451 related articles for article (PubMed ID: 11606636)
1. Huntingtin aggregate-associated axonal degeneration is an early pathological event in Huntington's disease mice.
Li H; Li SH; Yu ZX; Shelbourne P; Li XJ
J Neurosci; 2001 Nov; 21(21):8473-81. PubMed ID: 11606636
[TBL] [Abstract][Full Text] [Related]
2. Axonal transport of N-terminal huntingtin suggests early pathology of corticostriatal projections in Huntington disease.
Sapp E; Penney J; Young A; Aronin N; Vonsattel JP; DiFiglia M
J Neuropathol Exp Neurol; 1999 Feb; 58(2):165-73. PubMed ID: 10029099
[TBL] [Abstract][Full Text] [Related]
3. Mutant huntingtin causes context-dependent neurodegeneration in mice with Huntington's disease.
Yu ZX; Li SH; Evans J; Pillarisetti A; Li H; Li XJ
J Neurosci; 2003 Mar; 23(6):2193-202. PubMed ID: 12657678
[TBL] [Abstract][Full Text] [Related]
4. Proteasomal-dependent aggregate reversal and absence of cell death in a conditional mouse model of Huntington's disease.
Martín-Aparicio E; Yamamoto A; Hernández F; Hen R; Avila J; Lucas JJ
J Neurosci; 2001 Nov; 21(22):8772-81. PubMed ID: 11698589
[TBL] [Abstract][Full Text] [Related]
5. Full length mutant huntingtin is required for altered Ca2+ signaling and apoptosis of striatal neurons in the YAC mouse model of Huntington's disease.
Zhang H; Li Q; Graham RK; Slow E; Hayden MR; Bezprozvanny I
Neurobiol Dis; 2008 Jul; 31(1):80-8. PubMed ID: 18502655
[TBL] [Abstract][Full Text] [Related]
6. Time course of early motor and neuropathological anomalies in a knock-in mouse model of Huntington's disease with 140 CAG repeats.
Menalled LB; Sison JD; Dragatsis I; Zeitlin S; Chesselet MF
J Comp Neurol; 2003 Oct; 465(1):11-26. PubMed ID: 12926013
[TBL] [Abstract][Full Text] [Related]
7. Progressive and selective striatal degeneration in primary neuronal cultures using lentiviral vector coding for a mutant huntingtin fragment.
Zala D; Benchoua A; Brouillet E; Perrin V; Gaillard MC; Zurn AD; Aebischer P; Déglon N
Neurobiol Dis; 2005 Dec; 20(3):785-98. PubMed ID: 16006135
[TBL] [Abstract][Full Text] [Related]
8. 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; 22(18):8266-76. PubMed ID: 12223581
[TBL] [Abstract][Full Text] [Related]
9. Amino-terminal fragments of mutant huntingtin show selective accumulation in striatal neurons and synaptic toxicity.
Li H; Li SH; Johnston H; Shelbourne PF; Li XJ
Nat Genet; 2000 Aug; 25(4):385-9. PubMed ID: 10932179
[TBL] [Abstract][Full Text] [Related]
10. Characterization of neuron-specific huntingtin aggregates in human huntingtin knock-in mice.
Sawada H; Ishiguro H; Nishii K; Yamada K; Tsuchida K; Takahashi H; Goto J; Kanazawa I; Nagatsu T
Neurosci Res; 2007 Apr; 57(4):559-73. PubMed ID: 17335925
[TBL] [Abstract][Full Text] [Related]
11. The selective vulnerability of nerve cells in Huntington's disease.
Sieradzan KA; Mann DM
Neuropathol Appl Neurobiol; 2001 Feb; 27(1):1-21. PubMed ID: 11298997
[TBL] [Abstract][Full Text] [Related]
12. Adenovirus vector-based in vitro neuronal cell model for Huntington's disease with human disease-like differential aggregation and degeneration.
Dong X; Zong S; Witting A; Lindenberg KS; Kochanek S; Huang B
J Gene Med; 2012 Jul; 14(7):468-81. PubMed ID: 22700462
[TBL] [Abstract][Full Text] [Related]
13. Huntington aggregates may not predict neuronal death in Huntington's disease.
Kuemmerle S; Gutekunst CA; Klein AM; Li XJ; Li SH; Beal MF; Hersch SM; Ferrante RJ
Ann Neurol; 1999 Dec; 46(6):842-9. PubMed ID: 10589536
[TBL] [Abstract][Full Text] [Related]
14. 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; 354(1386):1035-45. PubMed ID: 10434303
[TBL] [Abstract][Full Text] [Related]
15. 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
[TBL] [Abstract][Full Text] [Related]
16. Cellular and subcellular localization of Huntingtin [corrected] aggregates in the brain of a rat transgenic for Huntington disease.
Petrasch-Parwez E; Nguyen HP; Löbbecke-Schumacher M; Habbes HW; Wieczorek S; Riess O; Andres KH; Dermietzel R; Von Hörsten S
J Comp Neurol; 2007 Apr; 501(5):716-30. PubMed ID: 17299753
[TBL] [Abstract][Full Text] [Related]
17. Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice.
Lloret A; Dragileva E; Teed A; Espinola J; Fossale E; Gillis T; Lopez E; Myers RH; MacDonald ME; Wheeler VC
Hum Mol Genet; 2006 Jun; 15(12):2015-24. PubMed ID: 16687439
[TBL] [Abstract][Full Text] [Related]
18. The early cellular pathology of Huntington's disease.
Li XJ
Mol Neurobiol; 1999; 20(2-3):111-24. PubMed ID: 10966117
[TBL] [Abstract][Full Text] [Related]
19. Ultrastructural localization and progressive formation of neuropil aggregates in Huntington's disease transgenic mice.
Li H; Li SH; Cheng AL; Mangiarini L; Bates GP; Li XJ
Hum Mol Genet; 1999 Jul; 8(7):1227-36. PubMed ID: 10369868
[TBL] [Abstract][Full Text] [Related]
20. Huntington's disease (HD): degeneration of select nuclei, widespread occurrence of neuronal nuclear and axonal inclusions in the brainstem.
Rüb U; Hentschel M; Stratmann K; Brunt E; Heinsen H; Seidel K; Bouzrou M; Auburger G; Paulson H; Vonsattel JP; Lange H; Korf HW; den Dunnen W
Brain Pathol; 2014 Apr; 24(3):247-60. PubMed ID: 24779419
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
