The bone marrow niche for haematopoietic stem cells

Targeting Hypoxia-Inducible Factors for the Treatment of Anemia in Chronic Kidney Disease Patients

Locatelli, F., Fishbane, S. N., Block, G. A., & Macdougall, I. C. (2017) · American Journal of Nephrology · doi:10.1159/000455166 · Cited by 4,836

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

A Direct Measurement of the Radiation Sensitivity of Normal Mouse Bone Marrow Cells1

Till, J. E., & McCulloch, E. A. (2010) · Radiation Research · doi:10.1667/rrxx28.1 · Cited by 4,036

A Direct Measurement of the Radiation Sensitivity of Normal Mouse Bone Marrow Cells

Till, J. E., & McCulloch, E. A. (1961) · Radiation Research · doi:10.2307/3570892 · Cited by 3,848

Osteoblastic cells regulate the haematopoietic stem cell niche

Calvi, L. M., Adams, G. B., Weibrecht, K. W., Weber, J. M., Olson, D. P., Knight, M. C., Martin, R. P., Schipani, E., Pajevic, P. D., Bringhurst, F. R., et al. (2003) · Nature · doi:10.1038/nature02040 · Cited by 3,559

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

Identification of the haematopoietic stem cell niche and control of the niche size

Zhang, J., Niu, C. S., Ye, L., Huang, H., He, X. C., Tong, W.-G., Ross, J., Haug, J., Johnson, T. J., Feng, J. Q., et al. (2003) · Nature · doi:10.1038/nature02041 · Cited by 2,948

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 2,908

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

Rapid selection of mesenchymal stem and progenitor cells in primary prostate stromal cultures

Brennen, W. N., Kisteman, L. N., & Isaacs, J. T. (2016) · The Prostate · doi:10.1002/pros.23145 · Cited by 26

Concise Review: The Malignant Hematopoietic Stem Cell Niche

Yao, J.-C., & Link, D. C. (2016) · Stem Cells · doi:10.1002/stem.2487 · Cited by 26

A New Chapter for Mesenchymal Stem Cells: Decellularized Extracellular Matrices

Anasiz, Y., Özgül, R. K., & Uçkan, D. (2017) · Stem Cell Reviews and Reports · doi:10.1007/s12015-017-9757-x · Cited by 25

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

Cellules souches mésenchymateuses et médecine régénératrice

Maumus, M., Pers, Y., Ruiz, M., Jørgensen, C., & Noël, D. (2018) · médecine/sciences · doi:10.1051/medsci/2018294 · Cited by 25

Connecting secretome to hematopoietic stem cell phenotype shifts in an engineered bone marrow niche

Gilchrist, A. E., & Harley, B. A. C. (2020) · Integrative Biology · doi:10.1093/intbio/zyaa013 · Cited by 23

Neuronal regulation of B-cell immunity: Anticipatory immune posturing?

You, Z., Liu, B., & Qi, H. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.014 · Cited by 25

Awakening of Dormant Breast Cancer Cells in the Bone Marrow

Wieder, R. (2023) · Cancers · doi:10.3390/cancers15113021 · Cited by 26

Mechanobiology of Dental Pulp Cells

Bryniarska, N., Basta‐Kaim, A., & Kubiak, A. (2024) · Cells · doi:10.3390/cells13050375 · Cited by 24

Leukemic Stem Cells and Hematological Malignancies

Choi, H.-S., Kim, B. S., Yoon, S., Oh, S., & Lee, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126639 · Cited by 26

Intelligent Manufacturing for Osteoarthritis Organoids

Lyu, X., Wang, J., & Su, J. (2025) · Cell Proliferation · doi:10.1111/cpr.70043 · Cited by 25

Bioengineering Hematopoietic Stem Cell Niche toward Regenerative Medicine

Sugimura, R. (2015) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2015.10.010 · Cited by 25

Is the risk of cardiovascular disease altered with anti‐inflammatory therapies? Insights from rheumatoid arthritis

