Spontaneous hepatic repopulation in transgenic mice expressing mutant human α1-antitrypsin by wild-type donor hepatocytes - Wikidata - wikimedia - TriplyDB

Spontaneous hepatic repopulation in transgenic mice expressing mutant human α1-antitrypsin by wild-type donor hepatocytes

Spontaneous hepatic repopulation in transgenic mice expressing mutant human α1-antitrypsin by wild-type donor hepatocytes

http://www.wikidata.org/entity/Q34876052

about

Liver tumors in children with metabolic disorders A universal system to select gene-modified hepatocytes in vivo Repopulation 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 mice Stem cells in liver diseases and cancer: recent advances on the path to new therapies.Stem cell-based therapy for α₁-antitrypsin deficiency New 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.

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Spontaneous hepatic repopulation in transgenic mice expressing mutant human α1-antitrypsin by wild-type donor hepatocytes

http://www.wikidata.org/entity/Q34876052

description

2011 nî lūn-bûn

@nan

2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2011 թվականի ապրիլին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes

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Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes

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Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes

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type

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Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes

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Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes

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Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes

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Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes

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Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes

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Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes

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Journal of Clinical Investigation

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Spontaneous hepatic repopulati ...... by wild-type donor hepatocytes

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Chandan Guha

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David H Perlmutter

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Govardhana R Yannam

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Hesham Basma

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Ira J Fox

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Jayanta Roy-Chowdhury

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Jianqiang Ding

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Namita Roy-Chowdhury

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Ronald J Wong

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Stephen I Rennard

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Principles of therapeutic liver repopulation.

The role of autophagy in alpha-1-antitrypsin deficiency: a specific cellular response in genetic diseases associated with aggregation-prone proteins.

Alpha 1-antitrypsin deficiency, emphysema, and liver disease. Genetic basis and strategies for therapy.

The mechanism of Z alpha 1-antitrypsin accumulation in the liver.

Worldwide racial and ethnic distribution of alpha1-antitrypsin deficiency: summary of an analysis of published genetic epidemiologic surveys.

Serial transplantation reveals the stem-cell-like regenerative potential of adult mouse hepatocytes

Tissue specific expression of the human alpha-1-antitrypsin gene in transgenic mice.

An autophagy-enhancing drug promotes degradation of mutant alpha1-antitrypsin Z and reduces hepatic fibrosis.

Alpha-1-antitrypsin mutant Z protein content in individual hepatocytes correlates with cell death in a mouse model.

A randomized clinical trial of alpha(1)-antitrypsin augmentation therapy.

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