On the public citation graph
Mindin is essential for cutaneous fibrogenesis in a new mouse model of systemic sclerosis
0 signed · 69 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/acr.21583openalex-snapshot
Clinical decision rule to predict the presence of interstitial lung disease in systemic sclerosis
inferredcites →https://doi.org/10.1002/art.23806openalex-snapshot
Endothelial/lymphocyte activation leads to prominent CD4+ T cell infiltration in the gastric mucosa of patients with systemic sclerosis
inferredcites →https://doi.org/10.1002/art.38098openalex-snapshot
2013 Classification Criteria for Systemic Sclerosis: An American College of Rheumatology/European League Against Rheumatism Collaborative Initiative
inferredcites →https://doi.org/10.1002/art.38990openalex-snapshot
Myofibroblasts in Murine Cutaneous Fibrosis Originate From Adiponectin‐Positive Intradermal Progenitors
inferredcites →https://doi.org/10.1002/path.2277openalex-snapshot
Cellular and molecular mechanisms of fibrosis
inferredcites →https://doi.org/10.1007/978-1-59745-060-7_14openalex-snapshot
Isolation and Culture of Epithelial Stem Cells
inferredcites →https://doi.org/10.1007/s00109-012-0883-2openalex-snapshot
Disruption of mindin exacerbates cardiac hypertrophy and fibrosis
inferredcites →https://doi.org/10.1007/s00281-015-0511-7openalex-snapshot
Cytokines in the immunopathology of systemic sclerosis
inferredcites →https://doi.org/10.1016/j.bbadis.2013.01.018openalex-snapshot
Strategies for biomarker discovery in fibrotic disease
inferredcites →https://doi.org/10.1016/j.jhep.2014.01.011openalex-snapshot
Mindin/Spondin 2 inhibits hepatic steatosis, insulin resistance, and obesity via interaction with peroxisome proliferator-activated receptor α in mice
inferredcites →https://doi.org/10.1016/j.jhep.2015.06.033openalex-snapshot
Mindin deficiency protects the liver against ischemia/reperfusion injury
inferredcites →https://doi.org/10.1016/j.semcdb.2009.11.017openalex-snapshot
Origin and function of tumor stroma fibroblasts
inferredcites →https://doi.org/10.1038/ncomms6797openalex-snapshot
Simultaneous downregulation of KLF5 and Fli1 is a key feature underlying systemic sclerosis
inferredcites →https://doi.org/10.1038/ncomms9574openalex-snapshot
The matrix protein Fibulin-5 is at the interface of tissue stiffness and inflammation in fibrosis
inferredcites →https://doi.org/10.1038/ni1021openalex-snapshot
The extracellular matrix protein mindin is a pattern-recognition molecule for microbial pathogens
inferredcites →https://doi.org/10.1038/nrm757openalex-snapshot
The snail superfamily of zinc-finger transcription factors
inferredcites →https://doi.org/10.1038/nrrheum.2009.26openalex-snapshot
Transforming growth factor β as a therapeutic target in systemic sclerosis
inferredcites →https://doi.org/10.1038/onc.2015.451openalex-snapshot
SPON2, a newly identified target gene of MACC1, drives colorectal cancer metastasis in mice and is prognostic for colorectal cancer patient survival
inferredcites →https://doi.org/10.1038/s41577-021-00540-zopenalex-snapshot
Fibroblasts as immune regulators in infection, inflammation and cancer
inferredcites →https://doi.org/10.1038/sj.emboj.7601289openalex-snapshot
Efficient dendritic cell priming of T lymphocytes depends on the extracellular matrix protein mindin
inferredcites →https://doi.org/10.1038/sj.emboj.7601421openalex-snapshot
Snail activation disrupts tissue homeostasis and induces fibrosis in the adult kidney
inferredcites →https://doi.org/10.1038/sj.gene.6364180openalex-snapshot