Kraakman, M. J., Dragoljevic, D., Kammoun, H. L., & Murphy, A. J. (2016) · Clinical & Translational Immunology · doi:10.1038/cti.2016.31 · Cited by 25

Engineered humanized bone organs maintain human hematopoiesis in vivo

Fritsch, K., Pigeot, S., Feng, X., Bourgine, P. E., Schroeder, T., Martín, I., Manz, M. G., & Takizawa, H. (2018) · Experimental Hematology · doi:10.1016/j.exphem.2018.01.004 · Cited by 24

Continuous cell supply from Krt7-expressing hematopoietic stem cells during native hematopoiesis revealed by targeted in vivo gene transfer method

Tajima, Y., Ito, K., Umino, A., Wilkinson, A. C., Nakauchi, H., & Yamazaki, S. (2017) · Scientific Reports · doi:10.1038/srep40684 · Cited by 23

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

How Hematopoietic Stem Cells Respond to Irradiation: Similarities and Differences between Low and High Doses of Ionizing Radiations

Henry, E., & Arcangeli, M.-L. (2020) · Experimental Hematology · doi:10.1016/j.exphem.2020.12.001 · Cited by 24

Colony Stimulating Factor 1 Receptor in Acute Myeloid Leukemia

Sletta, K. Y., Castells, O., & Gjertsen, B. T. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.654817 · Cited by 24

Prostate Cancer Dormancy and Reactivation in Bone Marrow

Singh, D. K., Patel, V. G., Oh, W. K., & Aguirre‐Ghiso, J. A. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10122648 · Cited by 27

Macrophage migration inhibitory factor in the pathogenesis of leukemia (Review)

Luo, Y., Wang, X., Shen, J., & Yao, J. (2021) · International Journal of Oncology · doi:10.3892/ijo.2021.5242 · Cited by 24

Review Cancer stem cells in haematological malignancies

Zagożdżon, R., & Gołąb, J. (2015) · Współczesna Onkologia · doi:10.5114/wo.2014.47127 · Cited by 24

Crosstalk between bone and other organs

Yuan, W., & Song, C. (2022) · Medical Review · doi:10.1515/mr-2022-0018 · Cited by 27

In vitro expansion of hematopoietic stem cells in a porous hydrogel-based 3D culture system

Liu, B., Jin, M. Y., & Wang, D. (2023) · Acta Biomaterialia · doi:10.1016/j.actbio.2023.01.057 · Cited by 25

Biophysical cues of bone marrow-inspired scaffolds regulate hematopoiesis of hematopoietic stem and progenitor cells

Li, W., Liang, H., Ao, Y., Tang, B., Li, J., Li, N., Wang, J., & Du, Y. (2023) · Biomaterials · doi:10.1016/j.biomaterials.2023.122111 · Cited by 25

Phenotypic, Morphological and Adhesive Differences of Human Hematopoietic Progenitor Cells Cultured on Murine versus Human Mesenchymal Stromal Cells

Reichert, D., Friedrichs, J., Ritter, S., Käubler, T., Werner, C., Bornhäuser, M., & Corbeil, D. (2015) · Scientific Reports · doi:10.1038/srep15680 · Cited by 24

Expression and role of RIP140/NRIP1 in chronic lymphocytic leukemia

Lapierre, M., Castet‐Nicolas, A., Gitenay, D., Jalaguier, S., Teyssier, C., Bret, C., Cartron, G., Moreaux, J., & Cavaillès, V. (2015) · Journal of Hematology & Oncology · doi:10.1186/s13045-015-0116-6 · Cited by 24

Three-dimensional ex vivo co-culture models of the leukaemic bone marrow niche for functional drug testing

Dhami, S. P. S., Kappala, S. S., Thompson, A., & Szegezdi, É. (2016) · Drug Discovery Today · doi:10.1016/j.drudis.2016.04.019 · Cited by 24

