Zobrazeno 1 - 10
of 295
pro vyhledávání: '"Outer dynein arm"'
Autor:
Nannan Zhou, Weilin Liang, Yanzhu Zhang, Guoli Quan, Ting Li, Siqing Huang, Yating Huo, Haiyan Cui, Yuanxiong Cheng
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder caused by defects in motile ciliary function and/or structure. Outer dynein arm docking complex subunit 1 (ODAD1) is an important component of the outer dynein arm docking compl
Externí odkaz:
https://doaj.org/article/420dcd0d9d364a7cad6b54f7050f3d56
Akademický článek
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Autor:
Maria Santa Rocca, Gioia Piatti, Angela Michelucci, Raffaella Guazzo, Veronica Bertini, Cinzia Vinanzi, Maria Adelaide Caligo, Angelo Valetto, Carlo Foresta
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Primary ciliary dyskinesia (PCD) is a highly heterogeneous genetic disorder caused by defects in motile cilia. The hallmark features of PCD are the chronic infections of the respiratory tract, moreover, clinical manifestations inc
Externí odkaz:
https://doaj.org/article/ec0418864d154a54a64a749b4eca1e68
Autor:
Edwards, Beatrice Freya Lucy, Wheeler, Richard John, Barker, Amy Rachel, Moreira-Leite, Flávia Fernandes, Gull, Keith, Sunter, Jack Daniel
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2018 Jul . 115(31), E7341-E7350.
Externí odkaz:
https://www.jstor.org/stable/26529390
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Safa Eltahir, Wadha Alotaibi, Khalid Al-Mobaireek, Abdulali P. Zada, Adnan Zafar, Gawahir Mukhtar, Mohammed Alzaid, Mohammed Almannai
Publikováno v:
International Journal of Pediatrics and Adolescent Medicine, Vol 8, Iss 4, Pp 258-263 (2021)
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics & Adolescent Medicine
Background Primary ciliary dyskinesia (PCD) is a ciliopathy with diverse clinical and genetic findings caused by abnormal motile cilia structure and function. In this study, we describe the clinical characteristics of confirmed PCD cases in our popul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f48bfe24a47f0b94d932573b0b03e4cf
https://doi.org/10.1016/j.ijpam.2021.03.002
https://doi.org/10.1016/j.ijpam.2021.03.002
Publikováno v:
Pharmacogenomics and Personalized Medicine
Chenyang Lu,1– 3,* Danhui Yang,1– 3,* Cheng Lei,1– 3 Rongchun Wang,1– 3 Ting Guo,1– 3 Hong Luo1– 3 1Department of Pulmonary and Critical Care Medicine, The Second Xiangya Hospital, Central South University, Changsha, People’s Republic o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c4fa980f41fa59f0499381f9332c9d1
https://doi.org/10.2147/pgpm.s338981
https://doi.org/10.2147/pgpm.s338981
Autor:
Xin Ni, Shunying Zhao, Xingfeng Yao, Yuhong Guan, Wentong Ge, Haiming Yang, Hui Liu, Xiaolei Tang, Chanjuan Hao, Hui Xu, Xiang zhang
Publikováno v:
Chest
Background Primary ciliary dyskinesia (PCD) is a heterogeneous disease with a diverse clinical and genetic spectrum among populations worldwide. Few cases of pediatric PCD have been reported from China. Research Question What are the clinical and gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fa52da5c3753b5b4b0d4c687028e8f5
https://doi.org/10.1016/j.chest.2021.02.006
https://doi.org/10.1016/j.chest.2021.02.006
Publikováno v:
Dev Biol
In cilia and flagella, dyneins form complexes which give rise to the inner and outer axonemal arms. Defects in the dynein arms are the leading cause of primary ciliary dyskinesia (PCD), which is characterized by chronic respiratory infections, situs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33fdf63426ba303d1e16fe37e45ca10b
https://doi.org/10.1016/j.ydbio.2020.04.006
https://doi.org/10.1016/j.ydbio.2020.04.006
Publikováno v:
Cells, Vol 7, Iss 9, p 124 (2018)
In the present study, we characterized CFAP70, a candidate of cilia-related protein in mice. As this protein has a cluster of tetratricopeptide repeat (TPR) domains like many components of the intraflagellar transport (IFT) complex, we investigated t
Externí odkaz:
https://doaj.org/article/18b9c592f5664079937e316db899f59c