Study of 1D stranged-charm meson family using HQET

Recently LHCb predicted spin 1 and spin 3 states D* s1(2860) and D* s3(2860) which are studied through their strong decays, and are assigned to fit the 13D1and 13D3 states in the charm spectroscopy. In this paper,using the heavy quark effective theory, we state that assigning D*s1(2860) as the mixing of 13D1 - 23S1 states, is rather a better justification to its observed experimental values than a pure state. We study its decay modes variation with hadronic coupling constant gxh and the mixing angle . We appoint spin 3 state D* s3(2860) as the missing 1D 3- JP state, and also study its decay channel behavior with coupling constant gyh. To appreciate the above results, we check the variation of decay modes for their spin partners states i.e. 1D2 and 1D'2 with their masses and strong coupling constant i.e. gxh and gyh. Our calculation using HQET approach give mixing angle between the 13D1 - 23S1 state for D* s1(2860) to lie in the range (-1.6 radians < theta < -1.2 radians). Our calculation for coupling constant values gives gxh to lie between value 0:17 < gxh < 0:20 and gyh to be 0.40. We expect from experiments to observe this mixing angle to verify our results.Comment: 11 pages, 9 figure and 5 Tables, EPJC 2015 communicate

Masses and Strong Decay properties of Radially Excited Bottom states B(2S)and B(2P) with their Strange Partners Bs(2S) and Bs(2P)

In this paper, we analyzed the experimentally available radially excited charm mesons to predict the similar spectra for the n=2 bottom mesons. In the heavy quark effective theory, we explore the flavor independent parameters to calculate the masses for the experimentally unknown n=2 bottom mesons B(2S), B(2P), Bs(2S) and Bs(2P). We have also analyzed these bottom masses by applying the QCD and 1/mQ corrections to the lagrangian leading to the modification of flavor symmetry parameters as. Further strong decay widths are determined using these calculated masses to check the sensitivity of these corrections for these radially excited mesons. The calculated decay widths are in the form of strong coupling constant geHH, egSH and egTH. We concluded that these corrections are less sensitive for n=2 masses as compared to n=1 masses. Branching ratios and branching fractions of these states are calculated to have a deeper understanding of these states. These predicted values can be confronted with the future experimental data.Comment: 11 Pages, 6 Table

Heavy-light charm mesons spectroscopy and decay widths

We present the mass formula for heavy-light charm meson for one loop, using heavy quark effective theory. Formulating an effective Lagrangian, the masses of the ground state heavy mesons have been studied in the heavy quark limit including leading corrections from finite heavy quark masses and nonzero light quark masses using a constrained fit for the eight equation having eleven parameters including three coupling constants g, h and g'. Masses determined from this approach is fitted to the experimentally known decay widths to estimate the strong coupling constants, showing a better match with available theoretical and experimental dataComment: 16 pages and 12 figures. arXiv admin note: text overlap with arXiv:hep-ph/0503134 by other author

Stem Cell Antigen CD34 In Native And Engineered Form Alter Its Binding Ability To Stromal Cells And Ligands: A Classical Example Of Clinical Benefits Of Therapeutic Genetic Engineering Of Stem Cells In Transplantation

CD34 is a highly glycosylated surface-expressed sialomucin and, because it is present on hematopoietic stem cells (HSCs), has demonstrated immense clinical utility in their enumeration in aphaeresis products, immunoaffinity purification for transplantation, and disease monitoring. The success of CD34 based reagents in identifying hematopoietic progenitors led to the assumption that CD34 is expressed on cells with regenerative potential and is sufficient for hematopoietic reconstitution in marrow-ablated recipients. However, its role has not been identified in substantial detail. &#xd;&#xa;&#xd;&#xa;With the advent of the fact that CD34 binds adapter protein like CRK-L in cytosol and CD34 knock out studies identified a a signaling role, CD34 antigen has been proposed to play a signaling function. Since it is a sialomucin, a member of the group adhesion molecules, we attempted to identify a role by over-expreesing its gene in cell lines. We report here that CD34 and engineered forms (Ser306 &#x26; Tyr318) significantly regulates adhesion to stromal cells, like mesenchymal stem cells and bone marrow ligands. These enhance binding of cells overexpressing CD34 by upregulating integrins and we therefore propose that such cells may effectively potentiate the success of transplantation through greater homing if they are used for transfusion