Adult haematopoietic stem cell niches

Cytokine-mediated regulation of CXCR4 expression in human neutrophils

Nagase, H., Miyamasu, M., Yamaguchi, M., Imanishi, M., Tsuno, N. H., Matsushima, K., Yamamoto, K., Morita, Y., & Hirai, K. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.71.4.711 · Cited by 4,713

Mesenchymal and haematopoietic stem cells form a unique bone marrow niche

Méndez‐Ferrer, S., Michurina, T. V., Ferraro, F., Mazloom, A. R., MacArthur, B. D., Lira, S. A., Scadden, D. T., Ma’ayan, A., Enikolopov, G., & Frenette, P. S. (2010) · Nature · doi:10.1038/nature09262 · Cited by 3,381

SLAM Family Receptors Distinguish Hematopoietic Stem and Progenitor Cells and Reveal Endothelial Niches for Stem Cells

Kiel, M. J., Yilmaz, Ö. H., Iwashita, T., Yilmaz, O. H., Terhorst, C., & Morrison, S. J. (2005) · Cell · doi:10.1016/j.cell.2005.05.026 · Cited by 3,168

Progenitor cell trafficking is regulated by hypoxic gradients through HIF-1 induction of SDF-1

Ceradini, D. J., Kulkarni, A. R., Callaghan, M. J., Tepper, O. M., Bastidas, N., Kleinman, M. E., Capla, J. M., Galiano, R. D., Levine, J. P., & Gurtner, G. C. (2004) · Nature Medicine · doi:10.1038/nm1075 · Cited by 2,600

Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development

Zou, Y.-R., Kottmann, A. H., Kuroda, M., Taniuchi, I., & Littman, D. R. (1998) · Nature · doi:10.1038/31269 · Cited by 2,531

The bone marrow niche for haematopoietic stem cells

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

Maintenance of the Hematopoietic Stem Cell Pool by CXCL12-CXCR4 Chemokine Signaling in Bone Marrow Stromal Cell Niches

Sugiyama, T., Kohara, H., Noda, M., & Nagasawa, T. (2006) · Immunity · doi:10.1016/j.immuni.2006.10.016 · Cited by 2,419

Defects of B-cell lymphopoiesis and bone-marrow myelopoiesis in mice lacking the CXC chemokine PBSF/SDF-1

Nagasawa, T., Hirota, S., Tachibana, K., Takakura, N., Nishikawa, S.-I., Kitamura, Y., Yoshida, N., Kikutani, H., & Kishimoto, T. (1996) · Nature · doi:10.1038/382635a0 · Cited by 2,338

The relationship between the spleen colony-forming cell and the haemopoietic stem cell.

Schofield, R. (1978) · PubMed · Cited by 2,304

Self-renewing osteoprogenitors in bone marrow sinusoids can organize a hematopoietic microenvironment

Sacchetti, B., Funari, A., Michienzi, S., Di Cesare, S., Piersanti, S., Saggio, I., Tagliafico, E., Ferrari, S., Robey, P. G., Riminucci, M., et al. (2007) · Cell · doi:10.1016/j.cell.2007.08.025 · Cited by 2,226

Intercellular Interactions of an Adipogenic CXCL12-Expressing Stromal Cell Subset in Murine Bone Marrow

Matsushita, Y., Chu, A. K. Y., Ono, W., Welch, J. D., & Ono, N. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4282 · Cited by 29

Exposure of the Bone Marrow Microenvironment to Simulated Solar and Galactic Cosmic Radiation Induces Biological Bystander Effects on Human Hematopoiesis

Almeida-Porada, G. D., Rodman, C., Kuhlman, B. M., Brudvik, E., Moon, J. H., George, S. K., Guida, P. M., Sajuthi, S. P., Langefeld, C. D., Walker, S. J., et al. (2018) · Stem Cells and Development · doi:10.1089/scd.2018.0005 · Cited by 30

Cadmium Activates Noncanonical Wnt Signaling to Impair Hematopoietic Stem Cell Function in Mice

Zhao, Y., Li, Q., Yang, Z., Shao, Y., Xue, P., Qu, W., Jia, X., Cheng, L., He, M., He, R., et al. (2018) · Toxicological Sciences · doi:10.1093/toxsci/kfy166 · Cited by 29

