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

Bone-marrow mimicking biomaterial niches for studying hematopoietic stem and progenitor cells

Nelson, M. R., & Roy, K. (2016) · Journal of Materials Chemistry B · doi:10.1039/c5tb02644j · Cited by 42

Jagged1 upregulation in prostate epithelial cells promotes formation of reactive stroma in the Pten null mouse model for prostate cancer

Su, Q., Zhang, B., Zhang, L., Dang, T., Rowley, D. R., Ittmann, M., & Xin, L. (2016) · Oncogene · doi:10.1038/onc.2016.232 · Cited by 41

The Mesenchymal Precursor Cell Marker Antibody STRO-1 Binds to Cell Surface Heat Shock Cognate 70

Fitter, S., Gronthos, S., Ooi, S. S., & Zannettino, A. C. W. (2016) · Stem Cells · doi:10.1002/stem.2560 · Cited by 40

Aberrant T cell responses in the bone marrow microenvironment of patients with poor graft function after allogeneic hematopoietic stem cell transplantation

Kong, Y., Wang, Y.-T., Cao, X.-N., Song, Y., Chen, Y., Sun, Y., Wang, Y., Zhang, X., Xu, L., & Huang, X. (2017) · Journal of Translational Medicine · doi:10.1186/s12967-017-1159-y · Cited by 41

Metabolic regulation of hematopoietic and leukemic stem/progenitor cells under homeostatic and stress conditions

Karigane, D., & Takubo, K. (2017) · International Journal of Hematology · doi:10.1007/s12185-017-2261-x · Cited by 40

Therapeutic Antibodies for Myeloid Neoplasms—Current Developments and Future Directions

Schürch, C. M. (2018) · Frontiers in Oncology · doi:10.3389/fonc.2018.00152 · Cited by 42

Spred1 Safeguards Hematopoietic Homeostasis against Diet-Induced Systemic Stress

Tadokoro, Y., Hoshii, T., Yamazaki, S., Eto, K., Ema, H., Kobayashi, M., Ueno, M., Ohta, K., Arai, Y., Hara, E., et al. (2018) · Cell stem cell · doi:10.1016/j.stem.2018.04.002 · Cited by 42

Multiplexed fluorescence microscopy reveals heterogeneity among stromal cells in mouse bone marrow sections

Holzwarth, K., Köhler, R., Philipsen, L., Tokoyoda, K., Ladyhina, V., Wählby, C., Niesner, R. A., & Hauser, A. E. (2018) · Cytometry Part A · doi:10.1002/cyto.a.23526 · Cited by 40

Age-related differences in the bone marrow stem cell niche generate specialized microenvironments for the distinct regulation of normal hematopoietic and leukemia stem cells

Lee, G., Jeong, S., Lee, H., & Oh, I. (2019) · Scientific Reports · doi:10.1038/s41598-018-36999-5 · Cited by 44

Beta-Adrenergic Signaling in Tumor Immunology and Immunotherapy

Wang, W., & Cao, X. (2019) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.2019031188 · Cited by 43

Similarities Between Stem Cell Niches in Glioblastoma and Bone Marrow: Rays of Hope for Novel Treatment Strategies

Hira, V. V. V., Breznik, B., Vittori, M., de Jong, A. L., Mlakar, J., Oostra, R., Khurshed, M., Molenaar, R. J., Lah, T. T., & Noorden, C. J. F. V. (2019) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155419878416 · Cited by 41

EBF1-deficient bone marrow stroma elicits persistent changes in HSC potential

Derecka, M., Herman, J. S., Cauchy, P., Ramamoorthy, S., Lupar, E., Grün, D., & Grosschedl, R. (2020) · Nature Immunology · doi:10.1038/s41590-020-0595-7 · Cited by 40

Controversies on the Consequences of Iron Overload and Chelation in MDS

Vinchi, F., Hell, S., & Platzbecker, U. (2020) · HemaSphere · doi:10.1097/hs9.0000000000000357 · Cited by 43