Megakaryocyte and Osteoblast Interactions Modulate Bone Mass and Hematopoiesis

Alvarez, M. B., Xu, L., Childress, P., Maupin, K. A., Mohamad, S., Chitteti, B. R., Himes, E. R., Olivos, D. J., Cheng, Y., Conway, S. J., et al. (2018) · Stem Cells and Development · doi:10.1089/scd.2017.0178 · 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

Effect of Hydroxyapatite Nanorods on the Fate of Human Adipose‐Derived Stem Cells Assessed In Situ at the Single Cell Level with a High‐Throughput, Real‐Time Microfluidic Chip

Hao, M., He, J., Wang, C., Wang, C., Ma, B., Zhang, S., Duan, J., Liu, F., Zhang, Y., Han, L. G., et al. (2019) · Small · doi:10.1002/smll.201905001 · Cited by 24

Understanding deregulated cellular and molecular dynamics in the haematopoietic stem cell niche to develop novel therapeutics for bone marrow fibrosis

Gleitz, H. F., Kramann, R., & Schneider, R. K. (2018) · The Journal of Pathology · doi:10.1002/path.5078 · Cited by 23

Proteomic analysis and functional validation reveal distinct therapeutic capabilities related to priming of mesenchymal stromal/stem cells with IFN-γ and hypoxia: potential implications for their clinical use

Calligaris, M., Zito, G., Busà, R., Bulati, M., Iannolo, G., Gallo, A., Carreca, A. P., Cuscino, N., Castelbuono, S., Carcione, C., et al. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1385712 · Cited by 23

An engineered model of metastatic colonization of human bone marrow reveals breast cancer cell remodeling of the hematopoietic niche

Baldassarri, I., Tavakol, D. N., Graney, P. L., Chramiec, A. G., Hibshoosh, H. H., & Vunjak‐Novakovic, G. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2405257121 · Cited by 25

TGFβ family signaling in human stem cell self-renewal and differentiation

Liu, S., Ren, J., Hu, Y., Zhou, F., & Zhang, L. (2024) · Cell Regeneration · doi:10.1186/s13619-024-00207-9 · Cited by 26

How age affects human hematopoietic stem and progenitor cells and the strategies to mitigate aging

Li, X., Wang, J., Hu, L., & Cheng, T. (2025) · Experimental Hematology · doi:10.1016/j.exphem.2025.104711 · Cited by 25

Profiling the spatial architecture of multiple myeloma in human bone marrow trephine biopsy specimens with spatial transcriptomics

Yip, R. K. H., Er, J. A. K., Qin, L., Nguyen, Q. H., Motyer, A., Rimes, J. S., Light, A., Mishi, R. D., Ling, L., Anttila, C. J. A., et al. (2025) · Blood · doi:10.1182/blood.2025028896 · Cited by 33

Biology of the bone marrow microenvironment and myelodysplastic syndromes

Rankin, E. B., Narla, A., Park, J. K., Lin, S., & Sakamoto, K. M. (2015) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2015.07.004 · Cited by 24

Developments in Hematopoietic Stem Cell Expansion and Gene Editing Technologies

Yücel, D., & Kocabaş, F. (2017) · Advances in experimental medicine and biology · doi:10.1007/5584_2017_114 · Cited by 23

Combinations of antioxidants and/or of epigenetic enzyme inhibitors allow for enhanced collection of mouse bone marrow hematopoietic stem cells in ambient air

Cai, Q., Capitano, M. L., Huang, X., Guo, B., Cooper, S. H., & Broxmeyer, H. E. (2018) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2018.01.005 · Cited by 23

The tetraspanin CD82 regulates bone marrow homing and engraftment of hematopoietic stem and progenitor cells

Reis, C. A. S., Marjon, K. D., Pascetti, E. M., Floren, M., & Gillette, J. M. (2018) · Molecular Biology of the Cell · doi:10.1091/mbc.e18-05-0305 · 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

CCN2 (Cellular Communication Network factor 2) in the bone marrow microenvironment, normal and malignant hematopoiesis

Leguit, R. J., Raymakers, R. A. P., Hebeda, K. M., & Goldschmeding, R. (2021) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-020-00602-2 · Cited by 23

