Titlebook: Gene Therapy and Cell Therapy Through the Liver; Current Aspects and Shuji Terai,Takeshi Suda Book 2016 Springer Japan 2016 CPC Isolator.a

連結(jié)

書目名稱Gene Therapy and Cell Therapy Through the Liver影響因子(影響力)




書目名稱Gene Therapy and Cell Therapy Through the Liver影響因子(影響力)學(xué)科排名




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書目名稱Gene Therapy and Cell Therapy Through the Liver網(wǎng)絡(luò)公開度學(xué)科排名




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書目名稱Gene Therapy and Cell Therapy Through the Liver被引頻次學(xué)科排名




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書目名稱Gene Therapy and Cell Therapy Through the Liver讀者反饋學(xué)科排名

Spinous-Process

Macrophage Therapy for Liver Fibrosis and Regenerationjury both the resident macrophages and circulating monocytes influence both liver regeneration and liver fibrosis. Kupffer cells can stimulate hepatocyte proliferation via the secretion of IL-6; macrophages stimulate a ductular proliferation via TWEAK secretion and also secrete Wnts which stimulate

infringe

MINT

Novel Immunotherapy Using Liver-Derived Natural Killer Cells for Preventing Hepatocellular Carcinomaants. However, no prevention or treatment exists for HCC recurrence after liver transplantation. Here, we describe an adoptive immunotherapy approach that uses natural killer (NK) cells derived from both living and deceased donor liver graft perfusates. Liver NK cells exhibited the vigorous cytotoxi

hedonic

voluble

voluble

Potential Usage of Human Artificial Chromosome for Regenerative Medicineneered creation) or a “bottom-up approach” (de novo creation). HACs with one or more acceptor sites exhibit several characteristics required by an ideal gene delivery vector, including stable episomal maintenance and the capacity to carry large genomic loci plus their regulatory elements, thus allow

antecedence

Image-Guided Hydrodynamic Gene Delivery to the Liver: Toward Clinical Applicationsn its cells. Conventional therapeutic methods are often insufficient or unavailable to manage genetic diseases in the liver; therefore, more efficient strategies are urgently needed. Gene therapy emerged as novel method of treatment relying on liver-directed transfer of a gene-coding sequence to pro

bioavailability

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