A Search for pair production of the LSP ντ~\tilde{\nu_{\tau}} at the CLIC via RPV Decays

In this work we consider pair production of LSP tau-sneutrinos at the Compact Lineer Collider. We assume that tau-sneutrinos decays in to e\textmu pair via RPV interactions. Backgroundless subprocess $e{}^{-}e^{+}\rightarrow\tilde{\nu}\bar{\tilde{\nu}}\rightarrow\mu^{+}\mu^{+}e^{-}e^{-}(\mu^{-}\mu^{-}e^{+}e^{+})$ is analyzed in details. Achievable limits on $Br\,(\tilde{\nu}_{\tau}\rightarrow\mu e)$ at $3\sigma$ and $5\sigma$ CL are obtained depending on $\tilde{\nu_{\tau}}$ mass.Comment: 8 pages, 5 figure

Graviton production through photon-quark scattering at the LHC

We have investigated real graviton emission in the ADD and RS model of extra dimensions through the photoproduction process pp-> p gamma p-> pGqX at the LHC. We have considered all contributions from the subprocesses gamma q -> G q, where q=u,d,c,s,b,anti-u,anti-d, anti-c, anti-s, anti-b quark. The constraints on model parameters of the ADD and RS model of extra dimensions have been calculated. During numerical calculations we have taken account of 3, 4, 5 and 6 large extra dimensional scenarios. The constraints on RS model parameters have been calculated by considering G -> gamma gamma, e^- e^+, mu^- mu^+ decay channels of the graviton.Comment: 27 pages, 12 figures; final version to appear in PR

The effect of vascular graft and human umbilical cord blood-derived CD34+ stem cell on peripheral nerve healing

AIM: There are many trials concerning peripheral nerve damage causes and treatment options. Unfortunately, nerve damage is still a major problem regarding health, social and economic issues. On this study, we used vascular graft and human cord blood derived stem cells to find an alternative treatment solution to this problem. MATERIAL AND METHODS: We used 21 female Wistar rats on our study. They were anesthetized with ketamine and we studied right hind limbs. On Group 1, we did a full layer cut on the right sciatic nerve. On Group 2, we did a full layer cut on the right sciatic nerve, and we covered synthetic vascular graft on cut area. On Group 3, we did a full layer cut on right sciatic nerve, and we covered the area with stem cell applied vascular graft. RESULTS: At the end of postoperative 8. weeks, we performed EMG on the rats. When we compared healthy and degenerated areas as a result of EMG, we found significant amplitude differences between the groups on healthy areas whereas there was no significant difference on degenerated areas between the groups. Then we re-opened the operated area again to reveal the sciatic nerve cut area, and we performed electron microscope evaluation. On the stem cell group, we observed that both the axon and the myelin sheet prevented degeneration. CONCLUSION: This study is a first on using synthetic vascular graft and cord blood derived CD34+ cells in peripheral nerve degeneration. On the tissues that were examined with electron microscope, we observed that CD34+ cells prevented both axonal and myelin sheath degeneration. Nerve tissue showed similar results to the control group, and the damage was minimal. © 2018 Ali Yilmaz, Abdullah Topcu, Cagdas Erdogan, Levent Sinan Bir, Barbaros Sahin, Gulcin Abban, Erdal Coskun, Ayca Ozkul

Phase imaging with intermodulation atomic force microscopy

Intermodulation atomic force microscopy (IMAFM) is a dynamic mode of atomic force microscopy (AFM) with two-tone excitation. The oscillating AFM cantilever in close proximity to a surface experiences the nonlinear tip-sample force which mixes the drive tones and generates new frequency components in the cantilever response known as intermodulation products (IMPs). We present a procedure for extracting the phase at each IMP and demonstrate phase images made by recording this phase while scanning. Amplitude and phase images at intermodulation frequencies exhibit enhanced topographic and material contrast.Comment: 6 pages, 6 page

Enzyme activities and growth promotion of spinach by indole-3-acetic acid-producing rhizobacteria

The objective of this study was to evaluate the effects of twelve plant growth-promoting rhizobacteria (PGPR; Bacillus mycoides FD07, B. sphaericus RC12, B. pumilus RC19, B. cereus RC18, Variovorax paradoxus RC21, Paenibacillus polymyxa RC35, Pseudomonas putida RC06, B. megaterium RC07, B. megaterium M-3, B. licheniformis RC08, B. subtilis RC11, and B. subtilis OSU-142) used as biofertilisers, on various enzyme activities [glucose-6-phosphate dehydrogenase (G6PD); 6-phosphogluconate dehydrogenase (6PGD); glutathione reductase (GR); and glutathione S-transferase (GST)] and on seedling growth in spinach (Spinacia oleracea L.). Enhanced plant growth could result from rhizobacterial production of indole-3-acetic acid (IAA). The highest IAA-producing rhizobacteria (RC35 and RC06) produced the highest root and shoot weights. PGPR improved N and P nutrition in spinach, and therefore stimulated plant growth and key enzyme activities. The responses to inoculation, compared to uninoculated control plants, were: –1.9% to +36.4% for shoot fresh weights (FWs), –5.5% to +30.1% for root FWs, –3.5% to +29.8% for shoot dry weights (DWs), –3.8% to +38.5% for root DWs, and –5.9% to +30.1% for leaf areas. Plant growth responses were variable and dependent on the inoculant strain used, as well as on the enzyme activity and growth parameter being evaluated. Close correlations between plant shoot growth, PGPR inoculation, and G6PD (r = 0.28*), 6PGD (r = 0.55**), GR (r = 0.73**), and GST (r = 0. 64**) enzyme activities in spinach have been demonstrated

A new method for fabrication of nanohydroxyapatite and TCP from the sea snail Cerithium vulgatum

Biphasic bioceramic nanopowders of hydroxyapatite (HA) and β-tricalcium phosphate (TCP) were prepared from shells of the sea snail Cerithium vulgatum (Bruguière, 1792) using a novel chemical method. Calcination of the powders produced was carried out at varying temperatures, specifically at 400°C and 800°C, in air for 4 hours. When compared to the conventional hydrothermal transformation method, this chemical method is very simple, economic, due to the fact that it needs inexpensive and safe equipment, because the transformation of the aragonite and calcite of the shells into the calcium phosphate phases takes place at 80°C under the atmospheric pressure. The powders produced were determined using infrared spectroscopy (FT-IR), X-ray diffraction, and scanning electron microscopy (SEM). The features of the powders produced along with the fact of their biological origin qualify these powders for further consideration and experimentation to fabricate nanoceramic biomaterials. © 2014 O. Gunduz et al