BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

247 related articles for article (PubMed ID: 32709945)

  • 1. Loss of Rsph9 causes neonatal hydrocephalus with abnormal development of motile cilia in mice.
    Zou W; Lv Y; Liu ZI; Xia P; Li H; Jiao J
    Sci Rep; 2020 Jul; 10(1):12435. PubMed ID: 32709945
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Rsph9 is critical for ciliary radial spoke assembly and central pair microtubule stability.
    Zhu L; Liu H; Chen Y; Yan X; Zhu X
    Biol Cell; 2019 Feb; 111(2):29-38. PubMed ID: 30383886
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Disruption of the mouse Jhy gene causes abnormal ciliary microtubule patterning and juvenile hydrocephalus.
    Appelbe OK; Bollman B; Attarwala A; Triebes LA; Muniz-Talavera H; Curry DJ; Schmidt JV
    Dev Biol; 2013 Oct; 382(1):172-85. PubMed ID: 23906841
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation.
    Ibañez-Tallon I; Pagenstecher A; Fliegauf M; Olbrich H; Kispert A; Ketelsen UP; North A; Heintz N; Omran H
    Hum Mol Genet; 2004 Sep; 13(18):2133-41. PubMed ID: 15269178
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SNX27 Deletion Causes Hydrocephalus by Impairing Ependymal Cell Differentiation and Ciliogenesis.
    Wang X; Zhou Y; Wang J; Tseng IC; Huang T; Zhao Y; Zheng Q; Gao Y; Luo H; Zhang X; Bu G; Hong W; Xu H
    J Neurosci; 2016 Dec; 36(50):12586-12597. PubMed ID: 27974614
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ultrastructure and movement of the ependymal and tracheal cilia in congenitally hydrocephalic WIC-Hyd rats.
    Shimizu A; Koto M
    Childs Nerv Syst; 1992 Feb; 8(1):25-32. PubMed ID: 1576603
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Loss of Dishevelleds disrupts planar polarity in ependymal motile cilia and results in hydrocephalus.
    Ohata S; Nakatani J; Herranz-Pérez V; Cheng J; Belinson H; Inubushi T; Snider WD; García-Verdugo JM; Wynshaw-Boris A; Alvarez-Buylla A
    Neuron; 2014 Aug; 83(3):558-71. PubMed ID: 25043421
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in Hydin impair ciliary motility in mice.
    Lechtreck KF; Delmotte P; Robinson ML; Sanderson MJ; Witman GB
    J Cell Biol; 2008 Feb; 180(3):633-43. PubMed ID: 18250199
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. MT1-MMP deficiency leads to defective ependymal cell maturation, impaired ciliogenesis, and hydrocephalus.
    Jiang Z; Zhou J; Qin X; Zheng H; Gao B; Liu X; Jin G; Zhou Z
    JCI Insight; 2020 May; 5(9):. PubMed ID: 32229724
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rethinking the cilia hypothesis of hydrocephalus.
    Duy PQ; Greenberg ABW; Butler WE; Kahle KT
    Neurobiol Dis; 2022 Dec; 175():105913. PubMed ID: 36341771
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Rsph4a is essential for the triplet radial spoke head assembly of the mouse motile cilia.
    Yoke H; Ueno H; Narita A; Sakai T; Horiuchi K; Shingyoji C; Hamada H; Shinohara K
    PLoS Genet; 2020 Mar; 16(3):e1008664. PubMed ID: 32203505
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.
    Castleman VH; Romio L; Chodhari R; Hirst RA; de Castro SC; Parker KA; Ybot-Gonzalez P; Emes RD; Wilson SW; Wallis C; Johnson CA; Herrera RJ; Rutman A; Dixon M; Shoemark A; Bush A; Hogg C; Gardiner RM; Reish O; Greene ND; O'Callaghan C; Purton S; Chung EM; Mitchison HM
    Am J Hum Genet; 2009 Feb; 84(2):197-209. PubMed ID: 19200523
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.