LIGHT/LTβR signaling regulates self-renewal and differentiation of hematopoietic and leukemia stem cells

Höpner, S., Raykova, A., Radpour, R., Amrein, M. A., Koller, D., Baerlocher, G. M., Riether, C., & Ochsenbein, A. F. (2021) · Nature Communications · doi:10.1038/s41467-021-21317-x · Cited by 25

ACE Inhibition Modulates Myeloid Hematopoiesis after Acute Myocardial Infarction and Reduces Cardiac and Vascular Inflammation in Ischemic Heart Failure

Rudi, W., Molitor, M., Garlapati, V. S., Finger, S., Wild, J., Münzel, T. F., Karbach, S. H., & Wenzel, P. (2021) · Antioxidants · doi:10.3390/antiox10030396 · Cited by 23

The role of heme oxygenase-1 in hematopoietic system and its microenvironment

Szade, A., Szade, K., Mahdi, M., & Józkowicz, A. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03803-z · Cited by 25

Engineering of fully humanized and vascularized 3D bone marrow niches sustaining undifferentiated human cord blood hematopoietic stem and progenitor cells

Born, G., Nikolova, M. T., Scherberich, A., Treutlein, B., García‐García, A., & Martín, I. (2021) · Journal of Tissue Engineering · doi:10.1177/20417314211044855 · Cited by 23

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

Development and clinical advancement of small molecules for ex vivo expansion of hematopoietic stem cell

Li, J., Wang, X., Ding, J., Zhu, Y., Min, W., Kuang, W., Yuan, K., Sun, C., & Yang, P. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.12.006 · Cited by 22

Microfluidic device engineered to study the trafficking of multiple myeloma cancer cells through the sinusoidal niche of bone marrow

Sui, C., Zilberberg, J., & Lee, W. (2022) · Scientific Reports · doi:10.1038/s41598-022-05520-4 · Cited by 23

Skeletal stem cells: origins, definitions, and functions in bone development and disease

Feng, H., Jiang, B., Xing, W., Sun, J., Greenblatt, M. B., & Zou, W. (2022) · Life Medicine · doi:10.1093/lifemedi/lnac048 · Cited by 24

Perivascular niche cells sense thrombocytopenia and activate hematopoietic stem cells in an IL-1 dependent manner

Luis, T. C., Barkas, N., Carrelha, J., Giustacchini, A., Mazzi, S., Norfo, R., Wu, B., Aliouat, A., Guerrero, J. A., Rodríguez-Meira, A., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-41691-y · Cited by 23

Bone marrow Schwann cells induce hematopoietic stem cell hibernation

Yamazaki, S., & Nakauchi, H. (2014) · International Journal of Hematology · doi:10.1007/s12185-014-1588-9 · Cited by 23

Challenges and Opportunities to Harnessing the (Hematopoietic) Stem Cell Niche

Choi, J. S., & Harley, B. A. C. (2016) · Current Stem Cell Reports · doi:10.1007/s40778-016-0031-y · Cited by 23

Impairment of bone marrow endothelial progenitor cells in acute graft‐versus‐host disease patients after allotransplant

Cao, X.-N., Kong, Y., Song, Y., Shi, M., Zhao, H., Wen, Q., Lyu, Z., Duan, C., Wang, Y., Xu, L., et al. (2018) · British Journal of Haematology · doi:10.1111/bjh.15456 · Cited by 23

Arrayed molecular barcoding identifies TNFSF13 as a positive regulator of acute myeloid leukemia-initiating cells

Chapellier, M., Peña-Martínez, P., Ramakrishnan, R., Eriksson, M., Talkhoncheh, M. S., Orsmark-Pietras, C., Lilljebjörn, H., Högberg, C., Hagström-Andersson, A. K., Fioretos, T., et al. (2019) · Haematologica · doi:10.3324/haematol.2018.192062 · Cited by 25

Clonal hematopoiesis of indeterminate potential and its impact on patient trajectories after stem cell transplantation