Cell-by-Cell Deconstruction of Stem Cell Niches

Tikhonova, A. N., Lasry, A., Austin, R. J., & Aifantis, I. (2020) · Cell stem cell · doi:10.1016/j.stem.2020.06.013 · Cited by 34

Getting blood out of a stone: Identification and management of patients with poor hematopoietic cell mobilization

Chen, J., Lazarus, H. M., Dahi, P. B., Avecilla, S. T., & Giralt, S. (2020) · Blood Reviews · doi:10.1016/j.blre.2020.100771 · Cited by 29

Endothelial cells: major players in acute myeloid leukaemia

Fodil, S., Arnaud, M., Vaganay, C., Puissant, A., Lengliné, É., Mooney, N., Itzykson, R., & Zafrani, L. (2022) · Blood Reviews · doi:10.1016/j.blre.2022.100932 · Cited by 29

Endogenous neural precursor cells in health and disease

Bacigaluppi, M., Sferruzza, G., Butti, E., Ottoboni, L., & Martino, G. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146619 · Cited by 29

Drosophila as a Model to Study Cellular Communication Between the Hematopoietic Niche and Blood Progenitors Under Homeostatic Conditions and in Response to an Immune Stress

Morin-Poulard, I., Tian, Y., Vanzo, N. F., & Crozatier, M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.719349 · Cited by 28

Approaches in Immunotherapy, Regenerative Medicine, and Bioengineering for Type 1 Diabetes

Kopan, C., Tucker, T. R., Alexander, M., Mohammadi, M. R., Pone, E. J., & Lakey, J. R. T. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01354 · Cited by 28

Pancreas organogenesis: The interplay between surrounding microenvironment(s) and epithelium-intrinsic factors

Cozzitorto, C., & Spagnoli, F. M. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2018.12.005 · Cited by 29

Bone Marrow Niches for Skeletal Progenitor Cells and their Inhabitants in Health and Disease

Herrmann, M., & Jakob, F. J. (2019) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x14666190123161447 · Cited by 28

Traditional and Advanced Cell Cultures in Hematopoietic Stem Cell Studies

Ribeiro-Filho, A. C., Levy, D., Ruiz, J. L. M., Mantovani, M. D. C., & Bydlowski, S. P. (2019) · Cells · doi:10.3390/cells8121628 · Cited by 28

Megakaryocyte in sepsis: the trinity of coagulation, inflammation and immunity

Hua, T., Yao, F.-H., Wang, H., Liu, W., Zhu, X., & Yongming, Y. (2024) · Critical Care · doi:10.1186/s13054-024-05221-6 · Cited by 27

Transplanted interleukin-4--secreting mesenchymal stromal cells show extended survival and increased bone mineral density in the murine femur

Lin, T., Pajarinen, J., Kohno, Y., Maruyama, M., Romero-López, M., Huang, J., Nathan, K., Khan, T. N., Yao, Z., & Goodman, S. B. (2018) · Cytotherapy · doi:10.1016/j.jcyt.2018.06.009 · Cited by 27

Development of Humanized Ossicles: Bridging the Hematopoietic Gap

Dupard, S. J., Grigoryan, A., Farhat, S., Coutu, D. L., & Bourgine, P. E. (2020) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2020.01.016 · Cited by 27

Indispensable role of Galectin-3 in promoting quiescence of hematopoietic stem cells

Jia, W., Kong, L., Kidoya, H., Naito, H., Muramatsu, F., Hayashi, Y., Hsieh, H., Yamakawa, D., Hsu, D. K., Liu, F., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22346-2 · Cited by 27

Recent Advancements in Poor Graft Function Following Hematopoietic Stem Cell Transplantation

Man, Y., Lu, Z., Yao, X., Gong, Y., Yang, T., & Wang, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.911174 · Cited by 27

Chemotherapy-induced niche perturbs hematopoietic reconstitution in B-cell acute lymphoblastic leukemia

