Can DCs be distinguished from macrophages by molecular signatures?

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

IDENTIFICATION OF A NOVEL CELL TYPE IN PERIPHERAL LYMPHOID ORGANS OF MICE

Steinman, R. M., & Cohn, Z. A. (1973) · The Journal of Experimental Medicine · doi:10.1084/jem.137.5.1142 · Cited by 2,443 · see citing works

Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages

the Immunological Genome Consortium, Gautier, E. L., Shay, T., Miller, J., Greter, M., Jakubzick, C., Ivanov, S., Helft, J., Chow, A., Elpek, K. G., et al. (2012) · Nature Immunology · doi:10.1038/ni.2419 · Cited by 1,972 · see citing works

Deciphering the transcriptional network of the dendritic cell lineage

Miller, J. C., Brown, B. D., Shay, T., Gautier, E. L., Jojic, V., Cohain, A. T., Pandey, G. S., Leboeuf, M., Elpek, K. G., Helft, J., et al. (2012) · Nature Immunology · doi:10.1038/ni.2370 · Cited by 779 · see citing works

Unravelling mononuclear phagocyte heterogeneity

Geissmann, F., Gordon, S., Hume, D. A., Mowat, A. M., & Randolph, G. J. (2010) · Nature reviews. Immunology · doi:10.1038/nri2784 · Cited by 529 · see citing works

An antibody against the colony-stimulating factor 1 receptor depletes the resident subset of monocytes and tissue- and tumor-associated macrophages but does not inhibit inflammation

MacDonald, K. P. A., Palmer, J. S., Cronau, S. L., Seppanen, E. J., Olver, S. D., Raffelt, N. C., Kuns, R. D., Pettit, A. R., Clouston, A. D., Wainwright, B. J., et al. (2010) · Blood · doi:10.1182/blood-2010-02-266296 · Cited by 507 · see citing works

Differentiation and heterogeneity in the mononuclear phagocyte system

Hume, D. A. (2008) · Mucosal Immunology · doi:10.1038/mi.2008.36 · Cited by 220 · see citing works

Applications of myeloid‐specific promoters in transgenic mice support in vivo imaging and functional genomics but do not support the concept of distinct macrophage and dendritic cell lineages or roles in immunity

Hume, D. A. (2011) · Journal of Leukocyte Biology · doi:10.1189/jlb.0810472 · Cited by 154 · see citing works

Isolation and characterization of antigen-presenting dendritic cells from the mouse intestinal lamina propria.

Pavli, P., Woodhams, C. E., Doe, W. F., & Hume, D. A. (1990) · PubMed Central · Cited by 140 · see citing works

Functional clustering and lineage markers: Insights into cellular differentiation and gene function from large-scale microarray studies of purified primary cell populations

Hume, D. A., SUMMERS, K. M., Raza, S., Baillie, J. K., & Freeman, T. C. (2010) · Genomics · doi:10.1016/j.ygeno.2010.03.002 · Cited by 88 · see citing works

Meta-analysis of lineage-specific gene expression signatures in mouse leukocyte populations

Mabbott, N. A., Baillie, J. K., Hume, D. A., & Freeman, T. C. (2010) · Immunobiology · doi:10.1016/j.imbio.2010.05.012 · Cited by 85 · see citing works

Plenary Perspective: The complexity of constitutive and inducible gene expression in mononuclear phagocytes

Hume, D. A. (2012) · Journal of Leukocyte Biology · doi:10.1189/jlb.0312166 · Cited by 33 · see citing works

Reference-based analysis of lung single-cell sequencing reveals a transitional profibrotic macrophage

Aran, D., Looney, A. P., Liu, L., Wu, E., Fong, V., Hsu, A., Chak, S., Naikawadi, R. P., Wolters, P. J., Abate, A. R., et al. (2019) · Nature Immunology · doi:10.1038/s41590-018-0276-y · Cited by 4,984 · see citing works

Microfold (M) cells: important immunosurveillance posts in the intestinal epithelium

