Dynamic reciprocity in the wound microenvironment. - Wikidata - wikimedia - TriplyDB

Dynamic reciprocity in the wound microenvironment.

Dynamic reciprocity in the wound microenvironment.

http://www.wikidata.org/entity/Q37848470

about

Serpina3n accelerates tissue repair in a diabetic mouse model of delayed wound healing Intracavity lavage and wound irrigation for prevention of surgical site infection Engineered Biopolymeric Scaffolds for Chronic Wound Healing Regenerative Medicine: Charting a New Course in Wound Healing Ovine-Based Collagen Matrix Dressing: Next-Generation Collagen Dressing for Wound Care Curbing Inflammation in Skin Wound Healing: A Review Challenges in the Treatment of Chronic Wounds.Fibronectin Interaction and Enhancement of Growth Factors: Importance for Wound Healing Diverse Roles of Heparan Sulfate and Heparin in Wound Repair Stem cell therapy for lower extremity diabetic ulcers: where do we stand?Growth Factor-Extracellular Matrix Interactions Regulate Wound Repair Cutaneous wound healing: recruiting developmental pathways for regeneration Interactions of the Extracellular Matrix and Progenitor Cells in Cutaneous Wound Healing Killing me softly--future challenges in apoptosis research Skin regeneration in adult axolotls: a blueprint for scar-free healing in vertebrates The stereotypical molecular cascade in neovascular age-related macular degeneration: the role of dynamic reciprocity Regulation of the innate immune response by fibronectin: synergism between the III-1 and EDA domains Individual versus collective fibroblast spreading and migration: regulation by matrix composition in 3D culture.FUT11 as a potential biomarker of clear cell renal cell carcinoma progression based on meta-analysis of gene expression data NGF accelerates cutaneous wound healing by promoting the migration of dermal fibroblasts via the PI3K/Akt-Rac1-JNK and ERK pathways.Utility of a human-mouse xenograft model and in vivo near-infrared fluorescent imaging for studying wound healing Joint pathology and platelet-rich plasma therapies.Skin wound healing and scarring: fetal wounds and regenerative restitution.The importance of both fibroblasts and keratinocytes in a bilayered living cellular construct used in wound healing Identification of biomarkers in sequential biopsies of patients with chronic wounds receiving simultaneous acute wounds: a genetic, histological, and noninvasive imaging study.Pericyte contractility controls endothelial cell cycle progression and sprouting: insights into angiogenic switch mechanics.Concentration of fibrin and presence of plasminogen affect proliferation, fibrinolytic activity, and morphology of human fibroblasts and keratinocytes in 3D fibrin constructs A prospective randomised comparative parallel study of amniotic membrane wound graft in the management of diabetic foot ulcers Lumican Accelerates Wound Healing by Enhancing α2β1 Integrin-Mediated Fibroblast Contractility Dense fibrillar collagen is a potent inducer of invadopodia via a specific signaling network.Type III collagen regulates osteoblastogenesis and the quantity of trabecular bone Microarray-based characterization of differential gene expression during vocal fold wound healing in rats.Revisiting the matricellular concept.Dynamic reciprocity between cells and their microenvironment in reproduction.Biodegradable Gelatin Microcarriers Facilitate Re-Epithelialization of Human Cutaneous Wounds - An In Vitro Study in Human Skin.Antitumor potential of a synthetic interferon-alpha/PLGF-2 positive charge peptide hybrid molecule in pancreatic cancer cells.A placental growth factor-positively charged peptide potentiates the antitumor activity of interferon-gamma in human brain glioblastoma U87 cells Identification and Characterization of Novel Matrix-Derived Bioactive Peptides: A Role for Collagenase from Santyl® Ointment in Post-Debridement Wound Healing?Pigment epithelium-derived factor as a multifunctional regulator of wound healing Prostaglandin E₂ induces oncostatin M expression in human chronic wound macrophages through Axl receptor tyrosine kinase pathway

