Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Gamze CÖMERTPAY"'
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 1, Pp 241-248 (2019)
Endoplazmik Retikulum (ER) ökaryotik hücrelerde bulunan, hücre içi kalsiyum homoastasizi, lipid sentezi, proteinlerin işlenmesi ve katlanmasından sorumlu olan bir organeldir. Hatalı katlanmış veya katlanmamış proteinlerin artması durumund
Externí odkaz:
https://doaj.org/article/ed647251121b46529076f2dc637f1ac8
Publikováno v:
Cukurova Medical Journal, Vol 43, Iss 1, Pp 7-12 (2018)
Amaç: Sigarada bulunan en önemli toksik bileşenlerden bir tanesi nikotindir. Prenatal dönemde sigara dumanına maruz kalmak yeni doğanda bilişsel, duygusal, davranışsal problemler ve çocukluk kanserleriyle birlikte birçok farklı problem or
Externí odkaz:
https://doaj.org/article/fd993df2f0e541339cb8efa2ea76e3ad
Autor:
Mehmet Bertan YILMAZ, İşıl ÖCAL, Eylül AKBAL, Tufan MERT, Turan TUFAN, Gamze CÖMERTPAY, Nermin Seda ILGAZ, Özgür TURGUT, İnayet Nur USLU
Publikováno v:
Cukurova Medical Journal, Vol 38, Iss 1, Pp 15-21 (2013)
Amaç: Normal ve streptozotosin ile indüklenen diyabetik sıçanlarda serum kolesterol, glikoz, ve trigliserid seviyelerinin normale dönmesini, damarsal hasarların giderilmesini ve özellikle aort halkalarında gevşeme yanıtının oluşmasında
Externí odkaz:
https://doaj.org/article/e3df4634248643e3b27e44bae6401267
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 1, Pp 241-248 (2019)
Endoplazmik Retikulum (ER) ökaryotik hücrelerde bulunan, hücre içi kalsiyum homoastasizi, lipid sentezi, proteinlerin işlenmesi ve katlanmasından sorumlu olan bir organeldir. Hatalı katlanmış veya katlanmamış proteinlerin artması durumund
ISL2 is an epigenetically silenced tumor suppressor and regulator of metabolism in pancreatic cancer
Autor:
Todd W. Bauer, Turan Tufan, Mazhar Adli, Ku-Lung Hsu, Nabeel Bardeesy, Sarbajeet Nagdas, Husnu Umit Luleyap, Sara J. Adair, Krishna S. Tummala, Dave F. Kashatus, Cem Kuscu, Bernadette J. Goudreau, Jiekun Yang, Gamze Cömertpay, Harun Cingoz
Pancreatic ductal adenocarcinoma (PDAC) remains one of the deadliest cancers. Uncovering mechanisms responsible for the heterogeneous clinical features of this disease is an essential step toward developing improved and more specific therapeutic appr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0deb28eaa9a043b5308e01cf61f0fb97
https://doi.org/10.1101/2020.05.23.112839
https://doi.org/10.1101/2020.05.23.112839
Autor:
Isil Ocal, Esma Deniz Barc, Hale Oksuz, Gamze Cömertpay, Sabriye Kocatürk-Sel, Mehmet Ali Erkoç, Mehmet Bertan Yilmaz, Turan Tufan
Publikováno v:
Bioelectromagnetics. 39:299-311
Diabetes mellitus is a metabolic disease that causes increased morbidity and mortality in developed and developing countries. With recent advancements in technology, alternative treatment methods have begun to be investigated in the world. This study
Publikováno v:
Volume: 43, Issue: 1 7-12
Cukurova Medical Journal
Cukurova Medical Journal
Purpose: The aim of this study was to show the effects of nicotine on expression levels of SOX2 and SOX4 genes, which are known for their master gene features, in human amniotic cell cultures. The study also aimed to show the effects of resveratrol,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0154748ba32cc6775809971c9a11df8
https://dergipark.org.tr/tr/pub/cumj/issue/28626/340086
https://dergipark.org.tr/tr/pub/cumj/issue/28626/340086
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
Autor:
Ferah, Sönmez, Melike, Güzünler-Şen, Dilek, Yılmaz, Gamze, Cömertpay, Marisol, Heise, Sebahattin, Çırak, Gökhan, Uyanık
Publikováno v:
The Turkish journal of pediatrics. 56(4)
Joubert syndrome (JS) is an autosomal recessive genetic disorder. To date, mutations in 20 genes of the genetically heterogeneous JS and JS-related disorders (JSRD) have been reported. Renal involvement occurs in 2-20% of JS cases. Identified renal a
Publikováno v:
otolaryngology.
Hearing loss (HL) is the most common sensory disorder, affecting all age groups, ethnicities, and genders. Several genes responsible for hearing loss are related to ion recycling and homeostasis in the inner ear. Mutations in GJB2 gene, the gene enco