Search Results - "Cim, Abdullah"

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  1. 1

    Association of polymorphisms in the vitamin D receptor gene and serum 25-hydroxyvitamin D levels in children with autism spectrum disorder by Coşkun, Salih, Şimşek, Şeref, Camkurt, Mehmet Akif, Çim, Abdullah, Çelik, Sercan Bulut

    Published in Gene (22-08-2016)
    “…Vitamin D is implicated in several aspects of human physiology, and polymorphisms in the vitamin D receptor gene (VDR) are associated with a variety of…”
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    Journal Article
  2. 2

    Serum IL-4 and IL-10 Levels Correlate with the Symptoms of the Drug-Naive Adolescents with First Episode, Early Onset Schizophrenia by Şimşek, Şeref, Yıldırım, Veli, Çim, Abdullah, Kaya, Savaş

    “…In this study, it was aimed to understand the underlying possible immunopathogenesis of first episode, early onset schizophrenia (EOS) through profiling the T…”
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    Journal Article
  3. 3

    Serum Cytokine Profiles of Children with Obsessive-Compulsive Disorder Shows the Evidence of Autoimmunity by Şimşek, Şeref, Yüksel, Tuğba, Çim, Abdullah, Kaya, Savaş

    “…Background: Previous reports have described an association between autoimmunity and primary obsessive compulsive disorder. This study aimed to investigate any…”
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    Journal Article
  4. 4

    Importance of DNA Sequencing for Abnormal Hemoglobins Detected by HPLC Screening by Canatan, Duran, Çim, Abdullah, Delibaş, Serpil, Altunsoy, Emel, Ceylaner, Serdar

    Published in Turkish journal of haematology (01-01-2020)
    “…Hemoglobinopathies are the most common health problem in Turkey. A hemoglobinopathy prevention program has been implemented by the Ministry of Health in Turkey…”
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    Journal Article
  5. 5

    The spectrum of MEFV gene mutations and genotypes in Van province, the eastern region of Turkey, and report of a novel mutation (R361T) by Coşkun, Salih, Ustyol, Lokman, Bayram, Yasemin, Selçuk Bektaş, M., Gulsen, Suleyman, Çim, Abdullah, Uluca, Unal, Savaş, Didem

    Published in Gene (10-05-2015)
    “…Familial Mediterranean fever (FMF) is the most common hereditary inflammatory periodic disease, characterized by recurrent episodes of fever and abdominal…”
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    Journal Article
  6. 6

    Elevated levels of tissue plasminogen activator and E-selectin in male children with autism spectrum disorder by Şimşek, Şeref, Çetin, İhsan, Çim, Abdullah, Kaya, Savaş

    Published in Autism research (01-12-2016)
    “…Although the etiopathology of autism spectrum disorder (ASD) is not clear, immune dysfunction has been proposed as a mechanism for the pathophysiology of ASD…”
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    Contribution of polymorphisms in ESR1, ESR2, FSHR, CYP19A1, SHBG and NRIP1 genes to migraine susceptibility in Turkish population by COŞKUN, SALIH, YÜCEL, YAVUZ, ÇIM, ABDULLAH, CENGIZ, BEYHAN, OZTUZCU, SERDAR, VAROL, SEFER, ÖZDEMIR, HASAN H., UZAR, ERTUĞRUL

    Published in Journal of genetics (01-03-2016)
    “…Migraine, a highly prevalent headache disorder, is regarded as a polygenic multifactorial disease. Single-nucleotide polymorphisms (SNPs) in the genes that…”
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    Journal Article
  10. 10

    Association between sequence variations of the Mediterranean fever gene and the risk of migraine: a case-control study by Coşkun, Salih, Varol, Sefer, Özdemir, Hasan H, Çelik, Sercan Bulut, Balduz, Metin, Camkurt, Mehmet Akif, Çim, Abdullah, Arslan, Demet, Çevik, Mehmet Uğur

