The DOI matches its Crossref record; 38 of the 39 references it cites were found in a registry or an index.
Inhibition of mTOR induces a paused pluripotent state
Open accessAbstract
Cultured pluripotent stem cells are a cornerstone of regenerative medicine owing to their ability to give rise to all cell types of the body. Although pluripotent stem cells can be propagated indefinitely in vitro, pluripotency is paradoxically a transient state in vivo, lasting 2-3 days around the time of blastocyst implantation. The exception to this rule is embryonic diapause, a reversible state of suspended development triggered by unfavourable conditions. Diapause is a physiological reproductive strategy widely employed across the animal kingdom, including in mammals, but its regulation remains poorly understood. Here we report that the partial inhibition of mechanistic target of rapamycin (mTOR), a major nutrient sensor and promoter of growth, induces reversible pausing of mouse blastocyst development and allows their prolonged culture ex vivo. Paused blastocysts remain pluripotent and competent-able to give rise to embryonic stem (ES) cells and live, fertile mice. We show that both naturally diapaused blastocysts in vivo and paused blastocysts ex vivo display pronounced reductions in mTOR activity, translation, histone modifications associated with gene activity and transcription. Pausing can be induced directly in cultured ES cells and sustained for weeks without appreciable cell death or deviations from cell cycle distributions. We show that paused ES cells display a remarkable global suppression of transcription, maintain a gene expression signature of diapaused blastocysts and remain pluripotent. These results uncover a new pluripotent stem cell state corresponding to the epiblast of the diapaused blastocyst and indicate that mTOR regulates developmental timing at the peri-implantation stage. Our findings have implications in the fields of assisted reproduction, regenerative medicine, cancer, metabolic disorders and ageing.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Similar intermediate states have been described during embryonic development, where cells enter a paused, pluripotent state in response to environmental stress.62”
From Paneth-like transition drives resistance to dual targeting of KRAS and EGFR in colorectal cancer (2026) · cites this paper as [62]
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“For example, of the 131 cells that undergo apoptosis in C. elegans, the great majority (105) are neurons, thus highlighting the importance of PCD for CNS development.22”
From The lysosome and proteostatic stress at the intersection of pediatric neurological disorders and adult neurodegenerative diseases (2025) · cites this paper as [22]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Lysosomes are also important in apoptosis, a form of programmed cell death (PCD) that is requisite for the appropriate development of the mammalian nervous system.21,22.”
From The lysosome and proteostatic stress at the intersection of pediatric neurological disorders and adult neurodegenerative diseases (2025) · cites this paper as [22]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
KEGG: Kyoto Encyclopedia of Genes and Genomes
Kanehisa, M. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.1.27 · Cited by 37,077
KEGG: Kyoto Encyclopedia of Genes and Genomes
Ogata, H., Goto, S., Sato, K., Fujibuchi, W., Bono, H., & Kanehisa, M. (1999) · Nucleic Acids Research · doi:10.1093/nar/27.1.29 · Cited by 31,232
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351
Kim, D., Pertea, G., Trapnell, C., Pimentel, H., Kelley, R., & Salzberg, S. L. (2013) · Genome Biology · doi:10.1186/gb-2013-14-4-r36 · Cited by 12,668
Establishment in culture of pluripotential cells from mouse embryos
Evans, M. J., & Kaufman, M. H. (1981) · Nature · doi:10.1038/292154a0 · Cited by 8,623
CellProfiler: image analysis software for identifying and quantifying cell phenotypes
Carpenter, A. E., Jones, T. R., Lamprecht, M. R., Clarke, C., Kang, I. H., Friman, O., Guertin, D. A., Chang, J. H., Lindquist, R. A., Moffat, J., et al. (2006) · Genome biology · doi:10.1186/gb-2006-7-10-r100 · Cited by 5,212
mTOR: from growth signal integration to cancer, diabetes and ageing
Zoncu, R., Efeyan, A., & Sabatini, D. M. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3025 · Cited by 3,941
Gene Ontology Consortium: going forward
The Gene Ontology Consortium (2015) · Nucleic Acids Research · doi:10.1093/nar/gku1179 · Cited by 3,492
The ground state of embryonic stem cell self-renewal
Ying, Q.-L., Wray, J., Nichols, J., Batlle-Morera, L., Doble, B., Woodgett, J., Cohen, P., & Smith, A. (2008) · Nature · doi:10.1038/nature06968 · Cited by 3,442
Derivation of completely cell culture-derived mice from early-passage embryonic stem cells.
