| Biallelic mutations in ADPRHL2, encoding ADP-ribosylhydrolase 3, lead to a degenerative pediatric stress-induced epileptic ataxia syndrome SG Ghosh, K Becker, H Huang, T Dixon-Salazar, G Chai, V Salpietro, ... The American Journal of Human Genetics 103 (3), 431-439, 2018 | 84 | 2018 |
| Periostin is temporally expressed as an extracellular matrix component in skeletal muscle regeneration and differentiation. C Ozdemir, U Akpulat, P Sharafi, Y Yıldız, I Onbaşılar, C Kocaefe Gene 553 (2), 130-139, 2014 | 55 | 2014 |
| LC-MS/HRMS Analysis, Anti-Cancer, Anti-Enzymatic and Anti-Oxidant Effects of Boerhavia diffusa Extracts: A Potential Raw Material for Functional Applications KI Sinan, U Akpulat, AA Aldahish, Y Celik Altunoglu, MC Baloğlu, ... Antioxidants 10 (12), 2003, 2021 | 40 | 2021 |
| Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization H Wang, CG Salter, O Refai, H Hardy, KES Barwick, U Akpulat, ... Brain 140 (11), 2838-2850, 2017 | 33 | 2017 |
| The vasorelaxant effect of hydrogen sulfide is enhanced in streptozotocin-induced diabetic rats M Denizalti, TE Bozkurt, U Akpulat, I Sahin-Erdemli, N Abacıoğlu Naunyn-Schmiedeberg's archives of pharmacology 383, 509-517, 2011 | 30 | 2011 |
| Shorter phosphorodiamidate morpholino splice-switching oligonucleotides may increase exon-skipping efficacy in DMD U Akpulat, H Wang, K Becker, A Contreras, TA Partridge, JS Novak, ... Molecular Therapy-Nucleic Acids 13, 534-542, 2018 | 13 | 2018 |
| Tenotomy immobilization as a model to investigate skeletal muscle fibrosis (with emphasis on Secreted frizzled-related protein 2) U Akpulat, İ Onbaşılar, YÇ Kocaefe Physiological genomics 48 (6), 397-408, 2016 | 12 | 2016 |
| Clinical and genetic characterization of PYROXD1‐related myopathy patients from Turkey HS Daimagüler, U Akpulat, Ö Özdemir, U Yis, S Güngör, B Talim, G Diniz, ... American Journal of Medical Genetics Part A 185 (6), 1678-1690, 2021 | 9 | 2021 |
| Türk toplumunda dopamin2 reseptör geninin ve kişilik özelliklerinin alkol bağımlılığındaki rolü. A DALMIŞ, Y AKVARDAR, Ç ERESEN, S KIZILDAĞ, U AKPULAT, ... Anatolian Journal of Psychiatry/Anadolu Psikiyatri Dergisi 15 (3), 2014 | 3 | 2014 |
| Fare miyoblast hücre hattında KLF5 geninin farklılaşma sürecine etkilerinin araştırılması U Akpulat Sağlık Bilimleri Enstitüsü, 2014 | 3 | 2014 |
| Biochemical parameters and relation to disease severity in COVID-19 patients S Gülten, U Akpulat, S Özcan, E Özcan, Ö Durak, VG Soylu, MM Gülhan, ... Kastamonu Medical Journal 1 (4), 93-96, 2021 | 2 | 2021 |
| P. 6. a. 005 The role of dopamine 2 receptor gene and personality characteristics in alcohol dependence in Turkish population A Kitis, Y Akvardar, C Eresen, S Kizildag, U Akpulat, S Yildirimcan, ... European Neuropsychopharmacology, S491, 2006 | 1 | 2006 |
| A scientific approach to improve Morpholino-based Exon-Skipping therapy for Duchenne Muscular Dystrophy S Cirak, H Wang, J Novak, TA Partridge, U Akpulat Nervenheilkunde 38 (05), V26, 2019 | | 2019 |
| Effect of Zoledronic Acid on Rats' Tissue SDF-1 Expression Z Arik, S Kilickap, U AKPULAT, M Nahit Sendur, Y KOCAEFE, M Erman UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI 26 (4), 2016 | | 2016 |
| Generation of targeted insertion in the Klf5 gene of mouse myoblasts (C2C12 cells) using CRISPR/Cas9 system D Akçay, U AKPULAT, Y KOCAEFE JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY 36 (6), 2015 | | 2015 |
| European Muscle Conference 2015 Abstracts YS Session J Muscle Res Cell Motil 36, 535-605, 2015 | | 2015 |
| AEBP1/ACLP is upregulated in differentiation, injury repair and fibrotic degeneration of skeletal muscle C Özdemir, U Akpulat, D Akçay, İ ONBAŞILAR, Y KOCAEFE JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY 36 (6), 2015 | | 2015 |
| EMC 2013 VU Amsterdam J Muscle Res Cell Motil 35, 55-63, 2014 | | 2014 |
| A consaquineous couple with a 44, XY, der (13; 14) der (13; 14) and 45, XXder (13; 14) karyotypes and genetic counseling GF Bal, U Alipulat, K Bozkurt, E Aktan CHROMOSOME RESEARCH 15, 105-106, 2007 | | 2007 |
| X/Y translocation in a family with 4 affected members in 3 generation showing Leri-Weill dyschondrosteosis phenotype AG Bal, B Karaman, A Baloglu, T Cokisilak, U Akpulat, S Basaran CHROMOSOME RESEARCH 15, 107-108, 2007 | | 2007 |
Sebahattin CirakProfessor, Uniklinikum Ulm, Klinik für Kinder- und Jugendmedizin, Sozialpädiatrisches Zentrum在 uniklinik-ulm.de 的电子邮件经过验证
