(Q52423188)

English

Genome editing: a tool for research and therapy: towards a functional understanding of variants for molecular diagnostics using genome editing.

scientific article published in October 2014

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

Genome editing: a tool for research and therapy: towards a functional understanding of variants for molecular diagnostics using genome editing. (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

3

object named as

J Keith Joung

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

author name string

Shengdar Q Tsai

1

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

A John Iafrate

2

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

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publication date

1 October 2014

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

Nature Medicine

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Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

20

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

10

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

1103-1104

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

https://scigraph.springernature.com/pub.10.1038/nm.3722

0 references

Standardized decision support in next generation sequencing reports of somatic cancer variants

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

A method and server for predicting damaging missense mutations

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

Progress and challenges in genome-wide association studies in humans

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

CRISPR-Cas systems for editing, regulating and targeting genomes

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

DNA sequencing and CRISPR-Cas9 gene editing for target validation in mammalian cells

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

Dimeric CRISPR RNA-guided FokI nucleases for highly specific genome editing

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

Generation of mouse models of myeloid malignancy with combinatorial genetic lesions using CRISPR-Cas9 genome editing.

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

Optimized cell transplantation using adult rag2 mutant zebrafish.

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells

1 reference

https://api.crossref.org/works/10.1038%2FNM.3722

21 January 2018

Identifiers

10.1038/NM.3722

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 May 2018

http://europepmc.org/abstract/MED/25295940

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