Interleukin-10 genotypes are associated with systemic sclerosis and influence disease-associated autoimmune responses
inferredcites →https://doi.org/10.1073/pnas.1117988108openalex-snapshot
Multiple stromal populations contribute to pulmonary fibrosis without evidence for epithelial to mesenchymal transition
inferredcites →https://doi.org/10.1093/ajcp/aqw192openalex-snapshot
Differential Expression of Hedgehog and Snail in Cutaneous Fibrosing Disorders
inferredcites →https://doi.org/10.1093/nar/28.1.27openalex-snapshot
KEGG: Kyoto Encyclopedia of Genes and Genomes
inferredcites →https://doi.org/10.1093/nar/gkz401openalex-snapshot
WebGestalt 2019: gene set analysis toolkit with revamped UIs and APIs
inferredcites →https://doi.org/10.1093/rheumatology/keh487openalex-snapshot
Localized scleroderma is an autoimmune disorder
inferredcites →https://doi.org/10.1093/rheumatology/ken310openalex-snapshot
Digital ulcers and outcomes assessment in scleroderma
inferredcites →https://doi.org/10.1111/1346-8138.15508openalex-snapshot
Interleukin (IL)‐17F and IL‐17E are related to fibrosis and vasculopathy in systemic sclerosis
inferredcites →https://doi.org/10.1111/imr.12971openalex-snapshot
The inflammatory speech of fibroblasts
inferredcites →https://doi.org/10.1111/j.1538-7836.2011.04209.xopenalex-snapshot
Fibroblast activation in vascular inflammation
inferredcites →https://doi.org/10.1111/jcmm.14618openalex-snapshot
Spondin 2 promotes the proliferation, migration and invasion of gastric cancer cells
inferredcites →https://doi.org/10.1111/jcmm.15236openalex-snapshot
Mindin deficiency alleviates renal fibrosis through inhibiting NF‐κB and TGF‐β/Smad pathways
inferredcites →https://doi.org/10.1128/mcb.01218-10openalex-snapshot
Hepatocyte-Derived Snail1 Propagates Liver Fibrosis Progression
inferredcites →https://doi.org/10.1136/annrheumdis-2018-213257openalex-snapshot
Association of circulating CXCL10 and CXCL11 with systemic sclerosis
inferredcites →https://doi.org/10.1136/annrheumdis-2019-215894openalex-snapshot
Global skin gene expression analysis of early diffuse cutaneous systemic sclerosis shows a prominent innate and adaptive inflammatory profile
inferredcites →https://doi.org/10.1136/ard.2008.091710openalex-snapshot
Systemic sclerosis and its pulmonary complications in The Netherlands: an epidemiological study
inferredcites →https://doi.org/10.1136/thx.2009.121798openalex-snapshot
SNAI transcription factors mediate epithelial-mesenchymal transition in lung fibrosis
inferredcites →https://doi.org/10.1152/physrev.00021.2018openalex-snapshot
Endothelial to Mesenchymal Transition: Role in Physiology and in the Pathogenesis of Human Diseases
inferredcites →https://doi.org/10.1155/2010/923743openalex-snapshot
Digital Ischemia in Scleroderma Spectrum of Diseases
inferredcites →https://doi.org/10.1155/2021/6628671openalex-snapshot
Development of Two Types of Skin Cancer in a Patient with Systemic Sclerosis: a Case Report and Overview of the Literature
inferredcites →https://doi.org/10.1158/0008-5472.can-10-0324openalex-snapshot
Expression of Snail in Epidermal Keratinocytes Promotes Cutaneous Inflammation and Hyperplasia Conducive to Tumor Formation
inferredcites →https://doi.org/10.1159/000163933openalex-snapshot
Mononuclear Cellular Infiltrates in Clinically Involved Skin from Patients with Systemic Sclerosis of Recent Onset Predominantly Consist of Monocytes/Macrophages
inferredcites →https://doi.org/10.1172/jci31487openalex-snapshot
Common and unique mechanisms regulate fibrosis in various fibroproliferative diseases
inferredcites →https://doi.org/10.1172/jci39104openalex-snapshot
