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Institution

Eskişehir Osmangazi University

EducationEskişehir, Turkey
About: Eskişehir Osmangazi University is a education organization based out in Eskişehir, Turkey. It is known for research contribution in the topics: Population & Thin film. The organization has 3427 authors who have published 7755 publications receiving 122977 citations. The organization is also known as: Eskişehir Osmangazi University & Eskişehir Osmangazi Üniversitesi.


Papers
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Journal ArticleDOI
TL;DR: A review of recent literature reports on the synthesis and applications of pH-responsive polymers can be found in this article, where the authors provide an analysis of some of the recent literature reported on the synthesizing and applications.

697 citations

Journal ArticleDOI
TL;DR: Treatment of progressive thoracic insufficiency syndrome should provide an acute increase in theThoracic volume with stabilization of any flail chest-wall defects and maintain these improvements as the patient grows, without the need for spine fusion.
Abstract: • Thoracic insufficiency syndrome is the inability of the thorax to support normal respiration or lung growth. • The rare condition of fused ribs and congenital scoliosis may result in a three-dimensional thoracic deformity with adverse effects on thoracic growth and function with development of thoracic insufficiency syndrome. • The normal thorax is defined by two characteristics: normal, stable volume and the ability to change that volume. Volume depends on the width and depth of the rib cage, and the thoracic spine provides height. The ability to change volume, termed thoracic function, is provided by the diaphragm and the secondary muscles of respiration. • On radiographs, the loss of the vertical height of the lung of the concave, restricted hemithorax is defined by the percentage of space available for the lung. • Spine rotation causes a windswept thorax, with both restriction of the volume of the convex hemithorax and restriction of the motion of the involved ribs. • Constrictive three-dimensional deformity of the thorax may cause extrinsic, restrictive lung disease. • Progressive thoracic insufficiency syndrome is diagnosed on the basis of clinical signs of respiratory insufficiency, loss of chest wall mobility as demonstrated by the thumb excursion test, worsening indices of three-dimensional thoracic deformity on radiographs and computed tomography scans, or a relative decline in percent predicted vital capacity due to thoracic "failure to thrive," as demonstrated by pulmonary function tests. • Treatment of progressive thoracic insufficiency syndrome should provide an acute increase in the thoracic volume with stabilization of any flail chest-wall defects and maintain these improvements as the patient grows, without the need for spine fusion.

552 citations

Journal ArticleDOI
01 Jun 2001-Polymer
TL;DR: In this paper, a group transfer polymerization of four tertiary amine methacrylates, 2-(dimethylamino)ethyl methacelate (DMA), 2-(diethylamino),ethyl methacricrylate (DEA), DPA, and 2-(N-morpholino) methyl methacylate (MEMA) produced a series of near-monodisperse homopolymers (Mw/Mn<1.15).

546 citations

Journal ArticleDOI
TL;DR: In this article, the changes of the properties for the rubberized concretes were investigated in terms of both size and amount of the rubber chips, and it was observed that plastic energy capacities began to increase when the high elastic energy capacity of normal concrete was reduced by adding rubber.

537 citations

Journal ArticleDOI
TL;DR: This work reports a fully integrated modular physical, biochemical, and optical sensing platform, interfaced through a fluidics-routing breadboard with a multi–organ-on-a-chip system to achieve in situ, continual, and automated sensing of microenvironment biophysical and biochemical parameters.
Abstract: Organ-on-a-chip systems are miniaturized microfluidic 3D human tissue and organ models designed to recapitulate the important biological and physiological parameters of their in vivo counterparts. They have recently emerged as a viable platform for personalized medicine and drug screening. These in vitro models, featuring biomimetic compositions, architectures, and functions, are expected to replace the conventional planar, static cell cultures and bridge the gap between the currently used preclinical animal models and the human body. Multiple organoid models may be further connected together through the microfluidics in a similar manner in which they are arranged in vivo, providing the capability to analyze multiorgan interactions. Although a wide variety of human organ-on-a-chip models have been created, there are limited efforts on the integration of multisensor systems. However, in situ continual measuring is critical in precise assessment of the microenvironment parameters and the dynamic responses of the organs to pharmaceutical compounds over extended periods of time. In addition, automated and noninvasive capability is strongly desired for long-term monitoring. Here, we report a fully integrated modular physical, biochemical, and optical sensing platform through a fluidics-routing breadboard, which operates organ-on-a-chip units in a continual, dynamic, and automated manner. We believe that this platform technology has paved a potential avenue to promote the performance of current organ-on-a-chip models in drug screening by integrating a multitude of real-time sensors to achieve automated in situ monitoring of biophysical and biochemical parameters.

533 citations


Authors

Showing all 3553 results

NameH-indexPapersCitations
Mehmet Kaya9575135759
Michael A. Gatzoulis8247832562
Ahmet Gül6250717351
Candan Gokceoglu5518610355
Hakan Ay532039340
Bill Triggs4910448821
Haner Direskeneli483149339
İlker Bekir Topçu472157379
Atilla Halil Elhan412295530
Mehmet Yilmaz406188292
Ahmet Bekir392334915
Sedat Kiraz372304508
Bulent Gorenek3718222408
Sonya V. Babu-Narayan351445680
Mehmet Gungor Kaya331563429
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202346
2022138
2021781
2020619
2019508
2018440