Tang, C. S., Li, M., Chen, Y., Sun, H., Liu, S.-L., Zheng, W., Zhang, M., Li, H., Fu, W. E., Zhang, W., et al. (2018) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-018-0859-3 · Cited by 27

Endothelial mTOR maintains hematopoiesis during aging

Ramalingam, P., Poulos, M. G., Gutkin, M. C., Katsnelson, L., Freire, A. G., Lazzari, E., & Butler, J. M. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20191212 · Cited by 27

Inflammatory stromal and T cells mediate human bone marrow niche remodeling in clonal hematopoiesis and myelodysplasia

Prummel, K. D., Woods, K., Kholmatov, M. M., Schmitt, E. C., Vlachou, E. P., Labyadh, M., Wehner, R., Poschmann, G., Stühler, K., Winter, S., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-65803-y · Cited by 30

Rejuvenation of Tissue Stem Cells by Intrinsic and Extrinsic Factors

Cai, Y., Wang, S., Qu, J. T., Belmonte, J. C. I., & Liu, G. (2021) · Stem Cells Translational Medicine · doi:10.1093/stcltm/szab012 · Cited by 28

Heterocellular molecular contacts in the mammalian stem cell niche

Ceafalan, L. C., Enciu, A., Fertig, T. E., Popescu, B. O., Gherghiceanu, M., Hinescu, M. E., & Radu, E. (2018) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2018.07.001 · Cited by 26

Single-cell and spatial transcriptomics approaches of the bone marrow microenvironment

Al-Sabah, J., Baccin, C., & Haas, S. F. (2019) · Current Opinion in Oncology · doi:10.1097/cco.0000000000000602 · Cited by 28

Three-Dimensional Human Bone Marrow Organoids for the Study and Application of Normal and Abnormal Hematoimmunopoiesis

de Janon, A., Mantalaris, A., & Panoskaltsis, N. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2200836 · Cited by 26

The regulation of normal and neoplastic hematopoiesis is dependent on microenvironmental cells

Kaushansky, K., & Zhan, H. (2018) · Advances in Biological Regulation · doi:10.1016/j.jbior.2018.06.003 · Cited by 25

Extracellular Vesicles Derived From Adult and Fetal Bone Marrow Mesenchymal Stromal Cells Differentially Promote ex vivo Expansion of Hematopoietic Stem and Progenitor Cells

Ghebes, C. A., Morhayim, J., Kleijer, M., Koroglu, M., Erkeland, S. J., Hoogenboezem, R. M., Bindels, E. M., van Alphen, F. P. J., van den Biggelaar, M., Nolte, M. A., et al. (2021) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2021.640419 · Cited by 24

Diversity, localization, and (patho)physiology of mature lymphocyte populations in the bone marrow

Schürch, C. M., Caraccio, C., & Nolte, M. A. (2021) · Blood · doi:10.1182/blood.2020007592 · Cited by 26

Mitochondrial Ca2+ and cell cycle regulation

Zhao, H., & Pan, X. (2021) · International review of cytology · doi:10.1016/bs.ircmb.2021.02.015 · Cited by 24

Lipid metabolism in focus: how the build-up and breakdown of lipids affects stem cells

Madsen, S., Ramosaj, M., & Knobloch, M. (2021) · Development · doi:10.1242/dev.191924 · Cited by 24

Mesenchymal stem cells and cancer‐associated fibroblasts as a therapeutic strategy for breast cancer

Borzone, F. R., Giorello, M. B., Sanmartin, M. C., Yannarelli, G., Martinez, L. M., & Chasseing, N. A. (2022) · British Journal of Pharmacology · doi:10.1111/bph.15861 · Cited by 24

Splenic red pulp macrophages provide a niche for CML stem cells and induce therapy resistance

Bührer, E. D., Amrein, M. A., Forster, S., Isringhausen, S., Schürch, C. M., Bhate, S. S., Brodie, T. M., Zindel, J., Stroka, D., Sayed, M. A., et al. (2022) · Leukemia · doi:10.1038/s41375-022-01682-2 · Cited by 24

Mesenchymal stem cells gene signature in high‐risk myeloma bone marrow linked to suppression of distinct IGFBP2‐expressing small adipocytes

