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 *

178 related articles for article (PubMed ID: 27261005)

  • 1. Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice.
    Ha S; Lindsay AM; Timms AE; Beier DR
    G3 (Bethesda); 2016 Aug; 6(8):2479-87. PubMed ID: 27261005
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport.
    Hartill VL; van de Hoek G; Patel MP; Little R; Watson CM; Berry IR; Shoemark A; Abdelmottaleb D; Parkes E; Bacchelli C; Szymanska K; Knoers NV; Scambler PJ; Ueffing M; Boldt K; Yates R; Winyard PJ; Adler B; Moya E; Hattingh L; Shenoy A; Hogg C; Sheridan E; Roepman R; Norris D; Mitchison HM; Giles RH; Johnson CA
    Hum Mol Genet; 2018 Feb; 27(3):529-545. PubMed ID: 29228333
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Mutations in the Motile Cilia Gene DNAAF1 Are Associated with Neural Tube Defects in Humans.
    Miao C; Jiang Q; Li H; Zhang Q; Bai B; Bao Y; Zhang T
    G3 (Bethesda); 2016 Oct; 6(10):3307-3316. PubMed ID: 27543293
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.
    Ta-Shma A; Hjeij R; Perles Z; Dougherty GW; Abu Zahira I; Letteboer SJF; Antony D; Darwish A; Mans DA; Spittler S; Edelbusch C; Cindrić S; Nöthe-Menchen T; Olbrich H; Stuhlmann F; Aprea I; Pennekamp P; Loges NT; Breuer O; Shaag A; Rein AJJT; Gulec EY; Gezdirici A; Abitbul R; Elias N; Amirav I; Schmidts M; Roepman R; Elpeleg O; Omran H
    PLoS Genet; 2018 Aug; 14(8):e1007602. PubMed ID: 30148830
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel hypomorphic allele of
    Abdelhamed Z; Lukacs M; Cindric S; Ali S; Omran H; Stottmann RW
    Dis Model Mech; 2020 Oct; 13(10):. PubMed ID: 32988999
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A mutation in
    Abdelhamed Z; Vuong SM; Hill L; Shula C; Timms A; Beier D; Campbell K; Mangano FT; Stottmann RW; Goto J
    Development; 2018 Jan; 145(1):. PubMed ID: 29317443
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. CFAP43 modulates ciliary beating in mouse and Xenopus.
    Rachev E; Schuster-Gossler K; Fuhl F; Ott T; Tveriakhina L; Beckers A; Hegermann J; Boldt K; Mai M; Kremmer E; Ueffing M; Blum M; Gossler A
    Dev Biol; 2020 Mar; 459(2):109-125. PubMed ID: 31884020
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia.
    Sironen A; Kotaja N; Mulhern H; Wyatt TA; Sisson JH; Pavlik JA; Miiluniemi M; Fleming MD; Lee L
    Biol Reprod; 2011 Oct; 85(4):690-701. PubMed ID: 21715716
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Functional loss of
    Chiani F; Orsini T; Gambadoro A; Pasquini M; Putti S; Cirilli M; Ermakova O; Tocchini-Valentini GP
    Dis Model Mech; 2019 Aug; 12(8):. PubMed ID: 31383820
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Defective motile cilia in Prickle2-deficient mice.
    Sowers LP; Yin T; Mahajan VB; Bassuk AG
    J Neurogenet; 2014; 28(1-2):146-52. PubMed ID: 24708399
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CFAP54 is required for proper ciliary motility and assembly of the central pair apparatus in mice.
    McKenzie CW; Craige B; Kroeger TV; Finn R; Wyatt TA; Sisson JH; Pavlik JA; Strittmatter L; Hendricks GM; Witman GB; Lee L
    Mol Biol Cell; 2015 Sep; 26(18):3140-9. PubMed ID: 26224312
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia.
    Lee L
    J Neurosci Res; 2013 Sep; 91(9):1117-32. PubMed ID: 23686703
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Accelerated mortality from hydrocephalus and pneumonia in mice with a combined deficiency of SPAG6 and SPAG16L reveals a functional interrelationship between the two central apparatus proteins.
    Zhang Z; Tang W; Zhou R; Shen X; Wei Z; Patel AM; Povlishock JT; Bennett J; Strauss JF
    Cell Motil Cytoskeleton; 2007 May; 64(5):360-76. PubMed ID: 17323374
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Transport of the outer dynein arm complex to cilia requires a cytoplasmic protein Lrrc6.
    Inaba Y; Shinohara K; Botilde Y; Nabeshima R; Takaoka K; Ajima R; Lamri L; Takeda H; Saga Y; Nakamura T; Hamada H
    Genes Cells; 2016 Jul; 21(7):728-39. PubMed ID: 27353389
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deletion of the Parkin co-regulated gene causes defects in ependymal ciliary motility and hydrocephalus in the quakingviable mutant mouse.
    Wilson GR; Wang HX; Egan GF; Robinson PJ; Delatycki MB; O'Bryan MK; Lockhart PJ
    Hum Mol Genet; 2010 Apr; 19(8):1593-602. PubMed ID: 20106870
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic interaction between central pair apparatus genes CFAP221, CFAP54, and SPEF2 in mouse models of primary ciliary dyskinesia.
    McKenzie CW; Lee L
    Sci Rep; 2020 Jul; 10(1):12337. PubMed ID: 32704025
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The FOXJ1 target
    Beckers A; Adis C; Schuster-Gossler K; Tveriakhina L; Ott T; Fuhl F; Hegermann J; Boldt K; Serth K; Rachev E; Alten L; Kremmer E; Ueffing M; Blum M; Gossler A
    Development; 2020 Jun; 147(21):. PubMed ID: 32376681
    [TBL] [Abstract][Full Text] [Related]  

  • 20. LRRC50, a conserved ciliary protein implicated in polycystic kidney disease.
    van Rooijen E; Giles RH; Voest EE; van Rooijen C; Schulte-Merker S; van Eeden FJ
    J Am Soc Nephrol; 2008 Jun; 19(6):1128-38. PubMed ID: 18385425
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.