Physiological Migration of Hematopoietic Stem and Progenitor Cells

Purification and Characterization of Mouse Hematopoietic Stem Cells

Spangrude, G. J., Heimfeld, S., & Weissman, I. L. (1988) · Science · doi:10.1126/science.2898810 · Cited by 2,889 · see citing works

A clonogenic common myeloid progenitor that gives rise to all myeloid lineages

Akashi, K., Traver, D., Miyamoto, T., & Weissman, I. L. (2000) · Nature · doi:10.1038/35004599 · Cited by 2,617 · see citing works

Purified hematopoietic stem cells can differentiate into hepatocytes in vivo

Lagasse, E., Connors, H., Al-Dhalimy, M., Reitsma, M., Dohse, M., Osborne, L., Wang, X., Finegold, M., Weissman, I. L., & Grompe, M. (2000) · Nature Medicine · doi:10.1038/81326 · Cited by 2,314 · see citing works

Turning Brain into Blood: A Hematopoietic Fate Adopted by Adult Neural Stem Cells in Vivo

Bjornson, C. R. R., Rietze, R. L., Reynolds, B. A., Magli, M. C., & Vescovi, A. L. (1999) · Science · doi:10.1126/science.283.5401.534 · Cited by 1,412 · see citing works

The long-term repopulating subset of hematopoietic stem cells is deterministic and isolatable by phenotype

Morrison, S. J., & Weissman, I. L. (1994) · Immunity · doi:10.1016/1074-7613(94)90037-x · Cited by 1,116 · see citing works

Hematopoietic potential of stem cells isolated from murine skeletal muscle

Jackson, K. A., Mi, T., & Goodell, M. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.25.14482 · Cited by 953 · see citing works

Evidence for Stem Cells in the Peripheral Blood of Mice

GOODMAN, J. W., & HODGSON, G. S. (1962) · Blood · doi:10.1182/blood.v19.6.702.702 · Cited by 469 · see citing works

Cyclophosphamide/granulocyte colony-stimulating factor induces hematopoietic stem cells to proliferate prior to mobilization

Morrison, S. J., Wright, D. E., & Weissman, I. L. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.5.1908 · Cited by 314 · see citing works

bcl-2 inhibits apoptosis of neutrophils but not their engulfment by macrophages.

Lagasse, E., & Weissman, I. L. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.3.1047 · Cited by 274 · see citing works

Primitive hemopoietic stem cells: direct assay of most productive populations by competitive repopulation with simple binomial, correlation and covariance calculations.

Harrison, D. E., Jordan, C. T., Zhong, R. K., & Astle, C. M. (1993) · PubMed · Cited by 273 · see citing works

An improved method of parabiosis

Bunster, E., & Meyer, R. K. (1933) · The Anatomical Record · doi:10.1002/ar.1090570404 · Cited by 222 · see citing works

Cyclophosphamide/granulocyte colony-stimulating factor causes selective mobilization of bone marrow hematopoietic stem cells into the blood after M phase of the cell cycle

Wright, D. E., Cheshier, S. H., Wagers, A. J., Randall, T. D., Christensen, J. L., & Weissman, I. L. (2001) · Blood · doi:10.1182/blood.v97.8.2278 · Cited by 208 · see citing works

Bone marrow transplantation: a review.

Thomas, E. D. (1999) · PubMed · Cited by 150 · see citing works

Steel factor influences the distribution and activity of murine hematopoietic stem cells in vivo.

