Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Oguzhan, Yarali"'
Autor:
Ayberk Turkyilmaz, Oguzhan Yarali
Publikováno v:
Medicine Science, Vol 10, Iss 2, Pp 293-8 (2021)
Cystic fibrosis (CF, OMIM: #219700), caused by biallelic pathogenic variations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, is the most common monogenic disease. The present study aimed to investigate CFTR gene variations i
Externí odkaz:
https://doaj.org/article/86422834145d465d95a495bf219a34a1
Publikováno v:
Medicine Science, Vol 10, Iss 2, Pp 328-33 (2021)
The aim of this study was to determine the prevalence of leptin (LEP), leptin receptors (LEPR), melanocortin-4-receptor (MC4R), proopiomelanocortin (POMC), single-minded 1 (SIM1), and SH2B1 gene variations in Turkish children and adolescents, and to
Externí odkaz:
https://doaj.org/article/e5b06e934747433eab31850a7a018493
Autor:
Ertugrul Erhan, Suat Terzi, Metin Celiker, Oguzhan Yarali, Murat Cankaya, Ferda Keskin Cimen, Ismail Malkoc, Bahadir Suleyman
Publikováno v:
Clinical and Experimental Otorhinolaryngology, Vol 10, Iss 2, Pp 181-187 (2017)
Objectives The objective of this study is to investigate and evaluate the effect of Hippophae rhamnoides extract (HRE) on oropharyngeal mucositis induced in rats with methotrexate (MTX) through biochemical, gene expression, and histopathological exam
Externí odkaz:
https://doaj.org/article/b82b4239678a4306b3b6621b14bd71ad
Autor:
Taner Karakaya, Ayberk Turkyilmaz, Gunes Sager, Rahsan Inan, Oguzhan Yarali, Alper Han Cebi, Yasemin Akin
Publikováno v:
neurogenetics. 23:213-221
Charcot-Marie-Tooth (CMT) disease represents a distinct subgroup of inherited peripheral neuropathies with a significant prevalence throughout the world and manifests both phenotypic and genetic heterogeneity. Electrophysiological studies subclassify
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5f9e15fe9e03f0473d1b59251ca03e9
https://doi.org/10.1007/s10048-022-00693-6
https://doi.org/10.1007/s10048-022-00693-6
Autor:
Emine Kartal Baykan, Ceren Alavanda, Erdal Kurnaz, Pinar Ata, Oguzhan Yarali, Ayberk Turkyilmaz, Atilla Cayir, Dilek Gogas Yavuz
Publikováno v:
Metabolic Syndrome and Related Disorders. 19:340-346
Background: Monogenic hypercholesterolemia with Mendelian inheritance is a heterogeneous group of diseases that are characterized by elevated plasma low-density lipoprotein cholesterol (LDL-C) leve...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::917e09b90c2cae45765ca6925d4185d8
https://doi.org/10.1089/met.2021.0004
https://doi.org/10.1089/met.2021.0004
Autor:
Ayberk Türkyılmaz, Huseyin Demirbilek, Emine Kartal Baykan, Oguzhan Yarali, Erdal Kurnaz, Atilla Cayir, Esra Arslan Ates
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 34:771-780
Objectives Hypogonadism is defined as inadequate sex hormone production due to defects in the hypothalamic-pituitary-gonadal axis. In recent years, rare single gene defects have been identified in both hypergonadotropic hypogonadism (Hh), and hypogon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e9d477bdb5ec24154d242c5b5bc8565
https://doi.org/10.1515/jpem-2020-0590
https://doi.org/10.1515/jpem-2020-0590
Autor:
Ayberk Turkyilmaz, Oguzhan Yarali
Publikováno v:
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics, Vol 23, Iss 1, Pp 103-108 (2020)
Balkan Journal of Medical Genetics, Vol 23, Iss 1, Pp 103-108 (2020)
Trisomy 16 is the most common type of autosomal trisomy associated with spontaneous abortion and is incompatible with life. Upon examining previously reported cases of partial chromosome 16q duplication, it was noted that the majority of cases had co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::978d8cef60de83368b2175b206cd6c48
http://europepmc.org/articles/PMC7474222
http://europepmc.org/articles/PMC7474222
Autor:
Erdal Kurnaz, Serap Turan, Zehra Yavas Abali, Abdullah Bereket, Oguzhan Yarali, Ayberk Türkyılmaz, Tulay Guran, Emine Kartal Baykan, Atilla Cayir
Publikováno v:
Hormone Research in Paediatrics. 93:558-566
Context: Steroid 17α-hydroxylase/17,20-lyase deficiency (17OHD) is characterized by decreased sex steroids and cortisol, and excessive mineralocorticoid action. The clinical symptoms of hypocortisolemia are subtle. Aim: The clinical, biochemical, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9982d2402e000e28f7a48b83022db9aa
https://doi.org/10.1159/000515079
https://doi.org/10.1159/000515079
Autor:
Oguzhan Yarali, Atilla Cayir, Duran Yildiz, Dogus Vuralli, Huseyin Demirbilek, Hasan Kahveci, Yasar Demirelli, Erdal Kurnaz
Publikováno v:
Hormone Research in Paediatrics. 91:175-185
Objective: The systemic form of pseudohypoaldosteronism type 1 (PHA1) is an autosomal recessive disorder characterized by defective sodium transport in multi-organ systems. Mutations in the genes encoding the amiloride-sensitive epithelial sodium cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::451d0172ea2b22a109bbbb95480139a2
https://doi.org/10.1159/000498860
https://doi.org/10.1159/000498860
Autor:
Oguzhan Yarali, Murat Cankaya, Metin Çeliker, Ismail Malkoc, Bahadir Suleyman, Ertugrul Erhan, Ferda Keskin Cimen, Suat Terzi
Publikováno v:
Clinical and Experimental Otorhinolaryngology
Malkoc, Ismail/0000-0002-9221-510X WOS: 000402589900010 PubMed: 27507269 Objectives. the objective of this study is to investigate and evaluate the effect of Hippophae rhamnoides extract (HRE) on oropharyngeal mucositis induced in rats with methotrex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39c73c17bad668f98a52a417de18181d
https://doi.org/10.21053/ceo.2016.00262
https://doi.org/10.21053/ceo.2016.00262