(Q45864903)

17 December 2017

http://europepmc.org/abstract/MED/24804755

title

CRISPR technology for gene therapy (English)

1 reference

17 December 2017

http://europepmc.org/abstract/MED/24804755

0 references

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24804755%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

author name string

Katherine High

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24804755%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

Charles Gersbach

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24804755%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

language of work or name

English

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publication date

1 May 2014

1 reference

17 December 2017

http://europepmc.org/abstract/MED/24804755

published in

Nature Medicine

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24804755%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24804755%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24804755%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

page(s)

476-477

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24804755%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/nm.3566

2 June 2020

exact match

0 references

cites work

Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome.

1 reference

Gene editing of CCR5 in autologous CD4 T cells of persons infected with HIV

21 January 2018

1 reference

Adenovirus-associated virus vector-mediated gene transfer in hemophilia B

21 January 2018

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In vivo genome editing restores haemostasis in a mouse model of haemophilia

21 January 2018

1 reference

Correction of a genetic disease in mouse via use of CRISPR-Cas9.

21 January 2018

1 reference

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

21 January 2018

1 reference

ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering

21 January 2018

1 reference

Cas9 as a versatile tool for engineering biology

21 January 2018

1 reference

Nonviral delivery of self-amplifying RNA vaccines

21 January 2018

1 reference

An unbiased genome-wide analysis of zinc-finger nuclease specificity

21 January 2018

1 reference

Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors

21 January 2018

1 reference

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24804755