Ex vivo transduction and transplantation of bone marrow cells for liver gene delivery of alpha1-antitrypsin - Wikidata - awgldk - TriplyDB

Ex vivo transduction and transplantation of bone marrow cells for liver gene delivery of alpha1-antitrypsin

Ex vivo transduction and transplantation of bone marrow cells for liver gene delivery of alpha1-antitrypsin

http://www.wikidata.org/entity/Q34080880

about

Challenges and Prospects for Alpha-1 Antitrypsin Deficiency Gene Therapy Recent advances in α-1-antitrypsin deficiency-related lung disease.Alpha-1 antitrypsin deficiency: new developments in augmentation and other therapies.

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P2860

Ex vivo transduction and transplantation of bone marrow cells for liver gene delivery of alpha1-antitrypsin

http://www.wikidata.org/entity/Q34080880

description

2010 nî lūn-bûn

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2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Ex vivo transduction and trans ...... delivery of alpha1-antitrypsin

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Ex vivo transduction and trans ...... delivery of alpha1-antitrypsin

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Ex vivo transduction and trans ...... delivery of alpha1-antitrypsin

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type

label

Ex vivo transduction and trans ...... delivery of alpha1-antitrypsin

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Ex vivo transduction and trans ...... delivery of alpha1-antitrypsin

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Ex vivo transduction and trans ...... delivery of alpha1-antitrypsin

@nl

prefLabel

Ex vivo transduction and trans ...... delivery of alpha1-antitrypsin

@ast

Ex vivo transduction and trans ...... delivery of alpha1-antitrypsin

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Ex vivo transduction and trans ...... delivery of alpha1-antitrypsin

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Molecular Therapy

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Ex vivo transduction and trans ...... delivery of alpha1-antitrypsin

@en

P2093

Bryon Petersen

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Hong Li

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Lung-Ji Chang

http://www.w3.org/2001/XMLSchema#string

Marda Jorgensen

http://www.w3.org/2001/XMLSchema#string

Rafal P Witek

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Sihong Song

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Yuanqing Lu

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P2860

Gene targeting of mutant COL1A2 alleles in mesenchymal stem cells from individuals with osteogenesis imperfecta

Gene targeting in stem cells from individuals with osteogenesis imperfecta

Alpha 1-antitrypsin deficiency. 3: Clinical manifestations and natural history

Alpha1-antitrypsin deficiency. 2: genetic aspects of alpha(1)-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema risk

Adipose-derived stem cells for regenerative medicine

Functional integration of hepatocytes derived from human mesenchymal stem cells into mouse livers.

Adipose-derived stem cells for the regeneration of damaged tissues.

Optimized lentiviral vector design improves titer and transgene expression of vectors containing the chicken beta-globin locus HS4 insulator element.

Correction of sickle cell disease in transgenic mouse models by gene therapy.

Rapid and highly efficient transduction by double-stranded adeno-associated virus vectors in vitro and in vivo.

P304

1553-1558

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scholarly article

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10.1038/MT.2010.116

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8

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18

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Martha Campbell-Thompson

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2010-06-15T00:00:00Z

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44676900

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20551917

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2927066

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