Mehdi, S. J., Johnson, S., Epstein, J., Zangari, M., Qu, P., Hoering, A., van Rhee, F., Schinke, C., Thanendrarajan, S., Barlogie, B., et al. (2018) · British Journal of Haematology · doi:10.1111/bjh.15669 · Cited by 24

The Periostin/Integrin-αv Axis Regulates the Size of Hematopoietic Stem Cell Pool in the Fetal Liver

Biswas, A., Roy, I. M., Babu, P., Manesia, J. K., Schouteden, S., Vijayakurup, V., Anto, R. J., Huelsken, J., Lacy‐Hulbert, A., Verfaillie, C. M., et al. (2020) · Stem Cell Reports · doi:10.1016/j.stemcr.2020.06.022 · Cited by 24

Histone methylation regulator PTIP is required to maintain normal and leukemic bone marrow niches

Das, P., Veazey, K. J., Van, H. T., Kaushik, S., Lin, K., Lu, Y., Ishii, M., Kikuta, J., Ge, K., Nussenzweig, A., et al. (2018) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1806019115 · Cited by 17

Imaging and spatial analysis of hematopoietic stem cell niches

Gomariz, Á., Isringhausen, S., Helbling, P. M., & Nombela‐Arrieta, C. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14184 · Cited by 23

Mechanoregulation in Hematopoiesis and Hematologic Disorders

Horton, P. D., Dumbali, S. P., & Wenzel, P. L. (2020) · Current Stem Cell Reports · doi:10.1007/s40778-020-00172-4 · Cited by 23

Understanding of the crosstalk between normal residual hematopoietic stem cells and the leukemic niche in acute myeloid leukemia

Batsivari, A., Grey, W., & Bonnet, D. A. (2021) · Experimental Hematology · doi:10.1016/j.exphem.2021.01.004 · Cited by 25

Hematopoietic progenitors polarize in contact with bone marrow stromal cells in response to SDF1

Bessy, T., Candelas, A., Souquet, B., Saadallah, K., Schaeffer, A., Vianay, B., Cuvelier, D., Gobaa, S., Nakid-Cordero, C., Lion, J., et al. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.202005085 · Cited by 23

Imaging methods used to study mouse and human HSC niches: Current and emerging technologies

Tjin, G., Figueroa, E. F., Duarte, D., Straszkowski, L., Scott, M., Khorshed, R., Purton, L. E., & Celso, C. L. (2018) · Bone · doi:10.1016/j.bone.2018.04.022 · Cited by 23

Tetraspanin Scaffold Proteins Function as Key Regulators of Hematopoietic Stem Cells

Balise, V. D., Reis, C. A. S., & Gillette, J. M. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00598 · Cited by 23

The role of immune cells settled in the bone marrow on adult hematopoietic stem cells

Xu, H., Li, Y., & Gao, Y. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05445-3 · Cited by 22

FLASH radiotherapy combined with immunotherapy: From biological mechanisms to blockbuster therapeutics

Wang, Y., Qi, S., Bi, N., & Li, Y. (2024) · Translational Oncology · doi:10.1016/j.tranon.2024.102183 · Cited by 22

The glycolytic enzyme PFKFB3 determines bone marrow endothelial progenitor cell damage after chemotherapy and irradiation

Lyu, Z., Tang, S.-Q., Xing, T., Zhou, Y., Lv, M., Fu, H., Wang, Y., Xu, L., Zhang, X., Lee, H., et al. (2022) · Haematologica · doi:10.3324/haematol.2021.279756 · Cited by 22

Megakaryocytes as the Regulator of the Hematopoietic Vascular Niche

Zhan, H., & Kaushansky, K. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.912060 · Cited by 23

The emergence of the calvarial hematopoietic niche in health and disease

Mills, W. A., Coburn, M., & Eyo, U. B. (2022) · Immunological Reviews · doi:10.1111/imr.13120 · Cited by 23

Exosomes: A New Hope for Angiogenesis-Mediated Bone Regeneration

Lange, M., Babczyk, P., & Tobiasch, E. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25105204 · Cited by 22

