Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Emrah, Yucesan"'
Publikováno v:
Acta Scientiarum: Biological Sciences, Vol 46, Iss 1 (2024)
The expression levels of certain genes or proteins may exhibit various features regardless of the tissue type. The housekeeping genes and reference proteins are often used during the normalization of expression studies. Herein, we aim to determine an
Externí odkaz:
https://doaj.org/article/535e659fb50349c8b89159fe2753f607
Autor:
Ozden Hatirnaz Ng, Ilayda Sahin, Yucel Erbilgin, Ozkan Ozdemir, Emrah Yucesan, Nazli Erturk, Merve Yemenici, Ozlem Akgun Dogan, Sibel Aylin Ugur Iseri, Ilhan Satman, Yasemin Alanay, Ugur Ozbek
Publikováno v:
Frontiers in Public Health, Vol 10 (2023)
Rare disease patients constitute a significant part of the healthcare system of all countries. However, the information on the experiences during disease processes and daily life of rare disease patients is still limited. So far, there is a small num
Externí odkaz:
https://doaj.org/article/04f3831b7dfa494d8f90a8d3bad42d91
Autor:
Emrah YUCESAN, Beyza GONCU, Oguz IDIZ, Ramazan UCAK, Burcu OZDEMIR, Ebru KANIMDAN, Yeliz Emine ERSOY, Erhan AYSAN
Publikováno v:
Kafkas Universitesi Veteriner Fakültesi Dergisi, Vol 26, Iss 6, Pp 765-770 (2020)
Parathyroid cell transplantation is an effective approach for the treatment of permanent hypoparathyroidism. Intramuscular and intraperitoneal routes were performed previously but intravenous adminstration has not been conducted previous studies. Our
Externí odkaz:
https://doaj.org/article/9ea1b9e65f0f4f2facd348fd41c8f05c
Autor:
Dovlat Khalilov, Garen Haryanyan, Baris Salman, Emrah Yucesan, Sibel Ugur Iseri, Nerses Bebek
Publikováno v:
Neurocase. 28:488-492
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::075a26b58a4bf56321a3ccce4544ccaf
https://doi.org/10.1080/13554794.2023.2176779
https://doi.org/10.1080/13554794.2023.2176779
Publikováno v:
Human Immunology. 83:113-118
Basic and clinical studies about parathyroid allotransplantation have to be utilized with more definitive criteria for longer graft survival. Several reports demonstrated different isolation and cultivation methods for parathyroid cells to minimize t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62e824ecf992483d4aa55ff13474a6d7
https://doi.org/10.1016/j.humimm.2021.12.003
https://doi.org/10.1016/j.humimm.2021.12.003
Autor:
Seda Susgun, Yesim Kesim, Dovlat Khalilov, Nermin Gorkem Sirin, Hasim Gezegen, Baris Salman, Emrah Yucesan, Gulden Gokcay, Huseyin Kutay Korbeyli, Mehmet Cihan Balci, Sibel Aylin Ugur Iseri, Betul Baykan, Nerses Bebek
Publikováno v:
Neurological Sciences.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66e4fa2a737c8b4001f947507f713c93
https://doi.org/10.1007/s10072-023-06699-8
https://doi.org/10.1007/s10072-023-06699-8
Background Variations in the TRAPPC12present many symptoms, including microcephaly, agenesis of corpus callosum, cerebellar atrophy, and epilepsy. These features indicate a broad range of mortality and morbidity. Identifying a variation with function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52b2e68b7428e89f0568722f29caccce
https://doi.org/10.21203/rs.3.rs-2552844/v1
https://doi.org/10.21203/rs.3.rs-2552844/v1
Autor:
Ayca Dilruba Aslanger, Beyza Goncu, Omer Faruk Duzenli, Emrah Yucesan, Esma Sengenc, Gozde Yesil
The trafficking protein particle (TRAPP) complex subunit 9 (C9) protein is a member of TRAPP-II complexes and regulates vesicle trafficking. Biallelic mutations in the TRAPPC9 gene are responsible for intellectual disability with expanded development
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::347f9360305639fa24e681d107f6e6ed
http://hdl.handle.net/20.500.12645/29981
http://hdl.handle.net/20.500.12645/29981
Autor:
Garen, Haryanyan, Ozkan, Ozdemir, Kemal, Tutkavul, Aysin, Dervent, Semih, Ayta, Cigdem, Ozkara, Baris, Salman, Emrah, Yucesan, Yesim, Kesim, Seda, Susgun, Ugur, Ozbek, Betul, Baykan, Sibel A, Ugur Iseri, Nerses, Bebek
Publikováno v:
Journal of human genetics. 66(12)
Lafora disease (LD) is a severe form of progressive myoclonus epilepsy inherited in an autosomal recessive fashion. It is associated with biallelic pathogenic variations in EPM2A or NHLRC1, which encode laforin and malin, respectively. The disease us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81a17b8dec85d8960d0d8f1e9390ce93
https://pubmed.ncbi.nlm.nih.gov/34117373
https://pubmed.ncbi.nlm.nih.gov/34117373
Autor:
Emrah Yucesan
Publikováno v:
Journal of Medical Biography. :096777202110653
Due to binomial classification system defined by Carl von Linné, it has been shown that living things that were thought to be independent from each other are actually in a relationship. This "binomial classification" idea corresponds to a leap in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86542b7f4d82c24d36ed0bb4313b3405
https://doi.org/10.1177/09677720211065352
https://doi.org/10.1177/09677720211065352