Nagy, A., Rossant, J., Nagy, R., Abramow-Newerly, W., & Roder, J. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.18.8424 · Cited by 2,328
Cited by
Sorted by citations
Items 101–200 of 291
The deubiquitinase Usp9x regulates PRC2-mediated chromatin reprogramming during mouse development
Macrae, T. A., & Ramalho‐Santos, M. (2021) · Nature Communications · doi:10.1038/s41467-021-21910-0 · Cited by 16
Self-citationdu Manoir, S., Delpech, H., Orsetti, B., Jacot, W., Pirot, N., Noel, J., Colombo, P., Sardet, C., & Theillet, C. G. (2022) · The Journal of Pathology · doi:10.1002/path.5896 · Cited by 19
Ribosomes: An Exciting Avenue in Stem Cell Research
Han, Z., Zhang, Q., Zhu, Y., Chen, J., & Li, W. (2020) · Stem Cells International · doi:10.1155/2020/8863539 · Cited by 19
Dormancy, Quiescence, and Diapause: Savings Accounts for Life
Ozguldez, H. O., & Bulut-Karslıoğlu, A. (2024) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-112122-022528 · Cited by 17
Suppression of ERK signalling promotes pluripotent epiblast in the human blastocyst
Simon, C. S., McCarthy, A., Woods, L. M., Staneva, D. P., Proks, M., Salehin, N., Lea, G., Huang, Q., Linneberg-Agerholm, M., Faulkner, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-61830-x · Cited by 24
The mTOR Pathway in Pluripotent Stem Cells: Lessons for Understanding Cancer Cell Dormancy
Alhasan, B. A., Gordeev, S. A., Knyazeva, A. R., Aleksandrova, K. V., Margulis, B. A., Guzhova, I. V., & Suvorova, I. I. (2021) · Membranes · doi:10.3390/membranes11110858 · Cited by 18
Metabolic regulation in pluripotent stem cells
Diamante, L., & Martello, G. (2022) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2022.101923 · Cited by 18
The mTORC1‐eIF4F axis controls paused pluripotency
Xu, X., Ahmed, T., Wang, L., Cao, X., Zhang, Z., Wang, M., Lv, Y., Kanwal, S., Tariq, M., Lin, R., et al. (2021) · EMBO Reports · doi:10.15252/embr.202153081 · Cited by 18
Nonninger, T. J., Mak, J., Gerisch, B., Ramponi, V., Kawamura, K., Ripa, R., Schilling, K., Latza, C., Kölschbach, J., Serrano, M., et al. (2025) · Nature Aging · doi:10.1038/s43587-025-00911-4 · Cited by 24
Aging by the clock and yet without a program
Meyer, D. H., Maklakov, A. A., & Schumacher, B. (2025) · Nature Aging · doi:10.1038/s43587-025-00975-2 · Cited by 20
Quiescence enables unrestricted cell fate in naive embryonic stem cells
Khoa, L. T. P., Yang, W., Shan, M., Zhang, L., Mao, F., Zhou, B. O., Li, Q., Malcore, R. M., Harris, C. E., Zhao, L., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-46121-1 · Cited by 17
Global Profiling of the Lysine Crotonylome in Different Pluripotent States
Lv, Y., Bu, C., Meng, J., Ward, C., Volpe, G., Hu, J., Jiang, M., Guo, L., Chen, J., Esteban, M. A., et al. (2021) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2021.01.004 · Cited by 16
Leucine and Arginine Availability Modulate Mouse Embryonic Stem Cell Proliferation and Metabolism
Correia, B., Sousa, M. I., Branco, A. F., Rodrigues, A. S., & Ramalho‐Santos, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232214286 · Cited by 16
Cellular response to moderate chromatin architectural defects promotes longevity
Yu, R., Sun, L., Sun, Y., Han, X., Qin, L., & Dang, W. (2019) · Science Advances · doi:10.1126/sciadv.aav1165 · Cited by 18
Sase, M., Sato, T., Sato, H., Miya, F., Zhang, S., Haeno, H., Kajita, M., Noguchi, T., Mori, Y., & Ohteki, T. (2024) · Developmental Cell · doi:10.1016/j.devcel.2024.10.007 · Cited by 17
