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BİLGİSAYAR DESTEKLİ NİTEL VERİ ANALİZİNDE GÖMÜLÜ TEORİ DESENİNİN KULLANIMI: ÇALIŞMA VE SOSYAL GÜVENLİK BAKANLIĞI DIŞ İLİŞKİLER EBÜLTENLERİ ÜZERİNE BİR ARAŞTIRMA.

Autor: METE, Hakan¹ hakanmete8@gmail.com

Publikováno v: Journal of Management & Economics Research. Mar2022, Vol. 20 Issue 1, p552-568. 17p.

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Further delineation of familial polycystic ovary syndrome (PCOS) via whole‐exome sequencing: PCOS ‐related rare FBN3 and FN1 gene variants are identified

Autor: Cengiz Karakaya, Aylin Pelin Çil, Kaya Bilguvar, Tunahan Çakir, Mete Hakan Karalok, Recep Onur Karabacak, Ahmet Okay Caglayan

Publikováno v: Journal of Obstetrics and Gynaecology Research. 48:1202-1211

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2d1e87a36e90ed75a8c57aaef0b63bb0
https://doi.org/10.1111/jog.15187

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Determining the most effective way of intervention in forest fires with fuzzy logic modeling : the case of Antalya/Türkiye

Autor: Ahmet Şahiner, Temel Ermiş, Mete Hakan Karakoyun, Muhammad Wasim Awan

Publikováno v: Natural Hazards.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1ad4a79c136384cf926296b4d498b733
https://doi.org/10.1007/s11069-022-05763-4

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Determining the Most Effective Way of Intervention in Forest Fires With Fuzzy Logic Modeling: The Case of Antalya/turkey

Autor: Temel Ermiş, Mete Hakan Karakoyun, Muhammad Wasim Awan

Forest fires in various parts of the world cause irreversible environmental and economic losses due to the increase in global warming. Determining the risk levels of forest fires is very important in terms of minimizing the negative effects of this f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::af7c1a2d569521117c85e1ddb1e76bae
https://doi.org/10.21203/rs.3.rs-1900652/v1

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Further Delineation of Familial Polycystic Ovary Syndrome Via Whole-Exome Sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified

Autor: Karakaya, Cengiz, Çil, Aylin Pelin, Bilguvar, Kaya, Çakir, Tunahan, Karalok, Mete Hakan, Karabacak, Recep Onur, Caglayan, Ahmet Okay

Publikováno v: J Obstet Gynaecol Res

AIM: To identify pathogenic rare coding Mendelian/high-effect size variant(s) by whole-exome sequencing in familial PCOS patients to elucidate PCOS related pathways. METHODS: Twenty women and their affected available relatives diagnosed with polycyst

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ce162984d370b285583f956a10c32aec
https://europepmc.org/articles/PMC9050819/

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Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified

Autor: ÇAKIR, TUNAHAN, KARAKAYA, CENGİZ, ÇAĞLAYAN, AHMET OKAY, KARABACAK, RECEP ONUR, Karalok, Mete Hakan, Cil, Aylin Pelin, Bilguvar, Kaya

Aim To identify pathogenic rare coding Mendelian/high-effect size variant(s) by whole-exome sequencing in familial polycystic ovary syndrome (PCOS) patients to elucidate PCOS-related pathways. Methods Twenty women and their affected available relativ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::9d39fa27696de57d8a6c8bb1fb06da67
https://avesis.deu.edu.tr/publication/details/e374fa2e-dfa6-4e62-a3dd-bf6f1cca1bcd/oai

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