35986841_10216840653711318_1105697261150535680_n

THE EFFECT OF MODULATION OF RNA EXPRESSION ON MYOCARDIAL INFARCTION RSPHO8.2 // GP // Dr. Mai Amin Zaafan (2018 - 2019) (Record no. 24969)

MARC details
000 -LEADER
fixed length control field 02448nam a22002537a 4500
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20190728115021.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 180715b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Transcribing agency MSA
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 616.1
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Amr Mohamed Alaa 150557
245 ## - TITLE STATEMENT
Title THE EFFECT OF MODULATION OF RNA<br/>EXPRESSION ON MYOCARDIAL INFARCTION RSPHO8.2 // GP // Dr. Mai Amin Zaafan (2018 - 2019)
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Giza :
Name of publisher, distributor, etc. MSA,
Date of publication, distribution, etc. 2019.
300 ## - PHYSICAL DESCRIPTION
Extent 29 p.
440 ## - SERIES STATEMENT/ADDED ENTRY--TITLE
Title PHARMACY DISTINGUISHED PROJECTS 2019
500 ## - GENERAL NOTE
General note Pharmacy - Pharmacology
520 ## - SUMMARY, ETC.
Summary, etc. Myocardial infarction (MI) is myocardial cell death due to severe and prolonged ischemia<br/>produced from atherosclerosis-related coronary artery disease. MI triggers a cascade of events<br/>and reparative phases end with myocardial cell necrosis. MicroRNA (miR) is non-coding single<br/><br/>stranded RNA that regulates protein expression. miR-103 is used to regulate expression of Fas-<br/>associated death domain (FADD) which decreases necroptosis of ischemic myocardium. The<br/><br/>study aims to investigate the modulatory effect of regulating mRNAs translation processes of<br/>myocardial infarction induced with Isoprenaline HCL 100 mg/kg (ISO) by injecting miR-103<br/>inhibitor. Eighteen mice (15-25 gm) were allocated into three groups; Group A (control)<br/>received normal saline, Group B received ISO and Group C received ISO and miR-103<br/>inhibitor. Mice were scarified by cervical dislocation under urethane anesthesia. Blood and<br/>hearts samples were collected for biochemical analysis of miR103, FADD, RIPK, IL-6 and<br/>Troponin-I. In addition, hearts were used for histopathological examination. Results showed<br/>that administration of miR-103 antagomir leads to increase in FADD protein levels in group C<br/>compared to group B. While miR-103, RIPK, and IL-6 showed high levels of expression in<br/>group B that is attenuated in group C. cardiac troponin-I also supported the previous results.<br/>Histopathological test showed normal histological structure in groups A and C while focal<br/>degeneration in myocardium in B. Accordingly, these results indicate a promising suppression<br/>of MI manifestations upon inhibition of miR-103.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Myocardial Infarction
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Ayman Selim Ahmed 151497
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Bana Ammar AlBarazi 154285
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Shahd Yehia AlWais 151775
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/1qGSlsIjxJXrGonraH1WNNweQrg7pMvOo/view">https://drive.google.com/file/d/1qGSlsIjxJXrGonraH1WNNweQrg7pMvOo/view</a>
Public note FULL TEXT PRESS HERE
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Distinguished Graduation Projects
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Shelving location Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
    Dewey Decimal Classification     Centeral Library Centeral Library Soft Copy located on library Cataloge 28.07.2019   GP68PH2019-COLOGY 82186 28.07.2019 28.07.2019 Distinguished Graduation Projects