Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Çağrı Güleç"'
Autor:
Sema Sırma Ekmekci, Zeliha Emrence, Neslihan Abacı, Melda Sarıman, Burcu Salman, Cumhur Gökhan Ekmekci, Çağrı Güleç
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 4, Pp 226-233 (2020)
Objective: T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive disease resulting from the accumulation of genetic changes that affect the development of T-cells. The precise role of lymphoid enhancerbinding factor 1 (LEF1) in T-ALL has been
Externí odkaz:
https://doaj.org/article/ab5f21f53d8345288e0d07ab581f2dbc
Autor:
Ayça Aslanger, Tuğba Kalaycı, Esma Konur, Çağrı Güleç, Şahin Avcı, Umut Altunoğlu, Volkan Karaman, Güven Toksoy, Birsen Karaman, Seher Başaran, Zehra Uyguner, Gözde Yeşil Sayın
Publikováno v:
Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2399b31a81c199ac94d349e9d57b17f4
https://doi.org/10.26650/iuitfd.1130578
https://doi.org/10.26650/iuitfd.1130578
Autor:
Hamdi Kale, Gozde Tutku Turgut, Çağrı Güleç, Gen Nishimura, Umut Altunoglu, Birsen Karaman, Tuğba Saraç Sivrikoz
Publikováno v:
American Journal of Medical Genetics Part A. 188:253-258
The lamin-B receptor (LBR) encodes a dual-functioning inner nuclear membrane protein essential for cholesterol biosynthesis and chromatin organization. LBR pathogenic variants cause distinct phenotypes due to the dual function of LBR, including Pelge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44787c5185a4418dac9b0f0360abf7ed
https://doi.org/10.1002/ajmg.a.62479
https://doi.org/10.1002/ajmg.a.62479
Autor:
Fatih Tepgec, Hasmet Hanagasi, Ebru Erzurumluoglu Gokalp, Bedia Samanci, Suleyman Guler, Gamze Guven, Hakan Gurvit, Oya Uyguner, Başar Bilgiç, Çağrı Güleç
Publikováno v:
Neurological Sciences. 42:2497-2504
Alzheimer’s disease (AD) can be either sporadic or familial, and familial forms of AD accounts for only 5% of the cases. So far, autosomal dominantly inherited mutations in “Presenilin 1” (PSEN1), “Presenilin 2” (PSEN2), and “Amyloid prec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a5f0a0142b39fcf124c67eed3cdd084
https://doi.org/10.1007/s10072-021-05243-w
https://doi.org/10.1007/s10072-021-05243-w
Autor:
Cumhur G. Ekmekçi, Neslihan Abaci, Sema Sirma Ekmekci, Burcu Salman, Melda Sariman, Zeliha Emrence, Çağrı Güleç
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 4, Pp 226-233 (2020)
Turkish Journal of Hematology
Turkish Journal of Hematology
Objective T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive disease resulting from the accumulation of genetic changes that affect the development of T-cells. The precise role of lymphoid enhancer-binding factor 1 (LEF1) in T-ALL has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2971123e1074cc64e977ecac14f5bc0
https://tjh.com.tr/jvi.aspx?pdir=tjh&plng=eng&un=TJH-33239&look4=
https://tjh.com.tr/jvi.aspx?pdir=tjh&plng=eng&un=TJH-33239&look4=
Autor:
Beyhan Tüysüz, Leyla Elkanova, Dilek Uludağ Alkaya, Çağrı Güleç, Güven Toksoy, Nilay Güneş, Hakan Yazan, A. Ilhan Bayhan, Timur Yıldırım, Gözde Yeşil, Z. Oya Uyguner
Publikováno v:
Bone. 155
Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous group of diseases characterized by increased bone fragility and deformities. Although most patients with OI have heterozygous mutations in COL1A1 or COL1A2, 17 genes have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::308baee0e5eaf3a3a86f729ea9c053f1
https://pubmed.ncbi.nlm.nih.gov/34902613
https://pubmed.ncbi.nlm.nih.gov/34902613
Autor:
Haşmet A. Hanağasi, Çağrı Güleç, Ebru Özer, Ebba Lohmann, Gamze Guven, Nihan Erginel Ünaltuna, Başar Bilgiç, Hakan Gurvit
Publikováno v:
İstanbul Tıp Fakültesi̇ Dergi̇si̇ 84(2), 165-174 (2021). doi:10.26650/IUITFD.2020.0061
Volume: 84, Issue: 2 165-174
Journal of Istanbul Faculty of Medicine
Volume: 84, Issue: 2 165-174
Journal of Istanbul Faculty of Medicine
Objective: Inflammation and associated microRNAs (miRNA) both play essential roles in the pathogenesis of Alzheimer’s disease (AD). The expression profile of miRNA’s in an AD brain, also reflected in the peripheral blood mononuclear cells, may gi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8750bb4787e7e4bff3ed59cf7566d1f3
https://pub.dzne.de/record/164579
https://pub.dzne.de/record/164579
Publikováno v:
Volume: 8, Issue: 2 58-61
Experimed
Experimed
DOI: 10.26650/experimed.2018.18004Objectives: Alzheimer’s disease (AD) is anirreversible, neurodegenerative disease with an increasing worldwideprevalence. Several different factors are known to play a role in itspathogenesis and genetic predisposi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31d23efc7e44ef9cb2a19e6d7e9b0cb2
https://doi.org/10.26650/experimed.2018.18004
https://doi.org/10.26650/experimed.2018.18004
Publikováno v:
Atherosclerosis. 331:e45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4dbd7dad05bc2e4cd2a47fd25d0fe46
https://doi.org/10.1016/j.atherosclerosis.2021.06.128
https://doi.org/10.1016/j.atherosclerosis.2021.06.128
Autor:
Neslihan Çoban, Nihan Erginel-Unaltuna, Çağrı Güleç, Özlem Yıldırım, Bilge Ozsait-Selcuk, Sema Sirma-Ekmekci
Publikováno v:
Experimental Cell Research. 353:6-15
ROR-alpha is a nuclear receptor, activity of which can be modulated by natural or synthetic ligands. Due to its possible involvement in, and potential therapeutic target for atherosclerosis, we aimed to identify ROR-alpha target genes in monocytic an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a721f1a0649b6b1ff3ccd9c26d4ac0c
https://doi.org/10.1016/j.yexcr.2017.02.028
https://doi.org/10.1016/j.yexcr.2017.02.028