Role for Leptin and Leptin Receptors in Stem Cells During Health and Diseases

Trinh, T. L. P., & Broxmeyer, H. E. (2021) · Stem Cell Reviews and Reports · doi:10.1007/s12015-021-10132-y · Cited by 46

Hypoxia promotes erythroid differentiation through the development of progenitors and proerythroblasts

Bapat, A., Schippel, N., Shi, X., Jasbi, P., Gu, H., Kala, M., Sertil, A., & Sharma, S. (2021) · Experimental Hematology · doi:10.1016/j.exphem.2021.02.012 · Cited by 39

Culturing patient-derived malignant hematopoietic stem cells in engineered and fully humanized 3D niches

García‐García, A., Klein, T., Born, G., Hilpert, M., Scherberich, A., Lengerke, C., Skoda, R. C., Bourgine, P. E., & Martín, I. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2114227118 · Cited by 41

Genetic and Epigenetic Mechanisms That Maintain Hematopoietic Stem Cell Function

Kosan, C., & Godmann, M. (2015) · Stem Cells International · doi:10.1155/2016/5178965 · Cited by 47

The Role of Inflammation in the Initiation and Progression of Myeloid Neoplasms

Balandrán, J. C., Lasry, A., & Aifantis, I. (2023) · Blood Cancer Discovery · doi:10.1158/2643-3230.bcd-22-0176 · Cited by 44

Regenerating human skeletal muscle forms an emerging niche in vivo to support PAX7 cells

Hicks, M. R., Saleh, K. K., Clock, B., Gibbs, D. E., Yang, M., Younesi, S., Gane, L., Gutierrez-Garcia, V., Xi, H., & Pyle, A. D. (2023) · Nature Cell Biology · doi:10.1038/s41556-023-01271-0 · Cited by 38

Oncostatin M Maintains the Hematopoietic Microenvironment in the Bone Marrow by Modulating Adipogenesis and Osteogenesis

Sato, F., Miyaoka, Y., Miyajima, A., & Tanaka, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0116209 · Cited by 40

Polymeric Electrospinning for Musculoskeletal Regenerative Engineering

Narayanan, N., Jiang, C., Uzunallı, G., Thankappan, S. K., Laurencin, C. T., & Deng, M. (2016) · Regenerative Engineering and Translational Medicine · doi:10.1007/s40883-016-0013-8 · Cited by 40

Runx1 downregulates stem cell and megakaryocytic transcription programs that support niche interactions

Behrens, K., Triviai, I., Schwieger, M., Tekin, N. S., Alawi, M., Spohn, M., Indenbirken, D., Ziegler, M., Müller, U., Alexander, W. S., et al. (2016) · Blood · doi:10.1182/blood-2015-09-668129 · Cited by 40

Inducible Nitric Oxide Synthase (iNOS) Is a Novel Negative Regulator of Hematopoietic Stem/Progenitor Cell Trafficking

Adamiak, M., Abdelbaset‐Ismail, A., Moore, J. B., Zhao, J. Z., Abdel‐Latif, A., Wysoczynski, M., & Ratajczak, M. Z. (2016) · Stem Cell Reviews and Reports · doi:10.1007/s12015-016-9693-1 · Cited by 40

Ontogenic Identification and Analysis of Mesenchymal Stromal Cell Populations during Mouse Limb and Long Bone Development

Nusspaumer, G., Jaiswal, S., Barbero, A., Reinhardt, R., Ishay-Ronen, D., Haumer, A., Lufkin, T., Martín, I., & Zeller, R. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.08.007 · Cited by 40

Periarteriolar Glioblastoma Stem Cell Niches Express Bone Marrow Hematopoietic Stem Cell Niche Proteins

Hira, V. V. V., Wormer, J. R., Kakar, H., Breznik, B., van der Swaan, B., Hulsbos, R., Tigchelaar, W., Tonar, Z., Khurshed, M., Molenaar, R. J., et al. (2018) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155417749174 · Cited by 42

Addressing the Manufacturing Challenges of Cell-Based Therapies

Fuzeta, M. D. A., Branco, A. D. D. M., Fernandes‐Platzgummer, A., da Silva, C. L., & Cabral, J. M. S. (2019) · Advances in biochemical engineering, biotechnology · doi:10.1007/10_2019_118 · Cited by 42

The vascular niche controls Drosophila hematopoiesis via fibroblast growth factor signaling

Letourneau, M., Morin-Poulard, I., Tian, Y., Vanzo, N. F., & Crozatier, M. (2021) · eLife · doi:10.7554/elife.64672 · Cited by 40

Therapeutic Treatments for Osteoporosis—Which Combination of Pills Is the Best among the Bad?

