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Serial progression of cortical and medullary thymic epithelial microenvironments
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/eji.200737131openalex-snapshot
Promiscuous gene expression and the developmental dynamics of medullary thymic epithelial cells
inferredcites →https://doi.org/10.1002/eji.200737275openalex-snapshot
Redefining epithelial progenitor potential in the developing thymus
inferredcites →https://doi.org/10.1002/eji.200839175openalex-snapshot
Thymus‐specific serine protease regulates positive selection of a subset of CD4+ thymocytes
inferredcites →https://doi.org/10.1002/eji.200939501openalex-snapshot
Absence of thymus crosstalk in the fetus does not preclude hematopoietic induction of a functional thymus in the adult
inferredcites →https://doi.org/10.1002/eji.200939628openalex-snapshot
Why Aire? Compensating for late bloomers
inferredcites →https://doi.org/10.1002/eji.201041375openalex-snapshot
Ontogeny of thymic cortical epithelial cells expressing the thymoproteasome subunit β5t
inferredcites →https://doi.org/10.1002/eji.201243209openalex-snapshot
Generation of both cortical and A ire + medullary thymic epithelial compartments from CD 205 + progenitors
inferredcites →https://doi.org/10.1016/j.celrep.2013.08.038openalex-snapshot
Lineage Tracing and Cell Ablation Identify a Post-Aire-Expressing Thymic Epithelial Cell Population
inferredcites →https://doi.org/10.1016/j.immuni.2009.10.009openalex-snapshot
Thymoproteasome Shapes Immunocompetent Repertoire of CD8+ T Cells
inferredcites →https://doi.org/10.1016/j.it.2009.07.010openalex-snapshot
Thymic epithelial cells: the multi-tasking framework of the T cell “cradle”
inferredcites →https://doi.org/10.1016/j.it.2009.11.002openalex-snapshot
Control of central self-tolerance induction by autoreactive CD4+ thymocytes
inferredcites →https://doi.org/10.1016/j.it.2012.03.005openalex-snapshot
Thymic epithelial cells: working class heroes for T cell development and repertoire selection
inferredcites →https://doi.org/10.1016/s0022-1759(01)00493-8openalex-snapshot
Analysis of thymic stromal cell populations using flow cytometry
inferredcites →https://doi.org/10.1016/s1074-7613(02)00321-7openalex-snapshot
Identification and Characterization of Thymic Epithelial Progenitor Cells
inferredcites →https://doi.org/10.1038/414763aopenalex-snapshot
Thymus medulla consisting of epithelial islets each derived from a single progenitor
inferredcites →https://doi.org/10.1038/nature04813openalex-snapshot
Clonal analysis reveals a common progenitor for thymic cortical and medullary epithelium
inferredcites →https://doi.org/10.1038/nature04850openalex-snapshot
Formation of a functional thymus initiated by a postnatal epithelial progenitor cell
inferredcites →https://doi.org/10.1038/ni1064openalex-snapshot
Functional evidence for a single endodermal origin for the thymic epithelium
inferredcites →https://doi.org/10.1038/ni1438openalex-snapshot
Medullary thymic epithelial cells expressing Aire represent a unique lineage derived from cells expressing claudin
inferredcites →https://doi.org/10.1038/ni723openalex-snapshot
Promiscuous gene expression in medullary thymic epithelial cells mirrors the peripheral self
inferredcites →https://doi.org/10.1038/ni812openalex-snapshot
Generation of a complete thymic microenvironment by MTS24+ thymic epithelial cells
inferredcites →https://doi.org/10.1038/nri1781openalex-snapshot
Journey through the thymus: stromal guides for T-cell development and selection
inferredcites →https://doi.org/10.1038/nri3534openalex-snapshot
Thymus involution and regeneration: two sides of the same coin?
inferredcites →https://doi.org/10.1073/pnas.0809559106openalex-snapshot
Characterization of the thymic IL-7 niche in vivo
inferredcites →https://doi.org/10.1073/pnas.1118823109openalex-snapshot
Regenerative capacity of adult cortical thymic epithelial cells
inferredcites →https://doi.org/10.1073/pnas.1301799110openalex-snapshot
Aire-expressing thymic medullary epithelial cells originate from β5t-expressing progenitor cells
inferredcites →https://doi.org/10.1073/pnas.93.12.5742openalex-snapshot
The nu gene acts cell-autonomously and is required for differentiation of thymic epithelial progenitors.
