Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yusuf Ȍzkul"'
Autor:
Zeynep Yilmaz Sukranli, Keziban Korkmaz Bayram, Serpil Taheri, Francois Cuzin, Yusuf Ozkul, Minoo Rassoulzadegan
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-17 (2024)
Abstract We previously identified a unique genetic feature of Autism Spectrum Disorder (ASD) in human patients and established mouse models, a low to very low level of six microRNAs, miR-19a-3p, miR-361-5p, miR-3613-3p, miR-150-5p, miR-126-3p and miR
Externí odkaz:
https://doaj.org/article/f974551c620b47448dd9fc9edfebe50e
Autor:
Busra Aynekin, Hilal Akalin, I. Ipek Muderris, Gokhan Acmaz, Hulya Akgun, Izem Olcay Şahin, Nuriye Coşkun Gokce, Zahraa Alzaidi, Gözde Erturk Zararsiz, Yusuf Ozkul, Munis Dundar, Çetin Saatci
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-6 (2022)
Abstract Background Circulating tumor cells represent an opportunity for the assessment of early recurrent disease or for real-time tracing of cancer. Glucose Regulated Protein 78 (GRP78) is known in the literature as a stress factor in endometrial c
Externí odkaz:
https://doaj.org/article/8e2dcfbb42284ac5b9fcf6fc2d604e86
Autor:
Zeynep Yilmaz Sukranli, Keziban Korkmaz Bayram, Ecmel Mehmetbeyoglu, Zuleyha Doganyigit, Feyzullah Beyaz, Elif Funda Sener, Serpil Taheri, Yusuf Ozkul, Minoo Rassoulzadegan
Publikováno v:
Biomolecules, Vol 14, Iss 2, p 201 (2024)
Recently, we described the alteration of six miRNAs in the serum of autistic children, their fathers, mothers, siblings, and in the sperm of autistic mouse models. Studies in model organisms suggest that noncoding RNAs participate in transcriptional
Externí odkaz:
https://doaj.org/article/1184744af79549c988e597d18396455f
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 52, Iss 4, Pp 270-275 (2022)
Objectives:Hereditary retinal dystrophies are a rare group of diseases which are heterogeneous in genotype and phenotype and result in total blindness. One of the genetic defects that cause hereditary retinal dystrophy is mutation of the RPE65 gene.
Externí odkaz:
https://doaj.org/article/dad5e2e310ab48c2846b2c62327a7717
Publikováno v:
Ahi Evran Medical Journal, Vol 6, Iss 2, Pp 126-131 (2022)
Purpose: Colorectal cancers, which are one of the most common types of cancer, take the first ranks in terms of mortality. Various factors, such as smoking, are considered risk factors in CRC. In this study, germline mutations in 18 genes were examin
Externí odkaz:
https://doaj.org/article/55a912580af3406aa4e2baed583c4eee
Autor:
Fethi Gül, Zeynep Burcin Gonen, Olcay Y. Jones, Neslihan Pakize Taşlı, Gökmen Zararsız, Ekrem Ünal, Aykut Özdarendeli, Fikrettin Şahin, Ahmet Eken, Semih Yılmaz, Musa Karakukçu, Oğuz Kaan Kırbaş, Nur Seda Gökdemir, Batuhan Turhan Bozkurt, Yusuf Özkul, Burçin Doruk Oktay, Muhammet Ali Uygut, Ismail Cinel, Mustafa Çetin
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
This is a single-center prospective, open-label, single arm interventional study to test the safety and efficacy of recently described ChipEXO™ for severe COVID-19 pneumonia. The ChipEXO™ is a natural product derived from convalescent human immun
Externí odkaz:
https://doaj.org/article/9057f474e0f247abb2e31d2e2ab4ceab
Publikováno v:
Pathophysiology, Vol 28, Iss 2, Pp 238-249 (2021)
Limb girdle muscular dystrophy type R1 disease is a progressive disease that is caused by mutations in the CAPN3 gene and involves the extremity muscles of the hip and shoulder girdle. The CAPN3 protein has proteolytic and non-proteolytic properties.
Externí odkaz:
https://doaj.org/article/5c2b0550356a4973a334237ee52338e6
Autor:
Neslihan Pakize Taşlı, Zeynep Burçin Gönen, Oğuz Kaan Kırbaş, Nur Seda Gökdemir, Batuhan Turhan Bozkurt, Buse Bayrakcı, Derya Sağraç, Ezgi Taşkan, Sevda Demir, Nur Ekimci Gürcan, Melike Bayındır Bilgiç, Ömer Faruk Bayrak, Hazel Yetişkin, Büşra Kaplan, Shaikh Terkıs Islam Pavel, Gökçen Dinç, Müge Serhatlı, Gamze Çakırca, Ahmet Eken, Vedat Aslan, Mehmet Yay, Musa Karakukcu, Ekrem Unal, Fethi Gül, Kemal Erdem Basaran, Yusuf Ozkul, Fikrettin Şahin, Olcay Y. Jones, Şaban Tekin, Aykut Özdarendeli, Mustafa Cetin
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The scale of the COVID-19 pandemic forced urgent measures for the development of new therapeutics. One of these strategies is the use of convalescent plasma (CP) as a conventional source for passive immunity. Recently, there has been interest in CP-d
Externí odkaz:
https://doaj.org/article/29030acd84a84397aaf33a65520ad6ba
Autor:
Stephanie Ascough, Rebecca J. Ingram, Karen K. Y. Chu, Stephen J. Moore, Theresa Gallagher, Hugh Dyson, Mehmet Doganay, Gökhan Metan, Yusuf Ozkul, Les Baillie, E. Diane Williamson, John H. Robinson, Bernard Maillere, Rosemary J. Boyton, Daniel M. Altmann
Publikováno v:
Vaccines, Vol 10, Iss 10, p 1571 (2022)
The causative agent of anthrax, Bacillus anthracis, evades the host immune response and establishes infection through the production of binary exotoxins composed of Protective Antigen (PA) and one of two subunits, lethal factor (LF) or edema factor (
Externí odkaz:
https://doaj.org/article/f4a45dbbf1d740b49ccfbc1e65929d9a
Publikováno v:
Eurasian Journal of Medicine, Vol 51, Iss 2, Pp 177-185 (2019)
Externí odkaz:
https://doaj.org/article/f15a6d34460a44db8b516b5481080a5a