Analysis of Cellular Resistance Mechanisms to Viral Oncolysis: Dissertation - Robert Strauss - Grāmatas - Südwestdeutscher Verlag für Hochschulsch - 9783838124858 - 2011. gada 21. jūnijs
Ja vāks un nosaukums nesakrīt, pareizs ir nosaukums

Analysis of Cellular Resistance Mechanisms to Viral Oncolysis: Dissertation German edition

Cena
€ 62,99

Pasūtīts no attālās noliktavas

Paredzamā piegāde . gada 30. sept. - . gada 8. okt.
Saņemiet paziņojumus par jauniem Robert Strauss izdevumiem
Pievienot savam iMusic vēlmju sarakstam

Not rated yet

Vectors based on adenoviruses have been designed as targeted anti-cancer therapeutics that showed promising results in pre-clinical applications. Particularly, efforts have focused on the development of oncolytic vectors that can eliminate cancer cells and replicate in a tumor-selective fashion to amplify the input dose. In clinical trials, these oncolytic adenoviruses have generally been proved safe in patients, but have fallen short of their expected therapeutic value as monotherapies. A number of obstacles that hamper the efficacy of adenoviral vectors have been identified. These include several soluble and cellular blood components, the lack of viral receptors, and the extracellular matrix sequestered by tumor stroma. However, the apparent inability of adenoviruses to spread throughout solid tumors could not be fully explained yet. The work in this book sheds light on obstacles that previously had not been taken into account. It was identified that the epithelial phenotype of ovarian cancer cells represents a barrier for adenovirus infection and virus-mediated oncolysis. Furthermore, major discrepancies between phenotypes of tumors in situ and cultured cells were discovered.

Mediji Grāmatas     Paperback Book   (Grāmata ar mīksto vāku un līmēto muguru)
Izlaists 2011. gada 21. jūnijs
ISBN13 9783838124858
Izdevēji Südwestdeutscher Verlag für Hochschulsch
Lapas 140
Izmēri 150 × 8 × 226 mm   ·   227 g
Valoda Vācu  

Vairāk no Robert Strauss

Rādīt visu

Vairāk no tā paša izdevēja