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164 related items for PubMed ID: 11353291

  • 1. Progressive formation of inclusions in the striatum and hippocampus of mice transgenic for the human Huntington's disease mutation.
    Morton AJ, Lagan MA, Skepper JN, Dunnett SB.
    J Neurocytol; 2000 Sep; 29(9):679-702. PubMed ID: 11353291
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  • 2. Intranuclear inclusions in subtypes of striatal neurons in Huntington's disease transgenic mice.
    Kosinski CM, Cha JH, Young AB, Mangiarini L, Bates G, Schiefer J, Schwarz M.
    Neuroreport; 1999 Dec 16; 10(18):3891-6. PubMed ID: 10716229
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  • 3. Cellular localization and development of neuronal intranuclear inclusions in striatal and cortical neurons in R6/2 transgenic mice.
    Meade CA, Deng YP, Fusco FR, Del Mar N, Hersch S, Goldowitz D, Reiner A.
    J Comp Neurol; 2002 Jul 29; 449(3):241-69. PubMed ID: 12115678
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  • 9. Resistance to NMDA toxicity correlates with appearance of nuclear inclusions, behavioural deficits and changes in calcium homeostasis in mice transgenic for exon 1 of the huntington gene.
    Hansson O, Guatteo E, Mercuri NB, Bernardi G, Li XJ, Castilho RF, Brundin P.
    Eur J Neurosci; 2001 Nov 29; 14(9):1492-504. PubMed ID: 11722611
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  • 10. Light and electron microscopic characterization of the evolution of cellular pathology in the R6/1 Huntington's disease transgenic mice.
    Bayram-Weston Z, Jones L, Dunnett SB, Brooks SP.
    Brain Res Bull; 2012 Jun 01; 88(2-3):104-12. PubMed ID: 21801812
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  • 12. Early motor dysfunction and striosomal distribution of huntingtin microaggregates in Huntington's disease knock-in mice.
    Menalled LB, Sison JD, Wu Y, Olivieri M, Li XJ, Li H, Zeitlin S, Chesselet MF.
    J Neurosci; 2002 Sep 15; 22(18):8266-76. PubMed ID: 12223581
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  • 13. Huntingtin inclusions do not down-regulate specific genes in the R6/2 Huntington's disease mouse.
    Sadri-Vakili G, Menon AS, Farrell LA, Keller-McGandy CE, Cantuti-Castelvetri I, Standaert DG, Augood SJ, Yohrling GJ, Cha JH.
    Eur J Neurosci; 2006 Jun 15; 23(12):3171-5. PubMed ID: 16820007
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  • 14. Promyelocytic leukemia protein is redistributed during the formation of intranuclear inclusions independent of polyglutamine expansion: an immunohistochemical study on Marinesco bodies.
    Kumada S, Uchihara T, Hayashi M, Nakamura A, Kikuchi E, Mizutani T, Oda M.
    J Neuropathol Exp Neurol; 2002 Nov 15; 61(11):984-91. PubMed ID: 12430715
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  • 15. Neuronal distribution of intranuclear inclusions in Huntington's disease with adult onset.
    Gourfinkel-An I, Cancel G, Duyckaerts C, Faucheux B, Hauw JJ, Trottier Y, Brice A, Agid Y, Hirsch EC.
    Neuroreport; 1998 Jun 01; 9(8):1823-6. PubMed ID: 9665608
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  • 16. Mice transgenic for the human Huntington's disease mutation have reduced sensitivity to kainic acid toxicity.
    Morton AJ, Leavens W.
    Brain Res Bull; 2000 May 01; 52(1):51-9. PubMed ID: 10779703
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  • 17. Transgenic mice expressing mutated full-length HD cDNA: a paradigm for locomotor changes and selective neuronal loss in Huntington's disease.
    Reddy PH, Charles V, Williams M, Miller G, Whetsell WO, Tagle DA.
    Philos Trans R Soc Lond B Biol Sci; 1999 Jun 29; 354(1386):1035-45. PubMed ID: 10434303
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  • 18. Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?
    Davies SW, Beardsall K, Turmaine M, DiFiglia M, Aronin N, Bates GP.
    Lancet; 1998 Jan 10; 351(9096):131-3. PubMed ID: 9439509
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  • 19. Huntington's disease intranuclear inclusions contain truncated, ubiquitinated huntingtin protein.
    Sieradzan KA, Mechan AO, Jones L, Wanker EE, Nukina N, Mann DM.
    Exp Neurol; 1999 Mar 10; 156(1):92-9. PubMed ID: 10192780
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  • 20. Abnormal synaptic plasticity and impaired spatial cognition in mice transgenic for exon 1 of the human Huntington's disease mutation.
    Murphy KP, Carter RJ, Lione LA, Mangiarini L, Mahal A, Bates GP, Dunnett SB, Morton AJ.
    J Neurosci; 2000 Jul 01; 20(13):5115-23. PubMed ID: 10864968
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