Fleming, W., Alpern, E., Uchida, N., Ikuta, K., & Weissman, I. L. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.8.3760 · Cited by 124 · see citing works

Mobilization of early hematopoietic progenitor cells with BB-10010: a genetically engineered variant of human macrophage inflammatory protein- 1 alpha

Lord, B. I., Woolford, L. B., Wood, L. M., Czaplewski, L. G., McCourt, M., Hunter, M., & Edwards, R. (1995) · Blood · doi:10.1182/blood.v85.12.3412.bloodjournal85123412 · Cited by 114 · see citing works

Physiology of Inflammation

(2001) · Springer eBooks · doi:10.1007/978-1-4614-7512-5 · Cited by 88 · see citing works

Stable multilineage hematopoietic chimerism in alpha-thalassemic mice induced by a bone marrow subpopulation that excludes the majority of day-12 spleen colony-forming units

van der Loo, J., van den Bos, C., Baert, M., et al. (1994) · Blood · doi:10.1182/blood.v83.7.1769.1769 · Cited by 40 · see citing works

The spleen as a hematological organ

Spencer, R. P., & Pearson, H. A. (1975) · Seminars in Nuclear Medicine · doi:10.1016/s0001-2998(75)80007-9 · Cited by 27 · see citing works

Turnover of circulating hematopoietic stem cells.

Dorie, M. J., Maloney, M. A., & Patt, H. M. (1979) · PubMed · Cited by 25 · see citing works

Development of Monocytes, Macrophages, and Dendritic Cells

Geissmann, F., Manz, M. G., Jung, S., Sieweke, M. H., Merad, M., & Ley, K. (2010) · Science · doi:10.1126/science.1178331 · Cited by 3,049 · see citing works

The bone marrow niche for haematopoietic stem cells

Morrison, S. J., & Scadden, D. T. (2014) · Nature · doi:10.1038/nature12984 · Cited by 2,451 · see citing works

Local self-renewal can sustain CNS microglia maintenance and function throughout adult life

Ajami, B., Bennett, J. L., Krieger, C., Tetzlaff, W., & Rossi, F. M. V. (2007) · Nature Neuroscience · doi:10.1038/nn2014 · Cited by 1,643 · see citing works

Signals from the Sympathetic Nervous System Regulate Hematopoietic Stem Cell Egress from Bone Marrow

Katayama, Y., Battista, M., Kao, W.-M., Hidalgo, A., Peired, A. J., Thomas, S. A., & Frenette, P. S. (2006) · Cell · doi:10.1016/j.cell.2005.10.041 · Cited by 1,412 · see citing works

Clonal hematopoiesis in human aging and disease

Jaiswal, S., & Ebert, B. L. (2019) · Science · doi:10.1126/science.aan4673 · Cited by 1,156 · see citing works

Vascular and Neurogenic Rejuvenation of the Aging Mouse Brain by Young Systemic Factors

Katsimpardi, L., Litterman, N. K., Schein, P. A., Miller, C. M., Loffredo, F. S., Wojtkiewicz, G. R., Chen, J. W., Lee, R. T., Wagers, A. J., & Rubin, L. L. (2014) · Science · doi:10.1126/science.1251141 · Cited by 1,037 · see citing works

Growth Differentiation Factor 11 Is a Circulating Factor that Reverses Age-Related Cardiac Hypertrophy

Loffredo, F. S., Steinhauser, M. L., Jay, S. M., Gannon, J., Pancoast, J. R., Yalamanchi, P., Sinha, M., Dall’Osso, C., Khong, D., Shadrach, J. L., et al. (2013) · Cell · doi:10.1016/j.cell.2013.04.015 · Cited by 948 · see citing works

Emergency granulopoiesis

Manz, M. G., & Boettcher, S. (2014) · Nature Reviews Immunology · doi:10.1038/nri3660 · Cited by 855 · see citing works

Adult haematopoietic stem cell niches

Crane, G. M., Jeffery, E., & Morrison, S. J. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2017.53 · Cited by 712 · see citing works

Rejuvenation of Regeneration in the Aging Central Nervous System

Ruckh, J. M., Zhao, J.-W., Shadrach, J. L., van Wijngaarden, P., Rao, T. N., Wagers, A. J., & Franklin, R. J. M. (2012) · Cell Stem Cell · doi:10.1016/j.stem.2011.11.019 · Cited by 649 · see citing works

The Chemokine Receptor CX3CR1 Defines Three Antigen-Experienced CD8 T Cell Subsets with Distinct Roles in Immune Surveillance and Homeostasis

