Research ArticleGene Therapy
A universal system to select gene-modified hepatocytes in vivo
- Sean Nygaard1,
- Adi Barzel2,
- Annelise Haft1,
- Angela Major3,
- Milton Finegold3,
- Mark A. Kay2 and
- Markus Grompe1,*
- 1Oregon Stem Cell Center, Oregon Health & Science University, Portland, OR 97239, USA.
- 2Departments of Pediatrics and Genetics, Stanford Medical School, Stanford, CA 94305, USA.
- 3Department of Pathology, Baylor College of Medicine, Houston, TX 77030, USA.
- ↵*Corresponding author. Email: grompem{at}ohsu.edu
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Science Translational Medicine 08 Jun 2016:
Vol. 8, Issue 342, pp. 342ra79
DOI: 10.1126/scitranslmed.aad8166
Vol. 8, Issue 342, pp. 342ra79
DOI: 10.1126/scitranslmed.aad8166
Sean Nygaard
Oregon Stem Cell Center, Oregon Health & Science University, Portland, OR 97239, USA.
Adi Barzel
Departments of Pediatrics and Genetics, Stanford Medical School, Stanford, CA 94305, USA.
Annelise Haft
Oregon Stem Cell Center, Oregon Health & Science University, Portland, OR 97239, USA.
Angela Major
Department of Pathology, Baylor College of Medicine, Houston, TX 77030, USA.
Milton Finegold
Department of Pathology, Baylor College of Medicine, Houston, TX 77030, USA.
Mark A. Kay
Departments of Pediatrics and Genetics, Stanford Medical School, Stanford, CA 94305, USA.
Markus Grompe
Oregon Stem Cell Center, Oregon Health & Science University, Portland, OR 97239, USA.
