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.
436 related articles for article (PubMed ID: 17959817)
1. Expression profiling of Huntington's disease models suggests that brain-derived neurotrophic factor depletion plays a major role in striatal degeneration. Strand AD; Baquet ZC; Aragaki AK; Holmans P; Yang L; Cleren C; Beal MF; Jones L; Kooperberg C; Olson JM; Jones KR J Neurosci; 2007 Oct; 27(43):11758-68. PubMed ID: 17959817 [TBL] [Abstract][Full Text] [Related]
2. Brain-derived neurotrophic factor regulates the onset and severity of motor dysfunction associated with enkephalinergic neuronal degeneration in Huntington's disease. Canals JM; Pineda JR; Torres-Peraza JF; Bosch M; Martín-Ibañez R; Muñoz MT; Mengod G; Ernfors P; Alberch J J Neurosci; 2004 Sep; 24(35):7727-39. PubMed ID: 15342740 [TBL] [Abstract][Full Text] [Related]
3. Selective reduction of striatal mature BDNF without induction of proBDNF in the zQ175 mouse model of Huntington's disease. Ma Q; Yang J; Li T; Milner TA; Hempstead BL Neurobiol Dis; 2015 Oct; 82():466-477. PubMed ID: 26282324 [TBL] [Abstract][Full Text] [Related]
4. BDNF overexpression in the forebrain rescues Huntington's disease phenotypes in YAC128 mice. Xie Y; Hayden MR; Xu B J Neurosci; 2010 Nov; 30(44):14708-18. PubMed ID: 21048129 [TBL] [Abstract][Full Text] [Related]
5. Decreased BDNF Release in Cortical Neurons of a Knock-in Mouse Model of Huntington's Disease. Yu C; Li CH; Chen S; Yoo H; Qin X; Park H Sci Rep; 2018 Nov; 8(1):16976. PubMed ID: 30451892 [TBL] [Abstract][Full Text] [Related]
6. Brain-derived neurotrophic factor over-expression in the forebrain ameliorates Huntington's disease phenotypes in mice. Gharami K; Xie Y; An JJ; Tonegawa S; Xu B J Neurochem; 2008 Apr; 105(2):369-79. PubMed ID: 18086127 [TBL] [Abstract][Full Text] [Related]
7. Relationship between BDNF expression in major striatal afferents, striatum morphology and motor behavior in the R6/2 mouse model of Huntington's disease. Samadi P; Boutet A; Rymar VV; Rawal K; Maheux J; Kvann JC; Tomaszewski M; Beaubien F; Cloutier JF; Levesque D; Sadikot AF Genes Brain Behav; 2013 Feb; 12(1):108-24. PubMed ID: 23006318 [TBL] [Abstract][Full Text] [Related]
8. Imbalance of p75(NTR)/TrkB protein expression in Huntington's disease: implication for neuroprotective therapies. Brito V; Puigdellívol M; Giralt A; del Toro D; Alberch J; Ginés S Cell Death Dis; 2013 Apr; 4(4):e595. PubMed ID: 23598407 [TBL] [Abstract][Full Text] [Related]
9. Early striatal dendrite deficits followed by neuron loss with advanced age in the absence of anterograde cortical brain-derived neurotrophic factor. Baquet ZC; Gorski JA; Jones KR J Neurosci; 2004 Apr; 24(17):4250-8. PubMed ID: 15115821 [TBL] [Abstract][Full Text] [Related]
11. TRiC subunits enhance BDNF axonal transport and rescue striatal atrophy in Huntington's disease. Zhao X; Chen XQ; Han E; Hu Y; Paik P; Ding Z; Overman J; Lau AL; Shahmoradian SH; Chiu W; Thompson LM; Wu C; Mobley WC Proc Natl Acad Sci U S A; 2016 Sep; 113(38):E5655-64. PubMed ID: 27601642 [TBL] [Abstract][Full Text] [Related]
12. Compensatory changes in the ubiquitin-proteasome system, brain-derived neurotrophic factor and mitochondrial complex II/III in YAC72 and R6/2 transgenic mice partially model Huntington's disease patients. Seo H; Kim W; Isacson O Hum Mol Genet; 2008 Oct; 17(20):3144-53. PubMed ID: 18640989 [TBL] [Abstract][Full Text] [Related]
13. Loss of striatal 90-kDa ribosomal S6 kinase (Rsk) is a key factor for motor, synaptic and transcription dysfunction in Huntington's disease. Anglada-Huguet M; Giralt A; Rué L; Alberch J; Xifró X Biochim Biophys Acta; 2016 Jul; 1862(7):1255-66. PubMed ID: 27063456 [TBL] [Abstract][Full Text] [Related]
14. Reduced expression of the TrkB receptor in Huntington's disease mouse models and in human brain. Ginés S; Bosch M; Marco S; Gavaldà N; Díaz-Hernández M; Lucas JJ; Canals JM; Alberch J Eur J Neurosci; 2006 Feb; 23(3):649-58. PubMed ID: 16487146 [TBL] [Abstract][Full Text] [Related]
15. Partial resistance to malonate-induced striatal cell death in transgenic mouse models of Huntington's disease is dependent on age and CAG repeat length. Hansson O; Castilho RF; Korhonen L; Lindholm D; Bates GP; Brundin P J Neurochem; 2001 Aug; 78(4):694-703. PubMed ID: 11520890 [TBL] [Abstract][Full Text] [Related]
16. Reduced striatal acetylcholine efflux in the R6/2 mouse model of Huntington's disease: an examination of the role of altered inhibitory and excitatory mechanisms. Farrar AM; Callahan JW; Abercrombie ED Exp Neurol; 2011 Dec; 232(2):119-25. PubMed ID: 21864528 [TBL] [Abstract][Full Text] [Related]
17. 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]