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Author Details
Full Name
Matthew H Porteus
Affiliation
Stanford University
ORCID
Career Start Year
1984
Papers
173
H Index
61
Expertise
CM4AI Collaborator
Prashant Mali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37537500
High-efficiency transgene integration by homology-directed repair in human primary cells using DNA-PKcs inhibition.
Nat Biotechnol
2024
38019608
Small-molecule correctors divert CFTR-F508del from ERAD by stabilizing sequential folding states.
Mol Biol Cell
2024
36793210
Comparative analysis of CRISPR off-target discovery tools following ex vivo editing of CD34<sup>+</sup> hematopoietic stem and progenitor cells.
Mol Ther
2023
37745470
Small molecule correctors divert CFTR-F508del from ERAD by stabilizing sequential folding states.
bioRxiv
2023
37773046
Epitope-engineered human hematopoietic stem cells are shielded from CD123-targeted immunotherapy.
J Exp Med
2023
38091985
iPSC-derived hypoimmunogenic tissue resident memory TÂ cells mediate robust anti-tumor activity against cervical cancer.
Cell Rep Med
2023
37637384
Molecular dynamics of genome editing with CRISPR-Cas9 and rAAV6 virus in human HSPCs to treat sickle cell disease.
Mol Ther Methods Clin Dev
2023
36685559
CRISPR-Cas9-AAV versus lentivector transduction for genome modification of X-linked severe combined immunodeficiency hematopoietic stem cells.
Front Immunol
2023
34735685
Treatment decision-making in sickle cell disease patients.
J Community Genet
2022
35773054
A Curative DNA Code for Hematopoietic Defects: Novel Cell Therapies for Monogenic Diseases of the Blood and Immune System.
Hematol Oncol Clin North Am
2022
35738284
Generating human artery and vein cells from pluripotent stem cells highlights the arterial tropism of Nipah and Hendra viruses.
Cell
2022
35763671
Reengineering Ponatinib to Minimize Cardiovascular Toxicity.
Cancer Res
2022
35414059
Author Correction: Investigation of Cas9 antibodies in the human eye.
Nat Commun
2022
35953477
Ultra-deep sequencing validates safety of CRISPR/Cas9 genome editing in human hematopoietic stem and progenitor cells.
Nat Commun
2022
33794364
Targeted replacement of full-length CFTR in human airway stem cells by CRISPR-Cas9 for pan-mutation correction in the endogenous locus.
Mol Ther
2022
35227602
Design of experiments as a decision tool for cell therapy manufacturing.
Cytotherapy
2022
35217666
Investigation of Cas9 antibodies in the human eye.
Nat Commun
2022
34973360
Hematopoietic stem cell gene editing and expansion: State-of-the-art technologies and recent applications.
Exp Hematol
2022
32241852
Genome editing of donor-derived T-cells to generate allogenic chimeric antigen receptor-modified T cells: Optimizing αβ T cell-depleted haploidentical hematopoietic stem cell transplantation.
Haematologica
2021
33623984
Enhanced homology-directed repair for highly efficient gene editing in hematopoietic stem/progenitor cells.
Blood
2021
33737751
Gene replacement of α-globin with β-globin restores hemoglobin balance in β-thalassemia-derived hematopoietic stem and progenitor cells.
Nat Med
2021
33712802
Correction of X-CGD patient HSPCs by targeted CYBB cDNA insertion using CRISPR/Cas9 with 53BP1 inhibition for enhanced homology-directed repair.
Gene Ther
2021
33678249
Improved Genome Editing through Inhibition of FANCM and Members of the BTR Dissolvase Complex.
Mol Ther
2021
33650026
Gene Editing Rescues In vitro T Cell Development of RAG2-Deficient Induced Pluripotent Stem Cells in an Artificial Thymic Organoid System.
J Clin Immunol
2021
33514718
Cas9-AAV6 gene correction of beta-globin in autologous HSCs improves sickle cell disease erythropoiesis in mice.
Nat Commun
2021
33821398
Correction to: Gene Editing Rescues in Vitro T Cell Development of RAG2-Deficient Induced Pluripotent Stem Cells in an Artificial Thymic Organoid System.
J Clin Immunol
2021
33609734
Correction of recessive dystrophic epidermolysis bullosa by homology-directed repair-mediated genome editing.
