The wound healing, chronic fibrosis, and cancer progression triad
about
The Epithelial Sodium Channel and the Processes of Wound HealingCancer Microenvironment: What Can We Learn from the Stem Cell NicheCells activated for wound repair have the potential to direct collective invasion of an epithelium.Transmembrane proteoglycans control stretch-activated channels to set cytosolic calcium levels.The Runt-related transcription factor 1 in prostate cancer-associated fibroblastsThe host microenvironment influences prostate cancer invasion, systemic spread, bone colonization, and osteoblastic metastasis.Type III Collagen Directs Stromal Organization and Limits Metastasis in a Murine Model of Breast Cancer.Characterization of various cell lines from different ampullary cancer subtypes and cancer associated fibroblast-mediated responses.Human Mesenchymal Stem Cells of Diverse Origins Support Persistent Infection with Kaposi's Sarcoma-Associated Herpesvirus and Manifest Distinct Angiogenic, Invasive, and Transforming Phenotypes.Sphingosine kinase 1 is required for TGF-β mediated fibroblastto- myofibroblast differentiation in ovarian cancer.Collagen and fibronectin: threads linking obesity and breast cancer.Hyaluronan and RHAMM in wound repair and the "cancerization" of stromal tissues.Biomechanical and biochemical remodeling of stromal extracellular matrix in cancerClinical application of sonoelastography in thyroid, prostate, kidney, pancreas, and deep venous thrombosis.Proteomics of cell-cell interactions in health and disease.Immune suppressive mechanisms in the tumor microenvironment.Epithelial-to-mesenchymal transition transcription factors in cancer-associated fibroblasts.Stromal dynamic reciprocity in cancer: intricacies of fibroblastic-ECM interactions.Palladin mediates stiffness-induced fibroblast activation in the tumor microenvironment.The potential role of platelets in the consensus molecular subtypes of colorectal cancer.Invisible Shield: Review of the Corneal Epithelium as a Barrier to UV Radiation, Pathogens, and Other Environmental Stimuli.Preparation of Extracellular Matrices Produced by Cultured and Primary Fibroblasts.Aligned fibers direct collective cell migration to engineer closing and nonclosing wound gaps.Advanced Role of Hippo Signaling in Endometrial Fibrosis: Implications for Intrauterine Adhesion.Extracellular matrix directs phenotypic heterogeneity of activated fibroblasts.Comprehensive DNA microarray expression profiles of tumors in tenascin-C-knockout mice.Identification of a small-molecule ligand of β-arrestin1 as an inhibitor of stromal fibroblast cell migration accelerated by cancer cells.Editorial: Wound healing and fibrosis-two sides of the same coin.Skin indentation firmness and tissue dielectric constant assessed in face, neck, and arm skin of young healthy women.Stretching Reduces Tumor Growth in a Mouse Breast Cancer Model.Limited fibrosis accompanies triple-negative breast cancer metastasis in multiple model systems and is not a preventive target.The evolving relationship of wound healing and tumor stroma
P2860
Q26738777-B2AA84C0-8AC3-43A3-A198-C97102F1A71BQ26782463-35754173-F980-437C-B448-3D95D5E96D3EQ27305106-1534EB53-045F-45B1-BE57-CCC04BF7ADB5Q27310200-E58C40D1-2B6C-44F7-ABDF-B37F8A9C3FD8Q34581047-4972ED54-40B4-47DF-A291-F41D4EC0DEA9Q34699785-5A498B8C-32F7-42BF-B86C-9B612D641D8CQ35568107-B6B2A66D-7935-4969-A4C3-0B28071A2FC8Q35948210-3ACA68D7-6818-493D-BAB5-D0450C772EB7Q36548258-0A416D62-656C-4D65-8A3D-5392D528B095Q36782379-577FB223-0FFB-4F3A-B913-60EFD0E384AAQ37407832-5B6D0981-2E3B-4BFE-872F-0F0E21E7950DQ38243335-40298FD2-5F8F-4C2C-89DC-FA32F37F562AQ38364631-AE81D791-A15A-4B59-A35E-26FE1DF0EB90Q38370216-4C6964BB-1577-45BA-8646-CAB87B3F18CBQ38629150-363E3632-6531-4767-8A7C-EC208CE04015Q38648567-EE2B4F6E-B89D-475E-8C11-15B7163D7CACQ38763748-0C9B9E42-50AD-4B5D-8889-20CE8385BCEBQ38841939-A622F763-C0A5-4342-A988-C312E8FFC6A0Q38850479-CAE4BD53-E339-43E2-8B2A-139947302285Q39417307-0548AE97-D4FA-44FA-BADE-BEE39A69D575Q41112869-E94E0A01-50A8-4807-BBF1-20BC8ED6AB17Q41412481-9E50213E-A0FD-498F-A8AA-0B149BF9742EQ45064204-E9C22854-381F-449C-B984-E850C7AF734EQ47122463-AB0742DE-CEF3-44EF-B88F-49FAD42053AFQ47285215-32B4F271-866E-4FDA-BFEA-0BB2BC9C52E9Q47852923-277BEEA6-A36B-472F-AA56-4278C5FF4D60Q48143870-D8E1BCBA-DB20-4150-B919-A87F326D01A4Q53059066-880BCF9C-2548-434D-ABBE-E23B3655E65BQ53777005-5587B7B7-33A8-4E90-B318-6C7CEFD1F3B8Q55215695-A5CFD0B6-5466-46A0-910F-1BDBAB4C1A62Q55339193-6EA3615A-BEC8-4D05-814C-8597F4F50BF8Q59134962-2735DE90-9190-496F-8155-D99A856A365A
P2860
The wound healing, chronic fibrosis, and cancer progression triad
description
2014 nî lūn-bûn
@nan
2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
The wound healing, chronic fibrosis, and cancer progression triad
@ast
The wound healing, chronic fibrosis, and cancer progression triad
@en
The wound healing, chronic fibrosis, and cancer progression triad
@nl
type
label
The wound healing, chronic fibrosis, and cancer progression triad
@ast
The wound healing, chronic fibrosis, and cancer progression triad
@en
The wound healing, chronic fibrosis, and cancer progression triad
@nl
prefLabel
The wound healing, chronic fibrosis, and cancer progression triad
@ast
The wound healing, chronic fibrosis, and cancer progression triad
@en
The wound healing, chronic fibrosis, and cancer progression triad
@nl
P2860
P3181
P1476
The wound healing, chronic fibrosis, and cancer progression triad
@en
P2093
Edna Cukierman
P2860
P304
P3181
P356
10.1152/PHYSIOLGENOMICS.00158.2013
P407
P577
2014-02-11T00:00:00Z