Tonk, C. H., Shoushrah, S. H., Babczyk, P., Khaldi-Hansen, B. E., Schulze, M., Herten, M., & Tobiasch, E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031393 · Cited by 44

p21-activated kinase 2 regulates HSPC cytoskeleton, migration, and homing via CDC42 activation and interaction with β-Pix

Reddy, P. N. G., Radu, M., Xu, K., Wood, J. A., Harris, C. E., Chernoff, J., & Williams, D. A. (2016) · Blood · doi:10.1182/blood-2016-01-693572 · Cited by 40

Critical requirement of VEGF-C in transition to fetal erythropoiesis

Fang, S., Nurmi, H. J., Heinolainen, K., Chen, S., Salminen, E., Saharinen, P., Mikkola, H. K. A., & Alitalo, K. K. (2016) · Blood · doi:10.1182/blood-2015-12-687970 · Cited by 40

Sigma‐1 receptor attenuates osteoclastogenesis by promoting ER‐associated degradation of SERCA2

Wei, X., Zheng, Z., Feng, Z., Zheng, L., Tao, S., Zheng, B., Huang, B. H., Zhang, X., Liu, J., Chen, Y., et al. (2022) · EMBO Molecular Medicine · doi:10.15252/emmm.202115373 · Cited by 38

Key Factors for Thymic Function and Development

Shichkin, V. P., & Antica, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.926516 · Cited by 42

Hematopoietic Stem Cells and Their Niche in Bone Marrow

Kwon, M., Kim, B. S., Yoon, S., Oh, S., & Lee, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25136837 · Cited by 42

Self-organization of the hematopoietic vascular niche and emergent innate immunity on a chip

Georgescu, A., Oved, J. H., Galarraga, J. H., Cantrell, T., Mehta, S., Dulmovits, B. M., Olson, T. S., Fattahi, P., Wang, A., Candarlioglu, P. L., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.11.003 · Cited by 40

Transcription factor‐mediated reprogramming toward hematopoietic stem cells

Ebina, W., & Rossi, D. J. (2015) · The EMBO Journal · doi:10.15252/embj.201490804 · Cited by 41

Prospective isolation of resident adult human mesenchymal stem cell population from multiple organs

Mabuchi, Y., & Matsuzaki, Y. (2015) · International Journal of Hematology · doi:10.1007/s12185-015-1921-y · Cited by 39

Bone marrow endothelial cell-derived interleukin-4 contributes to thrombocytopenia in acute myeloid leukemia

Gao, A., Gong, Y., Zhu, C., Yang, W., Li, Q., Zhao, M., Ma, S., Li, J., Hao, S., Cheng, H., et al. (2019) · Haematologica · doi:10.3324/haematol.2018.214593 · Cited by 38

Immune cell regulation of the hair cycle

Wang, E. C. E., & Higgins, C. A. (2020) · Experimental Dermatology · doi:10.1111/exd.14070 · Cited by 40

Diminished Reactive Hematopoiesis and Cardiac Inflammation in a Mouse Model of Recurrent Myocardial Infarction

Cremer, S., Schloss, M. J., Vinegoni, C., Foy, B. H., Zhang, S., Rohde, D., Hulsmans, M., Feruglio, P. F., Schmidt, S., Wojtkiewicz, G. R., et al. (2020) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2019.12.056 · Cited by 40

