627 related articles for article (PubMed ID: 32943623)
1. Motile ciliopathies.
Wallmeier J; Nielsen KG; Kuehni CE; Lucas JS; Leigh MW; Zariwala MA; Omran H
Nat Rev Dis Primers; 2020 Sep; 6(1):77. PubMed ID: 32943623
[TBL] [Abstract][Full Text] [Related]
2. Primary ciliary dyskinesia: a major player in a bigger game.
Bhatt R; Hogg C
Breathe (Sheff); 2020 Jun; 16(2):200047. PubMed ID: 33304404
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Impact of Motile Ciliopathies on Human Development and Clinical Consequences in the Newborn.
Hyland RM; Brody SL
Cells; 2021 Dec; 11(1):. PubMed ID: 35011687
[TBL] [Abstract][Full Text] [Related]
5. Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus.
Fassad MR; Shoemark A; Legendre M; Hirst RA; Koll F; le Borgne P; Louis B; Daudvohra F; Patel MP; Thomas L; Dixon M; Burgoyne T; Hayes J; Nicholson AG; Cullup T; Jenkins L; Carr SB; Aurora P; Lemullois M; Aubusson-Fleury A; Papon JF; O'Callaghan C; Amselem S; Hogg C; Escudier E; Tassin AM; Mitchison HM
Am J Hum Genet; 2018 Dec; 103(6):984-994. PubMed ID: 30471717
[TBL] [Abstract][Full Text] [Related]
6. Ciliopathy with special emphasis on kartageners syndrome.
Ul Hassan A; Hassan G; Khan SH; Rasool Z; Abida A
Int J Health Sci (Qassim); 2009 Jan; 3(1):65-9. PubMed ID: 21475513
[TBL] [Abstract][Full Text] [Related]
7. Biallelic variants in CEP164 cause a motile ciliopathy-like syndrome.
Devlin LA; Coles J; Jackson CL; Barroso-Gil M; Green B; Walker WT; Thomas NS; Thompson J; Rock SA; Neatu R; Powell L; Molinari E; ; Wilson IJ; Cordell HJ; Olinger E; Miles CG; Sayer JA; Wheway G; Lucas JS
Clin Genet; 2023 Mar; 103(3):330-334. PubMed ID: 36273371
[TBL] [Abstract][Full Text] [Related]
8. Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects.
Loges NT; Antony D; Maver A; Deardorff MA; Güleç EY; Gezdirici A; Nöthe-Menchen T; Höben IM; Jelten L; Frank D; Werner C; Tebbe J; Wu K; Goldmuntz E; Čuturilo G; Krock B; Ritter A; Hjeij R; Bakey Z; Pennekamp P; Dworniczak B; Brunner H; Peterlin B; Tanidir C; Olbrich H; Omran H; Schmidts M
Am J Hum Genet; 2018 Dec; 103(6):995-1008. PubMed ID: 30471718
[TBL] [Abstract][Full Text] [Related]
9. Motile ciliopathies.
Nat Rev Dis Primers; 2020 Sep; 6(1):76. PubMed ID: 32943641
[No Abstract] [Full Text] [Related]
10. Genetic defects in ciliary structure and function.
Zariwala MA; Knowles MR; Omran H
Annu Rev Physiol; 2007; 69():423-50. PubMed ID: 17059358
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Unique among ciliopathies: primary ciliary dyskinesia, a motile cilia disorder.
Praveen K; Davis EE; Katsanis N
F1000Prime Rep; 2015; 7():36. PubMed ID: 25926987
[TBL] [Abstract][Full Text] [Related]
13. A liquid-like organelle at the root of motile ciliopathy.
Huizar RL; Lee C; Boulgakov AA; Horani A; Tu F; Marcotte EM; Brody SL; Wallingford JB
Elife; 2018 Dec; 7():. PubMed ID: 30561330
[TBL] [Abstract][Full Text] [Related]
14.
Cindrić S; Dougherty GW; Olbrich H; Hjeij R; Loges NT; Amirav I; Philipsen MC; Marthin JK; Nielsen KG; Sutharsan S; Raidt J; Werner C; Pennekamp P; Dworniczak B; Omran H
Am J Respir Cell Mol Biol; 2020 Mar; 62(3):382-396. PubMed ID: 31545650
[TBL] [Abstract][Full Text] [Related]
15. De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry.
Wallmeier J; Frank D; Shoemark A; Nöthe-Menchen T; Cindric S; Olbrich H; Loges NT; Aprea I; Dougherty GW; Pennekamp P; Kaiser T; Mitchison HM; Hogg C; Carr SB; Zariwala MA; Ferkol T; Leigh MW; Davis SD; Atkinson J; Dutcher SK; Knowles MR; Thiele H; Altmüller J; Krenz H; Wöste M; Brentrup A; Ahrens F; Vogelberg C; Morris-Rosendahl DJ; Omran H
Am J Hum Genet; 2019 Nov; 105(5):1030-1039. PubMed ID: 31630787
[TBL] [Abstract][Full Text] [Related]
16. Truncating mutations in exons 20 and 21 of
Bukowy-Bieryllo Z; Rabiasz A; Dabrowski M; Pogorzelski A; Wojda A; Dmenska H; Grzela K; Sroczynski J; Witt M; Zietkiewicz E
J Med Genet; 2019 Nov; 56(11):769-777. PubMed ID: 31366608
[TBL] [Abstract][Full Text] [Related]
17. Advances in the Genetics of Primary Ciliary Dyskinesia: Clinical Implications.
Horani A; Ferkol TW
Chest; 2018 Sep; 154(3):645-652. PubMed ID: 29800551
[TBL] [Abstract][Full Text] [Related]
18. Changes of Motile Ciliary Phenotype in Patients with Primary Ciliopathies.
Brndiarova M; Kvassayova J; Vojtkova J; Igaz M; Buday T; Plevkova J
Adv Exp Med Biol; 2021; 1335():79-85. PubMed ID: 33687727
[TBL] [Abstract][Full Text] [Related]
19.
Rabiasz A; Ziętkiewicz E
Int J Mol Sci; 2023 Feb; 24(5):. PubMed ID: 36901899
[TBL] [Abstract][Full Text] [Related]
20. Primary ciliary dyskinesia: clinical presentation, diagnosis and genetics.
Storm van's Gravesande K; Omran H
Ann Med; 2005; 37(6):439-49. PubMed ID: 16203616
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]