Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Havva, Tezcan Unlu"'
Autor:
Havva Tezcan Unlu, Furkan Saridas, Ozlem Taskapilioglu, Gulsah Cecener, Unal Egeli, Omer Faruk Turan, Berrin Tunca, Mehmet Zarifoglu
Publikováno v:
Neurological Sciences and Neurophysiology, Vol 40, Iss 2, Pp 81-87 (2023)
Introduction: Recent research into multiple sclerosis (MS) has focused on the role of microRNAs (miRNAs) in the development of the disease. This study was designed to analyze miR-146a expression in whole blood and fecal samples of patients with MS. T
Externí odkaz:
https://doaj.org/article/f52e3ad439b74d22b5e615a8bb4914f1
Correlation between Ubiquitin E3 Ligases (SIAHs) and Heat Shock Protein 90 in Breast Cancer Patients
Autor:
Leila Sabour Takanlou, Gulsah Cecener, Maryam Sabour Takanlou, Hulya Ozturk Nazlioglu, Havva Tezcan Unlu, Ozgen Isik, Unal Egeli, Berrin Tunca, Erdem Cubukcu, Sahsine Tolunay, Mustafa Sehsuvar Gokgoz
Publikováno v:
Iranian Journal of Public Health, Vol 51, Iss 8 (2022)
Background: Breast cancer is a heterogeneous disease and differences in the expression levels of the ER, PR, and HER2 the triplet of established biomarkers used for clinical decision-making have been reported among breast cancer patients. Furthermore
Externí odkaz:
https://doaj.org/article/a7e0c5d247564e079a36c1c42e000b3d
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 15:97-102
Kenny-Caffey syndrome (KCS) is a rare autosomal recessive/dominant disease characterized by hypoparathyroidism, skeletal dysplasia, dwarfism, and dysmorphism. FAM111A or TBCE gene mutations are responsible for this syndrome. Osteocraniostenosis (OCS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a3770b34793916c7c91a39e2d119dfb
https://doi.org/10.4274/jcrpe.galenos.2021.2020.0315
https://doi.org/10.4274/jcrpe.galenos.2021.2020.0315
Autor:
Furkan Sarıdaş, Mehmet Zarifoglu, Havva Tezcan Unlu, Gulsah Cecener, Unal Egeli, Ömer Faruk Turan, Berrin Tunca, Maryam Sabour Takanlou, Leila Sabour Takanlou, Ozlem Taskapilioglu
Publikováno v:
Neurological Research. 44:217-223
Multiple sclerosis (MS) is an inflammatory, autoimmune demyelinating, and neurodegenerative disorder of the central nervous system. Interactions between environmental factors, predisposition genes, and determining genes appear to be involved in its e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b9f4e093d9f03669e3ceeb3e2b1b412
https://doi.org/10.1080/01616412.2021.1975221
https://doi.org/10.1080/01616412.2021.1975221
Autor:
Fuat, Aksoy, Havva, Tezcan Unlu, Gulsah, Cecener, Gamze, Guney Eskiler, Unal, Egeli, Berrin, Tunca, Ecem, Efendi Erdem, Kazım, Senol, Mustafa Sehsuvar, Gokgoz
Publikováno v:
Human heredity.
The CHEK2 gene is known to be an important signal transducer involved in DNA repair, apoptosis, or cell cycle arrest in response to DNA damage. The mutations in this gene have been associated with a wide range of cancers, both sporadic and hereditary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f4827cf39b1bfb43696dc99e4e43212
https://pubmed.ncbi.nlm.nih.gov/34991090
https://pubmed.ncbi.nlm.nih.gov/34991090
Publikováno v:
Journal of clinical research in pediatric endocrinology.
Kenny-Caffey syndrome (KCS) is a rare autosomal recessive/dominant disease characterized by hypoparathyroidism, skeletal dysplasia, dwarfism, and dysmorphism.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54e8c58b43926721327eeef2692e51c0
https://pubmed.ncbi.nlm.nih.gov/34382758
https://pubmed.ncbi.nlm.nih.gov/34382758
Autor:
Hulya Ozturk Nazlioglu, Berna Aytaç Vuruşkan, Onur Kaygisiz, Havva Tezcan Unlu, Ecem Efendi Erdem, Berrin Tunca, Hakan Vuruşkan, Ufuk Unal, Gulsah Cecener, Unal Egeli
Publikováno v:
Molecular biology reports. 49(3)
Background Clear cell type renal cell carcinoma (ccRCC) is the most common renal cell carcinoma (RCC). In this study, we examined the expressions of VHL and miR-223 in ccRCC patients׳ tissues to investigate the possible role in the development of cc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56464d52ce381e93be849a4db613c6ec
https://pubmed.ncbi.nlm.nih.gov/34851479
https://pubmed.ncbi.nlm.nih.gov/34851479
Autor:
Leila, Sabour Takanlou, Gulsah, Cecener, Maryam, Sabour Takanlou, Hulya, Ozturk Nazlioglu, Havva, Tezcan Unlu, Ozgen, Isik, Unal, Egeli, Berrin, Tunca, Erdem, Cubukcu, Sahsine, Tolunay, Mustafa Sehsuvar, Gokgoz
Publikováno v:
Iranian journal of public health. 51(8)
Breast cancer is a heterogeneous disease and differences in the expression levels of the ER, PR, and HER2 the triplet of established biomarkers used for clinical decision-making have been reported among breast cancer patients. Furthermore, resistance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f681bd58fab54292de96b94dfd802a36
https://pubmed.ncbi.nlm.nih.gov/36249118
https://pubmed.ncbi.nlm.nih.gov/36249118
Lösemi, hematopoietik hücrelerin malign transformasyonu sonucu gelişen, heterojen neoplastik hastalıklar grubudur. Philadelphia (Ph) benzeri akut lenfoblastik lösemi (ALL), yüksek risk sınıflamasında yer alan ve kötü prognoz gösteren B- h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b97abbd6cd9c76e59812e3da8eafda57
http://hdl.handle.net/11452/20160
http://hdl.handle.net/11452/20160