inferredcites →https://doi.org/10.1073/pnas.95.20.11822openalex-snapshot
Interdependence of cortical thymic epithelial cell differentiation and T-lineage commitment
inferredcites →https://doi.org/10.1084/jem.20062497openalex-snapshot
RANK signals from CD4+3− inducer cells regulate development of Aire-expressing epithelial cells in the thymic medulla
inferredcites →https://doi.org/10.1084/jem.20080134openalex-snapshot
Delta-like 4 is indispensable in thymic environment specific for T cell development
inferredcites →https://doi.org/10.1084/jem.20092144openalex-snapshot
Biphasic Aire expression in early embryos and in medullary thymic epithelial cells before end-stage terminal differentiation
inferredcites →https://doi.org/10.1084/jem.20102327openalex-snapshot
Aire-dependent production of XCL1 mediates medullary accumulation of thymic dendritic cells and contributes to regulatory T cell development
inferredcites →https://doi.org/10.1126/science.1075958openalex-snapshot
Projection of an Immunological Self Shadow Within the Thymus by the Aire Protein
inferredcites →https://doi.org/10.1126/science.1141915openalex-snapshot
Regulation of CD8 + T Cell Development by Thymus-Specific Proteasomes
inferredcites →https://doi.org/10.1126/science.272.5263.886openalex-snapshot
Two Genetically Separable Steps in the Differentiation of Thymic Epithelium
inferredcites →https://doi.org/10.1126/science.280.5362.450openalex-snapshot
Cathepsin L: Critical Role in Ii Degradation and CD4 T Cell Selection in the Thymus
inferredcites →https://doi.org/10.1146/annurev-immunol-020711-075038openalex-snapshot
VLR-Based Adaptive Immunity
inferredcites →https://doi.org/10.1146/annurev.immunol.26.021607.090408openalex-snapshot
Thymus Organogenesis
inferredcites →https://doi.org/10.1182/blood-2008-05-156265openalex-snapshot
Foxn1 is required to maintain the postnatal thymic microenvironment in a dosage-sensitive manner
inferredcites →https://doi.org/10.1371/journal.pgen.1002348openalex-snapshot
Foxn1 Regulates Lineage Progression in Cortical and Medullary Thymic Epithelial Cells But Is Dispensable for Medullary Sublineage Divergence
inferredcites →https://doi.org/10.1371/journal.pone.0053416openalex-snapshot
Normal T Cell Selection Occurs in CD205-Deficient Thymic Microenvironments
inferredcites →https://doi.org/10.1523/jneurosci.5497-07.2008openalex-snapshot
Early Neuronal and Glial Fate Restriction of Embryonic Neural Stem Cells
inferredcites →https://doi.org/10.3389/fimmu.2012.00019openalex-snapshot
Post-Aire Maturation of Thymic Medullary Epithelial Cells Involves Selective Expression of Keratinocyte-Specific Autoantigens
inferredcites →https://doi.org/10.4049/jimmunol.0804133openalex-snapshot
Autoimmune Regulator Deficiency Results in Decreased Expression of CCR4 and CCR7 Ligands and in Delayed Migration of CD4+ Thymocytes
inferredcites →https://doi.org/10.4049/jimmunol.1000601openalex-snapshot
Cutting Edge: A Thymocyte-Thymic Epithelial Cell Cross-Talk Dynamically Regulates Intrathymic IL-7 Expression In Vivo
inferredcites →https://doi.org/10.4049/jimmunol.1002151openalex-snapshot
Lymphotoxin Signals from Positively Selected Thymocytes Regulate the Terminal Differentiation of Medullary Thymic Epithelial Cells
inferredcites →https://doi.org/10.4049/jimmunol.1203042openalex-snapshot
Thymocyte Selection Regulates the Homeostasis of IL-7–Expressing Thymic Cortical Epithelial Cells In Vivo
inferredcites →https://doi.org/10.4049/jimmunol.1203203openalex-snapshot
Lymphotoxin β Receptor Regulates the Development of CCL21-Expressing Subset of Postnatal Medullary Thymic Epithelial Cells
inferredcites →https://doi.org/10.4049/jimmunol.151.5.2453openalex-snapshot
Medullary thymic epithelium expresses a ligand for CTLA4 in situ and in vitro.
