Co-regulation of primary mouse hepatocyte viability and function by oxygen and matrix-Reference-Cited by-同舟云学术

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Co-regulation of primary mouse hepatocyte viability and function by oxygen and matrix

Published:2014-01-31 Issue:5 Volume:111 Page:1018-1027
ISSN:0006-3592
Container-title:Biotechnology and Bioengineering
language:en
Short-container-title:Biotechnol. Bioeng.

Author:

Buck Lorenna D.¹,Inman S. Walker¹,Rusyn Ivan²,Griffith Linda G.¹

Affiliation:

1. Department of Biological Engineering; Massachusetts Institute of Technology; 77 Massachusetts Avenue, Room 16-429 Cambridge Massachusetts 02139

2. Department of Environmental Sciences and Engineering; University of North Carolina; Chapel Hill North Carolina

Funder

National Institutes of Health

Publisher

Wiley

Subject

Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Reference39 articles.

1. Evidence that hypoxia markers detect oxygen gradients in liver: pimonidazole and retrograde perfusion of rat liver;Arteel;Br J Cancer,1995

2. Chronic enteral ethanol treatment causes hypoxia in rat liver tissue in vivo;Arteel;Hepatology,1997

3. Transformation and action of extracellular NAD+ in perfused rat and mouse livers;Broetto-Biazon;Acta Pharmacol Sin,2008

4. Optimization of culture conditions for determining hepatobiliary disposition of taurocholate in sandwich-cultured rat hepatocytes;Chandra;In Vitro Cell Dev Biol,2001

5. Changes in Liver-specific compared to common gene transcription during primary culture of mouse hepatocytes;Clayton;Mol Cell Biol,1983

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