P2860

Q24563950-EEED07BC-DE9F-43C4-986F-E6C45B735F42 Q26471726-E770F1CF-2715-421F-AAAB-783E715978FA Q26740156-02AEE05A-31E2-4E0F-82CF-0D4FA55AB2DE Q26745626-524FB51B-CAA0-4041-8AA9-A7292BF85114 Q26767421-75480CBE-EEB9-4F70-819C-C7DCFB28C519 Q26781905-03114C8F-33CD-4AD7-9BBD-66131A0B0E05 Q26784576-CDB5AE6A-A741-44BA-B410-AFEF98145060 Q26798456-DCFF733D-683B-4A1D-87D4-41A815E76D31 Q26799832-904B65E7-3959-4D6F-80B4-B87D9A3360DB Q26824484-6463F04B-0D9A-4A48-ACB7-9D0CEDA6D834 Q26827591-602EBC9F-E0B9-4053-B2E3-DA440C430023 Q27004417-1F1F5D7C-0277-4C37-8CDC-9C33907FA19D Q27015024-C055B3BA-A326-4A10-B0F2-37DB4E2FD2C7 Q27025213-E66D8E16-6D9C-400F-B4BB-E0B314F2BF82 Q27307724-E4293DB3-FD81-4EDB-8699-3F09E9834EC8 Q28085495-99C40922-E4D3-4E89-9160-CB71D9786A75 Q28541049-75C21EDD-47FC-4D4A-BC1F-B5D320FB0134 Q30535725-BC95A98E-F267-4812-BEEE-C5BE4044676B Q30711138-CF404DA6-D872-45D0-A41A-B1A286DC53A5 Q33747664-440BFFB2-05C1-489A-92E0-A5E4F25AFCB7 Q33794168-5E7B452D-69D9-4771-83BD-BF374901E948 Q34240837-DF3F10C6-E8AD-4830-8ED3-D65892EA4DEB Q34383439-F56FCFC1-7769-4D3A-86D8-EFC09AF0E010 Q34413433-7E704884-5230-42D7-ACED-C8B6B55365FF Q34416627-CABDD936-D4FB-4153-9C1F-31C88434052B Q34439465-B1F7710F-FB7C-44B3-8CD8-F506C247E00B Q34500863-B864F940-8314-4502-9A52-258BAB6F833A Q34512571-C4E06049-B4F0-484C-8C91-6A65F1497FF6 Q34806507-8589323D-6164-47FF-9FFA-AAF25BE46B9C Q35042854-265ADE27-75F1-4F08-905F-7F2A8C49F0A6 Q35105491-F1A35968-889B-4855-9768-1F18DA13B18F Q35144043-A33622D7-0BF1-4817-BCCB-172C5A78A637 Q35233858-C0BBE878-0417-44C0-8525-E2CB24A2ABDF Q35617092-E94B9B23-C443-4C43-9032-0830D9F8CE9F Q35659958-59A6B321-2E38-4B6C-B71E-F55326E9B2BE Q35846233-8AAFF8CE-1889-4E2A-8EFD-32F3DD3AF3BC Q36019591-1026BBAE-E84B-422D-99B9-8AAA3C8E84BE Q36086178-18464D78-CDDC-4273-BE85-29FE153A29F1 Q36114293-AE36715E-1274-4923-BB9F-5ADD6CBC9F3B Q36222919-CB5E1AAB-5398-4A97-A48E-07ACE70B0039

P2860

Dynamic reciprocity in the wound microenvironment.

http://www.wikidata.org/entity/Q37848470

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on March 2011

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Dynamic reciprocity in the wound microenvironment.

@en

Dynamic reciprocity in the wound microenvironment.

@nl

type

label

Dynamic reciprocity in the wound microenvironment.

@en

Dynamic reciprocity in the wound microenvironment.

@nl

prefLabel

Dynamic reciprocity in the wound microenvironment.

@en

Dynamic reciprocity in the wound microenvironment.