Mabbott, N. A., Donaldson, D. S., Ohno, H., Williams, I. R., & Mahajan, A. (2013) · Mucosal Immunology · doi:10.1038/mi.2013.30 · Cited by 721 · see citing works

An expression atlas of human primary cells: inference of gene function from coexpression networks

Mabbott, N. A., Baillie, J. K., Brown, H. K., Freeman, T. C., & Hume, D. A. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-632 · Cited by 477 · see citing works

Macrophages Promote Osteoblastic Differentiation In Vivo: Implications in Fracture Repair and Bone Homeostasis

Vi, L., Baht, G. S., Whetstone, H., Ng, A., Wei, Q., Poon, R., Mylvaganam, S., Grynpas, M., & Alman, B. A. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2422 · Cited by 330 · see citing works

GM-CSF in inflammation

Hamilton, J. A. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20190945 · Cited by 310 · see citing works

The Many Alternative Faces of Macrophage Activation

Hume, D. A. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00370 · Cited by 303 · see citing works

Immune Cell Gene Signatures for Profiling the Microenvironment of Solid Tumors

Nirmal, A. J., Regan, T. W., Shih, B. B.-J., Hume, D. A., Sims, A. H., & Freeman, T. C. (2018) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-18-0342 · Cited by 219 · see citing works

Dendritic cells and macrophages in the kidney: a spectrum of good and evil

Rogers, N. M., Ferenbach, D. A., Isenberg, J. S., Thomson, A. W., & Hughes, J. (2014) · Nature Reviews Nephrology · doi:10.1038/nrneph.2014.170 · Cited by 199 · see citing works

Homeostasis in the mononuclear phagocyte system

Jenkins, S. J., & Hume, D. A. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.06.006 · Cited by 178 · see citing works

GM-CSF-Dependent Inflammatory Pathways

Hamilton, J. A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02055 · Cited by 141 · see citing works

Where are we? The anatomy of the murine cortical meninges revisited for intravital imaging, immunology, and clearance of waste from the brain

Coles, J. A., Myburgh, E., Brewer, J. M., & McMenamin, P. G. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.05.002 · Cited by 123 · see citing works

Mafb lineage tracing to distinguish macrophages from other immune lineages reveals dual identity of Langerhans cells

Wu, X., Briseño, C. G., Durai, V., Albring, J. C., Haldar, M., Bagadia, P., Kim, K.-W., Randolph, G. J., Murphy, T. L., & MURPHY, K. M. M. (2016) · The Journal of Experimental Medicine · doi:10.1084/jem.20160600 · Cited by 116 · see citing works

Network analysis of transcriptomic diversity amongst resident tissue macrophages and dendritic cells in the mouse mononuclear phagocyte system

SUMMERS, K. M., Bush, S. J., & Hume, D. A. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000859 · Cited by 111 · see citing works

Functional Immune Anatomy of the Liver—As an Allograft

Demetris, A. J., Bellamy, C. O. C., Gandhi, C. R., Prost, S., Nakanuma, Y., & Stolz, D. B. (2016) · American Journal of Transplantation · doi:10.1111/ajt.13749 · Cited by 115 · see citing works

Aging and the mucosal immune system in the intestine

Mabbott, N. A., Kobayashi, A., Sehgal, A., Bradford, B. M., Pattison, M., & Donaldson, D. S. (2015) · Biogerontology · doi:10.1007/s10522-014-9498-z · Cited by 95 · see citing works

A Discrete Subset of Monocyte-Derived Cells among Typical Conventional Type 2 Dendritic Cells Can Efficiently Cross-Present.

