Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Çetin Kocaefe"'
Autor:
Özge Boyacıoğlu, Elif Bilgiç, Cem Varan, Erem Bilensoy, Emirhan Nemutlu, Duygu Sevim, Çetin Kocaefe, Petek Korkusuz
Publikováno v:
Cell Death and Disease, Vol 12, Iss 1, Pp 1-14 (2021)
Abstract Therapeutic agents used for non-small cell lung cancer (NSCLC) have limited curative efficacy and may trigger serious adverse effects. Cannabinoid ligands exert antiproliferative effect and induce apoptosis on numerous epithelial cancers. We
Externí odkaz:
https://doaj.org/article/712ee169b20b43529e32681ed73968c0
Publikováno v:
Stem Cell Research & Therapy, Vol 10, Iss 1, Pp 1-10 (2019)
Abstract Background Autosomal recessive osteopetrosis is a genetically and phenotypically heterogeneous disease, caused by defects in osteoclast formation and function. The only available treatment is allogeneic stem cell transplantation that has sti
Externí odkaz:
https://doaj.org/article/9a55cddfc24f4ef48eb9c677aa4a72e2
Autor:
Arzu Yıldırım, Sadberk Lale Tokgözoğlu, Murat Yıldırım, Yusuf Ziya Şener, Metin Okşul, Duygu Akçay, Çetin Kocaefe, Gürhan Dönmez, Hikmet Yorgun, Necla Özer
Publikováno v:
The International Journal of Cardiovascular Imaging.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5e381e0a141c960c123e260e8223d76
https://doi.org/10.1007/s10554-023-02845-7
https://doi.org/10.1007/s10554-023-02845-7
Autor:
Goknur Haliloglu, Can Ebru Bekircan-Kurt, Y. Çetin Kocaefe, Haluk Topaloglu, Hasan Basri Kiliç, Sevim Erdem Özdamar, Bengisu Kevser Bulduk
Publikováno v:
Genetic Testing and Molecular Biomarkers. 24:165-170
Aim: Pathogenic variants within mitochondrial tRNA and rRNA genes negatively affect protein synthesis function and cause oxidative phosphorylation defects. The majority of mitochondrial cytopathies are caused by pathogenic point variants within the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f37bc96dd429d78bde03721672d2f89
https://doi.org/10.1089/gtmb.2019.0079
https://doi.org/10.1089/gtmb.2019.0079
Publikováno v:
Turkish Journal of Biochemistry. 44:769-777
Objective Detection of mtDNA copy number is required for diagnosis of mtDNA depletion. Multiplex quantification of mtDNA in blood samples was claimed via normalizing to a nuclear single copy gene using qPCR. This is not possible in high mtDNA samples
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f578244b0f689560b5daf6df517b4ca6
https://doi.org/10.1515/tjb-2018-0372
https://doi.org/10.1515/tjb-2018-0372
Autor:
Cem Varan, Elif Bilgiç, Erem Bilensoy, Çetin Kocaefe, Emirhan Nemutlu, Özge Boyacıoğlu, Duygu Gulmez Sevim, Petek Korkusuz
Publikováno v:
Cell Death and Disease, Vol 12, Iss 1, Pp 1-14 (2021)
Cell Death & Disease
Cell Death & Disease
Therapeutic agents used for non-small cell lung cancer (NSCLC) have limited curative efficacy and may trigger serious adverse effects. Cannabinoid ligands exert antiproliferative effect and induce apoptosis on numerous epithelial cancers. We confirme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d90f18dc89e00a7721a3726362a9574
https://doi.org/10.1038/s41419-020-03274-3
https://doi.org/10.1038/s41419-020-03274-3
Autor:
Bengisu Kevser, Bulduk, Hasan Basri, Kiliç, Can Ebru, Bekircan-Kurt, Göknur, Haliloğlu, Sevim, Erdem Özdamar, Haluk, Topaloğlu, Y Çetin, Kocaefe
Publikováno v:
Genetic testing and molecular biomarkers. 24(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4f51eae3042fb48ac82da501fd57aedd
https://pubmed.ncbi.nlm.nih.gov/32167396
https://pubmed.ncbi.nlm.nih.gov/32167396
Publikováno v:
Stem Cell Research & Therapy, Vol 10, Iss 1, Pp 1-10 (2019)
Stem Cell Research & Therapy
Stem Cell Research & Therapy
Background Autosomal recessive osteopetrosis is a genetically and phenotypically heterogeneous disease, caused by defects in osteoclast formation and function. The only available treatment is allogeneic stem cell transplantation that has still high m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f86af20e910fc83761dc7ec975df3e69
https://doi.org/10.1186/s13287-019-1316-8
https://doi.org/10.1186/s13287-019-1316-8
Autor:
Sukriye Ayter, Banu Anlar, Ali Varan, Çetin Kocaefe, Ibrahim Vargel, Beren Karaosmanoglu, Figen Soylemezoglu
Neurofibromatosis type 1 (NF1) is a common autosomal dominantly inherited disorder that affects both the skin and the nervous system. NF1 occurs due to the mutations in the NF1 gene. Neurofibromas are the most common Schwann cell-based tumors in NF1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82537f05964eebae8170ac469c99faa8
https://hdl.handle.net/20.500.11851/773
https://hdl.handle.net/20.500.11851/773
Publikováno v:
Physiological genomics. 48(6)
The pathological endpoint of congenital and senile myopathies is chronic muscle degeneration characterized by the atrophy of contractile elements, accompanied by fibrosis and fatty infiltration of the interstitium. Tenotomy is the release of preload
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6db25be8f93d21bed06a5cd4ea8c45d
https://pubmed.ncbi.nlm.nih.gov/27113532
https://pubmed.ncbi.nlm.nih.gov/27113532