Park, D. S., Akuffo, A. A., Muench, D. E., Grimes, H. L., Epling‐Burnette, P. K., Maini, P. K., Anderson, A. R. A., & Bonsall, M. B. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006913 · Cited by 23

miR-146b-5p regulates bone marrow mesenchymal stem cell differentiation by SIAH2/PPARγ in aplastic anemia children and benzene-induced aplastic anemia mouse model

Li, H., Xu, X., Wang, D. W., Zeng, L., Li, B., Zhang, Y., Su, S., Wei, L., You, H., Fang, Y., et al. (2020) · Cell Cycle · doi:10.1080/15384101.2020.1807081 · Cited by 23

Wharton’s Jelly Mesenchymal Stromal Cells Support the Expansion of Cord Blood–derived CD34 + Cells Mimicking a Hematopoietic Niche in a Direct Cell–cell Contact Culture System

Iacono, M. L., Russo, E., Anzalone, R., Baiamonte, E., Alberti, G., Gerbino, A., Maggio, A., Rocca, G. L., & Acuto, S. (2018) · Cell Transplantation · doi:10.1177/0963689717737089 · Cited by 23

Myeloid cells in cardiovascular organs

Nahrendorf, M. (2018) · Journal of Internal Medicine · doi:10.1111/joim.12844 · Cited by 25

The roles of neutrophils in cardiovascular diseases

Lian, Y., Lai, X., Wu, C., Wang, L., Shang, J., Zhang, H., Jia, S., Xing, W., & Liu, H. (2025) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2025.1526170 · Cited by 25

Hematopoietic stem and progenitor cells as a reservoir for trained immunity

Tran, B. T., Jeyanathan, V., Cao, R., Kaufmann, E., & King, K. Y. (2025) · eLife · doi:10.7554/elife.106610 · Cited by 25

Pathophysiological Significance of Store-Operated Calcium Entry in Megakaryocyte Function: Opening New Paths for Understanding the Role of Calcium in Thrombopoiesis

Buduo, C. A. D., Balduini, A., & Moccia, F. D. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17122055 · Cited by 22

Distinct signaling programs associated with progression of FGFR1 driven leukemia in a mouse model of stem cell leukemia lymphoma syndrome

Silva, J., Chang, C.-S., Hu, T., Qin, H., Kitamura, E., Hawthorn, L., Ren, M., & Cowell, J. K. (2018) · Genomics · doi:10.1016/j.ygeno.2018.10.015 · Cited by 22

Hematopoietic Stem Cells in Wound Healing Response

Urao, N., Liu, J., Takahashi, K., & Ganesh, G. (2021) · Advances in Wound Care · doi:10.1089/wound.2021.0065 · Cited by 23

The anti-apoptotic Bcl-2 protein regulates hair follicle stem cell function

Geueke, A., Mantellato, G., Küster, F., Schettina, P., Nelles, M., Seeger, J. M., Kashkar, H., & Niemann, C. (2021) · EMBO Reports · doi:10.15252/embr.202052301 · Cited by 22

CXCL12-abundant reticular cells are the major source of IL-6 upon LPS stimulation and thereby regulate hematopoiesis

Gerosa, R. C., Boettcher, S., Kovtonyuk, L. V., Hausmann, A., Hardt, W., Hidalgo, J., Nombela‐Arrieta, C., & Manz, M. G. (2021) · Blood Advances · doi:10.1182/bloodadvances.2021005531 · Cited by 24

Leukemia Stem Cells as a Potential Target to Achieve Therapy-Free Remission in Chronic Myeloid Leukemia

Ito, K., & Ito, K. (2021) · Cancers · doi:10.3390/cancers13225822 · Cited by 24

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

Nanoparticles targeting hematopoietic stem and progenitor cells: Multimodal carriers for the treatment of hematological diseases

Cruz, L. J., Rezaei, S., Grosveld, F. G., Philipsen, S., & Eich, C. (2022) · Frontiers in Genome Editing · doi:10.3389/fgeed.2022.1030285 · Cited by 23