inferredcites →https://doi.org/10.4049/jimmunol.181.12.8199openalex-snapshot
Cutting Edge: Thymic Crosstalk Regulates Delta-Like 4 Expression on Cortical Epithelial Cells
inferredcites →https://doi.org/10.4049/jimmunol.182.1.130openalex-snapshot
Checkpoints in the Development of Thymic Cortical Epithelial Cells
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9780470015902.a0027281openalex-snapshot
AIRE – The Autoimmune Regulator
inferred← citeshttps://doi.org/10.1002/9780470015902.a0029481openalex-snapshot
Thymus Microenvironment: Maintenance, Ageing and Strategies for Thymus Regeneration Following Damage
inferred← citeshttps://doi.org/10.1002/cbf.4009openalex-snapshot
Atypical chemokine receptor 4 (ACKR4/CCX‐CKR): A comprehensive exploration across physiological and pathological landscapes in contemporary research
inferred← citeshttps://doi.org/10.1002/eji.201444585openalex-snapshot
Intermediate expression of CCRL1 reveals novel subpopulations of medullary thymic epithelial cells that emerge in the postnatal thymus
inferred← citeshttps://doi.org/10.1002/eji.201445091openalex-snapshot
CCRL 1 marks heterogeneity in cortical and medullary thymic epithelial cells
inferred← citeshttps://doi.org/10.1002/eji.201445108openalex-snapshot
Thymus medulla fosters generation of natural Treg cells, invariant γδ T cells, and invariant NKT cells: What we learn from intrathymic migration
inferred← citeshttps://doi.org/10.1002/eji.201545677openalex-snapshot
Alternative NF‐κB signaling regulates mTEC differentiation from podoplanin‐expressing precursors in the cortico‐medullary junction
inferred← citeshttps://doi.org/10.1002/eji.201545844openalex-snapshot
Adult thymic epithelial cell (TEC) progenitors and TEC stem cells: Models and mechanisms for TEC development and maintenance
inferred← citeshttps://doi.org/10.1002/eji.201545995openalex-snapshot
Dynamic spatio‐temporal contribution of single β5t+ cortical epithelial precursors to the thymus medulla
inferred← citeshttps://doi.org/10.1002/eji.201546098openalex-snapshot
Switching on the Aire conditioner
inferred← citeshttps://doi.org/10.1002/eji.201546253openalex-snapshot
Relb acts downstream of medullary thymic epithelial stem cells and is essential for the emergence of RANK + medullary epithelial progenitors
inferred← citeshttps://doi.org/10.1002/eji.201646329openalex-snapshot
Thymus medulla under construction: Time and space oddities
inferred← citeshttps://doi.org/10.1002/eji.201746922openalex-snapshot
Thymic crosstalk restrains the pool of cortical thymic epithelial cells with progenitor properties
inferred← citeshttps://doi.org/10.1002/eji.201747006openalex-snapshot
Dissecting and modeling the emergent murine TEC compartment during ontogeny
inferred← citeshttps://doi.org/10.1002/eji.202048764openalex-snapshot
A novel method to identify Post‐Aire stages of medullary thymic epithelial cell differentiation
inferred← citeshttps://doi.org/10.1002/eji.202249915openalex-snapshot
Trappc1 deficiency impairs thymic epithelial cell development by breaking endoplasmic reticulum homeostasis
inferred← citeshttps://doi.org/10.1002/eji.202250202openalex-snapshot
T‐cell selection in the thymus: New routes toward the identification of the self‐peptide ligandome presented by thymic epithelial cells
inferred← citeshttps://doi.org/10.1002/eji.202451305openalex-snapshot
Neural Crest‐Derived Mesenchymal Cells Support Thymic Reconstitution After Lethal Irradiation
inferred← citeshttps://doi.org/10.1002/wdev.146openalex-snapshot
Developing stratified epithelia: lessons from the epidermis and thymus
inferred← citeshttps://doi.org/10.1007/978-3-030-12040-5_3openalex-snapshot
The Ins and Outs of Thymic Epithelial Cell Differentiation and Function
inferred← citeshttps://doi.org/10.1007/978-3-031-77921-3_3openalex-snapshot
The Ins and Outs of Thymic Epithelial Cell Differentiation and Function
inferred← citeshttps://doi.org/10.1007/978-3-319-47377-2_4openalex-snapshot
Development of Immune System Organs
inferred← citeshttps://doi.org/10.1007/978-4-431-56027-2_3openalex-snapshot
Strategies for Thymic Regeneration: Recent Advances Towards Clinical Therapy
inferred← citeshttps://doi.org/10.1007/s00018-015-2107-8openalex-snapshot