On time: developmental timing within and across species
García‐Ojalvo, J., & Bulut-Karslıoğlu, A. (2023) · Development · doi:10.1242/dev.201045 · Cited by 16
Review: Embryonic diapause in the European roe deer – slowed, but not stopped
Rüegg, A. B., & Ulbrich, S. E. (2023) · animal · doi:10.1016/j.animal.2023.100829 · Cited by 16
Unveiling the role of cellular dormancy in cancer progression and recurrence
Collignon, É. (2024) · Current Opinion in Oncology · doi:10.1097/cco.0000000000001013 · Cited by 16
Metabolic characterization of a paused-like pluripotent state
Sousa, M. I., Correia, B., Rodrigues, A. S., & Ramalho‐Santos, J. (2020) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2020.129612 · Cited by 16
Survival of salivary gland cancer stem cells requires mTOR signaling
de Andrade, N. P., Warner, K. A., Zhang, Z., Pearson, A. T., Mantesso, A., Guimarães, D. M., ALTEMANI, A. M. D. A. M., Mariano, F. V., Nunes, F. D., & Nor, J. E. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03391-7 · Cited by 16
Bora, P., Gahurová, L., Hauserová, A., Bohuslavová, M., Collier, R., Potěšil, D., Zdráhal, Z., & Bruce, A. W. (2021) · Open Biology · doi:10.1098/rsob.210092 · Cited by 16
Propagating pluripotency – The conundrum of self‐renewal
Smith, A. G. (2024) · BioEssays · doi:10.1002/bies.202400108 · Cited by 14
Lee, S. J., Kang, K., Kim, J.-H., Lee, B., Jung, J., Park, Y., Hong, S., & Kim, B. (2019) · Stem Cells and Development · doi:10.1089/scd.2019.0188 · Cited by 15
Cell Populations Expressing Stemness-Associated Markers in Vascular Anomalies
Kilmister, E. J., Hansen, L., Davis, P. F., Hall, S. R. R., & Tan, S. T. (2021) · Frontiers in Surgery · doi:10.3389/fsurg.2020.610758 · Cited by 15
Bessonnard, S., Vandormael‐Pournin, S., Coqueran, S., Cohen‐Tannoudji, M., & Artus, J. (2019) · Stem Cells · doi:10.1002/stem.3008 · Cited by 15
A Novel mTOR Inhibitor; Anthracimycin for the Treatment of Human Hepatocellular Carcinoma
Hayashi, T., Yamashita, T., Okada, H., OISHI, N., Sunagozaka, H., Nio, K., Hayashi, T., Hara, Y., Asahina, Y., Yoshida, M., et al. (2017) · Anticancer Research · doi:10.21873/anticanres.11706 · Cited by 14
New functions for old factors: the role of polyamines during the establishment of pregnancy
Fenelon, J. C., & Murphy, B. D. (2018) · Reproduction Fertility and Development · doi:10.1071/rd18235 · Cited by 14
Heterogeneity in leukemia cells that escape drug-induced senescence-like state
Miller, D., Kerkhofs, K., Aghababazadeh, F. A., Madahar, S. S., Minden, M. D., Hébert, J., Haibe‐Kains, B., Bayfield, M. A., & Benchimol, S. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06015-4 · Cited by 13
Ma, C., Li, Q., Yang, Y., Ge, L., Cai, J., Wang, J., Zhu, M., Xiong, Y., Zhang, W., Xie, J., et al. (2023) · Cell & Bioscience · doi:10.1186/s13578-023-01176-3 · Cited by 13
Metabolomics reveals novel insight on dormancy of aquatic invertebrate encysted embryos
Rozema, E., Kierszniowska, S., Almog-Gabai, O., Wilson, E. G., Choi, Y. H., Verpoorte, R., Hamo, R., Caspi, V. C., Assaraf, Y. G., & Lubzens, E. (2019) · Scientific Reports · doi:10.1038/s41598-019-45061-x · Cited by 15
Epigenetic metabolites license stem cell states
Somasundaram, L., Levy, S., Hussein, A. M., Ehnes, D. D., Mathieu, J., & Ruohola‐Baker, H. (2020) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2020.02.003 · Cited by 12
