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 *

244 related articles for article (PubMed ID: 37315079)

  • 1. IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.
    Bakey Z; Cabrera OA; Hoefele J; Antony D; Wu K; Stuck MW; Micha D; Eguether T; Smith AO; van der Wel NN; Wagner M; Strittmatter L; Beales PL; Jonassen JA; Thiffault I; Cadieux-Dion M; Boyes L; Sharif S; Tüysüz B; Dunstheimer D; Niessen HWM; Devine W; Lo CW; Mitchison HM; Schmidts M; Pazour GJ
    PLoS Genet; 2023 Jun; 19(6):e1010796. PubMed ID: 37315079
    [TBL] [Abstract][Full Text] [Related]  

  • 2.
    Bakey Z; Cabrera OA; Hoefele J; Antony D; Wu K; Stuck MW; Micha D; Eguether T; Smith AO; van der Wel NN; Wagner M; Strittmatter L; Beales PL; Jonassen JA; Thiffault I; Cadieux-Dion M; Boyes L; Sharif S; Tüysüz B; Dunstheimer D; Niessen HWM; Devine W; Lo CW; Mitchison HM; Schmidts M; Pazour GJ
    medRxiv; 2023 Feb; ():. PubMed ID: 36865301
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Defective airway intraflagellar transport underlies a combined motile and primary ciliopathy syndrome caused by IFT74 mutations.
    Fassad MR; Rumman N; Junger K; Patel MP; Thompson J; Goggin P; Ueffing M; Beyer T; Boldt K; Lucas JS; Mitchison HM
    Hum Mol Genet; 2023 Oct; 32(21):3090-3104. PubMed ID: 37555648
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Compound heterozygous IFT81 variations in a skeletal ciliopathy patient cause Bardet-Biedl syndrome-like ciliary defects.
    Tasaki K; Zhou Z; Ishida Y; Katoh Y; Nakayama K
    Hum Mol Genet; 2023 Sep; 32(19):2887-2900. PubMed ID: 37427975
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.
    Lorès P; Kherraf ZE; Amiri-Yekta A; Whitfield M; Daneshipour A; Stouvenel L; Cazin C; Cavarocchi E; Coutton C; Llabador MA; Arnoult C; Thierry-Mieg N; Ferreux L; Patrat C; Hosseini SH; Mustapha SFB; Zouari R; Dulioust E; Ray PF; Touré A
    Hum Genet; 2021 Jul; 140(7):1031-1043. PubMed ID: 33689014
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality Defects.
    Bonnefoy S; Watson CM; Kernohan KD; Lemos M; Hutchinson S; Poulter JA; Crinnion LA; Berry I; Simmonds J; Vasudevan P; O'Callaghan C; Hirst RA; Rutman A; Huang L; Hartley T; Grynspan D; Moya E; Li C; Carr IM; Bonthron DT; Leroux M; ; Boycott KM; Bastin P; Sheridan EG
    Am J Hum Genet; 2018 Nov; 103(5):727-739. PubMed ID: 30388400
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Getting tubulin to the tip of the cilium: one IFT train, many different tubulin cargo-binding sites?
    Bhogaraju S; Weber K; Engel BD; Lechtreck KF; Lorentzen E
    Bioessays; 2014 May; 36(5):463-7. PubMed ID: 24616010
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functional characterization of tektin-1 in motile cilia and evidence for TEKT1 as a new candidate gene for motile ciliopathies.
    Ryan R; Failler M; Reilly ML; Garfa-Traore M; Delous M; Filhol E; Reboul T; Bole-Feysot C; Nitschké P; Baudouin V; Amselem S; Escudier E; Legendre M; Benmerah A; Saunier S
    Hum Mol Genet; 2018 Jan; 27(2):266-282. PubMed ID: 29121203
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Together, the IFT81 and IFT74 N-termini form the main module for intraflagellar transport of tubulin.
    Kubo T; Brown JM; Bellve K; Craige B; Craft JM; Fogarty K; Lechtreck KF; Witman GB
    J Cell Sci; 2016 May; 129(10):2106-19. PubMed ID: 27068536
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease.
    Lewis WR; Malarkey EB; Tritschler D; Bower R; Pasek RC; Porath JD; Birket SE; Saunier S; Antignac C; Knowles MR; Leigh MW; Zariwala MA; Challa AK; Kesterson RA; Rowe SM; Drummond IA; Parant JM; Hildebrandt F; Porter ME; Yoder BK; Berbari NF
    PLoS Genet; 2016 Jul; 12(7):e1006220. PubMed ID: 27472056
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Loss of Ift74 Leads to Slow Photoreceptor Degeneration and Ciliogenesis Defects in Zebrafish.
    Zhu P; Xu J; Wang Y; Zhao C
    Int J Mol Sci; 2021 Aug; 22(17):. PubMed ID: 34502236
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular basis of tubulin transport within the cilium by IFT74 and IFT81.
    Bhogaraju S; Cajanek L; Fort C; Blisnick T; Weber K; Taschner M; Mizuno N; Lamla S; Bastin P; Nigg EA; Lorentzen E
    Science; 2013 Aug; 341(6149):1009-12. PubMed ID: 23990561
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The coiled-coil domain containing protein CCDC151 is required for the function of IFT-dependent motile cilia in animals.
    Jerber J; Baas D; Soulavie F; Chhin B; Cortier E; Vesque C; Thomas J; Durand B
    Hum Mol Genet; 2014 Feb; 23(3):563-77. PubMed ID: 24067530
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Assembly of IFT trains at the ciliary base depends on IFT74.
    Brown JM; Cochran DA; Craige B; Kubo T; Witman GB
    Curr Biol; 2015 Jun; 25(12):1583-93. PubMed ID: 26051893
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.
    Luo M; Lin Z; Zhu T; Jin M; Meng D; He R; Cao Z; Shen Y; Lu C; Cai R; Zhao Y; Wang X; Li H; Wu S; Zou X; Luo G; Cao L; Huang M; Jiao H; Gao H; Sui R; Zhao C; Ma X; Cao M
    Genet Med; 2021 Jun; 23(6):1041-1049. PubMed ID: 33531668
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics and centrosome cohesion.
    Dupont MA; Humbert C; Huber C; Siour Q; Guerrera IC; Jung V; Christensen A; Pouliet A; Garfa-Traoré M; Nitschké P; Injeyan M; Millar K; Chitayat D; Shannon P; Girisha KM; Shukla A; Mechler C; Lorentzen E; Benmerah A; Cormier-Daire V; Jeanpierre C; Saunier S; Delous M
    Hum Mol Genet; 2019 Aug; 28(16):2720-2737. PubMed ID: 31042281
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.