Autophagy in endothelial cells regulates their haematopoiesis-supporting ability

Lyu, Z., Cao, X.-N., Wen, Q., Mo, X., Zhao, H., Chen, Y., Wang, Y., Chang, Y., Xu, L., Zhang, X., et al. (2020) · EBioMedicine · doi:10.1016/j.ebiom.2020.102677 · Cited by 22

Bone Marrow Micro‐Environment in Normal and Deranged Hematopoiesis: Opportunities for Regenerative Medicine and Therapies

Sarkaria, S. M., Decker, M., & Ding, L. (2018) · BioEssays · doi:10.1002/bies.201700190 · Cited by 22

Molecular mechanism of bone metastasis in breast cancer

Sui, L., Wang, J., Jiang, W. G., Song, X., & Ye, L. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1401113 · Cited by 23

ASCs and their role in obesity and metabolic diseases

Milan, G., Conci, S., Sanna, M., Favaretto, F., Bettini, S., & Vettor, R. (2021) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2021.09.001 · Cited by 22

A rare subgroup of leukemia stem cells harbors relapse-inducing potential in acute lymphoblastic leukemia

Senft, D., & Jeremias, I. (2018) · Experimental Hematology · doi:10.1016/j.exphem.2018.09.006 · Cited by 23

The nuclear receptor corepressor NCoR1 regulates hematopoiesis and leukemogenesis in vivo

Wan, X., Liu, L., Zhou, P., Hui, X., He, Q., Yu, F., Zhang, W., Ding, X., Yuan, X., Zhang, N., et al. (2019) · Blood Advances · doi:10.1182/bloodadvances.2018022756 · Cited by 21

Induction of in Vivo Ectopic Hematopoiesis by a Three-Dimensional Structured Extracellular Matrix Derived from Decellularized Cancellous Bone

Nakamura, N., Kimura, T., Nam, K., Fujisato, T., Iwata, H., Tsuji, T., & Kishida, A. (2019) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.8b01491 · Cited by 21

Stabilizing hematopoietic stem cells in vitro

Wilkinson, A. C., & Nakauchi, H. (2020) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2020.05.035 · Cited by 21

Novel Approaches to Target Mutant FLT3 Leukaemia

Müller, J. P., & Schmidt‐Arras, D. (2020) · Cancers · doi:10.3390/cancers12102806 · Cited by 21

Membrane-bound SCF and VCAM-1 synergistically regulate the morphology of hematopoietic stem cells

Hao, J., Zhou, H., Nemes, K., Yen, D. P., Zhao, W., Bramlett, C. S., Wang, B., Lu, R., & Shen, K. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.202010118 · Cited by 21

Oncostatin M regulates hematopoietic stem cell (HSC) niches in the bone marrow to restrict HSC mobilization

Bisht, K., McGirr, C., Lee, S.-Y., Tseng, H., Fleming, W., Alexander, K. A., Matsumoto, T., Barbier, V., Sims, N. A., Müller‐Newen, G., et al. (2021) · Leukemia · doi:10.1038/s41375-021-01413-z · Cited by 22

Inhibition of TGFβ improves hematopoietic stem cell niche and ameliorates cancer-related anemia

Wang, B., Wang, Y., Chen, H., Yao, S., Lai, X., Qiu, Y., Cai, J., Huang, Y., Wei, X., Guan, Y., et al. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-02120-9 · Cited by 20

Lead in Synergism With IFNγ Acts on Bone Marrow-Resident Macrophages to Increase the Quiescence of Hematopoietic Stem Cells

Zhao, Y., Li, Q., Zhu, T., He, J., Xue, P., Zheng, W., Yao, Y., Qu, W., Zhou, Z., Lu, R., et al. (2021) · Toxicological Sciences · doi:10.1093/toxsci/kfab001 · Cited by 20

LepR+ niche cell–derived AREG compromises hematopoietic stem cell maintenance under conditions of DNA repair deficiency and aging

Wu, L., Lin, Q., Chatla, S., Amarachintha, S. P., Wilson, A. F., Atale, N., Gao, Z. J., Joseph, J., Wolff, E. V., & Du, W. (2023) · Blood · doi:10.1182/blood.2022018212 · Cited by 20

Time for revival of the red blood cell count and red cell mass in the differential diagnosis between essential thrombocythemia and polycythemia vera?

