These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
323 related articles for article (PubMed ID: 32764743)
1. Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesia. Bustamante-Marin XM; Horani A; Stoyanova M; Charng WL; Bottier M; Sears PR; Yin WN; Daniels LA; Bowen H; Conrad DF; Knowles MR; Ostrowski LE; Zariwala MA; Dutcher SK PLoS Genet; 2020 Aug; 16(8):e1008691. PubMed ID: 32764743 [TBL] [Abstract][Full Text] [Related]
2. C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia. Fassad MR; Shoemark A; le Borgne P; Koll F; Patel M; Dixon M; Hayward J; Richardson C; Frost E; Jenkins L; Cullup T; Chung EMK; Lemullois M; Aubusson-Fleury A; Hogg C; Mitchell DR; Tassin AM; Mitchison HM Am J Hum Genet; 2018 May; 102(5):956-972. PubMed ID: 29727692 [TBL] [Abstract][Full Text] [Related]
3. FAP57/WDR65 targets assembly of a subset of inner arm dyneins and connects to regulatory hubs in cilia. Lin J; Le TV; Augspurger K; Tritschler D; Bower R; Fu G; Perrone C; O'Toole ET; Mills KV; Dymek E; Smith E; Nicastro D; Porter ME Mol Biol Cell; 2019 Oct; 30(21):2659-2680. PubMed ID: 31483737 [TBL] [Abstract][Full Text] [Related]
4. Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia. Moore DJ; Onoufriadis A; Shoemark A; Simpson MA; zur Lage PI; de Castro SC; Bartoloni L; Gallone G; Petridi S; Woollard WJ; Antony D; Schmidts M; Didonna T; Makrythanasis P; Bevillard J; Mongan NP; Djakow J; Pals G; Lucas JS; Marthin JK; Nielsen KG; Santoni F; Guipponi M; Hogg C; Antonarakis SE; Emes RD; Chung EM; Greene ND; Blouin JL; Jarman AP; Mitchison HM Am J Hum Genet; 2013 Aug; 93(2):346-56. PubMed ID: 23891471 [TBL] [Abstract][Full Text] [Related]
5. TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella. Thomas L; Bouhouche K; Whitfield M; Thouvenin G; Coste A; Louis B; Szymanski C; Bequignon E; Papon JF; Castelli M; Lemullois M; Dhalluin X; Drouin-Garraud V; Montantin G; Tissier S; Duquesnoy P; Copin B; Dastot F; Couvet S; Barbotin AL; Faucon C; Honore I; Maitre B; Beydon N; Tamalet A; Rives N; Koll F; Escudier E; Tassin AM; Touré A; Mitchell V; Amselem S; Legendre M Am J Hum Genet; 2020 Feb; 106(2):153-169. PubMed ID: 31978331 [TBL] [Abstract][Full Text] [Related]
10. Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice. Wang R; Yang D; Tu C; Lei C; Ding S; Guo T; Wang L; Liu Y; Lu C; Yang B; Ouyang S; Gong K; Tan Z; Deng Y; Tan Y; Qing J; Luo H Front Med; 2023 Oct; 17(5):957-971. PubMed ID: 37314648 [TBL] [Abstract][Full Text] [Related]
11. Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice. Ma A; Zhou J; Ali H; Abbas T; Ali I; Muhammad Z; Dil S; Chen J; Huang X; Ma H; Zhao D; Zhang B; Zhang Y; Shah W; Shah B; Murtaza G; Iqbal F; Khan MA; Khan A; Li Q; Xu B; Wu L; Zhang H; Shi Q JCI Insight; 2023 Feb; 8(3):. PubMed ID: 36752199 [TBL] [Abstract][Full Text] [Related]
12. The ciliary inner dynein arm, I1 dynein, is assembled in the cytoplasm and transported by IFT before axonemal docking. Viswanadha R; Hunter EL; Yamamoto R; Wirschell M; Alford LM; Dutcher SK; Sale WS Cytoskeleton (Hoboken); 2014 Oct; 71(10):573-86. PubMed ID: 25252184 [TBL] [Abstract][Full Text] [Related]
13. Vertebrate Dynein-f depends on Wdr78 for axonemal localization and is essential for ciliary beat. Zhang Y; Chen Y; Zheng J; Wang J; Duan S; Zhang W; Yan X; Zhu X J Mol Cell Biol; 2019 May; 11(5):383-394. PubMed ID: 30060180 [TBL] [Abstract][Full Text] [Related]
14. The MIA complex is a conserved and novel dynein regulator essential for normal ciliary motility. Yamamoto R; Song K; Yanagisawa HA; Fox L; Yagi T; Wirschell M; Hirono M; Kamiya R; Nicastro D; Sale WS J Cell Biol; 2013 Apr; 201(2):263-78. PubMed ID: 23569216 [TBL] [Abstract][Full Text] [Related]
15. Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility. Aprea I; Raidt J; Höben IM; Loges NT; Nöthe-Menchen T; Pennekamp P; Olbrich H; Kaiser T; Biebach L; Tüttelmann F; Horvath J; Schubert M; Krallmann C; Kliesch S; Omran H PLoS Genet; 2021 Feb; 17(2):e1009306. PubMed ID: 33635866 [TBL] [Abstract][Full Text] [Related]
16. Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia. Pennarun G; Escudier E; Chapelin C; Bridoux AM; Cacheux V; Roger G; Clément A; Goossens M; Amselem S; Duriez B Am J Hum Genet; 1999 Dec; 65(6):1508-19. PubMed ID: 10577904 [TBL] [Abstract][Full Text] [Related]
17. Composition and function of ciliary inner-dynein-arm subunits studied in Chlamydomonas reinhardtii. Yamamoto R; Hwang J; Ishikawa T; Kon T; Sale WS Cytoskeleton (Hoboken); 2021 Mar; 78(3):77-96. PubMed ID: 33876572 [TBL] [Abstract][Full Text] [Related]
18. CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Merveille AC; Davis EE; Becker-Heck A; Legendre M; Amirav I; Bataille G; Belmont J; Beydon N; Billen F; Clément A; Clercx C; Coste A; Crosbie R; de Blic J; Deleuze S; Duquesnoy P; Escalier D; Escudier E; Fliegauf M; Horvath J; Hill K; Jorissen M; Just J; Kispert A; Lathrop M; Loges NT; Marthin JK; Momozawa Y; Montantin G; Nielsen KG; Olbrich H; Papon JF; Rayet I; Roger G; Schmidts M; Tenreiro H; Towbin JA; Zelenika D; Zentgraf H; Georges M; Lequarré AS; Katsanis N; Omran H; Amselem S Nat Genet; 2011 Jan; 43(1):72-8. PubMed ID: 21131972 [TBL] [Abstract][Full Text] [Related]
19. Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility. El Khouri E; Thomas L; Jeanson L; Bequignon E; Vallette B; Duquesnoy P; Montantin G; Copin B; Dastot-Le Moal F; Blanchon S; Papon JF; Lorès P; Yuan L; Collot N; Tissier S; Faucon C; Gacon G; Patrat C; Wolf JP; Dulioust E; Crestani B; Escudier E; Coste A; Legendre M; Touré A; Amselem S Am J Hum Genet; 2016 Aug; 99(2):489-500. PubMed ID: 27486783 [TBL] [Abstract][Full Text] [Related]