Thymic stromal cell subsets for T cell development
inferred← citeshttps://doi.org/10.1007/s00418-014-1296-9openalex-snapshot
Conditioned deletion of ephrinB1 and/or ephrinB2 in either thymocytes or thymic epithelial cells alters the organization of thymic medulla and favors the appearance of thymic epithelial cysts
inferred← citeshttps://doi.org/10.1007/s00418-019-01818-zopenalex-snapshot
FoxN1 mediates thymic cortex–medulla differentiation through modifying a developmental pattern based on epithelial tubulogenesis
inferred← citeshttps://doi.org/10.1007/s10238-015-0344-7openalex-snapshot
Expression of cell cycle and apoptosis regulators in thymus and thymic epithelial tumors
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.66176-7openalex-snapshot
Microenvironment Regulation of Thymic Progenitors: How Form Follows Function
inferred← citeshttps://doi.org/10.1016/b978-0-128-24465-4.00083-1openalex-snapshot
Thymocyte–TEC Cross Talk for Self-Tolerance in T Cells
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2016.11.054openalex-snapshot
Native thymic extracellular matrix improves in vivo thymic organoid T cell output, and drives in vitro thymic epithelial cell differentiation
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.10.012openalex-snapshot
Adult Thymic Medullary Epithelium Is Maintained and Regenerated by Lineage-Restricted Cells Rather Than Bipotent Progenitors
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.03.048openalex-snapshot
HDAC3 Is a Master Regulator of mTEC Development
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.05.045openalex-snapshot
Interplay between Follistatin, Activin A, and BMP4 Signaling Regulates Postnatal Thymic Epithelial Progenitor Cell Differentiation during Aging
inferred← citeshttps://doi.org/10.1016/j.imlet.2019.01.012openalex-snapshot
Medullary thymic epithelial cells: Deciphering the functional diversity beyond promiscuous gene expression
inferred← citeshttps://doi.org/10.1016/j.isci.2026.115161openalex-snapshot
KLF2 controls thymic epithelial cell homeostasis, impacting regulatory T cell development and immune tolerance
inferred← citeshttps://doi.org/10.1016/j.it.2017.11.001openalex-snapshot
Setting Up the Perimeter of Tolerance: Insights into mTEC Physiology
inferred← citeshttps://doi.org/10.1016/j.jaut.2015.12.004openalex-snapshot
Sonic Hedgehog regulates thymic epithelial cell differentiation
inferred← citeshttps://doi.org/10.1016/j.molimm.2016.02.015openalex-snapshot
TNF superfamily members play distinct roles in shaping the thymic stromal microenvironment
inferred← citeshttps://doi.org/10.1016/j.regen.2021.100052openalex-snapshot
Strategies for thymus regeneration and generating thymic organoids
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.3c00148openalex-snapshot
The Influence of Feeder Cell-Derived Extracellular Matrix Density on Thymic Epithelial Cell Culture
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.9b01610openalex-snapshot
Gelatin-Based 3D Microgels for In Vitro T Lineage Cell Generation
inferred← citeshttps://doi.org/10.1038/icb.2017.74openalex-snapshot
A key role for IL‐7R in the generation of microenvironments required for thymic dendritic cells
inferred← citeshttps://doi.org/10.1038/ni.3555openalex-snapshot
Progress on thymic function from Maui
inferred← citeshttps://doi.org/10.1038/nri.2017.12openalex-snapshot
Generation of diversity in thymic epithelial cells
inferred← citeshttps://doi.org/10.1038/s41423-023-01102-0openalex-snapshot
Insm1 regulates mTEC development and immune tolerance
inferred← citeshttps://doi.org/10.1038/s41467-023-37589-4openalex-snapshot
Embryonic keratin19+ progenitors generate multiple functionally distinct progeny to maintain epithelial diversity in the adult thymus medulla
inferred← citeshttps://doi.org/10.1038/s41467-025-62523-1openalex-snapshot
An iPSC-based in vitro model recapitulates human thymic epithelial development and multi-lineage specification
inferred← citeshttps://doi.org/10.1038/s41467-026-68675-yopenalex-snapshot
Combinatory differentiation of human induced pluripotent stem cells generates functional thymic epithelium driving dendritic cell and CD4/CD8 T cell development
