Publications by authors named "Hatice Mergen"

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Investigation of Fibrillar Aggregates Formed by Pathogenic Pre-pro-vasopressin Mutants that Cause ADNDI.
Refika Dilara Vaizoglu, Beril Erdem, Mehmet Gul, Ceren Acar, Huseyin Ozgur Ozdemirel, Hatice Mergen

J Clin Endocrinol Metab· May 2025

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A Novel Bioprotective Strain of  F2-Physiological, Genetical, and Antimicrobial Characterization.
Evrim Gunes Altuntas, Asena Aslihan Celık, Busra Sevım, Kenan Can Tok, Mehmet Gumustas, Hatice Mergen

Foodborne Pathog Dis· September 2024

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Composition of the colon microbiota in the individuals with inflammatory bowel disease and colon cancer.
Ceren Acar, Sibel Kucukyildirim Celik, H Ozgur Ozdemirel, Beril Erdem Tuncdemir, Saadet Alan, Hatice Mergen

Folia Microbiol (Praha)· April 2024

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Differential expression of Phlebotomus tobbi Adler, Theodor & Lourie, 1930 (Diptera: Psychodidae) genes under different environmental conditions.
Gizem Oguz, Hayriye Akel Bilgic, Cagatay Karaaslan, Hatice Mergen, Ozge Erisoz Kasap

Acta Trop· March 2023

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Design and Development of Gold-Loaded and Boron-Attached Multicore Manganese Ferrite Nanoparticles as a Potential Agent in Biomedical Applications.
Okan Icten, Beril Erdem Tuncdemir, Hatice Mergen

ACS Omega· June 2022

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Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus.
Merve Özcan Türkmen, Tugce Karaduman, Beril Erdem Tuncdemir, Mehmet Altay Ünal, Hatice Mergen

Endocrine· December 2021

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Low Base-Substitution Mutation Rate but High Rate of Slippage Mutations in the Sequence Repeat-Rich Genome of .
Sibel Kucukyildirim, Megan Behringer, Way Sung, Debra A Brock, Thomas G Doak, Hatice Mergen

G3 (Bethesda)· September 2020

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Molecular characterization of an aquaporin-2 mutation causing a severe form of nephrogenic diabetes insipidus.
Emel Saglar Ozer, Hanne B Moeller, Tugce Karaduman, Robert A Fenton, Hatice Mergen

Cell Mol Life Sci· March 2020

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Evaluation of pharmacochaperone-mediated rescue of mutant V2 receptor proteins.
Beril Erdem Tuncdemir, Hatice Mergen, Emel Saglar Ozer

Eur J Pharmacol· December 2019

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A Novel Mutation in the Gene Causing Congenital Nephrogenic Diabetes Insipidus.
Aslı Çelebi Tayfur, Tuğçe Karaduman, Merve Özcan Türkmen, Dilara Şahin, Aysun Çaltık Yılmaz, Hatice Mergen

J Clin Res Pediatr Endocrinol· November 2018

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Functional characterization of AVPR2 mutants found in Turkish patients with nephrogenic diabetes insipidus.
Beril Erdem, Angela Schulz, Emel Saglar, Ferhat Deniz, Torsten Schöneberg, Hatice Mergen

Endocr Connect· January 2018

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Identification of a Novel Deletion in AVP-NPII Gene in a Patient with Central Diabetes Insipidus.
Ferhat Deniz, Ceren Acar, Emel Saglar, Beril Erdem, Tugce Karaduman, Hatice Mergen

Ann Clin Lab Sci· October 2016

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AVP-NPII gene mutations and clinical characteristics of the patients with autosomal dominant familial central diabetes insipidus.
Doga Turkkahraman, Emel Saglar, Tugce Karaduman, Hatice Mergen

Pituitary· December 2015

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Association of VNTR polymorphisms in DRD4, 5-HTT and DAT1 genes with obesity.
Mustafa Uzun, Emel Saglar, Sibel Kucukyildirim, Beril Erdem, Hande Unlu, Hatice Mergen

Arch Physiol Biochem· May 2015

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Promoter hypermethylation of p16 and APC in gastrointestinal cancer patients.
Beril Erdem, Sibel Küçükyıldırım, Emel Sağlar, Zülfikar Polat, Hatice Mergen

Turk J Gastroenterol· October 2014

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Assessment of ER Stress and autophagy induced by ionizing radiation in both radiotherapy patients and ex vivo irradiated samples.
Emel Saglar, Sibel Unlu, Ibrahim Babalioglu, Saban Cakir Gokce, Hatice Mergen

J Biochem Mol Toxicol· September 2014

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A large deletion of the AVPR2 gene causing severe nephrogenic diabetes insipidus in a Turkish family.
Emel Saglar, Ferhat Deniz, Beril Erdem, Tugce Karaduman, Arif Yönem, Hatice Mergen

Endocrine· May 2014

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Mutations in the AVPR2, AVP-NPII, and AQP2 genes in Turkish patients with diabetes insipidus.
Duygu Duzenli, Emel Saglar, Ferhat Deniz, Omer Azal, Beril Erdem, Hatice Mergen

Endocrine· December 2012

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A prospective study of serotonin transporter gene promoter (5-HTT gene linked polymorphic region) and intron 2 (variable number of tandem repeats) polymorphisms as predictors of trauma response to mild physical injury.
Aslihan Sayin, Sibel Kucukyildirim, Taner Akar, Zekiye Bakkaloglu, Ahmet Demircan, Hatice Mergen

DNA Cell Biol· February 2010

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LEPR, ADBR3, IRS-1 and 5-HTT genes polymorphisms do not associate with obesity.
Hatice Mergen, Cağatay Karaaslan, Mehmet Mergen, Ergi Deniz Ozsoy, Metin Ozata

Endocr J· February 2007

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Early sign of atherosclerosis in slow coronary flow and relationship with angiotensin-converting enzyme I/D polymorphism.
Halil Tanriverdi, Harun Evrengul, Hatice Mergen, Ceren Acar, Deniz Seleci

Heart Vessels· January 2007

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Molecular scanning for mutations in the insulin receptor substrate-1 (IRS-1) gene in Turkish with type 2 diabetes mellitus.
Funda E Orkunoglu Suer, Hatice Mergen, Erol Bolu, Metin Ozata

Endocr J· October 2005

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Mitochondrial DNA sequence variation in the Anatolian Peninsula (Turkey).
Hatice Mergen, Reyhan Oner, Cihan Oner

J Genet· April 2004

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