Deterioration of hematopoietic autophagy is linked to osteoporosis

Yuan, Y., Fang, Y., Zhu, L., Gu, Y., Li, L., Qian, J., Zhao, R., Zhang, P., Li, J., Zhang, H., et al. (2020) · Aging Cell · doi:10.1111/acel.13114 · Cited by 39

The erythroblastic island niche: modeling in health, stress, and disease

May, A., & Forrester, L. M. (2020) · Experimental Hematology · doi:10.1016/j.exphem.2020.09.185 · Cited by 44

TNF-α-induced alterations in stromal progenitors enhance leukemic stem cell growth via CXCR2 signaling

Agarwal, P., Li, H., Choi, K., Hueneman, K. M., He, J., Welner, R. S., Starczynowski, D. T., & Bhatia, R. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109386 · Cited by 40

Modelling acute myeloid leukemia (AML): What’s new? A transition from the classical to the modern

Dozzo, A., Galvin, A., Shin, J., Scalia, S., O’Driscoll, C. M., & Ryan, K. B. (2022) · Drug Delivery and Translational Research · doi:10.1007/s13346-022-01189-4 · Cited by 40

Infectious Osteomyelitis: Marrying Bone Biology and Microbiology to Shed New Light on a Persistent Clinical Challenge

Novack, D. V., & Cassat, J. E. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4279 · Cited by 37

A Molecular Profile of the Endothelial Cell Response to Ionizing Radiation

Himburg, H. A., Sasine, J. P., Yan, X., Kan, J., Dressman, H. K., & Chute, J. P. (2016) · Radiation Research · doi:10.1667/rr14444.1 · Cited by 38

Live imaging of stem cells: answering old questions and raising new ones

Park, S., Greco, V., & Cockburn, K. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.07.004 · Cited by 36

Modular flow chamber for engineering bone marrow architecture and function

Buduo, C. A. D., Soprano, P. M., Tozzi, L., Marconi, S., Auricchio, F., Kaplan, D. L., & Balduini, A. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.08.006 · Cited by 38

A Chemoattractant-Guided Walk Through Lymphopoiesis

Lim, V., Zehentmeier, S., Fistonich, C., & Pereira, J. P. (2017) · Advances in immunology · doi:10.1016/bs.ai.2017.02.001 · Cited by 40

Efforts to enhance blood stem cell engraftment: Recent insights from zebrafish hematopoiesis

Perlin, J. R., Robertson, A. L., & Zon, L. I. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20171069 · Cited by 36

Hypoxia with Wharton’s jelly mesenchymal stem cell coculture maintains stemness of umbilical cord blood-derived CD34+ cells

Zhao, D., Liu, L., Chen, Q., Wang, F., Li, Q., Zeng, Q., Huang, J., Luo, M., Li, W., Zheng, Y., et al. (2018) · Stem Cell Research & Therapy · doi:10.1186/s13287-018-0902-5 · Cited by 38

Lack of Adipocytes Alters Hematopoiesis in Lipodystrophic Mice

Wilson, A., Fu, H., Schiffrin, M., Winkler, C., Koufany, M., Jouzeau, J., Bonnet, N., Gilardi, F., Renevey, F., Luther, S. A., et al. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02573 · Cited by 38

Blocking ATM-dependent NF-κB pathway overcomes niche protection and improves chemotherapy response in acute lymphoblastic leukemia

Chen, Y., Tang, C. S., Zhang, M., Huang, W., Xu, Y. K., Sun, H.-Y., Yang, F., Song, L., Wang, H., Mu, L., et al. (2019) · Leukemia · doi:10.1038/s41375-019-0458-0 · Cited by 37

Stress and catecholamines modulate the bone marrow microenvironment to promote tumorigenesis

Hanns, P., Paczulla, A., Medinger, M., Konantz, M., & Lengerke, C. (2019) · Cell Stress · doi:10.15698/cst2019.07.192 · Cited by 41

Caloric restriction maintains stem cells through niche and regulates stem cell aging

Maharajan, N., Vijayakumar, K. A., Jang, C. H., & Cho, G. (2019) · Journal of Molecular Medicine · doi:10.1007/s00109-019-01846-1 · Cited by 38

