Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Durkadin Demir"'
Autor:
Durkadin Demir Eksi, Huseyin Gunizi
Publikováno v:
Current Issues in Molecular Biology, Vol 46, Iss 9, Pp 9523-9533 (2024)
Allergic rhinitis (AR) is a prevalent inflammatory disorder of the upper respiratory tract, driven by allergen exposure. Understanding mechanisms and identifying biomarkers for AR could significantly impact diagnosis and treatment. This study aimed t
Externí odkaz:
https://doaj.org/article/dc5847548fe041179d2ae1f61f451cdb
Autor:
Durkadin Demir Eksi, Yiping Shen, Munire Erman, Lynn P. Chorich, Megan E. Sullivan, Meric Bilekdemir, Elanur Yılmaz, Guven Luleci, Hyung-Goo Kim, Ozgul M. Alper, Lawrence C. Layman
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-8 (2018)
Abstract Background Little is known about the genetic contribution to Müllerian aplasia, better known to patients as Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. Mutations in two genes (WNT4 and HNF1B) account for a small number of patients, but
Externí odkaz:
https://doaj.org/article/bcbb663442044972bea523c7d3c2c957
Akademický článek
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Copy Number Variation Analysis in Turkish Patients with Congenital Bilateral Absence of Vas Deferens
Autor:
Munire Erman, Elanur Yilmaz, Semra Kahraman, Yigit Akin, Özgül M. Alper, Durkadin Demir Eksi, Mehmet Murad Basar, Mustafa F. Usta
Publikováno v:
Acta Medica Alanya. 5:181-189
Aim: Congenital Bilateral Absence of the Vas Deferens (CBAVD) is a developmental abnormality that causes infertility in males. According to the literature, up to 88% of CBAVD cases have at least one pathogenic Cystic Fibrosis Transmembrane Conductanc
Autor:
Durkadin Demir Eksi, Elanur Yilmaz, A. Erdem Basaran, Gizem Erduran, Banu Nur, Ercan Mihci, Bulent Karadag, Aysen Bingol, Ozgul M. Alper
Objectives To determine the demographic, clinical, and genetic profile of Turkish Caucasian PCD cases. Methods Targeted next-generation sequencing (t-NGS) of 46 nuclear genes was performed in 21 unrelated PCD cases. Sanger sequencing confirmed of pot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::559621d1e5f2e6ea19c412c44d68a243
https://hdl.handle.net/11424/287645
https://hdl.handle.net/11424/287645
Akademický článek
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Autor:
Özgül M. Alper, Yiping Shen, Hyung Goo Kim, Lawrence C. Layman, Meric Bilekdemir, Guven Luleci, Megan E. Sullivan, Lynn P. Chorich, Elanur Yilmaz, Durkadin Demir Eksi, Munire Erman
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-8 (2018)
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-8 (2018)
Yilmaz, Elanur/0000-0001-7045-5068; Alper, Ozgul/0000-0003-1536-2111 WOS: 000424131300001 PubMed: 29434669 Background: Little is known about the genetic contribution to Mullerian aplasia, better known to patients as Mayer-Rokitansky-Kuster-Hauser (MR
Autor:
Yiping Shen, Lawrence C. Layman, Özgül M. Alper, Hyung Goo Kim, Megan E. Sullivan, Lynn P. Chorich, John A. Phillips, Durkadin Demir Eksi, Lacey S. Williams, Amy C. Lossie, Munire Erman
Publikováno v:
Fertility and sterility. 108(1)
Objective To study the genetic cause of Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH). Although a few candidate genes and genomic domains for have been reported for MRKH, the genetic underpinnings remain largely unknown. Some of the top candidate ge
Autor:
Murat Ozekinci, Munire Erman Akar, Guven Luleci, Sebahat Ozdem, Aylin Erman Daloglu, Gultekin Suleymanlar, Durkadin Demir, Asli Meric Bilekdemir, Gözde Öngüt, Can Çevikol, Özgül M. Alper, Yeşim Şenol, Gulbahar Uzun
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 41:12-16
Aim To review the medical charts of women who applied for the uterine transplant project from June 2008 to June 2011 in our hospital retrospectively (18–40 years). Methods The data for 144 women were retrieved, and information was collected on the
Akademický článek
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