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    <title>NOPR Community:</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/67252</link>
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        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/68636" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/68635" />
        <rdf:li rdf:resource="http://nopr.niscpr.res.in/handle/123456789/68634" />
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    <dc:date>2026-10-11T23:41:44Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/68636">
    <title>An overview of Livestock-Associated MRSA: prevalence, lineages, and treatment</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/68636</link>
    <description>Title: An overview of Livestock-Associated MRSA: prevalence, lineages, and treatment
Authors: Gurumurthy, Sanjana; Hritvik Nair, Kallumparambath; Kumari S, Chaitanya
Abstract: The objective of this review is to provide an updated overview of Livestock-Associated MRSA (LA-MRSA),&#xD;
highlighting its global prevalence, clonal lineages, transmission across animal host, and current treatment strategies with&#xD;
One Health perspective. Staphylococcus aureus is a Gram-positive, opportunistic, facultative anaerobe found in skin and&#xD;
mucosal layers of the human body. Livestock Associated Methicillin Resistant Staphylococcus aureus (LA-MRSA) is one of&#xD;
the three types of MRSA classified based on epidemiological characteristics. Notorious strains of MRSA were found&#xD;
majorly in cities within Eastern Asia, South America, Europe and smaller regions scattered across other continents. Several&#xD;
lineages (like CC398, CC130, CC97 etc.) affect a wide variety of animals and their species along with transfer of infection&#xD;
to humans. LA-MRSA could cause many different issues including contamination of meat sold in markets leading to&#xD;
sickness amongst humans and infection amongst domestic animals which live in the same homes as healthy people.&#xD;
Treatments related to MRSA have been discussed widely from using natural materials to synthesis of new generations of&#xD;
antibiotics. It is stated that antibiotic resistance could emerge as one of the major causes for high mortality rate worldwide&#xD;
by 2050. This review will give an overview on the threat, prevalence, lineages and treatment of LA-MRSA and peek into the&#xD;
future of antibiotic resistance.
Page(s): 897-914</description>
    <dc:date>2026-10-01T00:00:00Z</dc:date>
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  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/68635">
    <title>Pharmacological attribute, LC-MS/MS profiling and in-vitro bioactivity of Silene dichotoma aqueous extract</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/68635</link>
    <description>Title: Pharmacological attribute, LC-MS/MS profiling and in-vitro bioactivity of Silene dichotoma aqueous extract
Authors: HAZMAN, Ömer; AKSOY, Laçine; BÜYÜKBEN, Ahmet; Abdullah YILMAZ, Mustafa; ÇAKIR, Oğuz; EFĠLOĞLU, Feyza; Sena ARSLAN, Hanife; COġKUN, Emine; CANDAN, sevval
Page(s): 915-925</description>
    <dc:date>2026-10-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/68634">
    <title>Effects of Irisin Combined with Gefitinib on Expression Levels of miRNAs in the HepG2 Cell Line</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/68634</link>
    <description>Title: Effects of Irisin Combined with Gefitinib on Expression Levels of miRNAs in the HepG2 Cell Line
Authors: AYAZ, Lokman; Sancar, Hilal; ŞUMNULU, Deniz
Abstract: This study aims to investigate the effects of the combination of irisin and gefitinib on the expression of AKT1, FNCD5,&#xD;
VEGF, Bcl-2, EGFR, PI3K, CDK1, and ERBB2 genes, which play critical roles in the pathogenesis of hepatocellular&#xD;
carcinoma, beside the expression of miRNAs targeting these genes in the HepG2 cell line. MTT assay was applied to&#xD;
evaluate the cytotoxicity induced by irisin or gefitinib. Expressions of miR- 664b-5p, miR-3922-5p, miR-6843-3p, miR-&#xD;
8085, miR-381-5p, miR-1275, miR-1304, and miR-6801-5p, and the expression of target genes of these miRNAs were&#xD;
determined by RT-PCR. The most effective time for the combination of irisin and gefitinib in HepG2 cells was 48 hours,&#xD;
and the dose was 3.125 μM for irisin and 10.34 μM for gefitinib. PI3K, Akt, EGF, and ErbB2 expressions were significantly&#xD;
decreased in irisin groups compared to the control group. We found that irisin alone and in combination with gefitinib&#xD;
increased miR-664b-5p, miR-381-5p, miR-3922-5p, miR-1275, and miR-1304 gene expressions, whereas the combined&#xD;
treatment of irisin with gefitinib decreased miR-8085 expression. Our study shows that irisin can enhance the anticancer&#xD;
effects of gefitinib in the HepG2 cell line and dysregulated miRNA expressions contribute to HCC pathogenesis by&#xD;
decreasing cell proliferation and inducing apoptosis.
Page(s): 926-931</description>
    <dc:date>2026-10-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://nopr.niscpr.res.in/handle/123456789/68633">
    <title>Pathological and ultrastructural changes of Adrenal Cortex and their association with Adrenal insufficiency in a Rat Model of Severe Acute Pancreatitis</title>
    <link>http://nopr.niscpr.res.in/handle/123456789/68633</link>
    <description>Title: Pathological and ultrastructural changes of Adrenal Cortex and their association with Adrenal insufficiency in a Rat Model of Severe Acute Pancreatitis
Authors: Liu, Lilei; Zhang, Xingwen; Li, Xiang; Xu, Jing; Pei, Yanfang; Fan, Maiying; Yu, Fang; Wang, Xiangying; Han, Xiaotong
Page(s): 932-943</description>
    <dc:date>2026-10-01T00:00:00Z</dc:date>
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