Mol Ther
2021
34485608
Clinically relevant gene editing in hematopoietic stem cells for the treatment of pyruvate kinase deficiency.
Mol Ther Methods Clin Dev
2021
34122418
Answered and Unanswered Questions in Early-Stage Viral Vector Transduction Biology and Innate Primary Cell Toxicity for <i>Ex-Vivo</i> Gene Editing.
Front Immunol
2021
34232639
An Unusual "OR" Gate for Allosteric Regulation of Mammalian Transglutaminase 2 in the Extracellular Matrix.
J Am Chem Soc
2021
34135108
Development of β-globin gene correction in human hematopoietic stem cells as a potential durable treatment for sickle cell disease.
Sci Transl Med
2021
33427035
Safe and Effective <i>In Vivo</i> Targeting and Gene Editing in Hematopoietic Stem Cells: Strategies for Accelerating Development.
Hum Gene Ther
2021
33075720
The Binns Program for Cord Blood Research: A novel model of cord blood banking for academic biomedical research.
Placenta
2021
33473139
The TRACE-Seq method tracks recombination alleles and identifies clonal reconstitution dynamics of gene targeted human hematopoietic stem cells.
Nat Commun
2021
31513279
Early Tacrolimus Concentrations After Lung Transplant Are Predicted by Combined Clinical and Genetic Factors and Associated With Acute Kidney Injury.
Clin Pharmacol Ther
2020
31839569
High-Efficiency, Selection-free Gene Repair in Airway Stem Cells from Cystic Fibrosis Patients Rescues CFTR Function in Differentiated Epithelia.
Cell Stem Cell
2020
33136125
CD34 expression does not correlate with immunophenotypic stem cell or progenitor content in human cord blood products.
Blood Adv
2020
33273741
Generation of human striatal organoids and cortico-striatal assembloids from human pluripotent stem cells.
Nat Biotechnol
2020
32661439
Metabolic engineering generates a transgene-free safety switch for cell therapy.
Nat Biotechnol
2020
32991838
Loss of Extreme Long-Range Enhancers in Human Neural Crest Drives a Craniofacial Disorder.
Cell Stem Cell
2020
32820153
Author Correction: Engineering monocyte/macrophage-specific glucocerebrosidase expression in human hematopoietic stem cells using genome editing.
Nat Commun
2020
32620863
Engineering monocyte/macrophage-specific glucocerebrosidase expression in human hematopoietic stem cells using genome editing.
Nat Commun
2020
32989314
Neuronal defects in a human cellular model of 22q11.2 deletion syndrome.
Nat Med
2020
32355868
DNA Barcoding in Nonhuman Primates Reveals Important Limitations in Retrovirus Integration Site Analysis.
Mol Ther Methods Clin Dev
2020
32494707
CRISPR-based gene editing enables <i>FOXP3</i> gene repair in IPEX patient cells.
Sci Adv
2020
32483127
Improving the safety of human pluripotent stem cell therapies using genome-edited orthogonal safeguards.
Nat Commun
2020
32424320
Cas9-AAV6-engineered human mesenchymal stromal cells improved cutaneous wound healing in diabetic mice.
Nat Commun
2020
32531238
Macrophage Subpopulation Dynamics Shift following Intravenous Infusion of Mesenchymal Stromal Cells.
Mol Ther
2020
30692695
Identification of preexisting adaptive immunity to Cas9 proteins in humans.
Nat Med
2019
31836708
Functional significance of U2AF1 S34F mutations in lung adenocarcinomas.
Nat Commun
2019
1 - 50 of 173
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Morgan L Maeder
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Center for Cancer Research, National Cancer Institute, National Institutes of Health
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Vivien A Sheehan
Co-authored papers
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Jayakar V Nayak
Co-authored papers
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Linzhao Cheng
Johns Hopkins University School of Medicine
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Thomas J Montine
Stanford University
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James A Olzmann
Co-authored papers
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Benjamin P Kleinstiver
Center for Genomic Medicine, Massachusetts General Hospital
Co-authored papers
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Hanns Lochm??ller
Children's Hospital of Eastern Ontario Research Institute
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John A Stamatoyannopoulos
Altius Institute for Biomedical Sciences
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Diego Borges-Rivera
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