Hasselbalch, H. C. (2019) · Haematologica · doi:10.3324/haematol.2019.229039 · Cited by 20

Mouse Spermatogenesis Reflects the Unity and Diversity of Tissue Stem Cell Niche SystemsPreprint

Yoshida, S. (2020) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a036186 · Cited by 20

Mesenchymal stromal cells, metabolism, and mitochondrial transfer in bone marrow normal and malignant hematopoiesis

Singh, A. K., Prasad, P., & Cancelas, J. A. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1325291 · Cited by 21

The Influence of Metabolic Risk Factors on the Inflammatory Response Triggered by Myocardial Infarction: Bridging Pathophysiology to Treatment

Ramos-Regalado, L., Alcover, S., Badimón, L., & Vilahur, G. (2024) · Cells · doi:10.3390/cells13131125 · Cited by 19

Bone marrow microenvironment drives AML cell OXPHOS addiction and AMPK inhibition to resist chemotherapy

You, R., Hou, D., Wang, B., Liu, J., Wang, X., Xiao, Q., Pan, Z., Li, D., Feng, X., Kang, L., et al. (2021) · Journal of Leukocyte Biology · doi:10.1002/jlb.6a0821-409rr · Cited by 21

Mesenchymal stromal cells improve the transplantation outcome of CRISPR-Cas9 gene-edited human HSPCs

Crippa, S., Conti, A., Vavassori, V., Ferrari, S., Beretta, S., Rivis, S., Bosotti, R., Scala, S., Pirroni, S., Hernández, R. J., et al. (2022) · Molecular Therapy · doi:10.1016/j.ymthe.2022.08.011 · Cited by 19

A mechanosensitive vascular niche for Drosophila hematopoiesis

Tian, Y., Morin-Poulard, I., Liu, X., Vanzo, N. F., & Crozatier, M. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2217862120 · Cited by 20

Tumor-derived interleukin-1α and leukemia inhibitory factor promote extramedullary hematopoiesis

Barisas, D. A. G., Kim, M., Subramanian, M., Kabir, A. U., Krchma, K., Wu, J., Zinselmeyer, B. H., Stewart, C. L., & Choi, K. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3001746 · Cited by 19

Genistin: A Novel Estrogen Analogue Targeting ERβ to Alleviate Thrombocytopenia

Tang, X., Liao, R., Zhou, L. H., Yi, T., Ran, M., Luo, J., Huang, F., Wu, A., Mei, Q., Wang, L., et al. (2024) · International Journal of Biological Sciences · doi:10.7150/ijbs.90483 · Cited by 19

Transforming the Niche: The Emerging Role of Extracellular Vesicles in Acute Myeloid Leukaemia Progression

Mendes, M., Monteiro, A. C., Neto, E., Barrias, C. C., Simões, M. S., Duarte, D., & Caires, H. R. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084430 · Cited by 19

“Cell-Free Therapeutics” from Components Secreted by Mesenchymal Stromal Cells as a Novel Class of Biopharmaceuticals

Sagaradze, G. D., Nimiritsky, P., Akopyan, Z. A., Макаревич, П. И., & Efimenko, A. Y. (2018) · InTech eBooks · doi:10.5772/intechopen.78605 · Cited by 19

Evolutionary perspective on the hematopoietic system through a colonial chordate: allogeneic immunity and hematopoiesis

Rosental, B., Raveh, T., Voskoboynik, A., & Weissman, I. L. (2020) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.12.006 · Cited by 19

Commensal oral microbiota induces osteoimmunomodulatory effects separate from systemic microbiome in mice

Hathaway‐Schrader, J. D., Aartun, J. D., Poulides, N. A., Kuhn, M. B., McCormick, B. E., Chew, M. E., Huang, E., Darveau, R. P., Westwater, C., & Novince, C. M. (2022) · JCI Insight · doi:10.1172/jci.insight.140738 · Cited by 19

Loss of EfnB1 in the osteogenic lineage compromises their capacity to support hematopoietic stem/progenitor cell maintenance