Transitioning from Gamma Rays to X Rays for Comparable Biomedical Research Irradiations: Energy Matters

Poirier, Y. P., Belley, M. D., Dewhirst, M. W., Yoshizumic, T. T., & Down, J. D. (2020) · Radiation Research · doi:10.1667/rade-20-00039.1 · Cited by 38

TREM2 acts as a receptor for IL-34 to suppress acute myeloid leukemia in mice

Xie, X., Zhang, W., Xiao, M., Wei, T., Qiu, Y., Qiu, J., Wang, H., Qiu, Z., Zhang, S., Pan, Y., et al. (2023) · Blood · doi:10.1182/blood.2022018619 · Cited by 34

Bone marrow niches orchestrate stem-cell hierarchy and immune tolerance

Furuhashi, K., Kakiuchi, M., Ueda, R., Oda, H., Ummarino, S., Ebralidze, A. K., Bassal, M. A., Chen, M., Sato, T., Lyu, J., et al. (2025) · Nature · doi:10.1038/s41586-024-08352-6 · Cited by 39

Bone marrow microenvironment modulation of acute lymphoblastic leukemia phenotype

Moses, B. S., Slone, W. L., Thomas, P., Evans, R., Piktel, D., Angel, P. M., Walsh, C. M., Cantrell, P. S., Rellick, S. L., Martin, K. H., et al. (2015) · Experimental Hematology · doi:10.1016/j.exphem.2015.09.003 · Cited by 37

Computational modeling of the expansion of human cord blood CD133+ hematopoietic stem/progenitor cells with different cytokine combinations

Gullo, F., van der Garde, M., Russo, G. L., Pennisi, M. A., Motta, S., Pappalardo, F., & Watt, S. M. (2015) · Bioinformatics · doi:10.1093/bioinformatics/btv172 · Cited by 37

Sinusoidal ephrin receptor EPHB4 controls hematopoietic progenitor cell mobilization from bone marrow

Kwak, H., Salvucci, O., Weigert, R., Martinez-Torrecuadrada, J. L., Henkemeyer, M. J., Poulos, M. G., Butler, J. M., & Tosato, G. (2016) · Journal of Clinical Investigation · doi:10.1172/jci87848 · Cited by 39

Concise Review: The Deleterious Effects of Cigarette Smoking and Nicotine Usage and Mesenchymal Stem Cell Function and Implications for Cell-Based Therapies

Greenberg, J. M., Carballosa, C. M., & Cheung, H. S. (2017) · Stem Cells Translational Medicine · doi:10.1002/sctm.17-0060 · Cited by 38

Chemokines as a Conductor of Bone Marrow Microenvironment in Chronic Myeloid Leukemia

Mukaida, N., Tanabe, Y., & Baba, T. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081824 · Cited by 38

Geographic clonal tracking in macaques provides insights into HSPC migration and differentiation

Wu, C., Espinoza, D. A., Koelle, S., Potter, E. L., Lu, R., Li, B., Yang, D., Fan, X., Donahue, R. E., Roederer, M., et al. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20171341 · Cited by 37

Regulation of unfolded protein response in hematopoietic stem cells

Sigurðsson, V., & Miharada, K. (2018) · International Journal of Hematology · doi:10.1007/s12185-018-2458-7 · Cited by 38

Secretome within the bone marrow microenvironment: A basis for mesenchymal stem cell treatment and role in cancer dormancy

Eltoukhy, H. S., Sinha, G., Moore, C. A., Gergues, M., & Rameshwar, P. (2018) · Biochimie · doi:10.1016/j.biochi.2018.05.018 · Cited by 37

Mesenchymal stem cell-mediated Notch2 activation overcomes radiation-induced injury of the hematopoietic system

Kim, A., Shim, S., Kim, M., Myung, J. K., & Park, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-27666-w · Cited by 38

Interleukin-6 deletion stimulates revascularization and new bone formation following ischemic osteonecrosis in a murine model