    Published in Neuropsychiatric disease and treatment (01-01-2016)
    “…Migraine pathogenesis involves a complex interaction between hormones, neurotransmitters, and inflammatory pathways, which also influence the migraine…”
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    Journal Article
  11. 11

    Factors influencing insulin usage among type 2 diabetes mellitus patients: A study in Turkish primary care by Yilmaz, Ahmet, Ak, Muharrem, Cim, Abdullah, Palanci, Yilmaz, Kilinc, Faruk

    Published in The European journal of general practice (01-10-2016)
    “…Background: DM (diabetes mellitus) patients with poorly regulated blood glucose levels are at risk of increased morbidity and mortality. There are different…”
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    Journal Article
  12. 12

    Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene by Çim, Abdullah, Coşkun, Salih, Görükmez, Orhan, Yüksel, Hatice, Uluca, Ünal, Pietro, Erminia Di, Plourde, François, Braverman, Nancy Elise

    “…Peroxisomes are involved in various metabolic reactions. Rhizomelic chondrodysplasia punctata (RCDP) type 1 is one of the peroxisomal biogenesis disorders…”
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    Journal Article
  13. 13

    In vivo studies on non-viral transdifferentiation of liver cells towards pancreatic β cells by Cim, Abdullah, Sawyer, Greta J, Zhang, Xiaohong, Su, Haibin, Collins, Louise, Jones, Peter, Antoniou, Michael, Reynes, Jean-Paul, Lipps, Hans-Joachim, Fabre, John W

    Published in Journal of endocrinology (01-09-2012)
    “…Transdifferentiation in vivo is an attractive option for autologous replacement of pancreatic β cells in patients with type 1 diabetes. It has been achieved by…”
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    Effect of lisinopril on rat liver tissues in L-NAME induced hypertension model by Gokcimen, Alpaslan, Kocak, Ahmet, Kilbas, Serkan, Bayram, Dilek, Kilbas, Aynur, Cim, Abdullah, Kockar, Cem, Kutluhan, Suleyman

    Published in Molecular and cellular biochemistry (01-02-2007)
    “…N G-Nitro-l-arginine methyl ester hydrochloride (L-NAME) is a non-specific nitric oxide (NO) inhibitor and it has been used to eliminate the role of NO in many…”
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    Journal Article
  16. 16

    Increased Caspase-3 Immunoreactivity of Erythrocytes in STZ Diabetic Rats by Fırat, Uğur, Kaya, Savaş, Çim, Abdullah, Büyükbayram, Hüseyin, Gökalp, Osman, Dal, Mehmet Sinan, Tamer, Mehmet Numan

    Published in Experimental diabetes research (01-01-2012)
    “…Eryptosis is a term to define apoptosis of erythrocytes. Oxidative stress and hyperglycemia, both of which exist in the diabetic intravascular environment, can…”
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    Journal Article
  17. 17

    Circulating microRNAs as Potential Non-invasive Biomarkers for Breast Cancer Detection by Canatan, Duran, Yılmaz, Özlem, Sönmez, Yonca, Çim, Abdullah, Coşkun, Hasan Şenol, Sezgin Göksu, Sema, Ucar, Selda, Aktekin, Mehmet Rıfkı

    Published in Acta bio-medica de l'Ateneo Parmense (01-01-2021)
    “…Breast cancer is one of the most common cancers among women and is the second leading cause of cancer-related deaths. Mammography is currently the gold…”
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    Journal Article
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    A duplication mutation in KCNQ1 gene in Romano-Ward syndrome by Yıldırım,Yaşar, Çim,Abdullah, İslamoğlu,Yahya, Altunoğlu,Umut, Uyguner,Zehra Oya, Gökalp,Osman, Coşkun,Salih

    Published in Medical Genetics (2015)
    “…Romano-Ward syndrome (RWS, Long QT syndrome 1) is a rare familial congenital cardiac disorder characterized by a prolonged QT interval on electrocardiograph…”
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    Journal Article