Kilmister, E. J., & Tan, S. T. (2022) · Frontiers in Surgery · doi:10.3389/fsurg.2022.868187 · Cited by 13
Bora, P., Thamodaran, V., Šušor, A., & Bruce, A. W. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00276 · Cited by 13
Jentoft, I. M. A., & Schuh, M. (2025) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-101323-031045 · Cited by 13
Role of mTOR through Autophagy in Esophageal Cancer Stemness
Du, L., Wang, D., Nagle, P. W., Groen, A. H., Zhang, H., Muijs, C. T., Plukker, J. T. M., & Coppes, R. P. (2022) · Cancers · doi:10.3390/cancers14071806 · Cited by 12
Efficient cell chatting between embryo and uterus ensures embryo implantation
Deng, W., & Wang, H. (2022) · Biology of Reproduction · doi:10.1093/biolre/ioac135 · Cited by 13
Taslim, T. H., Hussein, A. M., Keshri, R., Ishibashi, J. R., Chan, T. C., Nguyen, B. N., Liu, S., Brewer, D. K., Harper, S., Lyons, S., et al. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.11.004 · Cited by 14
Jaber, M., Sebban, S., & Buganim, Y. (2017) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2017.06.012 · Cited by 12
Delay of human early development via in vitro diapausePreprint
Iyer, D. P., van der Weijden, V. A., Khoei, H. H., McCarthy, A., Rayón, T., Simon, C. S., Dunkel, I., Wamaitha, S. E., Elder, K. T., Snell, P., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.29.541316 · Cited by 14
Exploring and bypassing resistance to targeted therapies in colorectal cancer
Favier, S., Xiong, W., Chalabi-Dchar, M., Chettab, K., Piercey, O., Wu, T., Fenouil, T., Albaret, M.-A., Jordheim, L. P., Diaz, J.-J., et al. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118741 · Cited by 12
Hypertranscription: the invisible hand in stem cell biology
Kim, Y., Collignon, É., Martin, S.-B., & Ramalho‐Santos, M. (2024) · Trends in Genetics · doi:10.1016/j.tig.2024.08.005 · Cited by 11
Self-citationYang, X., Zhao, X., Zhao, Z., & Du, J. (2024) · BMC Biology · doi:10.1186/s12915-024-02000-1 · Cited by 11
The dynamics and functional impact of tRNA repertoires during early embryogenesis in zebrafish
Reimão-Pinto, M. M., Behrens, A., Forcelloni, S., Fröhlich, K., Shunji, K. A. Y. A., & Nedialkova, D. D. (2024) · The EMBO Journal · doi:10.1038/s44318-024-00265-4 · Cited by 11
Autophagy in reproduction and pregnancy-associated diseases
Singh, A., Perez, M. L., Kirsanov, O., Padilla‐Banks, E., & Guardia, C. M. A. (2024) · iScience · doi:10.1016/j.isci.2024.111268 · Cited by 14
Charting Developmental Dissolution of Pluripotency
Betschinger, J. (2016) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.12.017 · Cited by 11
Combinatorial metabolism drives the naive to primed pluripotent chromatin landscape
Ehnes, D. D., Hussein, A. M., Ware, C. B., Mathieu, J., & Ruohola‐Baker, H. (2020) · Experimental Cell Research · doi:10.1016/j.yexcr.2020.111913 · Cited by 12
The RNA helicase Ddx52 functions as a growth switch in juvenile zebrafish
Tseng, T.-L., Wang, Y.-T., Tsao, C.-Y., Ke, Y.-T., Lee, Y., Hsu, H., Poss, K. D., & Chen, C. (2021) · Development · doi:10.1242/dev.199578 · Cited by 11
Keller, A., Lei, Y., Krivec, N., de Deckersberg, E. C., Dziedzicka, D., Markouli, C., Sermon, K., Geens, M., & Spits, C. (2021) · doi:10.1101/2021.05.22.445238 · Cited by 10
Succinate as a New Actor in Pluripotency and Early Development?
