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  <title>DSpace Collection: Perfüzyonistlik Bölümü'ne ait koleksiyonları içerir.</title>
  <link rel="alternate" href="http://hdl.handle.net/11513/90" />
  <subtitle>Perfüzyonistlik Bölümü'ne ait koleksiyonları içerir.</subtitle>
  <id>http://hdl.handle.net/11513/90</id>
  <updated>2026-04-21T19:02:40Z</updated>
  <dc:date>2026-04-21T19:02:40Z</dc:date>
  <entry>
    <title>New prognostic biomarker in cardiovascular field: ST2 (IL1RL1)</title>
    <link rel="alternate" href="http://hdl.handle.net/11513/133" />
    <author>
      <name>Dikme, Reşat</name>
    </author>
    <author>
      <name>Padak, Mahmut</name>
    </author>
    <author>
      <name>Göz, Mustafa</name>
    </author>
    <author>
      <name>Aydın, Mehmet Salih</name>
    </author>
    <author>
      <name>Göç, Ömer</name>
    </author>
    <id>http://hdl.handle.net/11513/133</id>
    <updated>2019-06-10T11:16:13Z</updated>
    <published>2019-01-01T00:00:00Z</published>
    <summary type="text">Title: New prognostic biomarker in cardiovascular field: ST2 (IL1RL1)
Authors: Dikme, Reşat; Padak, Mahmut; Göz, Mustafa; Aydın, Mehmet Salih; Göç, Ömer
Abstract: As a result of natural immunity in the heart ST2 (IL1RL1) that protects the heart against excessive pressure load and tension, has two important isoforms&#xD;
(ST2L–membranebound, sST2-soluble). As ligand of ST2L and sST2 is interleukin 33 (IL33), the connection of ST2L to IL33 stimulates cardioprotective signal&#xD;
cascade whereas connection of sST2 to IL33 causes annihilation of these positive effects. As a high level of sST2 shows that the heart is under dense stress,&#xD;
this situation causes cell death, tissue fibrosis, decreased cardiac functions and an increase in progression rate of disease. That is why in cardiovascular disease sST2 is accepted as a biomarker of poor prognosis. It was obtained that the increase of sST2 over normal concentration multiplies negative situations&#xD;
related to cardiovascular diseases 3 times more. In 2013 in ACCF/AHA (American College of Cardiology Foundation/American Heart Association) guidelines,&#xD;
sST2 that was defined as “novel biomarker” for HF (Heart failure), is an independent biomarker from natriuretic peptides and cardiac troponins and is an&#xD;
important sign in cardiovascular diseases. ST2 is not affected by factors such as age, body mass index and kidney function disorder.</summary>
    <dc:date>2019-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Liquid reflecting the heart function: Pericardial fluid</title>
    <link rel="alternate" href="http://hdl.handle.net/11513/132" />
    <author>
      <name>Dikme, Reşat</name>
    </author>
    <author>
      <name>Padak, Mahmut</name>
    </author>
    <author>
      <name>Göz, Mustafa</name>
    </author>
    <author>
      <name>Aydın, Mehmet Salih</name>
    </author>
    <author>
      <name>Göç, Ömer</name>
    </author>
    <id>http://hdl.handle.net/11513/132</id>
    <updated>2019-06-10T11:12:53Z</updated>
    <published>2019-01-01T00:00:00Z</published>
    <summary type="text">Title: Liquid reflecting the heart function: Pericardial fluid
Authors: Dikme, Reşat; Padak, Mahmut; Göz, Mustafa; Aydın, Mehmet Salih; Göç, Ömer
Abstract: Pericardium is a sac surrounding the heart and big vessels, protecting them against injury and infection and fixing the heart to the mediastinum. As pericardium&#xD;
has an immunologic, paracrine, vasomotor and fibrinolytic activity; it affects myocyte structure, function and gene expression by synthesizing materials such as&#xD;
eicosanoids and prostaglandin. Pericardial fluid (PF) in two-walled pericardial sac surrounding the heart completely, has a potential of reflecting heart function&#xD;
and shows dynamic changes. Since many biomarkers associated with cardiovascular diseases pass to pericardial sac, PF analysis provides to be understood&#xD;
many pathophysiological mechanisms in various pericardial and cardiovascular diseases. The aim of this article is to give actual information about the content&#xD;
of PF that is thought to be passive ultrafiltrate of plasma produced with hydrostatic pressure difference and osmotic concentration gradient for years.</summary>
