BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

427 related articles for article (PubMed ID: 23354437)

  • 1. 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]  

  • 2. 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]  

  • 3. Detailed structural and biochemical characterization of the nexin-dynein regulatory complex.
    Oda T; Yanagisawa H; Kikkawa M
    Mol Biol Cell; 2015 Jan; 26(2):294-304. PubMed ID: 25411337
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation.
    Hjeij R; Onoufriadis A; Watson CM; Slagle CE; Klena NT; Dougherty GW; Kurkowiak M; Loges NT; Diggle CP; Morante NF; Gabriel GC; Lemke KL; Li Y; Pennekamp P; Menchen T; Konert F; Marthin JK; Mans DA; Letteboer SJ; Werner C; Burgoyne T; Westermann C; Rutman A; Carr IM; O'Callaghan C; Moya E; Chung EM; ; Sheridan E; Nielsen KG; Roepman R; Bartscherer K; Burdine RD; Lo CW; Omran H; Mitchison HM
    Am J Hum Genet; 2014 Sep; 95(3):257-74. PubMed ID: 25192045
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization.
    Jeanson L; Thomas L; Copin B; Coste A; Sermet-Gaudelus I; Dastot-Le Moal F; Duquesnoy P; Montantin G; Collot N; Tissier S; Papon JF; Clement A; Louis B; Escudier E; Amselem S; Legendre M
    Hum Mutat; 2016 Aug; 37(8):776-85. PubMed ID: 27120127
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia.
    Kott E; Duquesnoy P; Copin B; Legendre M; Dastot-Le Moal F; Montantin G; Jeanson L; Tamalet A; Papon JF; Siffroi JP; Rives N; Mitchell V; de Blic J; Coste A; Clement A; Escalier D; Touré A; Escudier E; Amselem S
    Am J Hum Genet; 2012 Nov; 91(5):958-64. PubMed ID: 23122589
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Scaffold subunits support associated subunit assembly in the
    Gui L; Song K; Tritschler D; Bower R; Yan S; Dai A; Augspurger K; Sakizadeh J; Grzemska M; Ni T; Porter ME; Nicastro D
    Proc Natl Acad Sci U S A; 2019 Nov; 116(46):23152-23162. PubMed ID: 31659045
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DRC2/CCDC65 is a central hub for assembly of the nexin-dynein regulatory complex and other regulators of ciliary and flagellar motility.
    Bower R; Tritschler D; Mills KV; Heuser T; Nicastro D; Porter ME
    Mol Biol Cell; 2018 Jan; 29(2):137-153. PubMed ID: 29167384
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The dynein regulatory complex is the nexin link and a major regulatory node in cilia and flagella.
    Heuser T; Raytchev M; Krell J; Porter ME; Nicastro D
    J Cell Biol; 2009 Dec; 187(6):921-33. PubMed ID: 20008568
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Drosophila orthologue of the primary ciliary dyskinesia-associated gene, DNAAF3, is required for axonemal dynein assembly.
    Zur Lage P; Xi Z; Lennon J; Hunter I; Chan WK; Bolado Carrancio A; von Kriegsheim A; Jarman AP
    Biol Open; 2021 Oct; 10(10):. PubMed ID: 34553759
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Axonemal structures reveal mechanoregulatory and disease mechanisms.
    Walton T; Gui M; Velkova S; Fassad MR; Hirst RA; Haarman E; O'Callaghan C; Bottier M; Burgoyne T; Mitchison HM; Brown A
    Nature; 2023 Jun; 618(7965):625-633. PubMed ID: 37258679
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia.
    Moore DJ; Onoufriadis A; Shoemark A; Simpson MA; zur Lage PI; de Castro SC; Bartoloni L; Gallone G; Petridi S; Woollard WJ; Antony D; Schmidts M; Didonna T; Makrythanasis P; Bevillard J; Mongan NP; Djakow J; Pals G; Lucas JS; Marthin JK; Nielsen KG; Santoni F; Guipponi M; Hogg C; Antonarakis SE; Emes RD; Chung EM; Greene ND; Blouin JL; Jarman AP; Mitchison HM
    Am J Hum Genet; 2013 Aug; 93(2):346-56. PubMed ID: 23891471
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse.
    Zhang J; He X; Wu H; Zhang X; Yang S; Liu C; Liu S; Hua R; Zhou S; Zhao S; Hu F; Zhang J; Liu W; Cheng H; Gao Y; Zhang F; Cao Y; Liu M
    Hum Mol Genet; 2021 Oct; 30(21):1996-2011. PubMed ID: 34169321
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. In situ localization of N and C termini of subunits of the flagellar nexin-dynein regulatory complex (N-DRC) using SNAP tag and cryo-electron tomography.
    Song K; Awata J; Tritschler D; Bower R; Witman GB; Porter ME; Nicastro D
    J Biol Chem; 2015 Feb; 290(9):5341-53. PubMed ID: 25564608
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans.
    Jreijiri F; Cavarocchi E; Amiri-Yekta A; Cazin C; Hosseini SH; El Khouri E; Patrat C; Thierry-Mieg N; Ray PF; Dulioust E; Whitfield M; Touré A
    Clin Genet; 2024 Mar; 105(3):317-322. PubMed ID: 37975235
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesia.
    Bustamante-Marin XM; Horani A; Stoyanova M; Charng WL; Bottier M; Sears PR; Yin WN; Daniels LA; Bowen H; Conrad DF; Knowles MR; Ostrowski LE; Zariwala MA; Dutcher SK
    PLoS Genet; 2020 Aug; 16(8):e1008691. PubMed ID: 32764743
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.