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For: Praveen K, Davis EE, Katsanis N. Unique among ciliopathies: primary ciliary dyskinesia, a motile cilia disorder. F1000Prime Rep 2015;7:36. [PMID: 25926987 DOI: 10.12703/P7-36] [Cited by in Crossref: 43] [Cited by in F6Publishing: 29] [Article Influence: 6.1] [Reference Citation Analysis]
Number Citing Articles
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2 Casar Tena T, Maerz LD, Szafranski K, Groth M, Blätte TJ, Donow C, Matysik S, Walther P, Jeggo PA, Burkhalter MD, Philipp M. Resting cells rely on the DNA helicase component MCM2 to build cilia. Nucleic Acids Res 2019;47:134-51. [PMID: 30329080 DOI: 10.1093/nar/gky945] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
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4 Yamamoto R, Obbineni JM, Alford LM, Ide T, Owa M, Hwang J, Kon T, Inaba K, James N, King SM, Ishikawa T, Sale WS, Dutcher SK. Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms. PLoS Genet 2017;13:e1006996. [PMID: 28892495 DOI: 10.1371/journal.pgen.1006996] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
5 Liu H, Zheng J, Zhu L, Xie L, Chen Y, Zhang Y, Zhang W, Yin Y, Peng C, Zhou J, Zhu X, Yan X. Wdr47, Camsaps, and Katanin cooperate to generate ciliary central microtubules. Nat Commun 2021;12:5796. [PMID: 34608154 DOI: 10.1038/s41467-021-26058-5] [Reference Citation Analysis]
6 Núnez-Ollé M, Jung C, Terré B, Balsiger NA, Plata C, Roset R, Pardo-Pastor C, Garrido M, Rojas S, Alameda F, Lloreta J, Martín-Caballero J, Flores JM, Stracker TH, Valverde MA, Muñoz FJ, Gil-Gómez G. Constitutive Cyclin O deficiency results in penetrant hydrocephalus, impaired growth and infertility. Oncotarget 2017;8:99261-73. [PMID: 29245899 DOI: 10.18632/oncotarget.21818] [Cited by in Crossref: 17] [Cited by in F6Publishing: 15] [Article Influence: 3.4] [Reference Citation Analysis]
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8 Nishijima Y, Hagiya Y, Kubo T, Takei R, Katoh Y, Nakayama K. RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly. Mol Biol Cell 2017;28:1652-66. [PMID: 28428259 DOI: 10.1091/mbc.E17-01-0017] [Cited by in Crossref: 44] [Cited by in F6Publishing: 38] [Article Influence: 8.8] [Reference Citation Analysis]
9 Al-Saiedy M, Gunasekara L, Green F, Pratt R, Chiu A, Yang A, Dennis J, Pieron C, Bjornson C, Winston B, Amrein M. Surfactant Dysfunction in ARDS and Bronchiolitis is Repaired with Cyclodextrins. Mil Med 2018;183:207-15. [PMID: 29635617 DOI: 10.1093/milmed/usx204] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
10 Abdelhamed Z, Vuong SM, Hill L, Shula C, Timms A, Beier D, Campbell K, Mangano FT, Stottmann RW, Goto J. A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice. Development 2018;145:dev154500. [PMID: 29317443 DOI: 10.1242/dev.154500] [Cited by in Crossref: 33] [Cited by in F6Publishing: 32] [Article Influence: 8.3] [Reference Citation Analysis]
11 Dai D, Ichikawa M, Peri K, Rebinsky R, Huy Bui K. Identification and mapping of central pair proteins by proteomic analysis. Biophys Physicobiol 2020;17:71-85. [PMID: 33178545 DOI: 10.2142/biophysico.BSJ-2019048] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
12 Santos-Carballal B, Fernández Fernández E, Goycoolea FM. Chitosan in Non-Viral Gene Delivery: Role of Structure, Characterization Methods, and Insights in Cancer and Rare Diseases Therapies. Polymers (Basel) 2018;10:E444. [PMID: 30966479 DOI: 10.3390/polym10040444] [Cited by in Crossref: 43] [Cited by in F6Publishing: 36] [Article Influence: 10.8] [Reference Citation Analysis]
13 Reck J, Schauer AM, VanderWaal Mills K, Bower R, Tritschler D, Perrone CA, Porter ME. The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas. Mol Biol Cell 2016;27:2404-22. [PMID: 27251063 DOI: 10.1091/mbc.E16-03-0191] [Cited by in Crossref: 32] [Cited by in F6Publishing: 23] [Article Influence: 5.3] [Reference Citation Analysis]
14 Knowles MR, Zariwala M, Leigh M. Primary Ciliary Dyskinesia. Clin Chest Med 2016;37:449-61. [PMID: 27514592 DOI: 10.1016/j.ccm.2016.04.008] [Cited by in Crossref: 92] [Cited by in F6Publishing: 71] [Article Influence: 15.3] [Reference Citation Analysis]
15 Watson CM, Crinnion LA, Berry IR, Harrison SM, Lascelles C, Antanaviciute A, Charlton RS, Dobbie A, Carr IM, Bonthron DT. Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping. BMC Med Genet 2016;17:1. [PMID: 26729329 DOI: 10.1186/s12881-015-0265-z] [Cited by in Crossref: 34] [Cited by in F6Publishing: 15] [Article Influence: 5.7] [Reference Citation Analysis]