Gerlach, C., Moseman, E. A., Loughhead, S. M., Alvarez, D., Zwijnenburg, A. J., Waanders, L., Garg, R., de la Torre, J. C., & von Andrian, U. H. (2016) · Immunity · doi:10.1016/j.immuni.2016.10.018 · Cited by 567 · see citing works

MAIT cells are imprinted by the microbiota in early life and promote tissue repair

Constantinides, M. G., Link, V. M., Tamoutounour, S., Wong, A. C., Perez-Chaparro, P. J., Han, S.-J., Chen, Y. E., Li, K., Farhat, S., Weckel, A., et al. (2019) · Science · doi:10.1126/science.aax6624 · Cited by 567 · see citing works

A mucosal vaccine against <i>Chlamydia trachomatis</i> generates two waves of protective memory T cells

Stary, G., Olive, A., Radovic-Moreno, A. F., Gondek, D., Alvarez, D., Basto, P. A., Perro, M., Vrbanac, V. D., Tager, A. M., Shi, J., et al. (2015) · Science · doi:10.1126/science.aaa8205 · Cited by 379 · see citing works

Aged skeletal stem cells generate an inflammatory degenerative niche

Ambrosi, T. H., Marecic, O., McArdle, A., Sinha, R., Gulati, G. S., Tong, X., Wang, Y., Steininger, H. M., Hoover, M. Y., Koepke, L. S., et al. (2021) · Nature · doi:10.1038/s41586-021-03795-7 · Cited by 392 · see citing works

Neutrophils at the crossroads of innate and adaptive immunity

Rosales, C. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.4mir0220-574rr · Cited by 372 · see citing works

Hoxb5 marks long-term haematopoietic stem cells and reveals a homogenous perivascular niche

Chen, J. Y., Miyanishi, M., Wang, S. K., Yamazaki, S., Sinha, R., Kao, K. S., Seita, J., Sahoo, D., Nakauchi, H., & Weissman, I. L. (2016) · Nature · doi:10.1038/nature16943 · Cited by 345 · see citing works

Chemokines in the systemic organization of immunity

Campbell, D. J., Kim, C. H., & Butcher, E. C. (2003) · Immunological Reviews · doi:10.1034/j.1600-065x.2003.00067.x · Cited by 330 · see citing works

Bone marrow-derived cells that populate the adult mouse brain preserve their hematopoietic identity

Vallières, L., & Sawchenko, P. E. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-12-05197.2003 · Cited by 245 · see citing works

In vivo tracking of human hematopoiesis reveals patterns of clonal dynamics during early and steady-state reconstitution phases

Biasco, L., Pellin, D., Scala, S., Dionisio, F., Basso-Ricci, L., Leonardelli, L., Scaramuzza, S., Baricordi, C., Ferrua, F., Cicalese, M. P., et al. (2016) · Cell stem cell · doi:10.1016/j.stem.2016.04.016 · Cited by 243 · see citing works

Tumor-associated fibroblasts predominantly come from local and not circulating precursors

Arina, A., Idel, C., Hyjek, E. M., Alegre, M.-L., Wang, Y., Bindokas, V. P., Weichselbaum, R. R., & Schreiber, H. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1600363113 · Cited by 238 · see citing works

Proliferation of parenchymal microglia is the main source of microgliosis after ischaemic stroke

Li, T., Pang, S., Yu, Y., Wu, X., Guo, J., & Zhang, S. (2013) · Brain · doi:10.1093/brain/awt287 · Cited by 199 · see citing works

A mouse model with high clonal barcode diversity for joint lineage, transcriptomic, and epigenomic profiling in single cells

Li, L., Bowling, S., McGeary, S. E., Yu, Q., Lemke, B., Alcedo, K., Jia, Y., Liu, X., Ferreira, M., Klein, A. M., et al. (2023) · Cell · doi:10.1016/j.cell.2023.09.019 · Cited by 167 · see citing works

Irradiation selects for p53-deficient hematopoietic progenitors.

