Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Basak Isildar"'
Autor:
Basak Isildar, Serbay Ozkan, Merve Ercin, Selda Gezginci-Oktayoglu, Mahmut Oncul, Meral Koyuturk
Publikováno v:
Inflammation and Regeneration, Vol 42, Iss 1, Pp 1-18 (2022)
Abstract Background Type 1 diabetes (T1D) is a T-cell-mediated autoimmune disease characterized by the irreversible destruction of insulin-producing β-cells in pancreatic islets. Helper and cytotoxic T-cells and cytokine production, which is impaire
Externí odkaz:
https://doaj.org/article/53f8fcd48115491191168bb322389e60
Autor:
Serbay Ozkan, Basak Isildar, Merve Ercin, Selda Gezginci-Oktayoglu, Dildar Konukoglu, Neşet Neşetoğlu, Mahmut Oncul, Meral Koyuturk
Publikováno v:
Stem Cell Research & Therapy, Vol 13, Iss 1, Pp 1-19 (2022)
Abstract Background The therapeutic potential of mesenchymal stem cells (MSCs)-derived conditioned media (CM) can be increased after preconditioning with various chemical agents. The aim of this study is comparative evaluation of effects of N-CM and
Externí odkaz:
https://doaj.org/article/3faadae4c2de4177b24cd1b276810f4a
Publikováno v:
Balkan Medical Journal, Vol 41, Iss 5, Pp 369-376 (2024)
Background: Mesenchymal stem cells (MSCs) play a key role in regenerative medicine due to their capacity to differentiate into multiple cell lines, regulate the immune system, and exert paracrine effects. The therapeutic impact of MSCs is primarily m
Externí odkaz:
https://doaj.org/article/689c300222c541a78a7bca820726d8eb
Autor:
Tugce Eskazan, Ahmet Emre Eskazan, Salime Pelin Erturkuner, Mustafa Tasyurekli, Muhlis Cem Ar, Basak Isildar, Kadri Atay, Zafer Baslar
Publikováno v:
Ultrastructural Pathology. 43:94-98
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder consisting of oculocutaneous albinism, platelet storage pool deficiency, and lysosomal accumulation of ceroid lipofuscin. The storage pool deficiency of HPS is associated with the lac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff0600955c5093ed0cf6e1f762ffcddf
https://doi.org/10.1080/01913123.2019.1593269
https://doi.org/10.1080/01913123.2019.1593269
Autor:
Tugce, Eskazan, Salime Pelin, Erturkuner, Basak, Isildar, Ahmet Emre, Eskazan, Muhlis Cem, Ar, Kadri, Atay, Zafer, Baslar, Mustafa, Tasyurekli
Publikováno v:
Ultrastructural pathology. 43(1)
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder consisting of oculocutaneous albinism, platelet storage pool deficiency, and lysosomal accumulation of ceroid lipofuscin. The storage pool deficiency of HPS is associated with the lac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a22c6c4026ddc5ef790532bd485a3890
https://pubmed.ncbi.nlm.nih.gov/30932722
https://pubmed.ncbi.nlm.nih.gov/30932722
Autor:
Serbay Ozkan, Meral Koyuturk, Basak Isildar, Mustafa Tasyurekli, Mahmut Oncul, Semih Kaleli, Zafer Baslar
Publikováno v:
Acta histochemica. 121(3)
The main purpose of this study is to establish an effective cryopreservation protocol for the umbilical cord tissue as a source of mesenchymal stem cells (MSCs). In this context, it was aimed to use a cryoprotectant that could be an alternative to di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20ac39ecf2616c31b56512219b20bde0
https://pubmed.ncbi.nlm.nih.gov/30837094
https://pubmed.ncbi.nlm.nih.gov/30837094
Publikováno v:
Ultrastructural pathology. 42(3)
Mesenchymal stem cells (MSCs) are considered as an important tool for regenerative medicine and experimental treatments. Unveiling the ultrastructural changes during the differentiation of MSCs might help us to understand the nature of the process an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64d5b2b9b913685b71eb0cdebedf1b6c
https://pubmed.ncbi.nlm.nih.gov/29624114
https://pubmed.ncbi.nlm.nih.gov/29624114