Arthur, A., Nguyen, T. M., Paton, S., Zannettino, A. C. W., & Gronthos, S. (2018) · Experimental Hematology · doi:10.1016/j.exphem.2018.10.004 · Cited by 19

Stem cell homeostasis by integral feedback through the niche

Becker, N. B., Günther, M., Li, C., Jolly, A., & Höfer, T. (2018) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2018.12.029 · Cited by 19

Ecological immunology

Schmid‐Hempel, P. (2021) · Oxford University Press eBooks · doi:10.1093/oso/9780198832140.003.0005 · Cited by 19

The hematopoietic stem cell expansion niche in fetal liver: Current state of the art and the way forward

Agrawal, H., Mehatre, S. H., & Khurana, S. (2024) · Experimental Hematology · doi:10.1016/j.exphem.2024.104585 · Cited by 20

New insights on extramedullary granulopoiesis and neutrophil heterogeneity in the spleen and its importance in disease

Guo, R., Xie, X., Ren, Q., & Liew, P. X. (2024) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiae220 · Cited by 19

CGRP: A New Endogenous Cell Stemness Maintenance Molecule

Lv, X., Chen, Q., Zhang, S., Gao, F., & Liu, Q. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/4107433 · Cited by 18

Disruption of stem cell niche–confined R-spondin 3 expression leads to impaired hematopoiesis

Kurtova, A. V., Heinlein, M., Haas, S. F., Velten, L., Dijkgraaf, G. J. P., Storm, E. E., Kljavin, N. M., Boumahdi, S., Himmels, P., Hérault, A., et al. (2022) · Blood Advances · doi:10.1182/bloodadvances.2022007714 · Cited by 18

SARS-CoV-2 variants induce distinct disease and impact in the bone marrow and thymus of mice

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Context-dependent modification of PFKFB3 in hematopoietic stem cells promotes anaerobic glycolysis and ensures stress hematopoiesis

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Advances in HIV Gene Therapy

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Tissue adaptation of CD4 T lymphocytes in homeostasis and cancer

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The ATF4-RPS19BP1 axis modulates ribosome biogenesis to promote erythropoiesis

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Complexities of modeling the bone marrow microenvironment to facilitate hematopoietic research

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Identification of a panel of cytokines in neonates with hypoxic ischemic encephalopathy treated with hypothermia

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Hematopoietic Stem Cell Dynamics Are Regulated by Progenitor Demand: Lessons from a Quantitative Modeling Approach

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Interferon gamma inhibits the differentiation of mouse adult liver and bone marrow hematopoietic stem cells by inhibiting the activation of notch signaling

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Location, Location, Location: How Vascular Specialization Influences Hematopoietic Fates During Development

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Single-Cell Atlas Reveals Fatty Acid Metabolites Regulate the Functional Heterogeneity of Mesenchymal Stem Cells

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Aquaporins implicated in the cell proliferation and the signaling pathways of cell stemness

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Human, mouse, and dog bone marrow show similar mesenchymal stromal cells within a distinctive microenvironment

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Caspase-3/NLRP3 signaling in the mesenchymal stromal niche regulates myeloid-biased hematopoiesis

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CD44: a stemness driver, regulator, and marker—all in one?

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Developmental HSC Microenvironments: Lessons from Zebrafish

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CD44-mediated hyaluronan binding marks proliferating hematopoietic progenitor cells and promotes bone marrow engraftment

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Germline mutations in the bone marrow microenvironment and dysregulated hematopoiesis

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The haematopoietic stem cell niche: a new player in cardiovascular disease?

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Acute and late effects of combined internal and external radiation exposures on the hematopoietic system

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Niches that regulate stem cells and hematopoiesis in adult bone marrow

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Uncertainty in the niches that maintain haematopoietic stem cells

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Hematopoietic stem cell niches

Cheng, H., & Cheng, T. (2017) · Scientia Sinica Vitae · doi:10.1360/n052017-00273 · Cited by 3

Hierarchy of immature hematopoietic cells related to blood flow and niche

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Haematopoietic stem cell activity and interactions with the niche

Pinho, S., & Frenette, P. S. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-019-0103-9 · Cited by 1,064