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Deciphering the Regulatory Landscape of γδ T Cell Development by Single-Cell RNA-Sequencing

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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.201343801openalex-snapshot
TLRs to cytokines: Mechanistic insights from the imiquimod mouse model of psoriasis
inferredcites →https://doi.org/10.1002/eji.201646753openalex-snapshot
Eomes expression reports the progressive differentiation of IFN‐γ‐producing Th1‐like γδ T cells
inferredcites →https://doi.org/10.1007/978-1-59745-060-7_14openalex-snapshot
Isolation and Culture of Epithelial Stem Cells
inferredcites →https://doi.org/10.1016/j.cell.2006.07.035openalex-snapshot
The Orphan Nuclear Receptor RORγt Directs the Differentiation Program of Proinflammatory IL-17+ T Helper Cells
inferredcites →https://doi.org/10.1016/j.cell.2016.10.052openalex-snapshot
Impaired Epidermal to Dendritic T Cell Signaling Slows Wound Repair in Aged Skin
inferredcites →https://doi.org/10.1016/j.cellimm.2015.03.007openalex-snapshot
Gamma delta T-cell differentiation and effector function programming, TCR signal strength, when and how much?
inferredcites →https://doi.org/10.1016/j.immuni.2005.03.014openalex-snapshot
TCR Signal Strength Influences αβ/γδ Lineage Fate
inferredcites →https://doi.org/10.1016/j.immuni.2005.04.003openalex-snapshot
Attenuation of γδTCR Signaling Efficiently Diverts Thymocytes to the αβ Lineage
inferredcites →https://doi.org/10.1016/j.immuni.2006.05.010openalex-snapshot
Stage-Specific and Differential Notch Dependency at the αβ and γδ T Lineage Bifurcation
inferredcites →https://doi.org/10.1016/j.immuni.2009.08.006openalex-snapshot
γδ T Cells and the Lymphoid Stress-Surveillance Response
inferredcites →https://doi.org/10.1016/j.immuni.2010.03.005openalex-snapshot
Fate Mapping Reveals Separate Origins of T Cells and Myeloid Lineages in the Thymus
inferredcites →https://doi.org/10.1016/j.immuni.2011.08.001openalex-snapshot
Pivotal Role of Dermal IL-17-Producing γδ T Cells in Skin Inflammation
inferredcites →https://doi.org/10.1016/j.immuni.2012.06.003openalex-snapshot
Development of Interleukin-17-Producing γδ T Cells Is Restricted to a Functional Embryonic Wave
inferredcites →https://doi.org/10.1016/j.immuni.2013.01.010openalex-snapshot
A Network of High-Mobility Group Box Transcription Factors Programs Innate Interleukin-17 Production
inferredcites →https://doi.org/10.1016/j.it.2017.01.007openalex-snapshot
Thymic Determinants of γδ T Cell Differentiation
inferredcites →https://doi.org/10.1016/j.stem.2016.05.010openalex-snapshot
De Novo Prediction of Stem Cell Identity using Single-Cell Transcriptome Data
inferredcites →https://doi.org/10.1038/322836a0openalex-snapshot
Diversity of murine gamma genes and expression in fetal and adult T lymphocytes
inferredcites →https://doi.org/10.1038/nature25500openalex-snapshot
c-MAF-dependent regulatory T cells mediate immunological tolerance to a gut pathobiont
inferredcites →https://doi.org/10.1038/ni.2247openalex-snapshot
Intrathymic programming of effector fates in three molecularly distinct γδ T cell subtypes
inferredcites →https://doi.org/10.1038/ni.2585openalex-snapshot
Deficiency in IL-17-committed Vγ4+ γδ T cells in a spontaneous Sox13-mutant CD45.1+ congenic mouse substrain provides protection from dermatitis
inferredcites →https://doi.org/10.1038/ni.3514openalex-snapshot
Asynchronous combinatorial action of four regulatory factors activates Bcl11b for T cell commitment
inferredcites →https://doi.org/10.1038/ni1022openalex-snapshot
An essential function for the nuclear receptor RORγt in the generation of fetal lymphoid tissue inducer cells
inferredcites →https://doi.org/10.1038/ni1371openalex-snapshot
Visualization of the earliest steps of γδ T cell development in the adult thymus
inferredcites →https://doi.org/10.1038/ni944openalex-snapshot
BTLA is a lymphocyte inhibitory receptor with similarities to CTLA-4 and PD-1
inferredcites →https://doi.org/10.1038/nmeth.2930openalex-snapshot
Validation of noise models for single-cell transcriptomics
inferredcites →https://doi.org/10.1038/nmeth.4662openalex-snapshot
FateID infers cell fate bias in multipotent progenitors from single-cell RNA-seq data
inferredcites →https://doi.org/10.1038/nmeth1005-731openalex-snapshot
The External RNA Controls Consortium: a progress report
inferredcites →https://doi.org/10.1038/nri2781openalex-snapshot
γδ T cell effector functions: a blend of innate programming and acquired plasticity
inferredcites →https://doi.org/10.1038/nri3384openalex-snapshot
