نتایج جستجو برای: primary cell culture

تعداد نتایج: 2385497  

Journal: :cell journal 0

objective: in all protocols for isolation of mesenchymal stem cells (mscs), a few days after culture initiation, the medium were discarded along with its contents of non-adherent cells and the adherent cell population kept and expanded as mscs population. in the present study, attempt was made to expand the cells suspended in removed medium of primary culture and compare them with the adherent ...

F. Yekani, M. Azarnia M. Massumi T. Peirouvi

Hippocampal neural stem/progenitor cells (hipp-NS/PCs) of the adult mammalian brain are important sources of neuronal and gial cell production. In this study, the main goal is to investigate the plasticity of these cells in neuronal/astroglial differentiations. To this end, the differentiation of the hipp-NS/PCs isolated from 3-month-old Wistar rats was investigated in response to the embryonic...

K. Khedmati L. Pishraft Sabet S. Mahdavi,

Herein, we presented the first report on bluetongue (BT) disease in 10 pregnant camels in a herd fromKerman province, Iran. All sera samples were tested serologically (AGID, C-ELISA). We also used the Razi-BK cell line, performed primary culture of ovine kidney and inoculated intravenously the embryonatedchicken eggs (ECE) to culture and isolate the BT virus. Efforts to culture and isolation of...

Journal: :razavi international journal of medicine 0
federico ferro orthopaedic trauma institute, san francisco general hospital, university of california, san francisco, usa; orthopaedic trauma institute, san francisco general hospital, university of california, 2550 23rd street, san francisco, usa. tel: +1-4152065362 chelsea shields baheney orthopaedic trauma institute, san francisco general hospital, university of california, san francisco, usa renza spelat school of veterinary medicine, university of california, davis, usa

conclusions our underlying hypothesis is that recapitulating the three-dimensional early embryonic structure, in order to reproduce better in vitro the three-dimensional morphogenetic-like re-arrangements, would improve cells differentiation, when in vivo transplanted; moreover, it could be used as a simplified cancer disease model and reliable drug evaluation method as well. results the proces...

ژورنال: Anatomical Sciences Journal 2008
Sadeghian Nodoushan, Fatemeh, Dalman, Azam, Eftekhari Yazdi, Popak, Imani, Hossein, Sepehri, Houri,

Purpose: To investigate the effect of different methods of synchronization on sheep granulosa cell cycle. Materials and Methods: Granulosa cells were aspirated from ovarian follicles and plated in a DMEM medium containing 15% FBS. Upon 70-80% confluency, the medium of the primarycultured as well as the passaged-5 cells were replaced with the medium containing either 0.5% FBS for 24, 48 and 72 h...

Journal: :international journal of hematology-oncology and stem cell research 0
ahmad shariftabrizi department of pathology, tufts university school of medicine, boston, ma 02111, usa. ilenia pellicciotta department of radiation oncology, new york university college of medicine, new york, ny 10016, usa. amer abdullah department of obstetrics, gynecology and reproductive biology, danbury hospital, 24 hospital avenue, danbury, ct 06810, usa. charis anne venditti department of obstetrics, gynecology and reproductive biology, danbury hospital, 24 hospital avenue, danbury, ct 06810, usa. robert samuelson department of obstetrics, gynecology and reproductive biology, danbury hospital, 24 hospital avenue, danbury, ct 06810, usa. shohreh shahabi department of obstetrics, gynecology and reproductive biology, danbury hospital, 24 hospital avenue, danbury, ct 06810, usa.

we have refined the technique for isolating and propagating cultures of primary ovarian carcinosarcoma cells (oscs) derived from ascites, which allowed the cells to obtain the biphasic features of carcinosarcoma in cell culture conditions (presence of both carcinoma and mesenchymal morphologic types). this protocol involves a simple yet rapid method for the growth and propagation of ascites osc...

Journal: :Cancer research 1995
S H Dairkee G Deng M R Stampfer F M Waldman H S Smith

We have used culture conditions which simulate the microenvironment of breast tumors for the isolation and propagation of primary breast tumor cells in vitro. In this monolayer setup, the mixture of cells dissociated from primary breast tumors is subjected to self-created gradients of oxygen and nutrients as well as metabolic waste and extracellular pH. The tumor populations isolated under thes...

2006
Shanaz H. Dairkee Guoren Deng Martha R. Stampfer Frederic M. Waldman S. Smith

We have used culture conditions which simulate the microenvironment of breast tumors for the isolation and propagation of primary breast tumor cells in vitro. In this monolayer setup, the mixture of cells dissoci ated from primary breast tumors is subjected to self-created gradients of oxygen and nutrients as well as metabolic waste and extracellular pH. The tumor populations isolated under the...

Journal: :jundishapur journal of microbiology 0
marzieh jamalidoust department of virology, faculty of medical sciences, tarbiat modares university, tehran, ir iran; alborzi clinical microbiology research center, nemazi hospital, shiraz university of medical sciences, shiraz, ir iran mehrdad ravanshad department of virology, faculty of medical sciences, tarbiat modares university, tehran, ir iran; department of virology, faculty of medical sciences, tarbiat modares university, tehran, ir iran. tel: +98-2182883836, fax: +98-2188013030 mandana namayandeh alborzi clinical microbiology research center, nemazi hospital, shiraz university of medical sciences, shiraz, ir iran maryam zare alborzi clinical microbiology research center, nemazi hospital, shiraz university of medical sciences, shiraz, ir iran sadaf asaei alborzi clinical microbiology research center, nemazi hospital, shiraz university of medical sciences, shiraz, ir iran mazyar ziyaeyan alborzi clinical microbiology research center, nemazi hospital, shiraz university of medical sciences, shiraz, ir iran

results aβ (1-42) stimulated the production of the proinflammatory cytokines il6, il1β, tnfα, and il18 in both the primary microglia cell culture and the b92 cell line. both the raav-il4 construct and the ril-4 protein were found to inhibit production of the most important aβ (1-42)-induced proinflammatory cytokine mrnas in the two types of cells with different patterns. conclusions it seems th...

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