Loss of bisecting GlcNAcylation on MCAM of bone marrow stoma determined pro-tumoral niche in MDS/AML

Feng, J., Wang, Y., Li, B., Yu, X., Lei, L., Wu, J., Zhang, X., Chen, Q., Zhou, Y., Gou, J., et al. (2022) · Leukemia · doi:10.1038/s41375-022-01748-1 · Cited by 22

Metabolic crosstalk between stromal and malignant cells in the bone marrow niche

Tirado, H. A., Balasundaram, N., Laaouimir, L., Erdem, A., & van Gastel, N. (2023) · Bone Reports · doi:10.1016/j.bonr.2023.101669 · Cited by 25

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

Stroma-Derived Connective Tissue Growth Factor Maintains Cell Cycle Progression and Repopulation Activity of Hematopoietic Stem Cells In Vitro

Istvánffy, R., Vilne, B., Schreck, C., Ruf, F., Pagel, C., Grziwok, S., Henkel, L., da Costa, O. P., Berndt, J., Stümpflen, V., et al. (2015) · Stem Cell Reports · doi:10.1016/j.stemcr.2015.09.018 · Cited by 21

Physiological, Tumor, and Metastatic Niches: Opportunities and Challenges for Targeting the Tumor Microenvironment

Murgai, M., Giles, A. J., & Kaplan, R. N. (2015) · Critical Reviews™ in Oncogenesis · doi:10.1615/critrevoncog.2015013668 · Cited by 23

RUNX1 haploinsufficiency results in granulocyte colony-stimulating factor hypersensitivity

Chin, D. W. L., Sakurai, M., Nah, G. S. S., Du, L. Z., Jacob, B., Yokomizo, T., Matsumura, T., Suda, T., Huang, G., Fu, X.-Y., et al. (2016) · Blood Cancer Journal · doi:10.1038/bcj.2015.105 · Cited by 22

Unraveling Myelodysplastic Syndromes: Current Knowledge and Future Directions

Chamseddine, A. N., Jabbour, E. J., Kantarjian, H. M., Bohannan, Z. S., & Garcia‐Manero, G. (2015) · Current Oncology Reports · doi:10.1007/s11912-015-0489-2 · Cited by 22

Ptk7-Deficient Mice Have Decreased Hematopoietic Stem Cell Pools as a Result of Deregulated Proliferation and Migration

Lhoumeau, A., Arcangeli, M.-L., Grandis, M. D., Giordano, M., Orsoni, J.-C., Lembo, F., Bardin, F., Marchetto, S., Aurrand‐Lions, M., & Borg, J. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1500680 · Cited by 22

Hematopoietic Stem Cells, Their Niche, and the Concept of Co-Culture Systems: A Critical Review.

Vaidya, A., & Kale, V. (2015) · PubMed · Cited by 21

Cellular and Molecular Networks in Chronic Myeloid Leukemia: The Leukemic Stem, Progenitor and Stromal Cell Interplay

Perrotti, D., Silvestri, G., Stramucci, L., Yu, J. E., & Trotta, R. (2016) · Current Drug Targets · doi:10.2174/1389450117666160615074120 · Cited by 22

Hematopoietic defects in response to reduced Arhgap21

Xavier-Ferrucio, J. M., Ricon, L., Vieira, K. P., Longhini, A. L. F., Lazarini, M., Bigarella, C. L., Franchi, G. C., Krause, D. S., & Saad, S. T. O. (2017) · Stem Cell Research · doi:10.1016/j.scr.2017.11.014 · Cited by 22

Functional compensation between hematopoietic stem cell clones in vivo

Nguyen, L., Wang, Z., Chowdhury, A. Y., Chu, E., Eerdeng, J., Du, J., & Lu, R. (2018) · EMBO Reports · doi:10.15252/embr.201745702 · Cited by 22

The Role of (Modified) Lipoproteins in Vascular Function: A Duet Between Monocytes and the Endothelium

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Impact of bone marrow-derived signals on NK cell development and functional maturation.

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