Marusyk, A., Porter, C. C., Zaberezhnyy, V., & DeGregori, J. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000324 · Cited by 151 · see citing works

Bone-marrow-derived microglia: myth or reality?

Soulet, D., & Rivest, S. (2008) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2008.04.002 · Cited by 139 · see citing works

Multi-omic rejuvenation and lifespan extension on exposure to youthful circulation

Zhang, B., Lee, D. E., Trapp, A., Tyshkovskiy, A., Lu, A. T., Bareja, A., Kerepesi, C., McKay, L. K., Shindyapina, A. V., Dmitriev, S. E., et al. (2023) · Nature Aging · doi:10.1038/s43587-023-00451-9 · Cited by 134 · see citing works

Molecular Signatures of Quiescent, Mobilized and Leukemia-Initiating Hematopoietic Stem Cells

Forsberg, E. C., Passegué, E., Prohaska, S. S., Wagers, A. J., Koeva, M., Stuart, J. M., & Weissman, I. L. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008785 · Cited by 127 · see citing works

Origin and distribution of bone marrow-derived cells in the central nervous system in a mouse model of amyotrophic lateral sclerosis

Solomon, J. N., Lewis, C. B., Ajami, B., Corbel, S. Y., Rossi, F. M. V., & Krieger, C. (2006) · Glia · doi:10.1002/glia.20331 · Cited by 105 · see citing works

Metabolic regulation of somatic stem cells in vivo

Meacham, C. E., DeVilbiss, A. W., & Morrison, S. J. (2022) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00462-1 · Cited by 85 · see citing works

Cyclical mobilization and gated importation of thymocyte progenitors in the adult mouse: evidence for a thymus‐bone marrow feedback loop

Goldschneider, I. (2006) · Immunological Reviews · doi:10.1111/j.0105-2896.2006.00354.x · Cited by 51 · see citing works

Sleep disruption impairs haematopoietic stem cell transplantation in mice

Rolls, A., Pang, W. W., Ibarra, I., Colas, D., Bonnavion, P., Korin, B., Heller, H. C., Weissman, I. L., & de Lecea, L. (2015) · Nature Communications · doi:10.1038/ncomms9516 · Cited by 48 · see citing works

Endogenous resident c-Kit cardiac stem cells increase in mice with an exercise-induced, physiologically hypertrophied heart

Leite, C. F., Lopes, C. S., Alves, A. C., Fuzaro, C. S. C., Silva, M. V., Oliveira, L. F. D., Garcia, L. P., Farnesi, T. S., Cuba, M. B. D., Rocha, L. B., et al. (2015) · Stem Cell Research · doi:10.1016/j.scr.2015.05.011 · Cited by 23 · see citing works

Tcf7l1 is required for spinal cord progenitor maintenance

Kim, H., & Dorsky, R. I. (2011) · Developmental Dynamics · doi:10.1002/dvdy.22716 · Cited by 12 · see citing works

1015 – HUMAN HAEMATOPOIETIC STEM AND PROGENITOR CELL LANDSCAPES: LOCATION MATTERS

Laurenti, E., Bastos, H. P., & Mende, N. (2020) · Experimental Hematology · doi:10.1016/j.exphem.2020.09.014

Defining the contribution of Troy -positive progenitor cells to the mouse esophageal epitheliumPreprint

Grommisch, D., Wang, M., Eenjes, E., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.11.575258 · Cited by 1 · see citing works

Lifelong multilineage contribution by embryonic-born blood progenitors

Patel, S. H., Christodoulou, C., Weinreb, C., Yu, Q., da Rocha, E. L., Pepe-Mooney, B. J., Bowling, S., Li, L., Osorio, F. G., Daley, G. Q., et al. (2022) · Nature · doi:10.1038/s41586-022-04804-z · Cited by 170 · see citing works

Radioprotective effect of WR-2721 on haematopoiesis in mice. III. Changes in peripheral blood.

Macková, N., & Brezáni, P. (1988) · PubMed