inferred← citeshttps://doi.org/10.1038/s41577-019-0238-0openalex-snapshot
Thymic epithelial cell heterogeneity: TEC by TEC
inferred← citeshttps://doi.org/10.1038/srep12895openalex-snapshot
Sex hormones have pervasive effects on thymic epithelial cells
inferred← citeshttps://doi.org/10.1038/srep44481openalex-snapshot
Epithelial LTβR signaling controls the population size of the progenitors of medullary thymic epithelial cells in neonatal mice
inferred← citeshttps://doi.org/10.1073/pnas.2214989119openalex-snapshot
Central tolerance promoted by cell chimerism
inferred← citeshttps://doi.org/10.1084/jem.20230894openalex-snapshot
Generation and repair of thymic epithelial cells
inferred← citeshttps://doi.org/10.1093/intimm/dxag031openalex-snapshot
Thymic cortical epithelial Psmb11 -encoded β5t in mouse and human
inferred← citeshttps://doi.org/10.1101/2025.08.28.672880openalex-snapshot
Ly6d expression delineates two putative postnatal thymus epithelial progenitor cells that are differentially affected by ageing
inferred← citeshttps://doi.org/10.1101/791103openalex-snapshot
A wave of embryonic bipotent T/lymphoid tissue inducer progenitors regulates the maturation of medullary thymic epithelial cells
inferred← citeshttps://doi.org/10.1101/gr.171645.113openalex-snapshot
Population and single-cell genomics reveal the Aire dependency, relief from Polycomb silencing, and distribution of self-antigen expression in thymic epithelia
inferred← citeshttps://doi.org/10.1111/imm.12831openalex-snapshot
Update on Aire and thymic negative selection
inferred← citeshttps://doi.org/10.1111/imr.12404openalex-snapshot
Development and developmental potential of cortical thymic epithelial cells
inferred← citeshttps://doi.org/10.1111/imr.12406openalex-snapshot
Control of the thymic medulla and its influence on αβT‐cell development
inferred← citeshttps://doi.org/10.1111/imr.12412openalex-snapshot
Medullary thymic epithelial stem cells: role in thymic epithelial cell maintenance and thymic involution
inferred← citeshttps://doi.org/10.1111/imr.70049openalex-snapshot
Cortical Thymic Epithelial Cells: Key Developers of the Code of T‐Cell Selection and TCR Repertoire Diversity
inferred← citeshttps://doi.org/10.1111/sji.13094openalex-snapshot
Regulation of thymic T regulatory cell differentiation by TECs in health and disease
inferred← citeshttps://doi.org/10.1126/sciadv.abd9585openalex-snapshot
Retracing the evolutionary emergence of thymopoiesis
inferred← citeshttps://doi.org/10.1126/sciadv.aec2253openalex-snapshot
Ly6d expression delineates two putative postnatal thymus epithelial progenitor cells that are differentially affected by aging
inferred← citeshttps://doi.org/10.1146/annurev-immunol-051116-052320openalex-snapshot
Thymic Epithelial Cells
inferred← citeshttps://doi.org/10.1182/blood.2020006779openalex-snapshot
A wave of bipotent T/ILC-restricted progenitors shapes the embryonic thymus microenvironment in a time-dependent manner
inferred← citeshttps://doi.org/10.1186/s13148-021-01197-0openalex-snapshot
Epigenetic modifications in thymic epithelial cells: an evolutionary perspective for thymus atrophy
inferred← citeshttps://doi.org/10.1242/dev.178582openalex-snapshot
Canonical Notch signaling controls the early thymic epithelial progenitor cell state and emergence of the medullary epithelial lineage in fetal thymus development
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005776openalex-snapshot
Requirement of Stat3 Signaling in the Postnatal Development of Thymic Medullary Epithelial Cells
inferred← citeshttps://doi.org/10.14348/molcells.2015.0044openalex-snapshot
Expression Analyses Revealed Thymic Stromal Co-Transporter/Slc46A2 Is in Stem Cell Populations and Is a Putative Tumor Suppressor
inferred← citeshttps://doi.org/10.15252/embr.201540096openalex-snapshot
The thymic cortical epithelium determines the TCR repertoire of IL‐17‐producing γδT cells
inferred← citeshttps://doi.org/10.1556/650.2019.31224openalex-snapshot
A thymus szerkezete a huszonegyedik század elején
inferred← citeshttps://doi.org/10.3389/fcell.2014.00013openalex-snapshot
The antigenic determinant that defines thymic nurse cells is expressed by thymic epithelial progenitor cells
