£>r lltS MASItK CUfi Kfctr ittlS COPY FOR REPRODUCTION PURPOSES
نویسنده
چکیده
PuM« moorwto Dun» (Of mis c&wxon at ntomiauon » uanalM lo av*rag* 1 hour Of moorv. fiduOing tn» tm» tor nvawng «mruaion». Marcnmc »nstng 0""|f?*gammg ine miranng trw «u nMdad. «no compMono «nd fw»wng tn. coiMctnn ot ntomuiion Samt commam ragaraing mo ouroanaaarnataa or iy«n« •*°yjl2£zL couaaon ol «formation, nöuong sugoaanons tw raauano mn Ouroan. to Wamngton Haaoouanari Sarre»* Diraetorata tor «format OoaranorMand fl««^" Janaraon ■ay SUM 120« Armgjon. VA 22202-4302. ino to 9» Ofhoa ol Manaoamant «no Buooat. Paoarwort« Raauaion Proiact (0704-01M). Waaringion, DC 20303. 0«vn Hionway. SU 1204. Ar gion.
منابع مشابه
Ad - a 263 766 Iii : R Copy - Keep This Copy for Reproduction Purposes
This paper is concerned with gradient estimation techniques for steady-state performance measures associated with regenerative stochastic processes. The principal emphasis is on the discussion of conditions under which likelihood ratio methods and infinitesimal perturbation analysis techniques are valid.
متن کاملTroxel , S . W . , Delanoy , R . L . , “ Machine Intelligent Approach to Automated Gust Front
copy may be made for personal use only. Systematic reproduction and distribution, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper are prohibited.
متن کاملJunctional abnormalities in human airway epithelial cells expressing F508del CFTR.
Cystic fibrosis (CF) has a profound impact on airway physiology. Accumulating evidence suggests that intercellular junctions are impaired in CF. We examined changes to CF transmembrane conductance regulator (CFTR) function, tight junctions, and gap junctions in NuLi-1 (CFTR(wt/wt)) and CuFi-5 (CFTR(ΔF508/ΔF508)) cells. Cells were studied at air-liquid interface (ALI) and compared with primary h...
متن کاملI-44: Concurrent Whole-Genome Haplotyping and Copy-Number Profiling of Single Cells
Background Methods for haplotyping and DNA copynumber typing of single cells are paramount for studying genomic heterogeneity and enabling genetic diagnosis. Before analyzing the DNA of a single cell by microarray or next-generation sequencing, a whole-genome amplification (WGA) process is required, but it substantially distorts the frequency and composition of the cell’s alleles. As a conseque...
متن کاملEGF and K+ channel activity control normal and cystic fibrosis bronchial epithelia repair.
Severe lesions of airway epithelia are observed in cystic fibrosis (CF) patients. The regulatory mechanisms of cell migration and proliferation processes, involved in the repair of injured epithelia, then need to be better understood. A model of mechanical wounding of non-CF (NuLi) and CF (CuFi) bronchial monolayers was employed to study the repair mechanisms. We first observed that wound repai...
متن کامل