Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Öge Gözütok"'
Autor:
Barış Genç, Mukesh Gautam, Öge Gözütok, Ina Dervishi, Santana Sanchez, Gashaw M. Goshu, Nuran Koçak, Edward Xie, Richard B. Silverman, P. Hande Özdinler
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 2, Pp n/a-n/a (2021)
Abstract Background Upper motor neurons (UMNs) are a key component of motor neuron circuitry. Their degeneration is a hallmark for diseases, such as hereditary spastic paraplegia (HSP), primary lateral sclerosis (PLS), and amyotrophic lateral scleros
Externí odkaz:
https://doaj.org/article/5370d3704c9349de99b927f4e9b91ea3
Autor:
Barış Genç, Boram Nho, Hana Seung, Benjamin Helmold, Huiwon Park, Öge Gözütok, Seunghyun Kim, Jinil Park, Sanghyun Ye, Haneul Lee, Nayeon Lee, Seung-Shin Yu, Sunyoung Kim, Junghun Lee, Hande Özdinler
Publikováno v:
Gene Therapy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dbf3261a1d263fdece95e52c2997492
https://doi.org/10.1038/s41434-023-00383-4
https://doi.org/10.1038/s41434-023-00383-4
Autor:
Öge Gözütok
Publikováno v:
BSAVA Congress Proceedings 2016 ISBN: 9781905319992
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f3063abf5d182c855aad1d64f664a84
https://doi.org/10.22233/9781910443446.54.13
https://doi.org/10.22233/9781910443446.54.13
Akademický článek
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Autor:
Mukesh Gautam, Renata Del Carratore, Benjamin Helmold, Alessandra Tessa, Oge Gozutok, Navdeep Chandel, Halil Idrisoglu, Paolo Bongioanni, Roberta Battini, P.Hande Ozdinler
Publikováno v:
Metabolites, Vol 12, Iss 2, p 174 (2022)
Pathogenic variants in ALS2 have been detected mostly in juvenile cases of amyotrophic lateral sclerosis (ALS), affecting mainly children and teenagers. Patients with ALS2 mutations demonstrate early onset cortical involvement in ALS. Currently, ther
Externí odkaz:
https://doaj.org/article/9dd60907849b4ab3b3bd9c5fb1d6b964
Publikováno v:
Brain Sciences, Vol 11, Iss 5, p 578 (2021)
Hereditary spastic paraplegia (HSP) and primary lateral sclerosis (PLS) are rare motor neuron diseases, which affect mostly the upper motor neurons (UMNs) in patients. The UMNs display early vulnerability and progressive degeneration, while other cor
Externí odkaz:
https://doaj.org/article/1adf1f94e64647c98c30ceb5f3da2b6c
Publikováno v:
Cells, Vol 9, Iss 2, p 502 (2020)
Understanding the cellular and molecular basis of selective vulnerability has been challenging, especially for motor neuron diseases. Developing drugs that improve the health of neurons that display selective vulnerability relies on in vivo cell-base
Externí odkaz:
https://doaj.org/article/2fff28d4bc034e88985efb9a06fb6151