Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Mehmet Ture"'
Autor:
Sahin Erdol MD, Mehmet Ture MD, Tahsin Yakut PhD, Halil Saglam PhD, Hideo Sasai MD, Elsayed Abdelkreem MD, Hiroki Otsuka MD, Toshiyuki Fukao MD, PhD
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 4 (2016)
Succinyl-CoA:3-oxoacid CoA transferase (SCOT) deficiency is an autosomal recessive disorder of ketone body utilization that is clinically characterized with intermittent ketoacidosis crises. We report here the second Turkish case with SCOT deficiency
Externí odkaz:
https://doaj.org/article/1f6beff17898491787ca450ad33d0315
Autor:
Mustafa Ferhat Öksuz, Mutlu Karkucak, Orhan Görukmez, Gökhan Ocakoğlu, Abdulmecit Yıldız, Mehmet Ture, Tahsin Yakut, Kamil Dilek
Publikováno v:
Revista Brasileira de Reumatologia, Vol 57, Iss 6, Pp 501-506
Abstract Aim: Various mutations have been identified in the Mediterranean fever (MEFV) gene which is reported to be responsible from Familial Mediterranean fever (FMF). In our study, we aimed to determine the frequency of the MEFV mutations in our re
Externí odkaz:
https://doaj.org/article/e9df650824be4705a663d07ac8d72b56
Publikováno v:
PeerJ, Vol 12, p e17741 (2024)
Background Psychological distress has been a growing challenge to healthy living worldwide. Special attention has been concentrated on examining the cost of psychological distress on the life satisfaction of college students who are vulnerable groups
Externí odkaz:
https://doaj.org/article/b2e98193313e449c9405e3bfd83d6d3f
Autor:
Mustafa Ferhat Öksüz, Orhan Gorukmez, Mehmet Ture, Gokhan Ocakoglu, Kamil Dilek, Tahsin Yakut, Mutlu Karkucak, Abdulmecit Yildiz
Publikováno v:
Revista Brasileira de Reumatologia. 57:501-506
ResumoObjetivoIdentificaram‐se mutações no gene da febre mediterrânica (MEFV) relatadas como responsáveis pela febre mediterrânica familiar (FMF). Este estudo teve como objetivo determinar a frequência de mutações no MEFV na região sul do
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eae60fefc77bbfd1a5aa4290936b88d
https://doi.org/10.1016/j.rbr.2015.09.006
https://doi.org/10.1016/j.rbr.2015.09.006
Autor:
Mehmet Ture, Emine Tuna Gülten, Şebnem Özemri Sağ, Betul Eser, Serdar Şahintürk, Tahsin Yakut, Bilge Çetinkaya Demir
Publikováno v:
Turkiye Klinikleri Journal of Gynecology and Obstetrics. 26:125-128
Partial trisomy of distal 17q is rare. Until now, 32 cases of partial trisomy for the distal region of 17q were reported. Our case has multiple anomalies, such as increased nuchal translucency, hypoplastic left heart syndrome and cerebral anomalies b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa67a958a3bbfe7e3c8903759e77b6be
https://doi.org/10.5336/gynobstet.2014-40704
https://doi.org/10.5336/gynobstet.2014-40704
Publikováno v:
International Journal of Human Genetics. 15:183-189
The aim of the present study is to investigate the relationship between angiotensin-converting enzyme (ACE) gene polymorphism and pulmonary embolism by comparing the frequency of ACE gene polymorphism between cases diagnosed with pulmonary embolism w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20bf3fdab698bef0de3e5863be45bf35
https://doi.org/10.1080/09723757.2015.11886266
https://doi.org/10.1080/09723757.2015.11886266
Autor:
Erdem Cubukcu, Turkkan Evrensel, Ömer Fatih Ölmez, Mehmet Ture, Nilufer Avci, Ali Topak, Adem Deligonul, Tahsin Yakut, Ender Kurt, Serdar Şahintürk, Ahmet Z. Sahin
Publikováno v:
Pathology & Oncology Research. 21:1243-1247
WOS: 000360385400050 PubMed ID: 26156886 Matrix metalloproteinases (MMPs) are a group of zinc-dependent peptidases that participate in matrix turnover in solid malignancies. The aim of this study was twofold. First, we sought to investigate under a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29f89c185158684ffd242f49781a903d
https://doi.org/10.1007/s12253-015-9950-7
https://doi.org/10.1007/s12253-015-9950-7
Autor:
Turkkan Evrensel, Erdem Cubukcu, Adem Deligonul, Tahsin Yakut, Mehmet Ture, Tuna Gulten, Mutlu Karkucak, Sebnem Ozemri Sag, Mustafa Hartavi
Publikováno v:
International Journal of Human Genetics. 15:7-12
KEYWORDS Lung Cancer. FGFR4 Gene. Polymorphism. Gly388Arg. Fibroblast ABSTRACT Several studies have shown relationships between predisposition to various types of cancer and polymorphisms of the fibroblast growth factor receptor 4 (FGFR4) gene. In th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5827bb9eee5a56e71b03e4fda2f42554
https://doi.org/10.1080/09723757.2015.11886245
https://doi.org/10.1080/09723757.2015.11886245
Autor:
Serdar Şahintürk, Ali Topak, Orhan Gorukmez, Ozlem Gorukmez, Rıdvan Ali, Tahsin Yakut, Sebnem Ozemri Sag, Tuna Gulten, Mehmet Ture, Gokhan Ocakoglu
Publikováno v:
Asian Pacific Journal of Cancer Prevention. 16:443-449
Background Myeloproliferative disorders (MPDs) are clonal hematologic malignancies originating at the level of the pluripotent hematopoietic stem cell. Matrix metalloproteases (MMPs) are proteolytic enzymes that contribute to all stages of malignancy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42d5e4af82a8f4782e373951d19ffdc8
https://doi.org/10.7314/apjcp.2015.16.2.443
https://doi.org/10.7314/apjcp.2015.16.2.443
Autor:
Tahsin Yakut, Ahmet Tuncer Özmen, Mehmet Ture, Meral Yildiz, Deniz Siğirli, Emine Tuna Gülten, Mutlu Karkucak
Publikováno v:
Volume: 45, Issue: 1 164-169
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
Retinopathy of prematurity (ROP) is one of the most frequent causes of blindness in newborn babies. Currently, its etiology is not fully understood. In this study we aimed to investigate the correlation between a patient group with ROP and a control
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faf3045d7b3a86c4cafd0d3a31e1aa5b
https://doi.org/10.3906/sag-1307-94
https://doi.org/10.3906/sag-1307-94