Search Results - Kocakap, Derya

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  1. 1
    Do CCR5 (CCR5Δ32) and TLR3 (RS5743313) gene polymorphisms prevent chronic hepatitis B infection?

    Do CCR5 (CCR5Δ32) and TLR3 (RS5743313) gene polymorphisms prevent chronic hepatitis B infection? by Tuncel, Burçin, Kaygusuz, Sedat, Sayın Kocakap, Derya Beyza, Aksoy, Emel, Azkur, Ahmet Kürşat

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  2. 2
    Clinical significance of MEFV gene variation R202Q

    Clinical significance of MEFV gene variation R202Q by Kandur, Yaşar, Kocakap, Derya Beyza Sayın, Alpcan, Aysegul, Tursun, Serkan

    Published in Clinical rheumatology
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  3. 3
    Adverse effect of VEGFR-2 (rs1870377) polymorphism on the clinical course of COVID-19 in females and males in an age-dependent manner

    Adverse effect of VEGFR-2 (rs1870377) polymorphism on the clinical course of COVID-19 in females and males in an age-dependent manner by Sayın Kocakap, Derya Beyza, Kaygusuz, Sedat, Aksoy, Emel, Şahin, Ömer, Baççıoğlu, Ayşe, Ekici, Aydanur, Kalpaklıoğlu, Ayşe Füsun, Ekici, Mehmet Savaş, Gül, Serdar, Kaçmaz, Birgül, Ayaşlıoğlu Açıkgöz, Ergin, Alyılmaz Bekmez, Sibel, Rouse, Barry T, Azkur, Ahmet Kürşat

    Published in Microbes and infection
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  4. 4
    The frequency of Familial Mediterranean fever gene mutations and genotypes at Kirikkale and comparison with the mean of regional MEFV mutation frequency of Turkey

    The frequency of Familial Mediterranean fever gene mutations and genotypes at Kirikkale and comparison with the mean of regional MEFV mutation frequency of Turkey by Sayın Kocakap, Derya Beyza, Günel-Özcan, Ayşen, Çabuk, Feryal, Ensari, Cüneyt

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  5. 5
    The association of paraoxonase 1 gene L55M polymorphism with the extent and severity of coronary artery disease in the Turkish population and its dependence on gender

    The association of paraoxonase 1 gene L55M polymorphism with the extent and severity of coronary artery disease in the Turkish population and its dependence on gender by Sayın Kocakap, Derya Beyza, Doğru, Mehmet Tolga, Şimşek, Vedat, Çabuk, Feryal, Yıldırım, Nesligül, Çelik, Yunus, Alyılmaz Bekmez, Sibel, Erdem, Solmaz

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  6. 6
    A Case Report of a Prenatally Missed Mowat-Wilson Syndrome With Isolated Corpus Callosum Agenesis

    A Case Report of a Prenatally Missed Mowat-Wilson Syndrome With Isolated Corpus Callosum Agenesis by Şenbil, Nesrin, Arslan, Zeynep, Sayın Kocakap, Derya Beyza, Bilgili, Yasemin

    Published in Child neurology open
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  7. 7
    Interleukin (IL)-17F (H161R) and IL-23R (R381Q) Gene Polymorphisms in Turkish Population with Periodontitis

    Interleukin (IL)-17F (H161R) and IL-23R (R381Q) Gene Polymorphisms in Turkish Population with Periodontitis by Erdemir, Ebru, Hendek, Meltem, Kocakap, Derya, Ozkan, Serdar

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  8. 8
    A Case Report of a Prenatally Missed Mowat-Wilson Syndrome With Isolated Corpus Callosum Agenesis

    A Case Report of a Prenatally Missed Mowat-Wilson Syndrome With Isolated Corpus Callosum Agenesis by Şenbil, Nesrin, Arslan, Zeynep, Sayın Kocakap, Derya Beyza, Bilgili, Yasemin

    Published in Child neurology open
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