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 *

421 related articles for article (PubMed ID: 16893913)

  • 1. The microtubule-severing protein Spastin is essential for axon outgrowth in the zebrafish embryo.
    Wood JD; Landers JA; Bingley M; McDermott CJ; Thomas-McArthur V; Gleadall LJ; Shaw PJ; Cunliffe VT
    Hum Mol Genet; 2006 Sep; 15(18):2763-71. PubMed ID: 16893913
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic and chemical modulation of spastin-dependent axon outgrowth in zebrafish embryos indicates a role for impaired microtubule dynamics in hereditary spastic paraplegia.
    Butler R; Wood JD; Landers JA; Cunliffe VT
    Dis Model Mech; 2010; 3(11-12):743-51. PubMed ID: 20829563
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary spastic paraplegia SPG4: what is known and not known about the disease.
    Solowska JM; Baas PW
    Brain; 2015 Sep; 138(Pt 9):2471-84. PubMed ID: 26094131
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of spastin function results in disease-specific axonal defects in human pluripotent stem cell-based models of hereditary spastic paraplegia.
    Denton KR; Lei L; Grenier J; Rodionov V; Blackstone C; Li XJ
    Stem Cells; 2014 Feb; 32(2):414-23. PubMed ID: 24123785
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The SMN binding protein Gemin2 is not involved in motor axon outgrowth.
    McWhorter ML; Boon KL; Horan ES; Burghes AH; Beattie CE
    Dev Neurobiol; 2008 Feb; 68(2):182-94. PubMed ID: 18000835
    [TBL] [Abstract][Full Text] [Related]  

  • 6. BMP- and neuropilin 1-mediated motor axon navigation relies on spastin alternative translation.
    Jardin N; Giudicelli F; Ten Martín D; Vitrac A; De Gois S; Allison R; Houart C; Reid E; Hazan J; Fassier C
    Development; 2018 Sep; 145(17):. PubMed ID: 30082270
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Evaluation of loss of function as an explanation for SPG4-based hereditary spastic paraplegia.
    Solowska JM; Garbern JY; Baas PW
    Hum Mol Genet; 2010 Jul; 19(14):2767-79. PubMed ID: 20430936
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gene dosage-dependent rescue of HSP neurite defects in SPG4 patients' neurons.
    Havlicek S; Kohl Z; Mishra HK; Prots I; Eberhardt E; Denguir N; Wend H; Plötz S; Boyer L; Marchetto MC; Aigner S; Sticht H; Groemer TW; Hehr U; Lampert A; Schlötzer-Schrehardt U; Winkler J; Gage FH; Winner B
    Hum Mol Genet; 2014 May; 23(10):2527-41. PubMed ID: 24381312
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Drosophila spastin regulates synaptic microtubule networks and is required for normal motor function.
    Sherwood NT; Sun Q; Xue M; Zhang B; Zinn K
    PLoS Biol; 2004 Dec; 2(12):e429. PubMed ID: 15562320
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing.
    Evans KJ; Gomes ER; Reisenweber SM; Gundersen GG; Lauring BP
    J Cell Biol; 2005 Feb; 168(4):599-606. PubMed ID: 15716377
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Role of spastin and protrudin in neurite outgrowth.
    Zhang C; Li D; Ma Y; Yan J; Yang B; Li P; Yu A; Lu C; Ma X
    J Cell Biochem; 2012 Jul; 113(7):2296-307. PubMed ID: 22573551
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics.
    Errico A; Ballabio A; Rugarli EI
    Hum Mol Genet; 2002 Jan; 11(2):153-63. PubMed ID: 11809724
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients.
    Kasher PR; De Vos KJ; Wharton SB; Manser C; Bennett EJ; Bingley M; Wood JD; Milner R; McDermott CJ; Miller CC; Shaw PJ; Grierson AJ
    J Neurochem; 2009 Jul; 110(1):34-44. PubMed ID: 19453301
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pleiotropic effects of spastin on neurite growth depending on expression levels.
    Riano E; Martignoni M; Mancuso G; Cartelli D; Crippa F; Toldo I; Siciliano G; Di Bella D; Taroni F; Bassi MT; Cappelletti G; Rugarli EI
    J Neurochem; 2009 Mar; 108(5):1277-88. PubMed ID: 19141076
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Microtubule-targeting drugs rescue axonal swellings in cortical neurons from spastin knockout mice.
    Fassier C; Tarrade A; Peris L; Courageot S; Mailly P; Dalard C; Delga S; Roblot N; Lefèvre J; Job D; Hazan J; Curmi PA; Melki J
    Dis Model Mech; 2013 Jan; 6(1):72-83. PubMed ID: 22773755
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spastin-interacting protein NA14/SSNA1 functions in cytokinesis and axon development.
    Goyal U; Renvoisé B; Chang J; Blackstone C
    PLoS One; 2014; 9(11):e112428. PubMed ID: 25390646
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spastin accumulation and motor neuron defects caused by a novel SPAST splice site mutation.
    Luo M; Wang Y; Liang J; Wan X
    J Transl Med; 2024 Sep; 22(1):872. PubMed ID: 39334479
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [AAA ATPases and hereditary spastic paraplegia].
    Wang YG; Shen L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):298-301. PubMed ID: 19504443
    [TBL] [Abstract][Full Text] [Related]  

  • 19. SPG4 gene promoter regulation via Elk1 transcription factor.
    Canbaz D; Kırımtay K; Karaca E; Karabay A
    J Neurochem; 2011 May; 117(4):724-34. PubMed ID: 21395583
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.
    Hazan J; Fonknechten N; Mavel D; Paternotte C; Samson D; Artiguenave F; Davoine CS; Cruaud C; Dürr A; Wincker P; Brottier P; Cattolico L; Barbe V; Burgunder JM; Prud'homme JF; Brice A; Fontaine B; Heilig B; Weissenbach J
    Nat Genet; 1999 Nov; 23(3):296-303. PubMed ID: 10610178
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.