Center for Stem Cell and Regenerative Medicine,
Brown Foundation Institute of Molecular Medicine,
Center for Stem Cell and Regenerative Medicine, Brown Foundation Institute of Molecular Medicine
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Unprecedented diversity of genotypic revertants in lymphocytes of a patient with Wiskott-Aldrich syndrome.
Blood May, 2008 | Pubmed ID: 18332229
Revertant somatic mosaicism in the Wiskott-Aldrich syndrome.
Immunologic research , 2009 | Pubmed ID: 19129986
Somatic mosaicism in the Wiskott-Aldrich syndrome: molecular and functional characterization of genotypic revertants.
Clinical immunology (Orlando, Fla.) Apr, 2010 | Pubmed ID: 20123155
Genetics. Mosaicism--switch or spectrum?
Science (New York, N.Y.) Oct, 2010 | Pubmed ID: 20929800
New frontier in regenerative medicine: site-specific gene correction in patient-specific induced pluripotent stem cells.
Human gene therapy Jun, 2013 | Pubmed ID: 23675640
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
American journal of human genetics Feb, 2014 | Pubmed ID: 24507774
Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.
Circulation. Cardiovascular genetics Jun, 2014 | Pubmed ID: 24951659
Targeted correction and restored function of the CFTR gene in cystic fibrosis induced pluripotent stem cells.
Stem cell reports Apr, 2015 | Pubmed ID: 25772471
Long-term expandable SOX9+ chondrogenic ectomesenchymal cells from human pluripotent stem cells.
Stem cell reports Apr, 2015 | Pubmed ID: 25818812
Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.
Stem cell reports Dec, 2015 | Pubmed ID: 26549847
Fixing stem cells via genome editing: hope for cystic fibrosis?
Regenerative medicine Jan, 2016 | Pubmed ID: 26680627
Gene Correction of iPSCs from a Wiskott-Aldrich Syndrome Patient Normalizes the Lymphoid Developmental and Functional Defects.
Stem cell reports 08, 2016 | Pubmed ID: 27396937
Homology Requirements for Efficient, Footprintless Gene Editing at the CFTR Locus in Human iPSCs with Helper-dependent Adenoviral Vectors.
Molecular therapy. Nucleic acids Oct, 2016 | Pubmed ID: 27727248
Increased susceptibility to Aβ toxicity in neuronal cultures derived from familial Alzheimer's disease (PSEN1-A246E) induced pluripotent stem cells.
Neuroscience letters 02, 2017 | Pubmed ID: 28034781
Prospective isolation of NKX2-1-expressing human lung progenitors derived from pluripotent stem cells.
The Journal of clinical investigation Jun, 2017 | Pubmed ID: 28463226
Differentiation of Human Pluripotent Stem Cells into Functional Lung Alveolar Epithelial Cells.
Cell stem cell 10, 2017 | Pubmed ID: 28965766
Long-Term Engraftment of ESC-Derived B-1 Progenitor Cells Supports HSC-Independent Lymphopoiesis.
Stem cell reports 03, 2019 | Pubmed ID: 30745034
Hemogenic Endothelial Cells Can Transition to Hematopoietic Stem Cells through a B-1 Lymphocyte-Biased State during Maturation in the Mouse Embryo.
Stem cell reports 07, 2019 | Pubmed ID: 31231025
Highly Efficient Gene Editing of Cystic Fibrosis Patient-Derived Airway Basal Cells Results in Functional CFTR Correction.
Molecular therapy : the journal of the American Society of Gene Therapy 07, 2020 | Pubmed ID: 32402246
Correction of Airway Stem Cells: Genome Editing Approaches for the Treatment of Cystic Fibrosis.
Human gene therapy 09, 2020 | Pubmed ID: 32741223
Derivation of Airway Basal Stem Cells from Human Pluripotent Stem Cells.
Cell stem cell 01, 2021 | Pubmed ID: 33098807
Stem Cells, Cell Therapies, and Bioengineering in Lung Biology and Disease 2019.
ERJ open research Oct, 2020 | Pubmed ID: 33123557
Differentiation of human pluripotent stem cells into functional airway basal stem cells.
STAR protocols 09, 2021 | Pubmed ID: 34355203
Targeted Gene Insertion for Functional CFTR Restoration in Airway Epithelium.
Frontiers in genome editing , 2022 | Pubmed ID: 35330693
GDF5+ chondroprogenitors derived from human pluripotent stem cells preferentially form permanent chondrocytes.
Development (Cambridge, England) Jun, 2022 | Pubmed ID: 35451016
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