Kuroyanagi, G., Adapala, N. S., Yamaguchi, R., Kamiya, N., Deng, Z., Aruwajoye, O. O., Kutschke, M. J., Chen, E. Y., Jo, C.-H., Ren, Y., et al. (2018) · Bone · doi:10.1016/j.bone.2018.08.011 · Cited by 37

A Three-Dimensional Dense Collagen Hydrogel to Model Cancer Cell/Osteoblast Interactions

James-Bhasin, M., Siegel, P. M., & Nazhat, S. N. (2018) · Journal of Functional Biomaterials · doi:10.3390/jfb9040072 · Cited by 37

Adult Cardiac Stem Cell Aging: A Reversible Stochastic Phenomenon?

Cianflone, E., Torella, M., Chimenti, C., Angelis, A. D., Beltrami, A. P., Urbanek, K., Rota, M., & Torella, D. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/5813147 · Cited by 40

Macrophages and Their Organ Locations Shape Each Other in Development and Homeostasis – A Drosophila Perspective

Mase, A., Augsburger, J., & Brückner, K. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.630272 · Cited by 34

Treatment of skeletal and non-skeletal alterations of Mucopolysaccharidosis type IVA by AAV-mediated gene therapy

Bertolin, J., Sánchez, V., Ribera, A., Jaén, M. L., García, M., Pujol, A., Sánchez, X., MUÑOZ, S. A., Marcó, S., Pérez, J., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25697-y · Cited by 39

Genetic abnormalities associated with acute lymphoblastic leukemia

Yokota, T., & Kanakura, Y. (2016) · Cancer Science · doi:10.1111/cas.12927 · Cited by 37

Lipoprotein lipase regulates hematopoietic stem progenitor cell maintenance through DHA supply

Liu, C., Han, T., Stachura, D. L., Wang, H., Vaisman, B. L., Kim, J., Klemke, R. L., Remaley, A. T., Rana, T. M., Traver, D. J., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03775-y · Cited by 37

Regulation of Hematopoiesis and Hematological Disease by TGF-β Family Signaling MoleculesPreprint

Naka, K., & Hirao, A. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a027987 · Cited by 37

Interactions of B-lymphocytes and bone cells in health and disease

Grčević, D., Sanjay, A., & Lorenzo, J. (2023) · Bone · doi:10.1016/j.bone.2021.116296 · Cited by 36

HIV-1 Tat protein inhibits the hematopoietic support function of human bone marrow mesenchymal stem cells

Yuan, Y., Zhou, C., Yang, Q., Ma, S., Wang, X., Guo, X., Ding, Y., Tang, J., Zeng, Y., & Li, D. (2019) · Virus Research · doi:10.1016/j.virusres.2019.197756 · Cited by 36

EphB4 Expressing Stromal Cells Exhibit an Enhanced Capacity for Hematopoietic Stem Cell Maintenance

Nguyen, T. M., Arthur, A., Panagopoulos, R. A., Paton, S., Hayball, J. D., Zannettino, A. C. W., Purton, L. E., Matsuo, K., & Gronthos, S. (2015) · Stem Cells · doi:10.1002/stem.2069 · Cited by 36

Magnetic Macroporous Hydrogels as a Novel Approach for Perfused Stem Cell Culture in 3D Scaffolds via Contactless Motion Control

Rödling, L., Volz, E. M., Raić, A., Brändle, K., Franzreb, M., & Lee‐Thedieck, C. (2018) · Advanced Healthcare Materials · doi:10.1002/adhm.201701403 · Cited by 36

Role of Schwann cells in cutaneous wound healing

da Silva, W. N., Leonel, C., Prazeres, P. H. D. M., Sena, I. F. G., Guerra, D. A. P., Heller, D., Diniz, I. M. A., Fortuna, V., Mintz, A., & Birbrair, A. (2018) · Wound Repair and Regeneration · doi:10.1111/wrr.12647 · Cited by 36

Hematopoietic stem cells and lineage cells undergo dynamic alterations under microgravity and recovery conditions

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Single‐cell transcriptomes of murine bone marrow stromal cells reveal niche‐associated heterogeneity

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