Zobrazeno 1 - 7
of 7
pro vyhledávání: '"K D, Knebel"'
Autor:
K. J. Gorelick, E. Lim, D. M. Fishwild, D. M. Wood, D. T. Reardan, K. D. Knebel, J. B. Parent, P. J. Conlon, P. W. Trown
Publikováno v:
Host Defense Dysfunction in Trauma, Shock and Sepsis ISBN: 9783642774072
Sepsis is a common, life-threatening complication of infection with gram-negative bacteria. While the pathophysiology of gram-negative sepsis has not been fully elucidated, a significant portion of the clinical syndrome can probably be attributed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7e4a79125a68e7c3f0e0a675e63734e
https://doi.org/10.1007/978-3-642-77405-8_156
https://doi.org/10.1007/978-3-642-77405-8_156
Publikováno v:
Journal of the National Cancer Institute. 64(6)
Publikováno v:
Journal of neurosurgery. 49(1)
Flow cytometry (FCM) is a technique that measures the quantity of DNA contained in individual nuclei and records a frequency distribution of the DNA content per nucleus in the sampled cell population. Nuclei from a variety of human brain-tumor types
Publikováno v:
Cancer research. 35(6)
An in vitro colony formation assay was used to determine the efficacy of in vitro therapy with 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) on a rat brain tumor. The fraction of clonogenic cells surviving in vivo therapy was determined by a comparison
Publikováno v:
Cancer research. 36(10)
An in vitro colony formation assay was modified to determine the effects of in vivo 1,3-bis(2-chloroethyl)-1-nitrosourea therapy on tumor cell kill and subsequent clonogenic cell kinetics. The measured surviving fraction must be multiplied by the rel
Publikováno v:
Cancer. 50(5)
Malignant human gliomas have a highly variable distribution of cell nuclei, consisting of diploid and/or other populations in terms of nuclear DNA content. In order to study in vitro clonogenicity of each population, dissociated or cultured human gli
Publikováno v:
Cancer treatment reports. 62(12)
Kinetic changes induced by dianhydrogalactitol (DAG) in cultured 9L rat brain tumor cells were studied using conventional autoradiography and flow cytometry. Cell cycle parameters for the untreated cell line were: G1, 8.5 hours; S, 8.2 hours; G2, 3.2