@nl

P1433

Q37848470-5FEB77A2-E6DA-4738-994B-1E1E940233A4

P1476

Q37848470-B000FD1E-4237-400A-B2CB-DD1E020C861E

P2093

Q37848470-5931E297-2D64-41AE-B1A0-470D83183CF2

Q37848470-9413E744-9FE7-4157-9104-06D264404628

Q37848470-9CEDCBD3-0D2F-4D22-A1AE-C20E7FD331E5

Q37848470-DB6A9720-ADFD-4914-A1EE-0903148E2EE4

Q37848470-E0E20B79-1E77-401C-91EE-9F8C4E0545DE

P2860

Q37848470-00A0503A-920F-46EB-86AC-92532693B7E0

Q37848470-03D6E880-6DB3-479A-B5E7-8DC5B4F5D6C8

Q37848470-05A784E1-3FE8-4EB7-A6AF-441B86CFACB4

Q37848470-0AB1DC34-383F-46C2-9D10-081FCC820B5F

Q37848470-0ABF67BF-A861-49CD-BD24-BD64E3DA5A2A

Q37848470-0B0FC9A7-796D-4A30-A5F5-B9D70DEF414B

Q37848470-0B698D01-C8AF-4455-8B88-49768C8B2E0C

Q37848470-0C8A11F9-9AB6-44D4-BB88-C3063D31A070

Q37848470-0D10B550-7E69-45D9-8C5B-045793FDF62C

Q37848470-1152023B-3598-48D2-8F3E-B345866F6934

P304

Q37848470-3BFFC880-3095-4A71-BC81-29ABE1B674DB

P31

Q37848470-9C6EA898-C12D-4C96-949F-B26D7DCDE50E

P356

Q37848470-E8A0A681-2043-4A7B-B32F-0BA0DF5FC9BE

P433

Q37848470-70C4F632-2F0D-427A-B221-95446FAC1C37

P478

Q37848470-92B59EF4-E5E2-4AB1-A45D-397A4F0A3FF8

P577

Q37848470-132EBE6C-F094-4D95-A7F3-AE9C9496ABA9

P698

Q37848470-AD1494CB-EDE5-4020-A384-016118A38D40

P932

Q37848470-DBBF8CDE-91F5-44D5-A0C4-36D285859160

P356

J.1524-475X.2011.00673.X

P1433

Wound Repair and Regeneration

P1476

Dynamic reciprocity in the wound microenvironment.

@en

P2093

Gregory S Schultz

http://www.w3.org/2001/XMLSchema#string

Ira M Herman

http://www.w3.org/2001/XMLSchema#string

Jeffrey M Davidson

http://www.w3.org/2001/XMLSchema#string

Paul Bornstein

http://www.w3.org/2001/XMLSchema#string

Robert S Kirsner

http://www.w3.org/2001/XMLSchema#string

P2860

Crystal structure of a ternary FGF-FGFR-heparin complex reveals a dual role for heparin in FGFR binding and dimerization

Appearance of heparin-binding EGF-like growth factor in wound fluid as a response to injury

Ectodomain shedding of epidermal growth factor receptor ligands is required for keratinocyte migration in cutaneous wound healing

Myofibroblast contraction activates latent TGF-beta1 from the extracellular matrix

Molecular markers in patients with chronic wounds to guide surgical debridement

Bacterial biofilms: a common cause of persistent infections

The integrin alpha v beta 6 binds and activates latent TGF beta 1: a mechanism for regulating pulmonary inflammation and fibrosis

Myofibroblasts and mechano-regulation of connective tissue remodelling

Protocol for the successful treatment of venous ulcers

Negative regulation of transforming growth factor-beta by the proteoglycan decorin

P304

134-148

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/J.1524-475X.2011.00673.X

http://www.w3.org/2001/XMLSchema#string

P433

2

http://www.w3.org/2001/XMLSchema#string

P478

19

http://www.w3.org/2001/XMLSchema#string

P577

2011-03-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

21362080

http://www.w3.org/2001/XMLSchema#string

P932

3051353

http://www.w3.org/2001/XMLSchema#string