Austin G. Smith
Affiliations: | Wellcome - MRC Cambridge Stem Cell Institute |
Google:
"Austin Smith"Mean distance: (not calculated yet)
Children
Sign in to add trainee| Balazs Viktor Varga | post-doc | 2008-2010 | Wellcome - MRC Cambridge Stem Cell Institute |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Agostinho de Sousa J, Wong CW, Dunkel I, et al. (2023) Epigenetic dynamics during capacitation of naïve human pluripotent stem cells. Science Advances. 9: eadg1936 |
| Ludwig TE, Andrews PW, Barbaric I, et al. (2023) ISSCR standards for the use of human stem cells in basic research. Stem Cell Reports. 18: 1744-1752 |
| Miroshnikova YA, Shahbazi MN, Negrete J, et al. (2023) Cell state transitions: catch them if you can. Development (Cambridge, England). 150 |
| Dattani A, Huang T, Liddle C, et al. (2022) Suppression of YAP safeguards human naïve pluripotency. Development (Cambridge, England) |
| Radley A, Corujo-Simon E, Nichols J, et al. (2022) Entropy sorting of single-cell RNA sequencing data reveals the inner cell mass in the human pre-implantation embryo. Stem Cell Reports |
| Huth M, Santini L, Galimberti E, et al. (2022) NMD is required for timely cell fate transitions by fine-tuning gene expression and regulating translation. Genes & Development. 36: 348-367 |
| Mulas C, Chaigne A, Smith A, et al. (2021) Cell state transitions: definitions and challenges. Development (Cambridge, England). 148 |
| Kinoshita M, Kobayashi T, Planells B, et al. (2021) Pluripotent stem cells related to embryonic disc exhibit common self-renewal requirements in diverse livestock species. Development (Cambridge, England). 148 |
| Kinoshita M, Barber M, Mansfield W, et al. (2021) Capture of Mouse and Human Stem Cells with Features of Formative Pluripotency. Cell Stem Cell. 28: 2180 |
| Kinoshita M, Li MA, Barber M, et al. (2021) Disabling de novo DNA methylation in embryonic stem cells allows an illegitimate fate trajectory. Proceedings of the National Academy of Sciences of the United States of America. 118 |