Sheng, J., Chen, Q., Soncin, I., Ng, S.-L., Karjalainen, K., & Ruedl, C. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.10.024 · Cited by 74 · see citing works

Specific Contributions of CSF-1 and GM-CSF to the Dynamics of the Mononuclear Phagocyte System

Louis, C., Cook, A. D., Lacey, D. C., Fleetwood, A. J., Vlahos, R., Anderson, G. P., & Hamilton, J. A. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1500369 · Cited by 82 · see citing works

Epithelial Basal Cells Are Distinct from Dendritic Cells and Macrophages in the Mouse Epididymis1

Shum, W. W., Smith, T., Cortez‐Retamozo, V., Grigoryeva, L. S., Roy, J. W., Hill, E., Pittet, M. J., Breton, S., & Silva, N. D. (2014) · Biology of Reproduction · doi:10.1095/biolreprod.113.116681 · Cited by 70 · see citing works

Regulation of Dendritic Cell Function in Inflammation

Said, A., & Weindl, G. (2015) · Journal of Immunology Research · doi:10.1155/2015/743169 · Cited by 67 · see citing works

Gut microbiota alterations and health status in aging adults: From correlation to causation

Wu, Y., Xu, J., Rong, X., Wang, F., Wang, H., & Zhao, C. (2021) · Aging Medicine · doi:10.1002/agm2.12167 · Cited by 66 · see citing works

Targeting GM-CSF in inflammatory and autoimmune disorders

Achuthan, A. A., Lee, M.-C., & Hamilton, J. A. (2021) · Seminars in Immunology · doi:10.1016/j.smim.2021.101523 · Cited by 62 · see citing works

Transcriptomic analysis of mononuclear phagocyte differentiation and activation

Hume, D. A., & Freeman, T. C. (2014) · Immunological Reviews · doi:10.1111/imr.12211 · Cited by 57 · see citing works

Dendritic Cell-Based Immunotherapy in Multiple Myeloma: Challenges, Opportunities, and Future Directions

Verheye, E., Melgar, J. B., Deschoemaeker, S., Raes, G., Maes, A., Bruyne, E. D., Menu, E., Vanderkerken, K., Laoui, D., & Veirman, K. D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23020904 · Cited by 54 · see citing works

Complement Receptor C5aR1/CD88 and Dipeptidyl Peptidase-4/CD26 Define Distinct Hematopoietic Lineages of Dendritic Cells

Nakano, H., Moran, T. P., Nakano, K., Gerrish, K., Bortner, C. D., & Cook, D. N. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402195 · Cited by 55 · see citing works

Distinct Molecular Signature of Human Skin Langerhans Cells Denotes Critical Differences in Cutaneous Dendritic Cell Immune Regulation

Polak, M. E., Thirdborough, S. M., Ung, C. Y., Elliott, T. J., Healy, E., Freeman, T. C., & Ardern‐Jones, M. R. (2013) · Journal of Investigative Dermatology · doi:10.1038/jid.2013.375 · Cited by 49 · see citing works

Identification of co‐expressed gene signatures in mouse B 1, marginal zone and B 2 B ‐cell populations

Mabbott, N. A., & Gray, D. (2013) · Immunology · doi:10.1111/imm.12171 · Cited by 48 · see citing works

Granulocyte macrophage colony-stimulating factor receptor α expression and its targeting in antigen-induced arthritis and inflammation

Cook, A. D., Louis, C., Robinson, M. J., Saleh, R., Sleeman, M. A., & Hamilton, J. A. (2016) · Arthritis Research & Therapy · doi:10.1186/s13075-016-1185-9 · Cited by 48 · see citing works

CD11c‐positive cells from brain, spleen, lung, and liver exhibit site‐specific immune phenotypes and plastically adapt to new environments

Immig, K., Gericke, M. T., Menzel, F., Merz, F., Krueger, M., Schiefenhövel, F., Lösche, A., Jäger, K., Hanisch, U., Biber, K. P. H., et al. (2014) · Glia · doi:10.1002/glia.22771 · Cited by 44 · see citing works

Sequential Immune Responses: The Weapons of Immunity

Mills, C. D., Ley, K. F., Buchmann, K., & Canton, J. (2015) · Journal of Innate Immunity · doi:10.1159/000380910 · Cited by 44 · see citing works

Combination of novel and public RNA-seq datasets to generate an mRNA expression atlas for the domestic chicken