16 Zhang Y, Chen Y, Zheng J, Wang J, Duan S, Zhang W, Yan X, Zhu X. Vertebrate Dynein-f depends on Wdr78 for axonemal localization and is essential for ciliary beat. J Mol Cell Biol 2019;11:383-94. [PMID: 30060180 DOI: 10.1093/jmcb/mjy043] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
17 Yuan S, Wang Z, Peng H, Ward SM, Hennig GW, Zheng H, Yan W. Oviductal motile cilia are essential for oocyte pickup but dispensable for sperm and embryo transport. Proc Natl Acad Sci U S A 2021;118:e2102940118. [PMID: 34039711 DOI: 10.1073/pnas.2102940118] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
18 Guo T, Tan ZP, Chen HM, Zheng DY, Liu L, Huang XG, Chen P, Luo H, Yang YF. An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families. Sci Rep 2017;7:7905. [PMID: 28801648 DOI: 10.1038/s41598-017-08510-z] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 3.2] [Reference Citation Analysis]
19 Beckers A, Fuhl F, Ott T, Boldt K, Brislinger MM, Walentek P, Schuster-Gossler K, Hegermann J, Alten L, Kremmer E, Przykopanski A, Serth K, Ueffing M, Blum M, Gossler A. The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus. Sci Rep 2021;11:13333. [PMID: 34172766 DOI: 10.1038/s41598-021-92495-3] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
20 Nevers Y, Prasad MK, Poidevin L, Chennen K, Allot A, Kress A, Ripp R, Thompson JD, Dollfus H, Poch O, Lecompte O. Insights into Ciliary Genes and Evolution from Multi-Level Phylogenetic Profiling. Mol Biol Evol 2017;34:2016-34. [PMID: 28460059 DOI: 10.1093/molbev/msx146] [Cited by in Crossref: 32] [Cited by in F6Publishing: 25] [Article Influence: 8.0] [Reference Citation Analysis]
21 Sugrue KF, Zohn IE. Mechanism for generation of left isomerism in Ccdc40 mutant embryos. PLoS One 2017;12:e0171180. [PMID: 28182636 DOI: 10.1371/journal.pone.0171180] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
22 Beckers A, Ott T, Schuster-Gossler K, Boldt K, Alten L, Ueffing M, Blum M, Gossler A. The evolutionary conserved FOXJ1 target gene Fam183b is essential for motile cilia in Xenopus but dispensable for ciliary function in mice. Sci Rep 2018;8:14678. [PMID: 30279523 DOI: 10.1038/s41598-018-33045-2] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
23 Zabeo D, Croft JT, Höög JL. Axonemal doublet microtubules can split into two complete singlets in human sperm flagellum tips. FEBS Lett 2019;593:892-902. [PMID: 30959570 DOI: 10.1002/1873-3468.13379] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
24 Dasgupta A, Amack JD. Cilia in vertebrate left-right patterning. Philos Trans R Soc Lond B Biol Sci 2016;371:20150410. [PMID: 27821522 DOI: 10.1098/rstb.2015.0410] [Cited by in Crossref: 47] [Cited by in F6Publishing: 38] [Article Influence: 9.4] [Reference Citation Analysis]
25 Grimes DT, Burdine RD. Left-Right Patterning: Breaking Symmetry to Asymmetric Morphogenesis. Trends Genet 2017;33:616-28. [PMID: 28720483 DOI: 10.1016/j.tig.2017.06.004] [Cited by in Crossref: 54] [Cited by in F6Publishing: 44] [Article Influence: 10.8] [Reference Citation Analysis]
26 Zabeo D, Heumann JM, Schwartz CL, Suzuki-Shinjo A, Morgan G, Widlund PO, Höög JL. A lumenal interrupted helix in human sperm tail microtubules. Sci Rep 2018;8:2727. [PMID: 29426884 DOI: 10.1038/s41598-018-21165-8] [Cited by in Crossref: 24] [Cited by in F6Publishing: 15] [Article Influence: 6.0] [Reference Citation Analysis]
27 Modarage K, Malik SA, Goggolidou P. Molecular Diagnostics of Ciliopathies and Insights Into Novel Developments in Diagnosing Rare Diseases. Br J Biomed Sci 2022;79:10221. [DOI: 10.3389/bjbs.2021.10221] [Reference Citation Analysis]
28 Eom TY, Han SB, Kim J, Blundon JA, Wang YD, Yu J, Anderson K, Kaminski DB, Sakurada SM, Pruett-Miller SM, Horner L, Wagner B, Robinson CG, Eicholtz M, Rose DC, Zakharenko SS. Schizophrenia-related microdeletion causes defective ciliary motility and brain ventricle enlargement via microRNA-dependent mechanisms in mice. Nat Commun 2020;11:912. [PMID: 32060266 DOI: 10.1038/s41467-020-14628-y] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
29 Patir A, Fraser AM, Barnett MW, McTeir L, Rainger J, Davey MG, Freeman TC. The transcriptional signature associated with human motile cilia. Sci Rep 2020;10:10814. [PMID: 32616903 DOI: 10.1038/s41598-020-66453-4] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 4.5] [Reference Citation Analysis]
30 Li C, Jensen VL, Park K, Kennedy J, Garcia-Gonzalo FR, Romani M, De Mori R, Bruel AL, Gaillard D, Doray B, Lopez E, Rivière JB, Faivre L, Thauvin-Robinet C, Reiter JF, Blacque OE, Valente EM, Leroux MR. MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone. PLoS Biol 2016;14:e1002416. [PMID: 26982032 DOI: 10.1371/journal.pbio.1002416] [Cited by in Crossref: 63] [Cited by in F6Publishing: 58] [Article Influence: 10.5] [Reference Citation Analysis]