inferred← citeshttps://doi.org/10.3389/fimmu.2017.00418openalex-snapshot
Differential Response of Mouse Thymic Epithelial Cell Types to Ionizing Radiation-Induced DNA Damage
inferred← citeshttps://doi.org/10.3389/fimmu.2018.01312openalex-snapshot
DN2 Thymocytes Activate a Specific Robust DNA Damage Response to Ionizing Radiation-Induced DNA Double-Strand Breaks
inferred← citeshttps://doi.org/10.3389/fimmu.2018.01663openalex-snapshot
Cultured Human Thymic-Derived Cells Display Medullary Thymic Epithelial Cell Phenotype and Functionality
inferred← citeshttps://doi.org/10.3389/fimmu.2020.00302openalex-snapshot
Gender Disparity Impacts on Thymus Aging and LHRH Receptor Antagonist-Induced Thymic Reconstitution Following Chemotherapeutic Damage
inferred← citeshttps://doi.org/10.3389/fimmu.2020.00858openalex-snapshot
Generation and Regeneration of Thymic Epithelial Cells
inferred← citeshttps://doi.org/10.3389/fimmu.2021.606860openalex-snapshot
Autoimmune Addison's Disease as Part of the Autoimmune Polyglandular Syndrome Type 1: Historical Overview and Current Evidence
inferred← citeshttps://doi.org/10.3389/fimmu.2021.668528openalex-snapshot
The Early Postnatal Life: A Dynamic Period in Thymic Epithelial Cell Differentiation
inferred← citeshttps://doi.org/10.3389/fimmu.2022.805451openalex-snapshot
The Lineage Differentiation and Dynamic Heterogeneity of Thymic Epithelial Cells During Thymus Organogenesis
inferred← citeshttps://doi.org/10.3389/fimmu.2022.867302openalex-snapshot
Abrogation of Notch Signaling in Embryonic TECs Impacts Postnatal mTEC Homeostasis and Thymic Involution
inferred← citeshttps://doi.org/10.3389/fimmu.2022.926516openalex-snapshot
Key Factors for Thymic Function and Development
inferred← citeshttps://doi.org/10.3389/fimmu.2022.930963openalex-snapshot
Differentiation of Pluripotent Stem Cells Into Thymic Epithelial Cells and Generation of Thymic Organoids: Applications for Therapeutic Strategies Against APECED
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1202163openalex-snapshot
Thymic epithelial cell fate and potency in early organogenesis assessed by single cell transcriptional and functional analysis
inferred← citeshttps://doi.org/10.3390/immuno2020025openalex-snapshot
Structural and Functional Thymic Biomarkers Are Involved in the Pathogenesis of Thymic Epithelial Tumors: An Overview
inferred← citeshttps://doi.org/10.3390/jdb4030022openalex-snapshot
Hedgehog Signalling in the Embryonic Mouse Thymus
inferred← citeshttps://doi.org/10.37349/etat.2024.00229openalex-snapshot
Immunotherapy in thymic epithelial tumors: tissue predictive biomarkers for immune checkpoint inhibitors
inferred← citeshttps://doi.org/10.4049/jimmunol.1502010openalex-snapshot
Foxn1 Protein Expression in the Developing, Aging, and Regenerating Thymus
inferred← citeshttps://doi.org/10.4049/jimmunol.1700203openalex-snapshot
Revisiting the Road Map of Medullary Thymic Epithelial Cell Differentiation
inferred← citeshttps://doi.org/10.4049/jimmunol.1800418openalex-snapshot
Retinoic Acid Signaling in Thymic Epithelial Cells Regulates Thymopoiesis
inferred← citeshttps://doi.org/10.4049/jimmunol.1801540openalex-snapshot
Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of Foxn1 in Thymic Epithelial Cells
inferred← citeshttps://doi.org/10.64898/2026.06.16.732438openalex-snapshot
Cross-species chromatin accessibility pinpoints HIVEP3 as a driver of thymic epithelial maturation and self-antigen expression, preventing chronic inflammation
inferred← citeshttps://doi.org/10.70675/42fcff10z3380z47f8zbffbz383cb7f17c67openalex-snapshot
Ontogeny of hematopoietic progenitor cells seeding the embryonic thymus
inferred← citeshttps://doi.org/10.70675/678b5ce6z1cbcz4ee6zb7ecz9eb09e7c4478openalex-snapshot
Étude de l’épissage alternatif des transcrits induits par Aire dans le thymus
inferred← citeshttps://doi.org/10.70675/96586792zd58bz497dza907zfe0a41d8d94dopenalex-snapshot
Génération et analyse d’un nouveau modèle de la maladie APECED par déficience pour Aire chez le rat
inferred← citeshttps://doi.org/10.7546/ama.30.3-4.2023.04openalex-snapshot
Evaluation of COVID-19 Vertical Maternal Transmission with Respect to Foetal Visceral Maturation
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