Bush, S. J., Freem, L. J., MacCallum, A. J., O’Dell, J., Wu, C., Afrasiabi, C., Psifidi, A., Stevens, M. P., Smith, J., SUMMERS, K. M., et al. (2018) · BMC Genomics · doi:10.1186/s12864-018-4972-7 · Cited by 39 · see citing works

A transcriptional perspective on human macrophage biology

Schultze, J. L., Freeman, T. C., Hume, D. A., & Latz, E. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2015.02.001 · Cited by 38 · see citing works

Identification of the macrophage-specific promoter signature in FANTOM5 mouse embryo developmental time course data

SUMMERS, K. M., & Hume, D. A. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.1a0417-150rr · Cited by 33 · see citing works

Oral Prion Disease Pathogenesis Is Impeded in the Specific Absence of CXCR5-Expressing Dendritic Cells

Bradford, B. M., Reizis, B., & Mabbott, N. A. (2017) · Journal of Virology · doi:10.1128/jvi.00124-17 · Cited by 34 · see citing works

Transcriptional Regulation and Macrophage Differentiation

Hume, D. A., SUMMERS, K. M., & Rehli, M. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0024-2015 · Cited by 31 · see citing works

CSF-1 receptor-mediated differentiation of a new type of monocytic cell with B cell-stimulating activity: its selective dependence on IL-34

Yamane, F., Nishikawa, Y., Matsui, K., Asakura, M., Iwasaki, E., Watanabe, K., Tanimoto, H., Sano, H., Fujiwara, Y., Stanley, E. R., et al. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.0613311 · Cited by 30 · see citing works

Characterization of regulatory dendritic cells differentiated from the bone marrow of UV ‐irradiated mice

Ng, R. L. X., Scott, N. M., Bisley, J. L., Lambert, M. J. M., Gorman, S., Norval, M., & Hart, P. H. (2013) · Immunology · doi:10.1111/imm.12145 · Cited by 21 · see citing works

Streptococcus pneumoniae Rapidly Translocate from the Nasopharynx through the Cribriform Plate to Invade the Outer Meninges

Audshasai, T., Coles, J. A., Panagiotou, S., Khandaker, S., Scales, H. E., Kjos, M., Baltazar, M., Vignau, J., Brewer, J. M., Kadioglu, A., et al. (2022) · mBio · doi:10.1128/mbio.01024-22 · Cited by 20 · see citing works

Multifunctional magnetic nanoparticles elicit anti-tumor immunity in a mouse melanoma model

Lafuente‐Gómez, N., de Lázaro, I., Dhanjani, M., García‐Soriano, D., Sobral, M. C., Salas, G., Mooney, D. J., & Somoza, Á. (2023) · Materials Today Bio · doi:10.1016/j.mtbio.2023.100817 · Cited by 20 · see citing works

Development of human dendritic cells and their role in HIV infection: antiviral immunity versus HIV transmission

Tsunetsugu-Yokota, Y., & Muhsen, M. (2013) · Frontiers in Microbiology · doi:10.3389/fmicb.2013.00178 · Cited by 13 · see citing works

Expression of Blimp-1 in Dendritic Cells Modulates the Innate Inflammatory Response in Dextran Sodium Sulfate-Induced Colitis

Kim, S. J., Goldstein, J., Dorso, K., Mérad, M., Mayer, L., Crawford, J. M., Gregersen, P. K., & Diamond, B. (2014) · Molecular Medicine · doi:10.2119/molmed.2014.00231 · Cited by 19 · see citing works

Hyaluronan Binding Identifies a Functionally Distinct Alveolar Macrophage–like Population in Bone Marrow–Derived Dendritic Cell Cultures

Poon, G. F. T., Dong, Y., Marshall, K. C., Arif, A., Deeg, C., Dosanjh, M., & Johnson, P. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402506 · Cited by 18 · see citing works

Transcriptional programming of human macrophages: on the way to systems immunology

Schultze, J. L. (2015) · Journal of Molecular Medicine · doi:10.1007/s00109-015-1286-y · Cited by 18 · see citing works

