Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Oktay I. Kaplan"'
Autor:
Merve G. Turan, Hanife Kantarci, Sadiye D. Temtek, Onur Cakici, Sebiha Cevik, Oktay I. Kaplan
Publikováno v:
STAR Protocols, Vol 3, Iss 3, Pp 101498- (2022)
Summary: Here, we present a protocol to image a fluorescent-labeled intraflagellar transport (IFT) component in Caenorhabditis elegans with fluorescence microscopy, including steps of sample preparations, in vivo live-cell imaging, and post-microscop
Externí odkaz:
https://doaj.org/article/c2ed62438fa141a8bda67b55d79247a3
Autor:
Mustafa S. Pir, Ferhan Yenisert, Aslı Karaman, Efe Begar, Sofia Tsiropoulou, Elif Nur Firat-Karalar, Oliver E Blacque, Sukru S. Oner, Osman Doluca, Sebiha Cevik, Oktay I. Kaplan
Discovering the entire list of human ciliary genes would help in the diagnosis of cilia-related human disorders known as ciliopathy, but at present the genetic diagnosis of many ciliopathies (over 30%) is far from complete (Bachmann-Gagescu et al., 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f695f3c659ece482d3ceaba43b74fcf
https://doi.org/10.1101/2023.03.31.535034
https://doi.org/10.1101/2023.03.31.535034
Rapid and low-cost sequencing, as well as computer analysis, have facilitated the diagnosis of many genetic diseases, resulting in a substantial rise in the number of disease-associated genes. However, genetic diagnosis of many disorders remains prob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::187b5391882d586aa2af94692b4a4502
https://doi.org/10.1101/2023.02.22.529565
https://doi.org/10.1101/2023.02.22.529565
Autor:
Pei Zhao, Fatih Coşkun, Yahong Kang, Sebiha Cevik, Halil I. Bilgin, Ahmet Sayici, Furkan M. Torun, Mustafa S. Pir, Oktay I. Kaplan
Publikováno v:
Nucleic Acids Research
The availability of genetic variants, together with phenotypic annotations from model organisms, facilitates comparing these variants with equivalent variants in humans. However, existing databases and search tools do not make it easy to scan for equ
Publikováno v:
Current protocolsLiterature Cited. 2(11)
ConVarT (https://convart.org/) is a search engine for searching for conjugate variants between humans and other species. The search engine is based on matching conjugate variants called MatchVars between species. Matching equivalent variants requires
Autor:
Ferhan Yenisert, Nazende Nur Bayram, Beyza Nur Köseoğlu, Murat Topuzoğulları, Sevil Dincer Isoglu, Oktay I. Kaplan
Gene therapy studies have been of great importance in the elimination of genetic diseases, and the capability of the CRISPR/Cas9 genome editing technique to correct genetic defects has shown great promise. As DNA-based Cas9 nuclease delivery is prefe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb091b5aca189f1be8348d008f37a9e4
https://doi.org/10.1101/2022.07.08.499239
https://doi.org/10.1101/2022.07.08.499239
Autor:
Sebiha Cevik, Xiaoyu Peng, Tina Beyer, Mustafa S Pir, Ferhan Yenisert, Franziska Woerz, Felix Hoffmann, Betul Altunkaynak, Betul Pir, Karsten Boldt, Asli Karaman, Miray Cakiroglu, S Sadik Oner, Ying Cao, Marius Ueffing, Oktay I Kaplan
Publikováno v:
Life Science Alliance. 6:e202201844
The correct intraflagellar transport (IFT) assembly at the ciliary base and the IFT turnaround at the ciliary tip are key for the IFT to perform its function, but we still have poor understanding about how these processes are regulated. Here, we iden
Autor:
Sadik Oner, Betul Pir, Felix Hoffmann, Betul Altunkaynak, Karsten Boldt, Xiaoyu Peng, Fowzan S. Alkuraya, Sebiha Cevik, Ying Cao, Asli Karaman, Lama Al-Abdi, Marius Ueffing, Franziska Woerz, Ferhan Yenisert, Ranad Shaheen, Miray Cakiroglu, Mustafa S. Pir, Atiyye Zorluer, Oktay I. Kaplan, Tina Beyer
The term “ciliopathy” refers to a group of over 35 rare disorders characterized by defective cilia and many overlapping clinical features, such as hydrocephalus, cerebellar vermis hypoplasia, polydactyly, and retinopathy. Even though many genes h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63a6f3e4894f80172c7bc15dca3f1880
https://doi.org/10.21203/rs.3.rs-622797/v1
https://doi.org/10.21203/rs.3.rs-622797/v1
Autor:
Sebiha Cevik, Xiaoyu Peng, Tina Beyer, Mustafa S. Pir, Ferhan Yenisert, Franziska Woerz, Felix Hoffmann, Betul Altunkaynak, Betul Pir, Karsten Boldt, Asli Karaman, Miray Cakiroglu, S. Sadik Oner, Ying Cao, Marius Ueffing, Oktay I. Kaplan
The correct intraflagellar transport (IFT) assembly at the ciliary base and the IFT turnaround at the ciliary tip are key for the IFT to perform its function, but we still have poor understanding about how these processes are regulated. Here, we iden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86fe6053f280e181442b5b918d90bac4
https://doi.org/10.1101/2021.06.10.445528
https://doi.org/10.1101/2021.06.10.445528
Autor:
Sebiha Cevik, Oktay I Kaplan
Publikováno v:
microPublication Biology
C. elegans EGL-36 displays extensive similarity to human KCNC proteins, the conserved potassium channel subfamily KV3 (the Shaw subfamily). This potassium channel subfamily contains four genes KCNC1, KCNC2, KCNC3, and KCNC4 encoding KV3.1 (Shaker), K