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 *

345 related articles for article (PubMed ID: 18250199)

  • 1. 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]  

  • 2. Chlamydomonas reinhardtii hydin is a central pair protein required for flagellar motility.
    Lechtreck KF; Witman GB
    J Cell Biol; 2007 Feb; 176(4):473-82. PubMed ID: 17296796
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hydin seek: finding a function in ciliary motility.
    Smith EF
    J Cell Biol; 2007 Feb; 176(4):403-4. PubMed ID: 17296793
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.
    Olbrich H; Schmidts M; Werner C; Onoufriadis A; Loges NT; Raidt J; Banki NF; Shoemark A; Burgoyne T; Al Turki S; Hurles ME; ; Köhler G; Schroeder J; Nürnberg G; Nürnberg P; Chung EM; Reinhardt R; Marthin JK; Nielsen KG; Mitchison HM; Omran H
    Am J Hum Genet; 2012 Oct; 91(4):672-84. PubMed ID: 23022101
    [TBL] [Abstract][Full Text] [Related]  

  • 5.
    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]  

  • 6. 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]  

  • 7. The hydrocephalus inducing gene product, Hydin, positions axonemal central pair microtubules.
    Dawe HR; Shaw MK; Farr H; Gull K
    BMC Biol; 2007 Aug; 5():33. PubMed ID: 17683645
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CFAP53 regulates mammalian cilia-type motility patterns through differential localization and recruitment of axonemal dynein components.
    Ide T; Twan WK; Lu H; Ikawa Y; Lim LX; Henninger N; Nishimura H; Takaoka K; Narasimhan V; Yan X; Shiratori H; Roy S; Hamada H
    PLoS Genet; 2020 Dec; 16(12):e1009232. PubMed ID: 33347437
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Biosynthesis of Wdr16, a marker protein for kinocilia-bearing cells, starts at the time of kinocilia formation in rat, and wdr16 gene knockdown causes hydrocephalus in zebrafish.
    Hirschner W; Pogoda HM; Kramer C; Thiess U; Hamprecht B; Wiesmüller KH; Lautner M; Verleysdonk S
    J Neurochem; 2007 Apr; 101(1):274-88. PubMed ID: 17394468
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Calaxin is required for cilia-driven determination of vertebrate laterality.
    Sasaki K; Shiba K; Nakamura A; Kawano N; Satouh Y; Yamaguchi H; Morikawa M; Shibata D; Yanase R; Jokura K; Nomura M; Miyado M; Takada S; Ueno H; Nonaka S; Baba T; Ikawa M; Kikkawa M; Miyado K; Inaba K
    Commun Biol; 2019; 2():226. PubMed ID: 31240264
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Impact of aquaporin-4 and CD11c + microglia in the development of ependymal cells in the aqueduct: inferences to hydrocephalus.
    Mayo F; González-Vinceiro L; Hiraldo-González L; Rodríguez-Gómez FD; Calle-Castillejo C; Mayo M; Netti V; Ramírez-Lorca R; Echevarría M
    Fluids Barriers CNS; 2024 Jul; 21(1):53. PubMed ID: 38956598
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heat shock transcription factor 1 is required for maintenance of ciliary beating in mice.
    Takaki E; Fujimoto M; Nakahari T; Yonemura S; Miyata Y; Hayashida N; Yamamoto K; Vallee RB; Mikuriya T; Sugahara K; Yamashita H; Inouye S; Nakai A
    J Biol Chem; 2007 Dec; 282(51):37285-92. PubMed ID: 17965413
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ventricular ependyma of normal and hydrocephalic subjects: a scanning electronmicroscopic study.
    Bannister CM; Chapman SA
    Dev Med Child Neurol; 1980 Dec; 22(6):725-35. PubMed ID: 7450299
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Alcohol consumption impairs the ependymal cilia motility in the brain ventricles.
    Omran AJA; Saternos HC; Althobaiti YS; Wisner A; Sari Y; Nauli SM; AbouAlaiwi WA
    Sci Rep; 2017 Oct; 7(1):13652. PubMed ID: 29057897
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene.
    Davy BE; Robinson ML
    Hum Mol Genet; 2003 May; 12(10):1163-70. PubMed ID: 12719380
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.