The basics of epithelial-mesenchymal transition
inferredcites →https://doi.org/10.1172/jci99088openalex-snapshot
PAI1 mediates fibroblast–mast cell interactions in skin fibrosis
inferredcites →https://doi.org/10.1177/0748730414553029openalex-snapshot
Detecting Rhythms in Time Series with RAIN
inferredcites →https://doi.org/10.1182/blood-2005-04-1658openalex-snapshot
The extracellular matrix protein mindin serves as an integrin ligand and is critical for inflammatory cell recruitment
inferredcites →https://doi.org/10.1371/journal.pbio.0030011openalex-snapshot
A Signaling Pathway Involving TGF-β2 and Snail in Hair Follicle Morphogenesis
inferredcites →https://doi.org/10.1371/journal.pone.0037225openalex-snapshot
Spondin-2 (SPON2), a More Prostate-Cancer-Specific Diagnostic Biomarker
inferredcites →https://doi.org/10.15252/emmm.201809085openalex-snapshot
Dual reporter genetic mouse models of pancreatic cancer identify an epithelial‐to‐mesenchymal transition‐independent metastasis program
inferredcites →https://doi.org/10.1590/abd1806-4841.20152890openalex-snapshot
Localized scleroderma: clinical spectrum and therapeutic update
inferredcites →https://doi.org/10.3389/fcell.2020.00794openalex-snapshot
Transcriptional Activation of Matricellular Protein Spondin2 (SPON2) by BRG1 in Vascular Endothelial Cells Promotes Macrophage Chemotaxis
inferredcites →https://doi.org/10.3389/fimmu.2018.02045openalex-snapshot
Vascular Leaking, a Pivotal and Early Pathogenetic Event in Systemic Sclerosis: Should the Door Be Closed?
inferredcites →https://doi.org/10.3389/fped.2021.669116openalex-snapshot
Genetic Signatures From RNA Sequencing of Pediatric Localized Scleroderma Skin
inferredcites →https://doi.org/10.3390/cancers12061439openalex-snapshot
SPON2 Is Upregulated through Notch Signaling Pathway and Promotes Tumor Progression in Gastric Cancer
inferredcites →https://doi.org/10.3748/wjg.v16.i9.1070openalex-snapshot
Mindin is upregulated during colitis and may activate NF-κB in a TLR-9 mediated manner
inferredcites →https://doi.org/10.3899/jrheum.111380openalex-snapshot
Vascular Leak Is a Central Feature in the Pathogenesis of Systemic Sclerosis
inferredcites →https://doi.org/10.5301/jsrd.5000236openalex-snapshot
Defining Skin Ulcers in Systemic Sclerosis: Systematic Literature Review and Proposed World Scleroderma Foundation (WSF) Definition
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-981-99-0846-2_43-1openalex-snapshot
Application of Single-Cell Sequencing on Stem Cell Research
inferred← citeshttps://doi.org/10.1007/978-981-99-7119-0_43openalex-snapshot
Application of Single-Cell Sequencing on Stem Cell Research
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111390openalex-snapshot
Snail maintains the stem/progenitor state of skin epithelial cells and carcinomas through the autocrine effect of matricellular protein Mindin
inferred← citeshttps://doi.org/10.1097/bor.0000000000000895openalex-snapshot
Contribution of keratinocytes to dermal fibrosis
inferred← citeshttps://doi.org/10.1101/2022.05.17.492347openalex-snapshot
Mindin differentially regulates fibroblast subpopulations via distinct members of the Src family kinases during fibrogenesis
inferred← citeshttps://doi.org/10.1101/2023.05.12.540570openalex-snapshot
Stable expression of Helicobacter pylori cagA oncoprotein in brinjal
inferred← citeshttps://doi.org/10.5530/ijper.20250081openalex-snapshot
Expression of Helicobacter pylori CagA in Solanum melongena L-A Cost Effective Strategy for Vaccine Development
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.