A Guide to Bioinformatics for Immunologists

Whelan, F., Yap, N. V. L., Surette, M. G., Golding, G. B., & Bowdish, D. M. E. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00416 · Cited by 17 · see citing works

Role of macrophages and phagocytes in orchestrating normal and pathologic hematopoietic niches

Lévesque, J.-P., SUMMERS, K. M., Millard, S. M., Bisht, K., Winkler, I. G., & Pettit, A. R. (2021) · Experimental Hematology · doi:10.1016/j.exphem.2021.07.001 · Cited by 14 · see citing works

Genomic and molecular control of cell type and cell type conversions

Fu, X., He, F., Li, Y., Shahveranov, A., & Hutchins, A. P. (2017) · Cell Regeneration · doi:10.1016/j.cr.2017.09.001 · Cited by 13 · see citing works

Flow cytometric characterization of brain dendritic cell subsets after murine stroke

Pösel, C., Uri, A., Schulz, I., Boltze, J., Weise, G., & Wagner, D. (2014) · Experimental & Translational Stroke Medicine · doi:10.1186/2040-7378-6-11 · Cited by 13 · see citing works

Immunology of Prion Protein and Prions

Mabbott, N. A. (2017) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.06.004 · Cited by 539 · see citing works

Integrated proteomics and scRNA-seq analyses of ovarian cancer reveal molecular subtype-associated cell landscapes and immunotherapy targets

Tan, R., Wen, M., Yang, W., Zhan, D., Zheng, N., Liu, M., Zhu, F., Chen, X., Wang, M., Yang, S., et al. (2024) · British Journal of Cancer · doi:10.1038/s41416-024-02894-2 · Cited by 12 · see citing works

Toward defining a ‘lineage’ – The case for dendritic cells

Perié, L., & Naik, S. H. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.02.004 · Cited by 11 · see citing works

The Good, the Bad, and the Ugly of Dendritic Cells during Prion Disease

Mabbott, N. A., & Bradford, B. M. (2015) · Journal of Immunology Research · doi:10.1155/2015/168574 · Cited by 10 · see citing works

Inhibitors of the 5-lipoxygenase arachidonic acid pathway induce ATP release and ATP-dependent organic cation transport in macrophages

Souza, H. A. D. S., de Lira, M. N., Costa‐Junior, H. M., da Cruz, C. M., Vasconcellos, J. S. S., Mendes, A. N., Pimenta-Reis, G., Alvarez, C. L., Faccioli, L. H., Serezani, C. H., et al. (2014) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2014.04.006 · Cited by 10 · see citing works

Alternatively Activated Mononuclear Phagocytes from the Skin Site of Infection and the Impact of IL-4Rα Signalling on CD4+T Cell Survival in Draining Lymph Nodes after Repeated Exposure to Schistosoma mansoni Cercariae

Prendergast, C. T., Sanin, D. E., & Mountford, A. P. (2016) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0004911 · Cited by 8 · see citing works

Increased susceptibility to oral Trichuris muris infection in the specific absence of CXCR 5+ CD 11c+ cells

Bradford, B. M., Donaldson, D. S., Forman, R. A., Else, K. J., & Mabbott, N. A. (2018) · Parasite Immunology · doi:10.1111/pim.12566 · Cited by 5 · see citing works

Erratum: Can DCs be distinguished from macrophages by molecular signatures?

Hume, D. A., Mabbott, N. A., Raza, S., & Freeman, T. C. (2013) · Nature Immunology · doi:10.1038/ni0813-876d · Cited by 4 · see citing works

Transcriptional Regulation and Macrophage Differentiation

Hume, D. A., SUMMERS, K. M., & Rehli, M. (2017) · ASM Press eBooks · doi:10.1128/9781555819194.ch8 · Cited by 5 · see citing works

Editorial

Schultze, J. L. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2015.04.001 · Cited by 3 · see citing works

A generalized protocol for the induction of M2-like macrophages from mouse and rat bone marrow mononuclear cells

