 30–40% of male infertility is due to unknown reasons. Genetic contributions to the disruption of spermatogenesis are suggested and amongst the genetic factors studied, Y chromosome microdeletions represent the most common one. Screening for microdeletions in AZFa, b and c region of Y chromosome showed a big variation among different studies. The purpose of this study was to investigate th...

About 30–40% of male infertility is due to unknown reasons. Genetic contributions to the disruption of spermatogenesis are suggested and amongst the genetic factors studied, Y chromosome microdeletions represent the most common one. Screening for microdeletions in AZFa, b and c region of Y chromosome showed a big variation among different studies. The purpose of this study was to investigate th...

About 30–40% of male infertility is due to unknown reasons. Genetic contributions to the disruption of spermatogenesis are suggested and amongst the genetic factors studied, Y chromosome microdeletions represent the most common one. Screening for microdeletions in AZFa, b and c region of Y chromosome showed a big variation among different studies. The purpose of this study was to investigate th...