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Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1

Marion G Ott
Manfred Schmidt
Manuel Grez
Research02 Apr 2006
Nature Medicine

Volume: 12, P: 401-409
CRISPR/Cas9-generated p47^phox-deficient cell line for Chronic Granulomatous Disease gene therapy vector development

Dominik Wrona
Ulrich Siler
Janine Reichenbach
ResearchOpen Access13 Mar 2017
Scientific Reports

Volume: 7, P: 1-6
Gene editing of NCF1 loci is associated with homologous recombination and chromosomal rearrangements

Simultaneous editing of the NCF1 and its pseudogenes in p47^phox-deficient chronic granulomatous disease is associated with homologous recombination and chromosomal rearrangements due to presence of multiple targets of high sequence similarity.

Federica Raimondi
Kah Mun Siow
Janine Reichenbach
ResearchOpen Access09 Oct 2024
Communications Biology

Volume: 7, P: 1-10
XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans

Dilafruz Juraeva
Jens Treutlein
Marcella Rietschel
Research18 Jul 2014
Neuropsychopharmacology

Volume: 40, P: 361-371
Signed outside: a surface marker system for transgenic cytoplasmic proteins

V Wohlgensinger
R Seger
U Siler
Research06 May 2010
Gene Therapy

Volume: 17, P: 1193-1199

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Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1

CRISPR/Cas9-generated p47^phox-deficient cell line for Chronic Granulomatous Disease gene therapy vector development

Gene editing of NCF1 loci is associated with homologous recombination and chromosomal rearrangements

XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans

Signed outside: a surface marker system for transgenic cytoplasmic proteins

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Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1

CRISPR/Cas9-generated p47phox-deficient cell line for Chronic Granulomatous Disease gene therapy vector development

Gene editing of NCF1 loci is associated with homologous recombination and chromosomal rearrangements

XRCC5 as a Risk Gene for Alcohol Dependence: Evidence from a Genome-Wide Gene-Set-Based Analysis and Follow-up Studies in Drosophila and Humans

Signed outside: a surface marker system for transgenic cytoplasmic proteins

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CRISPR/Cas9-generated p47^phox-deficient cell line for Chronic Granulomatous Disease gene therapy vector development