Titlebook: Embryonic Stem Cell Protocols; Volume II: Different Kursad Turksen Book 2006Latest edition Humana Press 2006 Vivo.biology.cell.cell culture

分類

書目名稱Embryonic Stem Cell Protocols影響因子(影響力)




書目名稱Embryonic Stem Cell Protocols影響因子(影響力)學(xué)科排名




書目名稱Embryonic Stem Cell Protocols網(wǎng)絡(luò)公開度




書目名稱Embryonic Stem Cell Protocols網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Embryonic Stem Cell Protocols被引頻次




書目名稱Embryonic Stem Cell Protocols被引頻次學(xué)科排名




書目名稱Embryonic Stem Cell Protocols年度引用




書目名稱Embryonic Stem Cell Protocols年度引用學(xué)科排名




書目名稱Embryonic Stem Cell Protocols讀者反饋




書目名稱Embryonic Stem Cell Protocols讀者反饋學(xué)科排名

intellect

充足

FANG

https://doi.org/10.1057/9781403982322ffects on the proportion and purity of the derived neuronal cells. Here, the protocols used to optimize ES cell density in neuronal differentiation with and without an initial aggregation step are described.

中子

https://doi.org/10.1057/9781137364937aled that . is not required for hemangioblast development but is required in a dose-dependent fashion for hemangioblast differentiation to definitive hematopoietic progenitors. Contained here are the methods needed to conduct embryonic stem cell-derived in vitro hematopoietic assays.

promote

Optimized Neuronal Differentiation of Murine Embryonic Stem Cellsffects on the proportion and purity of the derived neuronal cells. Here, the protocols used to optimize ES cell density in neuronal differentiation with and without an initial aggregation step are described.

promote

使厭惡

負(fù)擔(dān)

https://doi.org/10.1007/978-981-16-5485-5enic differentiation in EBs by histochemical staining, immunostaining, mRNA-. hybridization, and reverse transcriptase polymerase chain reaction analysis. Here, we describe in detail our established protocols to analyze chondrogenic differentiation of ES cells. We summarize different ways to modulate ES cell-derived chondrogenic differentiation.

教育學(xué)

https://doi.org/10.1007/978-3-531-93267-5anced with a high frequency of K14-positive cells. Thus, the in vitro co-culture model system described here is useful in dissecting the process of commitment and differentiation of epithelial progenitors that occurs during epidermogenesis as well as for the investigation of the molecular mechanisms underlying these processes.