Hasil Pencarian - Nazli Başak

Perbaiki Hasil
  1. 1
    Occlusal Radiographs in a Turkish Pediatric Subpopulation

    Occlusal Radiographs in a Turkish Pediatric Subpopulation oleh Bilal Ozmen, Nazlı Basak Ayna

    Diterbitkan 2024-01-01
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  2. 2
    Molecular Biology of Huntington’s Disease

    Molecular Biology of Huntington’s Disease oleh Nagehan Ersoy, A. Nazlı Başak

    Diterbitkan 2005-02-01
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  3. 3
    Molecular Biology of Alzheimer’s Disease

    Molecular Biology of Alzheimer’s Disease oleh M. Baki Yokeş, A. Nazlı Başak

    Diterbitkan 2005-04-01
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  4. 4
    TDP-43 Proteinopathies: A New Player in Neurodegenerative Diseases with Defective Protein Folding

    TDP-43 Proteinopathies: A New Player in Neurodegenerative Diseases with Defective Protein Folding oleh Suna Lahut, Burçak Özeş, Soykan Ağar, A. Nazlı Başak

    Diterbitkan 2012-03-01
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  5. 5
    TDP-43 Proteinopathies: A New Player in Neurodegenerative Diseases with Defective Protein Folding

    TDP-43 Proteinopathies: A New Player in Neurodegenerative Diseases with Defective Protein Folding oleh Suna Lahut, Burçak Özeş, Soykan Ağar, A. Nazlı Başak

    Diterbitkan 2012-03-01
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  6. 6
    Evaluation of the Hematological and Serum Biochemistry Parameters in the Pre-Symptomatic and Symptomatic Stages of ALS Disease to Support Early Diagnosis and Prognosis

    Evaluation of the Hematological and Serum Biochemistry Parameters in the Pre-Symptomatic and Symptomatic Stages of ALS Disease to Support Early Diagnosis and Prognosis oleh Duygu Aydemir, Selcuk Surucu, Ayse Nazli Basak, Nuriye Nuray Ulusu

    Diterbitkan 2022-11-01
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  7. 7
    Another de novo mutation in the SOD1 gene: the first Turkish patient with SOD1-His47Arg, a case report

    Another de novo mutation in the SOD1 gene: the first Turkish patient with SOD1-His47Arg, a case report oleh Elif Bayraktar, Vildan Çiftçi, Vildan Çiftçi, Hilmi Uysal, A. Nazlı Başak

    Diterbitkan 2023-08-01
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  8. 8
    Ophthalmic Features in SPA-8 with a Homozygous Missense Variant in the Homeobox Domain of the NKX6-2

    Ophthalmic Features in SPA-8 with a Homozygous Missense Variant in the Homeobox Domain of the NKX6-2 oleh Hidayet Şener, Duygu Gülmez Sevim, Murat Gültekin, Gülşah Şimşir, Ayşe Nazlı Başak

    Diterbitkan 2022-03-01
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  9. 9
    Case report: Revealing the rare—a Brody Disease patient from Turkey expanding the phenotype

    Case report: Revealing the rare—a Brody Disease patient from Turkey expanding the phenotype oleh Ayça Şahin, Esmer Zeynep Duru Badakal, Müge Kovancılar Koç, Hilmi Uysal, Ayşe Nazlı Başak

    Diterbitkan 2023-11-01
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  10. 10
    Atypical Features in a Large Turkish Family Affected with Friedreich Ataxia

    Atypical Features in a Large Turkish Family Affected with Friedreich Ataxia oleh Semiha Kurt, Betul Cevik, Durdane Aksoy, E. Irmak Sahbaz, Aslı Gundogdu Eken, A. Nazli Basak

    Diterbitkan 2016-01-01
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  11. 11
    Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS): a family with five affected sibs from Turkey

    Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS): a family with five affected sibs from Turkey oleh Figen Gökçay, Gülcan Neşem Baskan, Irmak Şahbaz, Müge Kovancılar Koç, A. Nazlı Başak, Nese Celebisoy

    Diterbitkan 2024-09-01
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  12. 12
    Two Families with SOD1 (L144F) and C9orf72 Gene Mutations and an Overview of Amyotrophic Lateral Sclerosis

    Two Families with SOD1 (L144F) and C9orf72 Gene Mutations and an Overview of Amyotrophic Lateral Sclerosis oleh Nazlı Gamze Bülbül, Yaprak Seçil, Nazlı Başak, Yeşim Beckmann, Hatice Sabiha Türe, Ceren Tunca, Aslıhan Özoğuz

    Diterbitkan 2018-06-01
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  13. 13
    Both ubiquitin ligases FBXW8 and PARK2 are sequestrated into insolubility by ATXN2 PolyQ expansions, but only FBXW8 expression is dysregulated.

    Both ubiquitin ligases FBXW8 and PARK2 are sequestrated into insolubility by ATXN2 PolyQ expansions, but only FBXW8 expression is dysregulated. oleh Melanie Vanessa Halbach, Tanja Stehning, Ewa Damrath, Marina Jendrach, Nesli Ece Şen, A Nazlı Başak, Georg Auburger

    Diterbitkan 2015-01-01
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  14. 14
    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 Protein Accumulation

    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... oleh Duygu Aydemir, Duygu Aydemir, Anjum Naeem Malik, Ibrahim Kulac, Ayse Nazli Basak, Ismail Lazoglu, Nuriye Nuray Ulusu, Nuriye Nuray Ulusu

    Diterbitkan 2022-02-01
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  15. 15
    Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia.

    Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia. oleh Zeynep Sena Agim, Melda Esendal, Laurent Briollais, Ozgun Uyan, Mehran Meschian, Luis Antonio Mendoza Martinez, Yongmei Ding, A Nazli Basak, Hilmi Ozcelik

    Diterbitkan 2013-01-01
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  16. 16
    Comprehensive Research on Past and Future Therapeutic Strategies Devoted to Treatment of Amyotrophic Lateral Sclerosis

    Comprehensive Research on Past and Future Therapeutic Strategies Devoted to Treatment of Amyotrophic Lateral Sclerosis oleh Belgin Sever, Halilibrahim Ciftci, Hasan DeMirci, Hilal Sever, Firdevs Ocak, Burak Yulug, Hiroshi Tateishi, Takahisa Tateishi, Masami Otsuka, Mikako Fujita, Ayşe Nazlı Başak

    Diterbitkan 2022-02-01
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  17. 17
    Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levels

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

    Diterbitkan 2016-12-01
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  18. 18
    Two new β-thalassemia deletions compromising prenatal diagnosis in an Italian and a Turkish couple seeking prevention

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

    Diterbitkan 2009-09-01
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  19. 19
    Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor.

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

    Diterbitkan 2013-01-01
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  20. 20
    ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population.

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

    Diterbitkan 2012-01-01
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