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138 related items for PubMed ID: 9928833
21. Protein surveillance machinery in brains with spinocerebellar ataxia type 3: redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions. Schmidt T, Lindenberg KS, Krebs A, Schöls L, Laccone F, Herms J, Rechsteiner M, Riess O, Landwehrmeyer GB. Ann Neurol; 2002 Mar; 51(3):302-10. PubMed ID: 11891825 [Abstract] [Full Text] [Related]
22. Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6. Ishikawa K, Fujigasaki H, Saegusa H, Ohwada K, Fujita T, Iwamoto H, Komatsuzaki Y, Toru S, Toriyama H, Watanabe M, Ohkoshi N, Shoji S, Kanazawa I, Tanabe T, Mizusawa H. Hum Mol Genet; 1999 Jul; 8(7):1185-93. PubMed ID: 10369863 [Abstract] [Full Text] [Related]
23. 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; 156(1):92-9. PubMed ID: 10192780 [Abstract] [Full Text] [Related]
24. SUMO-1 marks the nuclear inclusions in familial neuronal intranuclear inclusion disease. Pountney DL, Huang Y, Burns RJ, Haan E, Thompson PD, Blumbergs PC, Gai WP. Exp Neurol; 2003 Nov; 184(1):436-46. PubMed ID: 14637113 [Abstract] [Full Text] [Related]
25. Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats. Ito H, Kawakami H, Wate R, Matsumoto S, Imai T, Hirano A, Kusaka H. Neurology; 2006 Oct 24; 67(8):1479-81. PubMed ID: 17060579 [Abstract] [Full Text] [Related]
26. Presenile onset of spinocerebellar ataxia type 1 presenting with conspicuous psychiatric symptoms and widespread anti-expanded polyglutamine antibody- and fused in sarcoma antibody-immunopositive pathology. Iwasaki Y, Mori K, Ito M, Mimuro M, Yoshida M. Psychogeriatrics; 2015 Sep 24; 15(3):212-7. PubMed ID: 25920043 [Abstract] [Full Text] [Related]
27. Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length. Becher MW, Kotzuk JA, Sharp AH, Davies SW, Bates GP, Price DL, Ross CA. Neurobiol Dis; 1998 Apr 24; 4(6):387-97. PubMed ID: 9666478 [Abstract] [Full Text] [Related]
28. [Glial cytoskeletal abnormality in neurodegenerative diseases: multiple system atrophy]. Mizusawa H. No To Shinkei; 1996 Oct 24; 48(10):915-24. PubMed ID: 8921530 [No Abstract] [Full Text] [Related]
29. Intranuclear inclusions, neuronal loss and CAG mosaicism in two patients with Machado-Joseph disease. Muñoz E, Rey MJ, Milà M, Cardozo A, Ribalta T, Tolosa E, Ferrer I. J Neurol Sci; 2002 Aug 15; 200(1-2):19-25. PubMed ID: 12127671 [Abstract] [Full Text] [Related]
30. Intranuclear neuronal inclusions in DRPLA. Becher MW, Ross CA. Mov Disord; 1998 Sep 15; 13(5):852-3. PubMed ID: 9756163 [No Abstract] [Full Text] [Related]
31. Selective occurrence of TDP-43-immunoreactive inclusions in the lower motor neurons in Machado-Joseph disease. Tan CF, Yamada M, Toyoshima Y, Yokoseki A, Miki Y, Hoshi Y, Kaneko H, Ikeuchi T, Onodera O, Kakita A, Takahashi H. Acta Neuropathol; 2009 Oct 15; 118(4):553-60. PubMed ID: 19526244 [Abstract] [Full Text] [Related]
32. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion. Babovic-Vuksanovic D, Snow K, Patterson MC, Michels VV. Am J Med Genet; 1998 Oct 12; 79(5):383-7. PubMed ID: 9779806 [Abstract] [Full Text] [Related]
33. Attenuated nuclear shrinkage in neurones with nuclear inclusions of SCA1 brains. Nagaoka U, Uchihara T, Iwabuchi K, Konno H, Tobita M, Funata N, Yagishita S, Kato T. J Neurol Neurosurg Psychiatry; 2003 May 12; 74(5):597-601. PubMed ID: 12700301 [Abstract] [Full Text] [Related]
34. SUMO-1 co-localized with mutant atrophin-1 with expanded polyglutamines accelerates intranuclear aggregation and cell death. Terashima T, Kawai H, Fujitani M, Maeda K, Yasuda H. Neuroreport; 2002 Dec 03; 13(17):2359-64. PubMed ID: 12488827 [Abstract] [Full Text] [Related]
35. Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain. Hayashi Y, Kakita A, Yamada M, Koide R, Igarashi S, Takano H, Ikeuchi T, Wakabayashi K, Egawa S, Tsuji S, Takahashi H. Acta Neuropathol; 1998 Dec 03; 96(6):547-52. PubMed ID: 9845282 [Abstract] [Full Text] [Related]
36. Neuronal intranuclear hyaline inclusion disease with polyglutamine-immunoreactive inclusions. Takahashi J, Fukuda T, Tanaka J, Minamitani M, Fujigasaki H, Uchihara T. Acta Neuropathol; 2000 May 03; 99(5):589-94. PubMed ID: 10805106 [Abstract] [Full Text] [Related]
37. Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease. Lopes-Cendes I, Maciel P, Kish S, Gaspar C, Robitaille Y, Clark HB, Koeppen AH, Nance M, Schut L, Silveira I, Coutinho P, Sequeiros J, Rouleau GA. Ann Neurol; 1996 Aug 03; 40(2):199-206. PubMed ID: 8773601 [Abstract] [Full Text] [Related]
38. Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6). Ishikawa K, Watanabe M, Yoshizawa K, Fujita T, Iwamoto H, Yoshizawa T, Harada K, Nakamagoe K, Komatsuzaki Y, Satoh A, Doi M, Ogata T, Kanazawa I, Shoji S, Mizusawa H. J Neurol Neurosurg Psychiatry; 1999 Jul 03; 67(1):86-9. PubMed ID: 10369828 [Abstract] [Full Text] [Related]
39. Intranuclear aggregation of nonexpanded ataxin-3 in marinesco bodies of the nonhuman primate substantia nigra. Kettner M, Willwohl D, Hubbard GB, Rüb U, Dick EJ, Cox AB, Trottier Y, Auburger G, Braak H, Schultz C. Exp Neurol; 2002 Jul 03; 176(1):117-21. PubMed ID: 12093088 [Abstract] [Full Text] [Related]
40. Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals. Servadio A, Koshy B, Armstrong D, Antalffy B, Orr HT, Zoghbi HY. Nat Genet; 1995 May 03; 10(1):94-8. PubMed ID: 7647801 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]