Detraux, D., & Renard, P. (2022) · Metabolites · doi:10.3390/metabo12070651 · Cited by 11
Oxidative phosphorylation safeguards pluripotency via UDP-N-acetylglucosamine
Cao, J., Li, M., Liu, K., Shi, X.-X., Sui, N., Yao, Y., Wang, X., Li, S., Tian, Y., Tan, S., et al. (2022) · Protein & Cell · doi:10.1093/procel/pwac009 · Cited by 10
TET activity safeguards pluripotency throughout embryonic dormancy
Stötzel, M., Cheng, C.-Y., IIik, I. A., Kumar, A. S., Omgba, P. A., van der Weijden, V. A., Zhang, Y., Vingron, M., Meissner, A., Aktaş, T., et al. (2024) · Nature Structural & Molecular Biology · doi:10.1038/s41594-024-01313-7 · Cited by 11
Gahurová, L., Tománková, J., Cerna, P., Bora, P., Kubičková, M., Virnicchi, G., Kovačovicova, K. L., Potěšil, D., Hruška, P., Zdráhal, Z., et al. (2023) · Open Biology · doi:10.1098/rsob.230081 · Cited by 10
Proteostasis in cellular dormancy: lessons from yeast to oocytes
de Souza, S. R., Böke, E., & Zaffagnini, G. (2025) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2025.05.004 · Cited by 10
Epigenetic mechanisms in maternal-fetal crosstalk: inter- and trans-generational inheritance
Tisato, V., D’Aversa, E., Salvatori, F., Sbracia, M., Peluso, G., Scarpellini, F., & Gemmati, D. (2025) · Epigenomics · doi:10.1080/17501911.2025.2568369 · Cited by 11
From Intestinal Epithelial Homeostasis to Colorectal Cancer: Autophagy Regulation in Cellular Stress
Liu, Q.-L., Chen, Y., Zhou, L., Chen, H., & Zhou, Z. (2022) · Antioxidants · doi:10.3390/antiox11071308 · Cited by 9
Nutrient deprivation induces mouse embryonic diapause mediated by Gator1 and Tsc2
Ye, J. X., Xu, Y., Ren, Q., Liu, L., & Sun, Q. (2024) · Development · doi:10.1242/dev.202091 · Cited by 9
New insights into how to induce and maintain embryonic diapause in the blastocyst
Fenelon, J. C. (2024) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2024.102192 · Cited by 10
FOXO-like Gene Is Involved in the Regulation of 20E Pathway through mTOR in Eriocheir sinensis
Li, J., Ma, Y., Yang, Z., Wang, F., Li, J., Jiang, Y., Yang, D., Yi, Q., & Huang, S. (2023) · Journal of Marine Science and Engineering · doi:10.3390/jmse11061225 · Cited by 8
Oxytocin induces embryonic diapause
Minder, J. L., Winokur, S. B., Stephens, J., Tong, J., Cassel, N. L., Schuster, L., Issa, H. A., Cammer, M., Khatri, L., Moisan, G., et al. (2025) · Science Advances · doi:10.1126/sciadv.adt1763 · Cited by 8
The dual role of mTOR signaling in lung development and adult lung diseases
Bao, J., Bao, W., Song, Y., Li, Z., Kan, L., Fu, J., & Zhang, D. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01428-4 · Cited by 10
Selective Inhibition of mTORC1 Signaling Supports the Development and Maintenance of Pluripotency
Kim, J. K., Villa-Diaz, L. G., Saunders, T. L., Saul, R. P., Timilsina, S., Liu, F., Mishina, Y. M., & Krebsbach, P. H. (2023) · Stem Cells · doi:10.1093/stmcls/sxad079 · Cited by 10
Liu, X., Gao, L., Li, X., Liu, Y., Lou, X., Yang, M., Wu, W., & Liu, X. (2023) · Toxicology in Vitro · doi:10.1016/j.tiv.2023.105742 · Cited by 10
Hashimshony, T., Levin, L., Fröbius, A. C., Dahan, N., Caspi, V. C., Hamo, R., Almog-Gabai, O., Blais, I., Assaraf, Y. G., & Lubzens, E. (2024) · BMC Genomics · doi:10.1186/s12864-024-09961-1 · Cited by 9
