Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Ayfer Ulgenalp"'
Autor:
Mahafarin Maralani, Tufan Cankaya, Esra Ataman, Yavuz Tokgoz, Erkan Kaytankas, Nur Arslan, Behzad Baradaran, Khalil Hajiasgharzadeh, Ayfer Ulgenalp
Publikováno v:
Acta Medica Iranica, Vol 61, Iss 4 (2023)
Obesity is becoming a concerning disease in developing countries. Like other multifactorial diseases, genetics plays a substantial role in the development of this disease. We tried to investigate genetic variations (mutation/polymorphism) of GLP-1R g
Externí odkaz:
https://doaj.org/article/de66eda46179478393e716a6282a9b81
Publikováno v:
Hitit Medical Journal, Vol 2, Iss 2, Pp 49-55 (2020)
Bireylerin mevcut biyolojik cinsiyetlerinden hoşnutsuzlukları ve karşıt cinsiyete ait hissetme durumu cinsiyet disforisi olarak tanımlanır. Bu davranış özelliğinin oluşmasında çevresel birçok faktörün yanı sıra kişilerin kendine ha
Externí odkaz:
https://doaj.org/article/89d8947a9e0f48a2be111769ee8b5073
Autor:
Eser Dogan, Semra Gursoy, Giray Bozkaya, Secil Arslansoyu Camlar, Ozge Aksel Kilicarslan, Alper Soylu, Ayfer Ulgenalp, Salih Kavukcu, Ozlem Giray Bozkaya
Publikováno v:
Indian Journal of Rheumatology, Vol 14, Iss 4, Pp 297-303 (2019)
Introduction: In this study, we aimed to characterize the effect of methylation on clinical diversity and gene expression levels in familial Mediterranean fever. Materials and Methods: Forty children, who were diagnosed with FMF according to the Tel-
Externí odkaz:
https://doaj.org/article/bb2c6cf3cb114abc99e5a133eeadfcc0
Publikováno v:
Case Reports in Ophthalmology, Vol 9, Iss 2, Pp 375-380 (2018)
A 12-year-old girl with bilateral stage 2B Coats disease was screened meticulously for a possible underlying systemic disease as she was female and the disease was bilateral. Full systemic workout turned out to be unremarkable. However, an ABCA4 gene
Externí odkaz:
https://doaj.org/article/8c5c3291dc3b49318c6de400c0157ea2
Autor:
Tayfun Cinleti, Ali Gülen, Beria Sönmez, Semra Gürsoy, Özge Kangalli Boyacioğlu, Suna Asilsoy, Ayfer Ulgenalp, Özlem Giray Bozkaya, Ahmet Okay Çağlayan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7672510d1eb1b9a48c410b27aef67775
https://avesis.deu.edu.tr/publication/details/6394efc0-6d18-4302-afff-c1f02f964f75/oai
https://avesis.deu.edu.tr/publication/details/6394efc0-6d18-4302-afff-c1f02f964f75/oai
Autor:
Mehmet Kocabey, Tufan Cankaya, Meral Torum Bayram, Ayfer Ulgenalp, Ahmet Okay Caglayan, Ozlem Giray Bozkaya
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::973e27f49429fbf972f26806d6767390
https://avesis.deu.edu.tr/publication/details/577b1030-d42e-40fd-b114-f535c9c37b1f/oai
https://avesis.deu.edu.tr/publication/details/577b1030-d42e-40fd-b114-f535c9c37b1f/oai
Autor:
Elcin Bora, Ahmet Okay Caglayan, Altug Koc, Tufan Cankaya, Hande Ozkalayci, Mehmet Kocabey, Demet Kemer, Suleyman Aksoy, Zumre Arican Alicikus, Isil Basara Akin, Merih Guray Durak, Duygu Gurel, Tugba Yavuzsen, Ali Sevinc, Isil Somali, Ilknur Gorken, Pinar Balci, Aziz Karaoglu, Serdar Saydam, Ayfer Ulgenalp
Publikováno v:
Cancer Genetics. :118-133
Breast cancer, a worldwide leading cause of cancer in women, may occur in familial cases. Germline mutations in BRCA1/2 genes are responsible for 15% of the familial cases. With the power of next generation sequencing (NGS) analysis, it is possible t
Autor:
Meral Torun Bayram, Gizem Yildiz, Ahmet Okay Cağlayan, Ayfer Ulgenalp, Sadiye Mehtat Unlu, Alper Soylu, Salih Kavukcu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f0a5f39c5c4d1872f5cc540605456be
https://avesis.deu.edu.tr/publication/details/7f3617ac-5d0c-4289-be42-3cad9af2a7b7/oai
https://avesis.deu.edu.tr/publication/details/7f3617ac-5d0c-4289-be42-3cad9af2a7b7/oai
Autor:
Meral Torun Bayram, Gizem Yildiz, Ahmet Okay Cağlayan, Ayfer Ulgenalp, Sadiye Mehtat Unlu, Alper Soylu, Salih Kavukcu
Publikováno v:
Pediatric nephrology (Berlin, Germany). 38(1)
Autor:
Aycan Unalp, Elcin Bora, Tufan Cankaya, Ozlem Giray Bozkaya, Derya Ercal, Aysel Ozturk, Ayfer Ulgenalp
Publikováno v:
The Scientific World Journal, Vol 2012 (2012)
Brain-derived factor (BDNF) is a member of neurotrophin family and is localized and upregulated in areas implicated in epileptogenesis. Several lines of evidence make the BDNF gene a plausible candidate gene for predisposition to epilepsy. In this st
Externí odkaz:
https://doaj.org/article/92aea7cd000b42d9ba0e043b9711fcf1