Spontaneous hepatic repopulation in transgenic mice expressing mutant human α1-antitrypsin by wild-type donor hepatocytes
about
Liver tumors in children with metabolic disordersA universal system to select gene-modified hepatocytes in vivoRepopulation of the fibrotic/cirrhotic rat liver by transplanted hepatic stem/progenitor cells and mature hepatocytes.Persistent lung inflammation and fibrosis in serum amyloid P component (APCs-/-) knockout miceStem cells in liver diseases and cancer: recent advances on the path to new therapies.Stem cell-based therapy for α₁-antitrypsin deficiencyNew Tools in Experimental Cellular Therapy for the Treatment of Liver Diseases.Disorders of protein misfolding: alpha-1-antitrypsin deficiency as prototype.Characterization and use of HapT1-derived homologous tumors as a preclinical model to evaluate therapeutic efficacy of drugs against pancreatic tumor desmoplasia.Bile Duct Ligation Induces ATZ Globule Clearance in a Mouse Model of α-1 Antitrypsin Deficiency.Mysteries of α1-antitrypsin deficiency: emerging therapeutic strategies for a challenging disease.Novel treatment strategies for liver disease due to α1-antitrypsin deficiency.Broad spectrum of hepatocyte inclusions in humans, animals, and experimental models.Cell and tissue engineering for liver disease.Targeting the vascular and perivascular niches as a regenerative therapy for lung and liver fibrosis.Concise Review: Liver Regenerative Medicine: From Hepatocyte Transplantation to Bioartificial Livers and Bioengineered Grafts.In situ expansion of engineered human liver tissue in a mouse model of chronic liver disease.Human Urinary Epithelial Cells as a Source of Engraftable Hepatocyte-Like Cells Using Stem Cell Technology.Cell therapy from bench to bedside: Hepatocytes from fibroblasts - the truth and myth of transdifferentiation.Repeated transplantation of hepatocytes prevents fulminant hepatitis in a rat model of Wilson's disease.Survival Advantage of Both Human Hepatocyte Xenografts and Genome-Edited Hepatocytes for Treatment of α-1 Antitrypsin Deficiency.Human hepatocyte transplantation for liver disease: current status and future perspectives.A ZFN/piggyBac step closer to autologous liver cell therapy.Bone marrow stem cell therapy partially ameliorates pathological consequences in livers of mice expressing mutant human α1-antitrypsin.Therapeutic Genome Editing With CRISPR/Cas9 in a Humanized Mouse Model Ameliorates α1-antitrypsin Deficiency Phenotype.Alpha-1 antitrypsin deficiency: outstanding questions and future directions.
P2860
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P2860
Spontaneous hepatic repopulation in transgenic mice expressing mutant human α1-antitrypsin by wild-type donor hepatocytes
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes
@ast
Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes
@en
Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes
@nl
type
label
Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes
@ast
Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes
@en
Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes
@nl
prefLabel
Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes
@ast
Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes
@en
Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes
@nl
P2093
P2860
P356
P1476
Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes
@en
P2093
Chandan Guha
David H Perlmutter
Govardhana R Yannam
Hesham Basma
Jayanta Roy-Chowdhury
Jianqiang Ding
Namita Roy-Chowdhury
Ronald J Wong
Stephen I Rennard
P2860
P304
P356
10.1172/JCI45260
P407
P577
2011-04-18T00:00:00Z