Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Halil Kasap"'
Autor:
Sabriye KOCATÜRK SEL, Ayfer PAZARBAŞI, Mehmet Bertan YILMAZ, Sibel BAŞARAN, Tunay SARPEL, Lütfiye ÖZPAK, Seda ILGAZ, Hale ÖKSÜZ, Halil KASAP
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 3, Pp 936-946 (2019)
Amaç: Çalışmamızda, Çukurova bölgesinde, postmenopozal osteoporozlu hastalarda ve sağlıklı kadınlarda osteoporoz ile ilişkili aday genlerden VDR ve COL1A1 gen polimorfizmlerinin genotip ve allel sıklıkları ile biyokimyasal ve anatomik
Externí odkaz:
https://doaj.org/article/a17aaa2632f3459c88f55b07fe1ad814
Autor:
Umit Luleyap, Percin Pazarci, Gamze Comertpay, Halise Neslihan Onenli, Ayfer Pazarbasi, Davut Alptekin, Halil Kasap, Ursula Froster
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 41, Iss 4, Pp 702-708 (2016)
Purpose: Phenylketonuria is an autosomal recessive deficiency of the hepatic enzyme phenylalanine hydroxylase. With this study, detection of the most frequent phenylalanine hydroxylase gene mutations in Turkish population is aimed. Material and Metho
Externí odkaz:
https://doaj.org/article/d03793de224947058c2c2eae4a2966f9
Autor:
Seza BULCA, Halil KASAP, Tunay SARPEL, Sabriye Kocatürk SEL, Sibel BAŞARAN, Mehmet Bertan YILMAZ, Ayfer PAZARBAŞI
Publikováno v:
Cukurova Medical Journal, Vol 39, Iss 1, Pp 105-116 (2014)
Amaç: Osteoporoz, kemik mineral yoğunluğunun (KMY) azalmasına bağlı olarak kemik mikromimarisinin bozulması ile ortaya çıkan multifaktöriyel bir hastalıktır. Kemik mineral yoğunluğunu etkileyen birçok çevresel faktör bilinmesine rağ
Externí odkaz:
https://doaj.org/article/99afa80e06854f0fb2c3fb7e43adf851
Autor:
Seza Bulca, Halil Kasap, Tunay Sarpel, Sabriye Kocaturk Sel, Sibel Basaran, Mehmet Bertan Yilmaz, Ayfer Pazarbasi
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 39, Iss 1, Pp 105-116 (2014)
Purpose: Osteoporosis is a multifactorial disease characterized by a decrease bone mineral density (BMD) and micro-architectural deterioration of bone structure. Although several environmental factors are known to have influences on BMD, genetic cont
Externí odkaz:
https://doaj.org/article/30b52d0e40a148a6b8f70bafd3bbb939
Autor:
Mehmet Bertan YILMAZ, Mehmet Ali ERKOÇ, Sabriye KOCATÜRK-SEL, Erdal TUNÇ, Lütfiye ÖZPAK, Ayfer PAZARBAŞI, Ali İrfan GÜZEL, Davut ALPTEKİN, Hüsnü Ümit LÜLEYAP, Osman DEMİRHAN, Mülkiye KASAP, Halil KASAP
Publikováno v:
Cukurova Medical Journal, Vol 38, Iss 2, Pp 174-180 (2013)
Amaç: Bu çalışmadaki amacımız, gonodotropin salgılanması, cinsel dimorfik fetal beyin gelişimi ve yetişkinlerdeki cinsel tercih için çok önemli olan, aromatazın ve östrojen reseptör alfa (Esr1) ve progesteron reseptörlerinin (Pgr) ge
Externí odkaz:
https://doaj.org/article/8001471074a64a00bf213f51d871e8ac
Autor:
Mehmet Bertan Yilmaz, Mehmet Ali Erkoc, Sabriye Kocaturk-Sel, Erdal Tunc, Lutfiye Ozpak, Ayfer Pazarbasi, Ali Irfan Guzel, Davut Alptekin, Husnu Umit Luleyap, Osman Demirhan, Mulkiye Kasap, Halil Kasap
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 38, Iss 2, Pp 174-180 (2013)
Purpose: Aromatase (Cyp19a1) is crucial for the sexually dimorphic development of the fetal brain, regulation of gonadotropin secretion and sexual interest in adults. Our goal is to determine the developmental mRNA expression patterns of aromatase, e
Externí odkaz:
https://doaj.org/article/2b930f9906a24b94be1c89fe941bf3ea
Autor:
Halil Kasap, Osman Demirhan, Davut Alptekin, Mülkiye Kasap, A. İrfan Güzel, Ümit Lüleyap, Ayfer Pazarbaşı
Canlilari her yonu ile inceleyen Biyoloji oldukca genis kapsamli bilimlerden biridir. Bu durum goz onune alinarak kitap, ozellikle insan ve hayvan sagligi alaninda onemi olan temel biyoloji konulari ile sinirli tutulmustur. Universitelerde, ozellikle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f911bdd6500c1c92223dc861eaa761d
https://doi.org/10.37609/akya.502
https://doi.org/10.37609/akya.502
Publikováno v:
Volume: 45, Issue: 6 1228-1233
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
Background/aim: Spinocerebellar ataxias (SCAs) are complex clinical and genetically heterogeneous, mostly autosomal dominant neurodegenerative diseases. At present, more than 30 hereditary SCA types have been associated with different gene mutations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43f9eccbe6dc8e296a15e4396de069c2
https://doi.org/10.3906/sag-1402-101
https://doi.org/10.3906/sag-1402-101
Kocaturk Sel, Sabriye/0000-0003-2446-0979; GUZEL, Ali irfan/0000-0002-9720-5920 WOS: 000379331000005 PubMed: 28360782 Introduction: This study aimed to analyze the genotypic characteristics of Friedreich's ataxia (FA) and autosomal dominant ataxias [
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a672b94090afca26331b94ddfbad5f5a
https://europepmc.org/articles/PMC5353014/
https://europepmc.org/articles/PMC5353014/
Autor:
Gamze Cömertpay, Ümit Lüleyap, Ayfer Pazarbaşı, Ursula G. Froster, Davut Alptekin, Perçin Pazarcı, Halise Neslihan Önenli, Halil Kasap
Publikováno v:
Volume: 41, Issue: 4 702-708
Cukurova Medical Journal
Cukurova Medical Journal
Amaç: Fenilketonüri, hepatik bir enzim olan fenilalanin hidroksilazın otozomal resesif bozukluğu sonucu ortaya çıkan bir durumdur. Bu çalışmada, Türk popülasyonunda en sık görülen fenilalanin hidroksilaz geni mutasyonlarını belirlemek
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbe1e885188c8583a80c14991e0f84d0
https://dergipark.org.tr/tr/pub/cumj/issue/23861/254199
https://dergipark.org.tr/tr/pub/cumj/issue/23861/254199