Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Esra, Gunduz"'
Publikováno v:
Journal of the Pakistan Medical Association, Vol 71, Iss 1 (2020)
The case of a 69-year-old man with bilateral synchronous tonsillar carcinoma is reported. The patient complained of nasal closure, strange voice, and discomfort in his pharynx when he was admitted to the Department of Otolaryngology Head and Neck Sur
Externí odkaz:
https://doaj.org/article/55e8b86bd0a44c019fab5b10f4620da9
Autor:
Ayla Eser, Eylem Unlubilgin, Fatih Hizli, Muradiye Acar, Zeynep Kamalak, Aydin Kosus, Nermin Kosus, Deniz Hizli, Esra Gunduz
Publikováno v:
International Neurourology Journal, Vol 19, Iss 3, Pp 164-170 (2015)
Purpose: Pelvic organ prolapse is a multifactorial disorder in which extracellular matrix defects are implicated. Fibrillin-1 level is reduced in stress urinary incontinence. In Marfan syndrome, which is associated with mutations in Fibrillin-1, pelv
Externí odkaz:
https://doaj.org/article/4acdc6c03baf4418a3c77316773af404
Publikováno v:
Cancers, Vol 13, Iss 3878, p 3878 (2021)
Cancers
Cancers
Simple Summary Although there has been improvement in our understanding about cancer stem cells recently, we still don’t know much about cancer stem cells of oropharyngeal cancer. Lack of knowledge solely on oropharyngeal cancer together with the i
Autor:
Takashi Nishinaka, Satoshi Hirohata, Esra Gunduz, Junko Inagaki, Mehmet Gunduz, Gabriel Opoku, Shogo Watanabe, Takashi Ohtsuki, Kentaro Ikemura, Eyyup Uctepe, Hidenori Wake, Hideo Takahashi, Omer Faruk Hatipoglu
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 139, Iss, Pp 111633-(2021)
Idiopathic pulmonary fibrosis (IPF) is the most common and most deadly form of interstitial lung disease. Osteopontin (OPN), a matricellular protein with proinflammatory and profibrotic properties, plays a major role in several fibrotic diseases, inc
Autor:
Engin Sahna, Esra Gunduz
Publikováno v:
Journal of Biomedical Science and Engineering. 10:257-272
Aim: Ischemia and reperfusion (IR) injury is a serious problem that is occured during thrombolytic therapy, organ transplantation, coronary angioplasty, and cardiopulmonary bypass. There is an increase in the number of AT2 receptors in some pathologi
Publikováno v:
International Manual of Oncology Practice ISBN: 9783030162443
International Manual of Oncology Practice ISBN: 9783319216829
International Manual of Oncology Practice ISBN: 9783319216829
The variation between and among the many types of cancer presents a formidable challenge both to practicing clinicians and medical researchers. There are several characteristics that are common to all cancers such as unrestrained proliferation and ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7004bf6a4eb5df5bde8e518b946ab04
https://doi.org/10.1007/978-3-030-16245-0_5
https://doi.org/10.1007/978-3-030-16245-0_5
Autor:
Zeynep Ocak, Muhammet Ramazan Yigitoglu, Secil Aldemir, Ercan Dalbudak, Esra Gunduz, Muradiye Acar
Publikováno v:
Klinik Psikofarmakoloji Bülteni-Bulletin of Clinical Psychopharmacology. 26:134-140
Objective: Obsessive-compulsive disorder (OCD) is a frequent neuropsychiatric disorder, in which genetic factors play important causative roles. We investigated the roles of the (-1019 C/G) promoter region polymorphism of 5-HTR1A and the G861C coding
Autor:
Elif Nihan Cetin, Esra Gunduz, Ozlem Cemeroglu, Kevser Gok, Mehmet Gunduz, Muradiye Acar, Hasim Cakirbay, Kadir Demircan
Publikováno v:
International Journal of Rheumatic Diseases. 21:821-827
Objective The aim of this study is to determine the role of cytosine-adenine (CA) micro-satellite repeat sequence of ADAMTS9 gene on the development and progression of osteoarthritis (OA). Methods A total of 110 participants, including those with pri
Autor:
Mehmet Gunduz, Hüseyin Demirci, Zeliha Gormez, Eyyup Uctepe, Murat Oznur, Esra Gunduz, Seval Erpolat, Mahmut Şamil Sağıroğlu, Fatma Mujgan Sonmez
Publikováno v:
Intractable & Rare Diseases Research. 5:222-226
Coffin-Siris syndrome (CSS) (MIM 135900) is characterized by developmental delay, severe speech impairment, distinctive facial features, hypertrichosis, aplasia or hypoplasia of the distal phalanx or nail of the fifth digit and agenesis of the corpus
Publikováno v:
Precision Medicine in Cancers and Non-Communicable Diseases ISBN: 9781315154749
Precision Medicine in Cancers and Non-Communicable Diseases
Precision Medicine in Cancers and Non-Communicable Diseases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b1058b1f0967c22d6a1db2338f97add
https://doi.org/10.1201/9781315154749-1
https://doi.org/10.1201/9781315154749-1