In vivo genome editing partially restores alpha1-antitrypsin in a murine model of AAT deficiency. (Q52431137)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29597895%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

title

In Vivo Genome Editing Partially Restores Alpha1-Antitrypsin in a Murine Model of AAT Deficiency (English)

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21 March 2020

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2

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21 March 2020

author name string

Chun-Qing Song

1

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21 March 2020

Tingting Jiang

3

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21 March 2020

Kevin O'Connor

4

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21 March 2020

Qiushi Tang

5

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21 March 2020

Lingling Cai

6

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21 March 2020

Xiangrui Li

7

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21 March 2020

Zhiping Weng

8

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21 March 2020

Hao Yin

9

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21 March 2020

Guangping Gao

10

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21 March 2020

Christian Mueller

11

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21 March 2020

Terence R Flotte

12

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21 March 2020

Wen Xue

13

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21 March 2020

publication date

14 May 2018

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21 March 2020

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21 March 2020

volume

29

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21 March 2020

page(s)

853-860

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21 March 2020

issue

8

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Amelioration of Alpha-1 Antitrypsin Deficiency Diseases with Genome Editing in Transgenic Mice.

21 March 2020

cites work

1 reference

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29 September 2018

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Streamlined ex vivo and in vivo genome editing in mouse embryos using recombinant adeno-associated viruses.

29 September 2018

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Partial DNA-guided Cas9 enables genome editing with reduced off-target activity.

29 September 2018

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Survival Advantage of Both Human Hepatocyte Xenografts and Genome-Edited Hepatocytes for Treatment of α-1 Antitrypsin Deficiency.

29 September 2018

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Synthetically modified guide RNA and donor DNA are a versatile platform for CRISPR-Cas9 engineering

29 September 2018

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5 Year Expression and Neutrophil Defect Repair after Gene Therapy in Alpha-1 Antitrypsin Deficiency.

29 September 2018

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Genome-Wide CRISPR Screen Identifies Regulators of Mitogen-Activated Protein Kinase as Suppressors of Liver Tumors in Mice.

29 September 2018

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A multifunctional AAV-CRISPR-Cas9 and its host response

29 September 2018

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Gene Therapy for Alpha-1 Antitrypsin Deficiency Lung Disease

29 September 2018

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Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo

29 September 2018

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In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy.

29 September 2018

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Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy.

29 September 2018

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Recurrent AAV2-related insertional mutagenesis in human hepatocellular carcinomas

29 September 2018

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Adenovirus-Mediated Somatic Genome Editing of Pten by CRISPR/Cas9 in Mouse Liver in Spite of Cas9-Specific Immune Responses.

29 September 2018

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Intravenous augmentation treatment and lung density in severe α1 antitrypsin deficiency (RAPID): a randomised, double-blind, placebo-controlled trial.

29 September 2018

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Genome editing. The new frontier of genome engineering with CRISPR-Cas9

29 September 2018

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Efficient and allele-specific genome editing of disease loci in human iPSCs

29 September 2018

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Current status of gene therapy for α-1 antitrypsin deficiency

29 September 2018

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Easy quantitative assessment of genome editing by sequence trace decomposition

29 September 2018

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29 September 2018

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Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype.

29 September 2018

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Alpha-1-antitrypsin deficiency: from genoma to liver disease. PiZ mouse as model for the development of liver pathology in human.

29 September 2018

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29 September 2018

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Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients

29 September 2018

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Human Treg responses allow sustained recombinant adeno-associated virus-mediated transgene expression

29 September 2018

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29 September 2018

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Sustained miRNA-mediated knockdown of mutant AAT with simultaneous augmentation of wild-type AAT has minimal effect on global liver miRNA profiles.

29 September 2018

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Sustained transgene expression despite T lymphocyte responses in a clinical trial of rAAV1-AAT gene therapy

29 September 2018

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Therapeutic level of functional human alpha 1 antitrypsin (hAAT) secreted from murine muscle transduced by adeno-associated virus (rAAV1) vector

29 September 2018

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Sustained secretion of human alpha-1-antitrypsin from murine muscle transduced with adeno-associated virus vectors

29 September 2018

1 reference

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Expression of the cystic fibrosis transmembrane conductance regulator from a novel adeno-associated virus promoter.

29 September 2018

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Liver disease in adults with alpha-1 -antitrypsin deficiency.

29 September 2018

1 reference

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Replacement therapy for alpha 1-antitrypsin deficiency associated with emphysema

29 September 2018

1 reference

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29 September 2018

Identifiers

DOI

10.1089/HUM.2017.225

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29597895%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29597895%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

1 reference