Zhang, S., Wang, Z., Jiang, J., Feng, G., & Fan, S. (2024) · Food & Function · doi:10.1039/d3fo05422e · Cited by 8
Regulation of mRNA translation in stem cells; links to brain disorders
Statoulla, E., Chalkiadaki, K., Karozis, D., & Gkogkas, C. G. (2021) · Cellular Signalling · doi:10.1016/j.cellsig.2021.110166 · Cited by 8
ERG1 plays an essential role in rat cardiomyocyte fate decision by mediating AKT signaling
Wang, D., Liu, C., Liu, H., Meng, Y., Lin, F., Gu, Y., Wang, H., Shang, M., Tong, C., Sachinidis, A., et al. (2021) · Stem Cells · doi:10.1002/stem.3328 · Cited by 9
Li, M., Wang, X., He, W., & Zhou, H. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1586552 · Cited by 8
Epitranscriptomics as a Candidate Universal Modulator of Dormancy Transitions
Ahi, E. P. (2026) · Ecology and Evolution · doi:10.1002/ece3.73007 · Cited by 7
Metz, E. P., Wilder, P. J., Popay, T. M., Wang, J., Liu, Q., Kalluchi, A., Rowley, M. J., Tansey, W. P., & Rizzino, A. (2022) · Cancers · doi:10.3390/cancers14081946 · Cited by 7
Qin, Y., Ni, P., Zhang, Q., Wang, X., Du, X., Yin, Z., Wang, L., Ye, L., & Chen, L. (2022) · Development · doi:10.1242/dev.200527 · Cited by 7
Hiratsuka, D., Aikawa, S., Hirota, Y., Fukui, Y., Akaeda, S., Hiraoka, T., Matsuo, M., & Osuga, Y. (2022) · Reproductive Sciences · doi:10.1007/s43032-022-00988-x · Cited by 7
Zhou, P., Feng, F., Song, Y., Li, J., Li, Q., Xu, Z., Shi, J., Qin, L., He, F., Li, H., et al. (2022) · Materials & Design · doi:10.1016/j.matdes.2022.110762 · Cited by 7
Program freezing of diapausing embryos in the mouse
Amstislavsky, S. Y., Okotrub, S. V., Рожкова, И. Н., Rakhmanova, T., Igonina, T. N., Brusentsev, E. Y., Kozeneva, V. S., Lebedeva, D., Omelchenko, A. N., & Okotrub, K. A. (2024) · Theriogenology · doi:10.1016/j.theriogenology.2024.01.006 · Cited by 8
The Role of Nutrients in Maintaining Hematopoietic Stem Cells and Healthy Hematopoiesis for Life
Tadokoro, Y., & Hirao, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031574 · Cited by 11
Emerging roles of ribosome translation in stem cells and stem cell therapy - a review
Gao, Y., Guo, L., Shi, G., Wang, R., Wang, X., & Lou, J. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01412-y · Cited by 6
Using diapause as a platform to understand the biology of dormancy
Sweet, N. A., & Hu, C. (2025) · Open Biology · doi:10.1098/rsob.250104 · Cited by 6
Nuclear Dynamics in Quiescent Cells: Conserved Mechanisms from Yeasts to Mammals
Braun, S. J., Kilchert, C., Bulut-Karslıoğlu, A., Ruault, M., Taddei, A., Rabbani, F., & Wloch‐Salamon, D. (2026) · Biomolecules · doi:10.3390/biom16020203 · Cited by 9
Genome-scale transcriptome augmentation during Arabidopsis thaliana photomorphogenesis
Schivre, G., Wolff, L., Mirasole, F. M., Vidal, A., Davidson, M. L. H., Armanet, E., Dardalhon-Cuménal, D., Dumont, M., Bourge, M., Baroux, C., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-66359-7 · Cited by 6
The stem cell zoo for comparative studies of developmental tempo
Lázaro, J., Sochacki, J., & Ebisuya, M. (2024) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2023.102149 · Cited by 7
