215 related articles for article (PubMed ID: 34445067)
1. Zebrafish Motile Cilia as a Model for Primary Ciliary Dyskinesia.
Pinto AL; Rasteiro M; Bota C; Pestana S; Sampaio P; Hogg C; Burgoyne T; Lopes SS
Int J Mol Sci; 2021 Aug; 22(16):. PubMed ID: 34445067
[TBL] [Abstract][Full Text] [Related]
2. Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities.
Leslie JS; Hjeij R; Vivante A; Bearce EA; Dyer L; Wang J; Rawlins L; Kennedy J; Ubeyratna N; Fasham J; Irons ZH; Craig SB; Koenig J; George S; Pode-Shakked B; Bolkier Y; Barel O; Mane S; Frederiksen KK; Wenger O; Scott E; Cross HE; Lorentzen E; Norris DP; Anikster Y; Omran H; Grimes DT; Crosby AH; Baple EL
Genet Med; 2022 Nov; 24(11):2249-2261. PubMed ID: 36074124
[TBL] [Abstract][Full Text] [Related]
3. The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation.
Becker-Heck A; Zohn IE; Okabe N; Pollock A; Lenhart KB; Sullivan-Brown J; McSheene J; Loges NT; Olbrich H; Haeffner K; Fliegauf M; Horvath J; Reinhardt R; Nielsen KG; Marthin JK; Baktai G; Anderson KV; Geisler R; Niswander L; Omran H; Burdine RD
Nat Genet; 2011 Jan; 43(1):79-84. PubMed ID: 21131974
[TBL] [Abstract][Full Text] [Related]
4. DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.
Li Y; Yagi H; Onuoha EO; Damerla RR; Francis R; Furutani Y; Tariq M; King SM; Hendricks G; Cui C; Saydmohammed M; Lee DM; Zahid M; Sami I; Leatherbury L; Pazour GJ; Ware SM; Nakanishi T; Goldmuntz E; Tsang M; Lo CW
PLoS Genet; 2016 Feb; 12(2):e1005821. PubMed ID: 26918822
[TBL] [Abstract][Full Text] [Related]
5. Mutations in CCDC11, which encodes a coiled-coil containing ciliary protein, causes situs inversus due to dysmotility of monocilia in the left-right organizer.
Narasimhan V; Hjeij R; Vij S; Loges NT; Wallmeier J; Koerner-Rettberg C; Werner C; Thamilselvam SK; Boey A; Choksi SP; Pennekamp P; Roy S; Omran H
Hum Mutat; 2015 Mar; 36(3):307-18. PubMed ID: 25504577
[TBL] [Abstract][Full Text] [Related]
6. Sperm defects in primary ciliary dyskinesia and related causes of male infertility.
Sironen A; Shoemark A; Patel M; Loebinger MR; Mitchison HM
Cell Mol Life Sci; 2020 Jun; 77(11):2029-2048. PubMed ID: 31781811
[TBL] [Abstract][Full Text] [Related]
7. Motile cilia defects in diseases other than primary ciliary dyskinesia: The contemporary diagnostic and research role for transmission electron microscopy.
Mitchison HM; Shoemark A
Ultrastruct Pathol; 2017; 41(6):415-427. PubMed ID: 28925789
[TBL] [Abstract][Full Text] [Related]
8. Microtubular protofilaments and subunits of the outer dynein arm in cilia from dogs with primary ciliary dyskinesia.
Wilsman NJ; Morrison WB; Farnum CE; Fox LE
Am Rev Respir Dis; 1987 Jan; 135(1):137-43. PubMed ID: 2432809
[TBL] [Abstract][Full Text] [Related]
9. Ciliary ultrastructure in patients with chronic rhinosinusitis and primary ciliary dyskinesia.
Demarco RC; Tamashiro E; Rossato M; Ferreira MD; Valera FC; Anselmo-Lima WT
Eur Arch Otorhinolaryngol; 2013 Jul; 270(7):2065-70. PubMed ID: 23292041
[TBL] [Abstract][Full Text] [Related]
10. Systematic discovery of novel ciliary genes through functional genomics in the zebrafish.
Choksi SP; Babu D; Lau D; Yu X; Roy S
Development; 2014 Sep; 141(17):3410-9. PubMed ID: 25139857
[TBL] [Abstract][Full Text] [Related]
11. Primary Ciliary Dyskinesia: A Clinical Review.
Despotes KA; Zariwala MA; Davis SD; Ferkol TW
Cells; 2024 Jun; 13(11):. PubMed ID: 38891105
[TBL] [Abstract][Full Text] [Related]
12. Two novel mutations in the DNAH11 gene in primary ciliary dyskinesia (CILD7) with considerable variety in the clinical and beating cilia phenotype.
Schultz R; Elenius V; Lukkarinen H; Saarela T
BMC Med Genet; 2020 Nov; 21(1):237. PubMed ID: 33243178
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. DNAH11 Localization in the Proximal Region of Respiratory Cilia Defines Distinct Outer Dynein Arm Complexes.
Dougherty GW; Loges NT; Klinkenbusch JA; Olbrich H; Pennekamp P; Menchen T; Raidt J; Wallmeier J; Werner C; Westermann C; Ruckert C; Mirra V; Hjeij R; Memari Y; Durbin R; Kolb-Kokocinski A; Praveen K; Kashef MA; Kashef S; Eghtedari F; Häffner K; Valmari P; Baktai G; Aviram M; Bentur L; Amirav I; Davis EE; Katsanis N; Brueckner M; Shaposhnykov A; Pigino G; Dworniczak B; Omran H
Am J Respir Cell Mol Biol; 2016 Aug; 55(2):213-24. PubMed ID: 26909801
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesia.
Blanchon S; Legendre M; Bottier M; Tamalet A; Montantin G; Collot N; Faucon C; Dastot F; Copin B; Clement A; Filoche M; Coste A; Amselem S; Escudier E; Papon JF; Louis B
J Med Genet; 2020 Apr; 57(4):237-244. PubMed ID: 31772028
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.
Austin-Tse C; Halbritter J; Zariwala MA; Gilberti RM; Gee HY; Hellman N; Pathak N; Liu Y; Panizzi JR; Patel-King RS; Tritschler D; Bower R; O'Toole E; Porath JD; Hurd TW; Chaki M; Diaz KA; Kohl S; Lovric S; Hwang DY; Braun DA; Schueler M; Airik R; Otto EA; Leigh MW; Noone PG; Carson JL; Davis SD; Pittman JE; Ferkol TW; Atkinson JJ; Olivier KN; Sagel SD; Dell SD; Rosenfeld M; Milla CE; Loges NT; Omran H; Porter ME; King SM; Knowles MR; Drummond IA; Hildebrandt F
Am J Hum Genet; 2013 Oct; 93(4):672-86. PubMed ID: 24094744
[TBL] [Abstract][Full Text] [Related]
19. Survey of the Ciliary Motility Machinery of
Zur Lage P; Newton FG; Jarman AP
Front Genet; 2019; 10():24. PubMed ID: 30774648
[TBL] [Abstract][Full Text] [Related]
20. Notch/Her12 signalling modulates, motile/immotile cilia ratio downstream of
Tavares B; Jacinto R; Sampaio P; Pestana S; Pinto A; Vaz A; Roxo-Rosa M; Gardner R; Lopes T; Schilling B; Henry I; Saúde L; Lopes SS
Elife; 2017 Sep; 6():. PubMed ID: 28875937
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