Six-of-the-best: unique contributions of γδ T cells to immunology
inferredcites →https://doi.org/10.1038/nri3389openalex-snapshot
Shades of grey — the blurring view of innate and adaptive immunity
inferredcites →https://doi.org/10.1038/nri3702openalex-snapshot
Developmental gene networks: a triathlon on the course to T cell identity
inferredcites →https://doi.org/10.1038/nri797openalex-snapshot
γδ T cells: functional plasticity and heterogeneity
inferredcites →https://doi.org/10.1039/c5mb00663eopenalex-snapshot
ReactomePA: an R/Bioconductor package for reactome pathway analysis and visualization
inferredcites →https://doi.org/10.1073/pnas.0903895106openalex-snapshot
TCR-inducible PLZF transcription factor required for innate phenotype of a subset of γδ T cells with restricted TCR diversity
inferredcites →https://doi.org/10.1073/pnas.1312872111openalex-snapshot
Enforcement of γδ-lineage commitment by the pre–T-cell receptor in precursors with weak γδ-TCR signals
inferredcites →https://doi.org/10.1084/jem.20130791openalex-snapshot
Sox5 and c-Maf cooperatively induce Th17 cell differentiation via RORγt induction as downstream targets of Stat3
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp698openalex-snapshot
Fast and accurate long-read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1101/gr.1239303openalex-snapshot
Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks
inferredcites →https://doi.org/10.1111/jnc.13414openalex-snapshot
Sox13 functionally complements the related Sox5 and Sox6 as important developmental modulators in mouse spinal cord oligodendrocytes
inferredcites →https://doi.org/10.1126/science.1135344openalex-snapshot
Regulation of γδ Versus αß T Lymphocyte Differentiation by the Transcription Factor SOX13
inferredcites →https://doi.org/10.1186/gb-2010-11-10-r106openalex-snapshot
Differential expression analysis for sequence count data
inferredcites →https://doi.org/10.1186/s13059-016-0938-8openalex-snapshot
CEL-Seq2: sensitive highly-multiplexed single-cell RNA-Seq
inferredcites →https://doi.org/10.1371/journal.pone.0012776openalex-snapshot
Inferring Regulatory Networks from Expression Data Using Tree-Based Methods
inferredcites →https://doi.org/10.3389/fimmu.2013.00431openalex-snapshot
Molecular Mechanisms of Differentiation of Murine Pro-Inflammatory γδ T Cell Subsets
inferredcites →https://doi.org/10.3389/fimmu.2017.01399openalex-snapshot
Differentiation of IL-17-Producing Invariant Natural Killer T Cells Requires Expression of the Transcription Factor c-Maf
inferredcites →https://doi.org/10.4049/jimmunol.0802999openalex-snapshot
Imiquimod-Induced Psoriasis-Like Skin Inflammation in Mice Is Mediated via the IL-23/IL-17 Axis
inferredcites →https://doi.org/10.4049/jimmunol.0900123openalex-snapshot
c-Maf Regulates IL-10 Expression during Th17 Polarization
inferredcites →https://doi.org/10.4049/jimmunol.1000679openalex-snapshot
Fine-Scale Staging of T Cell Lineage Commitment in Adult Mouse Thymus
inferredcites →https://doi.org/10.4049/jimmunol.1002766openalex-snapshot
Unexpected Role for the B Cell-Specific Src Family Kinase B Lymphoid Kinase in the Development of IL-17–Producing γδ T Cells
inferredcites →https://doi.org/10.4049/jimmunol.1401813openalex-snapshot
Origins of γδ T Cell Effector Subsets: A Riddle Wrapped in an Enigma
inferredcites →https://doi.org/10.4049/jimmunol.1500939openalex-snapshot
PLZF Controls the Development of Fetal-Derived IL-17+Vγ6+ γδ T Cells
inferredcites →https://doi.org/10.4049/jimmunol.1501921openalex-snapshot
Effector γδ T Cell Differentiation Relies on Master but Not Auxiliary Th Cell Transcription Factors
inferredcites →https://doi.org/10.4049/jimmunol.1701134openalex-snapshot
Cutting Edge: c-Maf Is Required for Regulatory T Cells To Adopt RORγt+ and Follicular Phenotypes
inferredcites →https://doi.org/10.4049/jimmunol.181.9.5940openalex-snapshot
Identification of CD25+ γδ T Cells As Fetal Thymus-Derived Naturally Occurring IL-17 Producers
inferredcites →https://doi.org/10.4161/trns.21809openalex-snapshot
The transcription factor c-Maf in sensory neuron development

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1038/s41592-020-01050-xopenalex-snapshot
Joint probabilistic modeling of single-cell multi-omic data with totalVI
inferred← citeshttps://doi.org/10.1101/2020.05.14.094334openalex-snapshot
The cIAP ubiquitin ligases sustain type 3 γδ T and innate lymphoid cells during aging to allow normal cutaneous and mucosal responses
inferred← citeshttps://doi.org/10.3389/fimmu.2020.00042openalex-snapshot
Regulation of γδ T Cell Effector Diversification in the Thymus
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