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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

346 related articles for article (PubMed ID: 33279404)

  • 1. Motile cilia and airway disease.
    Legendre M; Zaragosi LE; Mitchison HM
    Semin Cell Dev Biol; 2021 Feb; 110():19-33. PubMed ID: 33279404
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Immunofluorescence staining of ciliated respiratory epithelial cells.
    Omran H; Loges NT
    Methods Cell Biol; 2009; 91():123-33. PubMed ID: 20409784
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system.
    Aprea I; Nöthe-Menchen T; Dougherty GW; Raidt J; Loges NT; Kaiser T; Wallmeier J; Olbrich H; Strünker T; Kliesch S; Pennekamp P; Omran H
    Mol Hum Reprod; 2021 Feb; 27(3):. PubMed ID: 33561200
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Primary ciliary dyskinesia: recent advances in epidemiology, diagnosis, management and relationship with the expanding spectrum of ciliopathy.
    Bush A; Hogg C
    Expert Rev Respir Med; 2012 Dec; 6(6):663-82. PubMed ID: 23234452
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. HEATR2 plays a conserved role in assembly of the ciliary motile apparatus.
    Diggle CP; Moore DJ; Mali G; zur Lage P; Ait-Lounis A; Schmidts M; Shoemark A; Garcia Munoz A; Halachev MR; Gautier P; Yeyati PL; Bonthron DT; Carr IM; Hayward B; Markham AF; Hope JE; von Kriegsheim A; Mitchison HM; Jackson IJ; Durand B; Reith W; Sheridan E; Jarman AP; Mill P
    PLoS Genet; 2014 Sep; 10(9):e1004577. PubMed ID: 25232951
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Primary Ciliary Dyskinesia Associated Disease-Causing Variants in
    Wilken A; Höben IM; Wolter A; Loges NT; Olbrich H; Aprea I; Dworniczak B; Raidt J; Omran H
    Cells; 2024 Jul; 13(14):. PubMed ID: 39056782
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 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. Gene editing of DNAH11 restores normal cilia motility in primary ciliary dyskinesia.
    Lai M; Pifferi M; Bush A; Piras M; Michelucci A; Di Cicco M; del Grosso A; Quaranta P; Cursi C; Tantillo E; Franceschi S; Mazzanti MC; Simi P; Saggese G; Boner A; Pistello M
    J Med Genet; 2016 Apr; 53(4):242-9. PubMed ID: 26729821
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DYX1C1 is required for axonemal dynein assembly and ciliary motility.
    Tarkar A; Loges NT; Slagle CE; Francis R; Dougherty GW; Tamayo JV; Shook B; Cantino M; Schwartz D; Jahnke C; Olbrich H; Werner C; Raidt J; Pennekamp P; Abouhamed M; Hjeij R; Köhler G; Griese M; Li Y; Lemke K; Klena N; Liu X; Gabriel G; Tobita K; Jaspers M; Morgan LC; Shapiro AJ; Letteboer SJ; Mans DA; Carson JL; Leigh MW; Wolf WE; Chen S; Lucas JS; Onoufriadis A; Plagnol V; Schmidts M; Boldt K; ; Roepman R; Zariwala MA; Lo CW; Mitchison HM; Knowles MR; Burdine RD; Loturco JJ; Omran H
    Nat Genet; 2013 Sep; 45(9):995-1003. PubMed ID: 23872636
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel genetic variant in DNAI2 detected by custom gene panel in a newborn with Primary Ciliary Dyskinesia: case report.
    Rocca MS; Piatti G; Michelucci A; Guazzo R; Bertini V; Vinanzi C; Caligo MA; Valetto A; Foresta C
    BMC Med Genet; 2020 Nov; 21(1):220. PubMed ID: 33167880
    [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. The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans.
    Wirschell M; Olbrich H; Werner C; Tritschler D; Bower R; Sale WS; Loges NT; Pennekamp P; Lindberg S; Stenram U; Carlén B; Horak E; Köhler G; Nürnberg P; Nürnberg G; Porter ME; Omran H
    Nat Genet; 2013 Mar; 45(3):262-8. PubMed ID: 23354437
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia.
    Boon M; Wallmeier J; Ma L; Loges NT; Jaspers M; Olbrich H; Dougherty GW; Raidt J; Werner C; Amirav I; Hevroni A; Abitbul R; Avital A; Soferman R; Wessels M; O'Callaghan C; Chung EM; Rutman A; Hirst RA; Moya E; Mitchison HM; Van Daele S; De Boeck K; Jorissen M; Kintner C; Cuppens H; Omran H
    Nat Commun; 2014 Jul; 5():4418. PubMed ID: 25048963
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 18.