    <dc:date>2019-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>MICRORNAS IN THE PERICARDIAL FLUID OF CORONARY ARTERY PATIENTS</title>
    <link rel="alternate" href="http://hdl.handle.net/11513/131" />
    <author>
      <name>Dikme, Reşat</name>
    </author>
    <author>
      <name>Gönel, Ataman</name>
    </author>
    <author>
      <name>Koyuncu, İsmail</name>
    </author>
    <author>
      <name>Akkafa, Feridun</name>
    </author>
    <author>
      <name>Göz, Mustafa</name>
    </author>
    <author>
      <name>Aydın, Mehmet Salih</name>
    </author>
    <author>
      <name>Temiz, Ebru</name>
    </author>
    <id>http://hdl.handle.net/11513/131</id>
    <updated>2019-06-10T11:09:09Z</updated>
    <published>2018-01-01T00:00:00Z</published>
    <summary type="text">Title: MICRORNAS IN THE PERICARDIAL FLUID OF CORONARY ARTERY PATIENTS
Authors: Dikme, Reşat; Gönel, Ataman; Koyuncu, İsmail; Akkafa, Feridun; Göz, Mustafa; Aydın, Mehmet Salih; Temiz, Ebru
Abstract: Background: microRNAs (miRNAs) that play important roles in organisms are associated&#xD;
with usual function of cells, development of living, biological processes as well as many&#xD;
diseases involving cardiovascular disease. miRNAs are effective in endothelium disfunction,&#xD;
atherosclerosis, inflammation, apoptosis and angiogenesis related with coronary artery disease&#xD;
(CAD). miRNAs that are explained differently in cells, exist extracellularly, in circulation and&#xD;
body fluids. Many biomarkers related with CAD can get through circulation and pericard&#xD;
fluid (PF), the closest place to heart. That is why in etiopathogenesis evaluation of CAD&#xD;
miRNAs can be used diagnostically in PF and circulation. Since PF has a potential of&#xD;
reflecting heart potential, PF concentration of some substances provides to be understood&#xD;
many pathophysiological mechanisms.</summary>
    <dc:date>2018-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Oxidative stress and DNA damage during cardiopulmonary bypass</title>
    <link rel="alternate" href="http://hdl.handle.net/11513/130" />
    <author>
      <name>Dikme, Reşat</name>
    </author>
    <author>
      <name>Göz, Mustafa</name>
    </author>
    <author>
      <name>Aydın, Mehmet Salih</name>
    </author>
    <author>
      <name>Çelik, Hakim</name>
    </author>
    <author>
      <name>Padak, Mahmut</name>
    </author>
    <author>
      <name>Göç, Ömer</name>
    </author>
    <author>
      <name>Taşkın, Abdullah</name>
    </author>
    <id>http://hdl.handle.net/11513/130</id>
    <updated>2019-06-10T11:04:38Z</updated>
    <published>2019-01-01T00:00:00Z</published>
    <summary type="text">Title: Oxidative stress and DNA damage during cardiopulmonary bypass
Authors: Dikme, Reşat; Göz, Mustafa; Aydın, Mehmet Salih; Çelik, Hakim; Padak, Mahmut; Göç, Ömer; Taşkın, Abdullah
Abstract: Aim: The aim of this study is to measure the oxidative stress index (OSI) and DNA damage in patients undergoing cardiopulmonary bypass (CPB) surgery due&#xD;
to coronary artery disease. Material and Method: 25 patients operated for CPB surgery due to coronary artery disease were included in the study. By collecting heparin containing blood from the patients at 5 different times (Before CPB, during pump inlet, during placing of cross clamp, during taking out of cross&#xD;
clamp and after CPB) DNA damage was studied by Comet Assay method from mononuclear leucocytes and OSI in plasma was studied. Results: At 5 different&#xD;
times plasma OSI value was found respectively as 4.92 ± 1.73, 5.20 ± 2.69, 5.70 ± 2.06, 9.88 ± 4.88, 9.57 ± 4.54 whereas Arbitrary unit (AU), DNA damage&#xD;
were determined respectively as 28.48 ± 11.30, 29.04 ± 9.43, 31.44 ± 11.74, 33.92 ± 7.96, 38.56 ± 6.20 AU and p&lt;0.001. Discussion: During CPB, OSI and&#xD;
DNA damage gradually increased and a positive meaningful correlation occured between these two parameters (r=0,882 p=0,048). As CPB period extended,&#xD;
oxidative stress and DNA damage increased as well as TOS and OSI increased, or vice versa.</summary>
    <dc:date>2019-01-01T00:00:00Z</dc:date>
  </entry>
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