Stem metabolism: Insights from oncometabolism and vice versa
Rodrigues, A. S., Pereira, S. L., & Ramalho‐Santos, J. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.165760 · Cited by 6
EIF3D safeguards the homeostasis of key signaling pathways in human primed pluripotency
Okubo, C., Nakamura, M., Sato, M., Shichino, Y., Mito, M., Takashima, Y., Iwasaki, S., & Takahashi, K. (2025) · Science Advances · doi:10.1126/sciadv.adq5484 · Cited by 5
Temperature-induced embryonic diapause in chickens is mediated by PKC-NF-κB-IRF1 signaling
Ren, J., Hu, Z., Li, Q., Gu, S., Lan, F., Wang, X., Li, J., Li, J., Shao, L., Yang, N., et al. (2023) · BMC Biology · doi:10.1186/s12915-023-01550-0 · Cited by 6
Sutherland, L., Ruhe, M., Gattegno-Ho, D., Mann, K., Greaves, J., Koscielniak, M., Meek, S. E., Lu, Z. H., Waterfall, M., Taylor, R., et al. (2018) · Journal of Cell Science · doi:10.1242/jcs.222257 · Cited by 5
Lineage-specific CDK activity dynamics characterize early mammalian development
Saykali, B., Tran, A. D., Cornwell, J. A., Caldwell, M. A., Sangsari, P. R., Morgan, N. Y., Kruhlak, M. J., Cappell, S. D., & Ruiz, S. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115558 · Cited by 6
New directions to understand and learn from embryonic diapause in mammals
Comizzoli, P. (2020) · Bioscientifica Proceedings · doi:10.1530/biosciprocs.10.016 · Cited by 5
Ishibashi, J. R., Keshri, R., Taslim, T. H., Brewer, D. K., Chan, T. C., Lyons, S., McManamen, A. M., Chen, A., del Castillo, D., & Ruohola‐Baker, H. (2021) · Cells · doi:10.3390/cells10102771 · Cited by 5
Metabolic enhancement of mammalian developmental pausingPreprint
van der Weijden, V. A., Stötzel, M., Fauler, B., Iyer, D. P., Shahraz, M., Meierhofer, D., Rulands, S., Alexandrov, T., Mielke, T., & Bulut-Karslıoğlu, A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.22.504730 · Cited by 5
Iyer, D. P., Moyon, L., Ringeling, F. R., Cheng, C.-Y., Wittler, L., Canzar, S., Marsico, A., & Bulut-Karslıoğlu, A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.20.572612 · Cited by 5
Menchero, S., Barrington, C., Critcher, C., Varsally, W., Alanis‐Lobato, G., Niakan, K. K., & Turner, J. M. A. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.06.037 · Cited by 4
Sun, M. S., Martin, B., Dembska, J., Lyublinskaya, E., Deluz, C., & Suter, D. M. (2025) · Cell Systems · doi:10.1016/j.cels.2025.101456 · Cited by 4
mTORC1 activity suppresses ferroptosis through a SCARB1-dependent HDL-tocopherol uptake pathway
O’Loughlin, T. A., Stiles, J. S., Acharya, P., Arab, A., Goudy, L., Dai, R., Borah, A. A., Weiss, W. A., Medoh, U. N., & Gilbert, L. A. (2026) · Molecular Cell · doi:10.1016/j.molcel.2026.03.019 · Cited by 5
Zhou, X., Ren, Z., Xu, J., Deng, C., Zhang, Z., Godoy-Parejo, C., Xu, F., Huang, E. C. C., Wang, J., Cai, Z., et al. (2022) · International Journal of Biological Sciences · doi:10.7150/ijbs.71199 · Cited by 4
Peixoto, P. M. G., Bromfield, J. J., Ribeiro, E. S., Santos, J. E. P., Thatcher, W. W., & Bisinotto, R. S. (2023) · Journal of Dairy Science · doi:10.3168/jds.2023-23398 · Cited by 4
