Key Cell Functions are Modulated by Compression in an Animal Model of Hypertrophic Scar. (Record no. 3835)

MARC details
000 -LEADER
fixed length control field 03087nam a22004217a 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 181102s20182018 xxu||||| |||| 00| 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1044-7946
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code WNDS20180930-1 [pii]
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 30304713
245 ## - TITLE STATEMENT
Title Key Cell Functions are Modulated by Compression in an Animal Model of Hypertrophic Scar.
251 ## - Source
Source Wounds-A Compendium of Clinical Research & Practice. 2018 Sep 30
252 ## - Abbreviated Source
Abbreviated source WOUNDS. 2018 Sep 30
253 ## - Journal Name
Journal name Wounds : a compendium of clinical research and practice
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Year 2018
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Manufacturer FY2019
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Publication status aheadofprint
266 ## - Date added to catalog
Date added to catalog 2018-11-02
520 ## - SUMMARY, ETC.
Abstract CONCLUSIONS: Compression modulates transcription and affects multiple biological functions associated with an improved scar appearance.
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Abstract INTRODUCTION: The value of compression studies and applications in hypertrophic scar (HTS) treatment is often undermined due to the lack of ideal controls, patient compliance, and clear action mechanisms.
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Abstract MATERIALS AND METHODS: An automated pressure delivery system (APDS) applied controlled doses of pressure to scars in a red Duroc swine HTS model. Full-thickness wounds were created by a skin grafting instrument on each animal's bilateral flanks and were observed through reepithelialization and scar development. On day 70, the APDSs were mounted on the developed scars; right flank scars received a pressure of 30 mm Hg, while left flank scars received APDSs with no pressure (sham) for 2 weeks. A genome-wide assessment of compression effect on transcription in scar specimens before (early), shortly after (mid), and long after (late) compression initiation were performed.
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Abstract OBJECTIVE: This study assesses the genome-wide compression effects on scars under well-controlled conditions.
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Abstract RESULTS: Analysis of early-phase biopsies showed similar transcriptome profiles, which diverged thereafter in gene numbers and functions between compression- and sham-treated scars in the mid phase. The majority of these changes persisted in the late-phase scar samples. Canonical pathway analysis of differentially regulated genes resulted in an almost identical list of pathways during the early phase prior to compression. In the mid and late phases after compression, many of the identified pathways shifted in significance, and new pathways such as calcium signaling and cholesterol synthesis emerged.
546 ## - LANGUAGE NOTE
Language note English
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element IN PROCESS -- NOT YET INDEXED
651 ## - SUBJECT ADDED ENTRY--GEOGRAPHIC NAME
Institution MedStar Health Research Institute
651 ## - SUBJECT ADDED ENTRY--GEOGRAPHIC NAME
Institution MedStar Washington Hospital Center
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Department Firefighters' Burn and Surgical Research Laboratory
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Department Surgery/Burn Services
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Medline publication type Journal Article
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Local Authors Alkhalil, Abdulnaser
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Local Authors Carney, Bonnie C
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Local Authors Moffatt, Lauren T
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Local Authors Shupp, Jeffrey W
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Local Authors Travis, Taryn E
790 ## - Authors
All authors Alkhalil A, Carney BC, Ghassemi P, Hammamieh R, Jett M, Miller SA, Moffatt LT, Muhie S, Ramella-Roman JC, Shupp JW, Travis TE
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
Item type description Article
Holdings
Withdrawn status Lost status Damaged status Not for loan Collection Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
          MedStar Authors Catalog MedStar Authors Catalog 11/02/2018   30304713 30304713 11/02/2018 11/02/2018 Journal Article

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