Brian Davis

Unprecedented diversity of genotypic revertants in lymphocytes of a patient with Wiskott-Aldrich syndrome.

Revertant somatic mosaicism in the Wiskott-Aldrich syndrome.

Somatic mosaicism in the Wiskott-Aldrich syndrome: molecular and functional characterization of genotypic revertants.

Genetics. Mosaicism--switch or spectrum?

New frontier in regenerative medicine: site-specific gene correction in patient-specific induced pluripotent stem cells.

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.

Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.

Targeted correction and restored function of the CFTR gene in cystic fibrosis induced pluripotent stem cells.

Long-term expandable SOX9+ chondrogenic ectomesenchymal cells from human pluripotent stem cells.

Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Fixing stem cells via genome editing: hope for cystic fibrosis?

Gene Correction of iPSCs from a Wiskott-Aldrich Syndrome Patient Normalizes the Lymphoid Developmental and Functional Defects.

Homology Requirements for Efficient, Footprintless Gene Editing at the CFTR Locus in Human iPSCs with Helper-dependent Adenoviral Vectors.

Increased susceptibility to Aβ toxicity in neuronal cultures derived from familial Alzheimer's disease (PSEN1-A246E) induced pluripotent stem cells.

Prospective isolation of NKX2-1-expressing human lung progenitors derived from pluripotent stem cells.

Differentiation of Human Pluripotent Stem Cells into Functional Lung Alveolar Epithelial Cells.

Long-Term Engraftment of ESC-Derived B-1 Progenitor Cells Supports HSC-Independent Lymphopoiesis.

Hemogenic Endothelial Cells Can Transition to Hematopoietic Stem Cells through a B-1 Lymphocyte-Biased State during Maturation in the Mouse Embryo.

Highly Efficient Gene Editing of Cystic Fibrosis Patient-Derived Airway Basal Cells Results in Functional CFTR Correction.

Correction of Airway Stem Cells: Genome Editing Approaches for the Treatment of Cystic Fibrosis.

Derivation of Airway Basal Stem Cells from Human Pluripotent Stem Cells.

Stem Cells, Cell Therapies, and Bioengineering in Lung Biology and Disease 2019.

Differentiation of human pluripotent stem cells into functional airway basal stem cells.

Targeted Gene Insertion for Functional CFTR Restoration in Airway Epithelium.

GDF5+ chondroprogenitors derived from human pluripotent stem cells preferentially form permanent chondrocytes.