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Burcak Ozes
Burcak Ozes
Research Scientist, The Abigail Wexner Research Institute, Nationwide Children's Hospital
nationwidechildrens.org üzerinde doğrulanmış e-posta adresine sahip
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Exome sequence analysis suggests that genetic burden contributes to phenotypic variability and complex neuropathy
C Gonzaga-Jauregui, T Harel, T Gambin, M Kousi, LB Griffin, ...
Cell reports 12 (7), 1169-1183, 2015
2452015
Motor protein mutations cause a new form of hereditary spastic paraplegia
AC Oteyza, E Battaloğlu, L Ocek, T Lindig, J Reichbauer, AP Rebelo, ...
Neurology 82 (22), 2007-2016, 2014
692014
PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia
B Ozes, N Karagoz, R Schüle, A Rebelo, MJ Sobrido, F Harmuth, ...
Clinical genetics 92 (5), 534-539, 2017
462017
Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach
M Zimoń, E Battaloğlu, Y Parman, S Erdem, J Baets, E De Vriendt, ...
neurogenetics 16, 33-42, 2015
462015
Gene therapy to promote regeneration in Charcot-Marie-Tooth disease
Z Sahenk, B Ozes
Brain research 1727, 146533, 2020
362020
Ultrasonographic findings in hereditary neuropathy with liability to pressure palsies
AO Bayrak, IK Bayrak, E Battaloglu, B Ozes, O Yildiz, MK Onar
Neurological research 37 (2), 106-111, 2015
362015
AAV1. NT-3 gene therapy for X-linked Charcot–Marie–Tooth neuropathy type 1
B Ozes, M Myers, K Moss, J Mckinney, A Ridgley, L Chen, S Bai, ...
Gene therapy 29 (3-4), 127-137, 2022
292022
SIK2 attenuates proliferation and survival of breast cancer cells with simultaneous perturbation of MAPK and PI3K/Akt pathways
N Zohrap, Ö Saatci, B Ozes, I Coban, HM Atay, E Battaloglu, Ö Şahin, ...
Oncotarget 9 (31), 21876, 2018
282018
AAV1.NT-3 gene therapy in a CMT2D model: phenotypic improvements in GarsP278KY/+ mice
B Ozes, K Moss, M Myers, A Ridgley, L Chen, D Murrey, Z Sahenk
Brain communications 3 (4), fcab252, 2021
182021
High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus–Merzbacher disease
B Bilir, Z Yapici, C Yalcinkaya, I Baris, CMB Carvalho, M Bartnik, B Ozes, ...
Clinical genetics 83 (1), 66-72, 2013
122013
Systemic delivery of AAVrh74. tMCK. hCAPN3 rescues the phenotype in a mouse model for LGMD2A/R1
Z Sahenk, B Ozes, D Murrey, M Myers, K Moss, ME Yalvac, A Ridgley, ...
Molecular Therapy-Methods & Clinical Development 22, 401-414, 2021
112021
AAV1. NT-3 gene therapy prevents age-related sarcopenia
B Ozes, L Tong, M Myers, K Moss, A Ridgley, Z Sahenk
Aging (Albany NY) 15 (5), 1306, 2023
42023
Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey
NH Akçakaya, BÖ Ak, MA Gonzalez, S Züchner, E Battaloğlu, Y Parman
Neurologia i neurochirurgia polska 54 (2), 176-184, 2020
22020
TDP-43 Proteinopatileri: Nörodejeneratif konformasyon bozukluğu hastalıklarında yeni bir oyuncu
S Lahut, B Özeş, S Ağar, AN Başak
Turkish Journal of Neurology 18, 1-10, 2012
22012
AAV1. NT‐3 gene therapy in the SOD1KO mouse model of accelerated sarcopenia
L Tong, B Ozes, K Moss, M Myers, A Ridgley, Z Sahenk
Journal of Cachexia, Sarcopenia and Muscle, 2023
12023
NT-3 gene transfer therapy attenuates muscle pathology in the GarsP278KY/+ mice model of CMT2D
B Ozes, K Moss, M Myers, A Ridgley, L Chen, D Murrey, Z Sahenk
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM 26 (3), 369-370, 2021
2021
AAV1. NT-3 Gene Therapy Improves Motor Function in Accelerated Aging Model SOD1KO Mice
B Ozes, M Myers, K Moss, A Ridgley, L Chen, D Murrey, Z Sahenk
MOLECULAR THERAPY 29 (4), 286-286, 2021
2021
AAV1. NT-3 gene therapy improves phenotype in GarsNmf249/+ mice, a Charcot-Marie-Tooth axonal type 2D (CMT2D) model
B Ozes, M Myers, K Moss, A Ridgley, L Chen, D Murrey, R Burgess, ...
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM 25 (4), 505-505, 2020
2020
AAV. CAPN3 gene therapy for Limb-girdle muscular dystrophy type 2A (LGMD2A): Phenotypic improvements in the calpain3 (CAPN3)-null mouse
B Ozes, D Murrey, M Myers, L Chen, K Moss, A Ridgley, C Wier, Z Sahenk
NEUROMUSCULAR DISORDERS 30, S66-S66, 2020
2020
Biopotency and Biodistribution/Toxicology Studies Following Systemic Gene Therapy with AAVrh74. tMCK. hCAPN3 in the Mouse Model for LGMD2A
DA Murrey, B Ozes, L Chen, M Myers, K Moss, A Ridgley, Z Sahenk
MOLECULAR THERAPY 28 (4), 490-490, 2020
2020
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