Reversible proliferative arrest induced by rapid depletion of RNase MRP
Liu, Y., He, S., Pyo, K., Franklin, R., Maaz, I. B., Cai, C., Shah, K., Cheloufi, S., Marzluff, W. F., & Murn, J. (2025) · Nature Communications · doi:10.1038/s41467-025-60471-4 · Cited by 3
Salilew‐Wondim, D., Hoelker, M., Held-Hoelker, E., Rings, F., Tholen, E., Große‐Brinkhaus, C., Schellander, K., Blaschka, C., Besenfelder, U., Havlicek, V., et al. (2024) · PLoS ONE · doi:10.1371/journal.pone.0298835 · Cited by 4
Lane-Donovan, C., Paredes, M., & Kao, A. W. (2025) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2025.102854 · Cited by 3
Putting mammalian early embryonic cells into dormancy
Iyer, D. P., Khoei, H. H., Rivron, N. C., & Bulut-Karslıoğlu, A. (2026) · Nature Protocols · doi:10.1038/s41596-025-01303-z · Cited by 3
Role of autophagy in embryogenesis
Tatsumi, T., & Tsukamoto, S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822003-0.00020-6 · Cited by 3
Selection and validation of reference genes for RT-qPCR normalization in dormant cancer cells
Iskhakova, E. R., Aleksandrova, K. V., & Suvorova, I. I. (2025) · Scientific Reports · doi:10.1038/s41598-025-02951-7 · Cited by 3
Diapause-like Drug-Tolerant Persister State: The Key to Nirvana Rebirth
Chen, H., & Jin, W. (2024) · Medicina · doi:10.3390/medicina60020228 · Cited by 3
Metadata
- Authors
- Bulut-Karslioglu, A., Biechele, S., Jin, H., Macrae, T. A., Hejna, M., Gertsenstein, M., Song, J. S., & Ramalho-Santos, M.
- Affiliations
- University of California, San Francisco (US)
- University of Illinois Urbana-Champaign (US)
- Toronto Centre for Phenogenomics (CA)
- Venue
- Nature
- Published
- 2016-11-23
- Volume
- 540
- Issue
- 7631
- Pages
- 119-123
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5143278
- OpenAlex
- W2553053943
- Cited by
- 283
- References
- 39
- Citations by year
- 2026: 17 · 2025: 40 · 2024: 37 · 2023: 32 · 2022: 32 · 2021: 42 · 2020: 23 · 2019: 27 · 2018: 17 · 2017: 14 · 2016: 2
- FWCI
- 10.40
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Science Foundation
- National Institutes of Health (R01OD012204)
- University of California, San Francisco
- National Cancer Institute (P30CA082103, R01CA163336)
- National Institute of General Medical Sciences (R01GM113014)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK063720)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Health Sciences › Medicine › Reproductive Medicine › Reproductive Biology and Fertility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- mTOR inhibition, delayed implantation, blastocyst development, pluripotency, epiblast, embryonic stem cells, long-term culture, transcriptional repression, histone modifications, peri-implantation development, developmental timing, assisted reproduction, regenerative medicine, rapamycin, mouse embryo, translational regulation, nutrient sensing
- MeSH terms
- Mouse Embryonic Stem Cells, Animals, Blastocyst, Cells, Cultured, Female, Germ Layers, Histones, Male, Transcription, Genetic, Protein Biosynthesis, Down-Regulation, Pluripotent Stem Cells, Embryonic Development, Mice, TOR Serine-Threonine Kinases, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review