Pluripotent stem cell biology; disease modeling with human iPSCs; hPSC-derived organoids
Integrating collecting systems in human kidney organoids through fusion of distal nephron to ureteric bud. Cell Stem Cell. 2025; 32(7):1055-1070.e8.
Human pluripotent stem cell-derived organoids repair damaged bowel in vivo. Cell Stem Cell. 2024; 31(10):1513-1523.e7.
Protocol for establishing inducible CRISPR interference system for multiple-gene silencing in human pluripotent stem cells. STAR Protocols. 2024; 5(3):103221.
Protocol for establishing inducible CRISPRd system for blocking transcription factor-binding sites in human pluripotent stem cells. STAR Protocols. 2024; 5(3):103233.
Pioneer and PRDM transcription factors coordinate bivalent epigenetic states to safeguard cell fate. Molecular Cell. 2024; 84(3):476-489.e10.
Development of functional resident macrophages in human pluripotent stem cell-derived colonic organoids and human fetal colon. Cell Stem Cell. 2023; 30(11):1434-1451.e9.
iPSC-derived neural precursor cells engineering GBA1 recovers acid β-glucosidase deficiency and diminishes α-synuclein and neuropathology. Molecular Therapy: Methods & Clinical Development. 2023; 29:185-201.
A review of protocols for brain organoids and applications for disease modeling. STAR Protocols. 2023; 4(1):101860.
Implementing Research Shared (Core) Facility Billing Systems. Journal of Biomolecular Techniques. 2022; 33(4).
Aggregation of cryopreserved mid-hindgut endoderm for more reliable and reproducible hPSC-derived small intestinal organoid generation. Stem Cell Reports. 2022; 17(8):1889-1902.
Christopher N. Mayhew, PhD7/28/2022