Occlusal Radiographs in a Turkish Pediatric Subpopulation

by Bilal Ozmen, Nazlı Basak Ayna
Published 2024-01-01

Molecular Biology of Huntington’s Disease

by Nagehan Ersoy, A. Nazlı Başak
Published 2005-02-01

Molecular Biology of Alzheimer’s Disease

by M. Baki Yokeş, A. Nazlı Başak
Published 2005-04-01

TDP-43 Proteinopathies: A New Player in Neurodegenerative Diseases with Defective Protein Folding

by Suna Lahut, Burçak Özeş, Soykan Ağar, A. Nazlı Başak
Published 2012-03-01

TDP-43 Proteinopathies: A New Player in Neurodegenerative Diseases with Defective Protein Folding

by Suna Lahut, Burçak Özeş, Soykan Ağar, A. Nazlı Başak
Published 2012-03-01

Evaluation of the Hematological and Serum Biochemistry Parameters in the Pre-Symptomatic and Symptomatic Stages of ALS Disease to Support Early Diagnosis and Prognosis

by Duygu Aydemir, Selcuk Surucu, Ayse Nazli Basak, Nuriye Nuray Ulusu
Published 2022-11-01

Another de novo mutation in the SOD1 gene: the first Turkish patient with SOD1-His47Arg, a case report

by Elif Bayraktar, Vildan Çiftçi, Vildan Çiftçi, Hilmi Uysal, A. Nazlı Başak
Published 2023-08-01

Ophthalmic Features in SPA-8 with a Homozygous Missense Variant in the Homeobox Domain of the NKX6-2

by Hidayet Şener, Duygu Gülmez Sevim, Murat Gültekin, Gülşah Şimşir, Ayşe Nazlı Başak
Published 2022-03-01

Case report: Revealing the rare—a Brody Disease patient from Turkey expanding the phenotype

by Ayça Şahin, Esmer Zeynep Duru Badakal, Müge Kovancılar Koç, Hilmi Uysal, Ayşe Nazlı Başak
Published 2023-11-01

Atypical Features in a Large Turkish Family Affected with Friedreich Ataxia

by Semiha Kurt, Betul Cevik, Durdane Aksoy, E. Irmak Sahbaz, Aslı Gundogdu Eken, A. Nazli Basak
Published 2016-01-01

Two Families with SOD1 (L144F) and C9orf72 Gene Mutations and an Overview of Amyotrophic Lateral Sclerosis

by Nazlı Gamze Bülbül, Yaprak Seçil, Nazlı Başak, Yeşim Beckmann, Hatice Sabiha Türe, Ceren Tunca, Aslıhan Özoğuz
Published 2018-06-01

Both ubiquitin ligases FBXW8 and PARK2 are sequestrated into insolubility by ATXN2 PolyQ expansions, but only FBXW8 expression is dysregulated.

by Melanie Vanessa Halbach, Tanja Stehning, Ewa Damrath, Marina Jendrach, Nesli Ece Şen, A Nazlı Başak, Georg Auburger
Published 2015-01-01

Impact of the Amyotrophic Lateral Sclerosis Disease on the Biomechanical Properties and Oxidative Stress Metabolism of the Lung Tissue Correlated With the Human Mutant SOD1G93A Pro...

by Duygu Aydemir, Duygu Aydemir, Anjum Naeem Malik, Ibrahim Kulac, Ayse Nazli Basak, Ismail Lazoglu, Nuriye Nuray Ulusu, Nuriye Nuray Ulusu
Published 2022-02-01

Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia.

by Zeynep Sena Agim, Melda Esendal, Laurent Briollais, Ozgun Uyan, Mehran Meschian, Luis Antonio Mendoza Martinez, Yongmei Ding, A Nazli Basak, Hilmi Ozcelik
Published 2013-01-01

Comprehensive Research on Past and Future Therapeutic Strategies Devoted to Treatment of Amyotrophic Lateral Sclerosis

by Belgin Sever, Halilibrahim Ciftci, Hasan DeMirci, Hilal Sever, Firdevs Ocak, Burak Yulug, Hiroshi Tateishi, Takahisa Tateishi, Masami Otsuka, Mikako Fujita, Ayşe Nazlı Başak
Published 2022-02-01

Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levels

by Nesli Ece Sen, Jessica Drost, Suzana Gispert, Sylvia Torres-Odio, Ewa Damrath, Michael Klinkenberg, Hamid Hamzeiy, Gülden Akdal, Halil Güllüoğlu, A. Nazlı Başak, Georg Auburger
Published 2016-12-01

Two new β-thalassemia deletions compromising prenatal diagnosis in an Italian and a Turkish couple seeking prevention

by Marion Phylipsen, Antonio Amato, Maria Pia Cappabianca, Jan Traeger-Synodinos, Emmanuel Kanavakis, Nazli Basak, Renzo Galanello, Teresa Tuveri, Giovanni Ivaldi, Cornelis L. Harteveld, Piero C. Giordano
Published 2009-09-01

Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor.

by Özgün Uyan, Özgür Ömür, Zeynep Sena Ağım, Aslıhan Özoğuz, Hong Li, Yeşim Parman, Feza Deymeer, Piraye Oflazer, Filiz Koç, Ersin Tan, Hilmi Özçelik, A Nazlı Başak
Published 2013-01-01

ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population.

by Suna Lahut, Özgür Ömür, Özgün Uyan, Zeynep Sena Ağım, Aslihan Özoğuz, Yeşim Parman, Feza Deymeer, Piraye Oflazer, Filiz Koç, Hilmi Özçelik, Georg Auburger, A Nazlı Başak
Published 2012-01-01

Blood RNA biomarkers in prodromal PARK4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson's disease

by Suna Lahut, Suzana Gispert, Özgür Ömür, Candan Depboylu, Kay Seidel, Jorge Antolio Domínguez-Bautista, Nadine Brehm, Hülya Tireli, Karl Hackmann, Caroline Pirkevi, Barbara Leube, Vincent Ries, Kerstin Reim, Nils Brose, Wilfred F. den Dunnen, Madrid Johnson, Zsuzsanna Wolf, Marc Schindewolf, Wiebke Schrempf, Kathrin Reetz, Peter Young, David Vadasz, Achilleas S. Frangakis, Evelin Schröck, Helmuth Steinmetz, Marina Jendrach, Udo Rüb, Ayşe Nazlı Başak, Wolfgang Oertel, Georg Auburger
Published 2017-05-01