Yakhshimurodov, U. R., Yamashita, K., Miki, K., Kawamura, T., Saito, S., & Miyagawa, S. (2025) · Biology Methods and Protocols · doi:10.1093/biomethods/bpaf020 · Cited by 2 · see citing works

Role of NF-κB Activation in Macrophages

Lawrence, T. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1311-4_21 · Cited by 2 · see citing works

Histomorphometrical and Immunohistochemical Study of the Maturation of Bursa of Fabricius in Rose Male Broiler Chicken at Post-Hatching Period

AMEEN, S. Z., Mohammed, Y., & Abdullah, M. A. (2024) · Egyptian Journal of Veterinary Science · doi:10.21608/ejvs.2024.268880.1837 · Cited by 2 · see citing works

The Macrophage Transcriptome

Milde, R., Pesant, M., Locati, M., & Martínez, F. O. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1311-4_28 · Cited by 2 · see citing works

Mechanisms of Psoriatic Plaque Formation in Mice

Wohn, C. R. (2015) · RePub (Erasmus University Rotterdam) · Cited by 2 · see citing works

Combination of novel and public RNA-seq datasets to generate an mRNA expression atlas for the domestic chickenPreprint

Bush, S. J., Freem, L. J., MacCallum, A. J., O’Dell, J., Wu, C., Afrasiabi, C., Psifidi, A., Stevens, M. P., Smith, J., SUMMERS, K. M., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/295535 · Cited by 2 · see citing works

Angefertigt mit Genehmigung der Mathematisch-Naturwissenschaftlichen Fakultät der

Bonn, R. F.-W.-U. (2012)

Immunology of Prion Disease

Mabbott, N. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-374279-7.13027-9

VISUALIZING THE DYNAMICS OF IMMUNE SURVEILLANCE IN BRAIN TUMORS BY INTRAVITAL MULTIPHOTON MICROSCOPY

Nwajei, F. (2017) · Digital Commons-TMC (Texas Medical Center)

Age-related changes of arginase activity and nitric oxide level in phagocytes and their modulation by thymic mesenchymal stromal cells

DOVHYI, R., Nikolsky, I. S., & Skivka, L. M. (2017) · Studia Biologica · doi:10.30970/sbi.1102.533

The Control of Gene Expression in Macrophages

Ostuni, R., & Natoli, G. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1311-4_26

Streptococcus pneumoniae rapidly translocates from the nasopharynx through the cribriform plate to invade and inflame the duraPreprint

Audshasai, T., Coles, J. A., Panagiotou, S., Khandaker, S., Scales, H. E., Kjos, M., Baltazar, M., Vignau, J., Brewer, J. M., Kadioglu, A., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.28.462246

Data from Immune Cell Gene Signatures for Profiling the Microenvironment of Solid Tumors

Nirmal, A. J., Regan, T. W., Shih, B. B.-J., Hume, D. A., Sims, A. H., & Freeman, T. C. (2023) · doi:10.1158/2326-6066.c.6548552.v1

Reply to: "Can DCs be distinguished from macrophages by molecular signatures?"

Randolph, G., & Merad, M. (2013) · Nature Immunology · doi:10.1038/ni.2517 · Cited by 13 · see citing works

Gene expression profiling during differentiation of human monocytes to macrophages or dendritic cells

Julkunen, I. (2014)

Monocyte and DC atlas

Fehervari, Z. T. (2017) · Nature Immunology · doi:10.1038/ni.3757

An mRNA expression atlas for the domestic chicken generated by the meta-analysis of RNA-seq datasets

Bush, S. J., Freem, L. J., MacCallum, A. J., O’Dell, J., Wu, C., Afrasiabi, C., Psifidi, A., Stevens, M. P., Smith, J., & Hume, D. A. (2017) · Edinburgh Research Explorer (University of Edinburgh) · doi:10.7488/ds/2137

Cloning and characterisation of the chicken orthologue of dendritic cell-lysosomal associated membrane protein (DC-LAMP)

Wu, Z., Hu, T., Butter, C., & Kaiser, P. (2009) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2009.09.007 · Cited by 20 · see citing works