Stuart Chambers, Ph.D.
Affiliations: | Memorial Sloan-Kettering Cancer Center, Rockville Centre, NY, United States |
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"Stuart Chambers"Mean distance: 17.37 (cluster 32) | S | N | B | C | P |
Parents
Sign in to add mentor| Lorenz Studer | post-doc | 2008-2012 | Memorial Sloan-Kettering Cancer Center |
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Publications
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| Fasano CA, Chambers SM, Lee G, et al. (2023) Retraction Notice to: Efficient Derivation of Functional Floor Plate Tissue from Human Embryonic Stem Cells. Cell Stem Cell. 30: 905 |
| Yamazaki T, Liu L, Lazarev D, et al. (2019) Corrigendum: TCF3 alternative splicing controlled by hnRNP H/F regulates E-cadherin expression and hESC pluripotency. Genes & Development. 33: 733-736 |
| Cornacchia D, Zhang C, Zimmer B, et al. (2019) Lipid Deprivation Induces a Stable, Naive-to-Primed Intermediate State of Pluripotency in Human PSCs. Cell Stem Cell |
| Yamazaki T, Liu L, Lazarev D, et al. (2018) TCF3 alternative splicing controlled by hnRNP H/F regulates E-cadherin expression and hESC pluripotency. Genes & Development |
| Chambers SM, Mica Y, Lee G, et al. (2013) Dual-SMAD Inhibition/WNT Activation-Based Methods to Induce Neural Crest and Derivatives from Human Pluripotent Stem Cells. Methods in Molecular Biology (Clifton, N.J.) |
| Chambers SM, Tchieu J, Studer L. (2013) Build-a-brain. Cell Stem Cell. 13: 377-8 |
| Mica Y, Lee G, Chambers SM, et al. (2013) Modeling neural crest induction, melanocyte specification, and disease-related pigmentation defects in hESCs and patient-specific iPSCs. Cell Reports. 3: 1140-52 |
| Harel S, Tu EY, Weisberg S, et al. (2012) ZFX controls the self-renewal of human embryonic stem cells. Plos One. 7: e42302 |
| Chambers SM, Qi Y, Mica Y, et al. (2012) Combined small-molecule inhibition accelerates developmental timing and converts human pluripotent stem cells into nociceptors. Nature Biotechnology. 30: 715-20 |
| Balmer NV, Weng MK, Zimmer B, et al. (2012) Epigenetic changes and disturbed neural development in a human embryonic stem cell-based model relating to the fetal valproate syndrome. Human Molecular Genetics. 21: 4104-14 |