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Journal Abstract Search


138 related items for PubMed ID: 34019998

  • 1. Disease-causing mutated ATLASTIN 3 is excluded from distal axons and reduces axonal autophagy.
    Behrendt L, Hoischen C, Kaether C.
    Neurobiol Dis; 2021 Jul; 155():105400. PubMed ID: 34019998
    [Abstract] [Full Text] [Related]

  • 2. A disease causing ATLASTIN 3 mutation affects multiple endoplasmic reticulum-related pathways.
    Behrendt L, Kurth I, Kaether C.
    Cell Mol Life Sci; 2019 Apr; 76(7):1433-1445. PubMed ID: 30666337
    [Abstract] [Full Text] [Related]

  • 3. ATL3 Is a Tubular ER-Phagy Receptor for GABARAP-Mediated Selective Autophagy.
    Chen Q, Xiao Y, Chai P, Zheng P, Teng J, Chen J.
    Curr Biol; 2019 Mar 04; 29(5):846-855.e6. PubMed ID: 30773365
    [Abstract] [Full Text] [Related]

  • 4. Sensory-Neuropathy-Causing Mutations in ATL3 Cause Aberrant ER Membrane Tethering.
    Krols M, Detry S, Asselbergh B, Almeida-Souza L, Kremer A, Lippens S, De Rycke R, De Winter V, Müller FJ, Kurth I, McMahon HT, Savvides SN, Timmerman V, Janssens S.
    Cell Rep; 2018 May 15; 23(7):2026-2038. PubMed ID: 29768202
    [Abstract] [Full Text] [Related]

  • 5. Sensory neuropathy-causing mutations in ATL3 affect ER-mitochondria contact sites and impair axonal mitochondrial distribution.
    Krols M, Asselbergh B, De Rycke R, De Winter V, Seyer A, Müller FJ, Kurth I, Bultynck G, Timmerman V, Janssens S.
    Hum Mol Genet; 2019 Feb 15; 28(4):615-627. PubMed ID: 30339187
    [Abstract] [Full Text] [Related]

  • 6. Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3.
    Kornak U, Mademan I, Schinke M, Voigt M, Krawitz P, Hecht J, Barvencik F, Schinke T, Gießelmann S, Beil FT, Pou-Serradell A, Vílchez JJ, Beetz C, Deconinck T, Timmerman V, Kaether C, De Jonghe P, Hübner CA, Gal A, Amling M, Mundlos S, Baets J, Kurth I.
    Brain; 2014 Mar 15; 137(Pt 3):683-92. PubMed ID: 24459106
    [Abstract] [Full Text] [Related]

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  • 8. RTN3L and CALCOCO1 function in parallel to maintain proteostasis in the endoplasmic reticulum.
    Kumar K, Chidambaram R, Parashar S, Ferro-Novick S.
    Autophagy; 2024 Sep 15; 20(9):2067-2075. PubMed ID: 38818751
    [Abstract] [Full Text] [Related]

  • 9. ATL3 gene mutation in a Chinese family with hereditary sensory neuropathy type 1F.
    Xu H, Zhang C, Cao L, Song J, Xu X, Zhang B, Chen B, Zhao G.
    J Peripher Nerv Syst; 2019 Mar 15; 24(1):150-155. PubMed ID: 30680846
    [Abstract] [Full Text] [Related]

  • 10. Drosophila Atlastin in motor neurons is required for locomotion and presynaptic function.
    De Gregorio C, Delgado R, Ibacache A, Sierralta J, Couve A.
    J Cell Sci; 2017 Oct 15; 130(20):3507-3516. PubMed ID: 28860117
    [Abstract] [Full Text] [Related]

  • 11. Spastin, atlastin, and ER relocalization are involved in axon but not dendrite regeneration.
    Rao K, Stone MC, Weiner AT, Gheres KW, Zhou C, Deitcher DL, Levitan ES, Rolls MM.
    Mol Biol Cell; 2016 Nov 01; 27(21):3245-3256. PubMed ID: 27605706
    [Abstract] [Full Text] [Related]

  • 12. Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphology.
    Zhao G, Zhu PP, Renvoisé B, Maldonado-Báez L, Park SH, Blackstone C.
    Exp Cell Res; 2016 Nov 15; 349(1):32-44. PubMed ID: 27669642
    [Abstract] [Full Text] [Related]

  • 13. SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development.
    Zhu PP, Soderblom C, Tao-Cheng JH, Stadler J, Blackstone C.
    Hum Mol Genet; 2006 Apr 15; 15(8):1343-53. PubMed ID: 16537571
    [Abstract] [Full Text] [Related]

  • 14. Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I.
    Guelly C, Zhu PP, Leonardis L, Papić L, Zidar J, Schabhüttl M, Strohmaier H, Weis J, Strom TM, Baets J, Willems J, De Jonghe P, Reilly MM, Fröhlich E, Hatz M, Trajanoski S, Pieber TR, Janecke AR, Blackstone C, Auer-Grumbach M.
    Am J Hum Genet; 2011 Jan 07; 88(1):99-105. PubMed ID: 21194679
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  • 16. Compartment-Specific Regulation of Autophagy in Primary Neurons.
    Maday S, Holzbaur EL.
    J Neurosci; 2016 Jun 01; 36(22):5933-45. PubMed ID: 27251616
    [Abstract] [Full Text] [Related]

  • 17. Human atlastin-3 is a constitutive ER membrane fusion catalyst.
    Bryce S, Stolzer M, Crosby D, Yang R, Durand D, Lee TH.
    J Cell Biol; 2023 Jul 03; 222(7):. PubMed ID: 37102997
    [Abstract] [Full Text] [Related]

  • 18. A novel nonsense variant in the ATL3 gene is associated with disturbed pain sensitivity, numbness of distal limbs and muscle weakness.
    Mohammadi S, Jafari Khamirani H, Baneshi M, Kamal N, Manoocheri J, Saffar M, Dianatpour M, Tabei SMB, Dastgheib SA.
    Ann Hum Genet; 2023 Jul 03; 87(4):147-157. PubMed ID: 36856139
    [Abstract] [Full Text] [Related]

  • 19. Atlastin GTPases are required for Golgi apparatus and ER morphogenesis.
    Rismanchi N, Soderblom C, Stadler J, Zhu PP, Blackstone C.
    Hum Mol Genet; 2008 Jun 01; 17(11):1591-604. PubMed ID: 18270207
    [Abstract] [Full Text] [Related]

  • 20. Atlastin Endoplasmic Reticulum-Shaping Proteins Facilitate Zika Virus Replication.
    Monel B, Rajah MM, Hafirassou ML, Sid Ahmed S, Burlaud-Gaillard J, Zhu PP, Nevers Q, Buchrieser J, Porrot F, Meunier C, Amraoui S, Chazal M, Salles A, Jouvenet N, Roingeard P, Blackstone C, Amara A, Schwartz O.
    J Virol; 2019 Dec 01; 93(23):. PubMed ID: 31534046
    [Abstract] [Full Text] [Related]


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