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Journal Abstract Search

179 related items for PubMed ID: 22705585

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  • 3. Mild functional effects of a novel GFAP mutant allele identified in a familial case of adult-onset Alexander disease.
    Bachetti T, Caroli F, Bocca P, Prigione I, Balbi P, Biancheri R, Filocamo M, Mariotti C, Pareyson D, Ravazzolo R, Ceccherini I.
    Eur J Hum Genet; 2008 Apr; 16(4):462-70. PubMed ID: 18197187
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  • 4. The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27.
    Der Perng M, Su M, Wen SF, Li R, Gibbon T, Prescott AR, Brenner M, Quinlan RA.
    Am J Hum Genet; 2006 Aug; 79(2):197-213. PubMed ID: 16826512
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  • 5. Oligomers of mutant glial fibrillary acidic protein (GFAP) Inhibit the proteasome system in alexander disease astrocytes, and the small heat shock protein alphaB-crystallin reverses the inhibition.
    Tang G, Perng MD, Wilk S, Quinlan R, Goldman JE.
    J Biol Chem; 2010 Apr 02; 285(14):10527-37. PubMed ID: 20110364
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  • 6. Alexander-disease mutation of GFAP causes filament disorganization and decreased solubility of GFAP.
    Hsiao VC, Tian R, Long H, Der Perng M, Brenner M, Quinlan RA, Goldman JE.
    J Cell Sci; 2005 May 01; 118(Pt 9):2057-65. PubMed ID: 15840648
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  • 7. Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander disease.
    Mignot C, Delarasse C, Escaich S, Della Gaspera B, Noé E, Colucci-Guyon E, Babinet C, Pekny M, Vicart P, Boespflug-Tanguy O, Dautigny A, Rodriguez D, Pham-Dinh D.
    Exp Cell Res; 2007 Aug 01; 313(13):2766-79. PubMed ID: 17604020
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  • 16. Alexander Disease Modeling in Zebrafish: An In Vivo System Suitable to Perform Drug Screening.
    Candiani S, Carestiato S, Mack AF, Bani D, Bozzo M, Obino V, Ori M, Rosamilia F, De Sarlo M, Pestarino M, Ceccherini I, Bachetti T.
    Genes (Basel); 2020 Dec 11; 11(12):. PubMed ID: 33322348
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  • 17. Gene expression analysis in mice with elevated glial fibrillary acidic protein and Rosenthal fibers reveals a stress response followed by glial activation and neuronal dysfunction.
    Hagemann TL, Gaeta SA, Smith MA, Johnson DA, Johnson JA, Messing A.
    Hum Mol Genet; 2005 Aug 15; 14(16):2443-58. PubMed ID: 16014634
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  • 18. Alexander disease-associated glial fibrillary acidic protein mutations in mice induce Rosenthal fiber formation and a white matter stress response.
    Hagemann TL, Connor JX, Messing A.
    J Neurosci; 2006 Oct 25; 26(43):11162-73. PubMed ID: 17065456
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  • 20. Glial fibrillary acidic protein filaments can tolerate the incorporation of assembly-compromised GFAP-delta, but with consequences for filament organization and alphaB-crystallin association.
    Perng MD, Wen SF, Gibbon T, Middeldorp J, Sluijs J, Hol EM, Quinlan RA.
    Mol Biol Cell; 2008 Oct 25; 19(10):4521-33. PubMed ID: 18685083
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