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.
202 related articles for article (PubMed ID: 20699355)
1. CHMP2B mutants linked to frontotemporal dementia impair maturation of dendritic spines. Belly A; Bodon G; Blot B; Bouron A; Sadoul R; Goldberg Y J Cell Sci; 2010 Sep; 123(Pt 17):2943-54. PubMed ID: 20699355 [TBL] [Abstract][Full Text] [Related]
2. Regulation of postsynaptic function by the dementia-related ESCRT-III subunit CHMP2B. Chassefeyre R; Martínez-Hernández J; Bertaso F; Bouquier N; Blot B; Laporte M; Fraboulet S; Couté Y; Devoy A; Isaacs AM; Pernet-Gallay K; Sadoul R; Fagni L; Goldberg Y J Neurosci; 2015 Feb; 35(7):3155-73. PubMed ID: 25698751 [TBL] [Abstract][Full Text] [Related]
3. TMEM106B, a frontotemporal lobar dementia (FTLD) modifier, associates with FTD-3-linked CHMP2B, a complex of ESCRT-III. Jun MH; Han JH; Lee YK; Jang DJ; Kaang BK; Lee JA Mol Brain; 2015 Dec; 8():85. PubMed ID: 26651479 [TBL] [Abstract][Full Text] [Related]
4. The role of CHMP2B Krasniak CS; Ahmad ST Brain Res; 2016 Oct; 1649(Pt B):151-157. PubMed ID: 26972529 [TBL] [Abstract][Full Text] [Related]
5. A novel synaptopathy-defective synaptic vesicle protein trafficking in the mutant CHMP2B mouse model of frontotemporal dementia. Clayton EL; Bonnycastle K; Isaacs AM; Cousin MA; Schorge S J Neurochem; 2022 Feb; 160(3):412-425. PubMed ID: 34855215 [TBL] [Abstract][Full Text] [Related]
6. Neuroprotective activity of ursodeoxycholic acid in CHMP2B West RJH; Ugbode C; Fort-Aznar L; Sweeney ST Neurobiol Dis; 2020 Oct; 144():105047. PubMed ID: 32801000 [TBL] [Abstract][Full Text] [Related]
7. Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathology. Clayton EL; Mizielinska S; Edgar JR; Nielsen TT; Marshall S; Norona FE; Robbins M; Damirji H; Holm IE; Johannsen P; Nielsen JE; Asante EA; Collinge J; ; Isaacs AM Acta Neuropathol; 2015 Oct; 130(4):511-23. PubMed ID: 26358247 [TBL] [Abstract][Full Text] [Related]
8. ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration. Lee JA; Beigneux A; Ahmad ST; Young SG; Gao FB Curr Biol; 2007 Sep; 17(18):1561-7. PubMed ID: 17683935 [TBL] [Abstract][Full Text] [Related]
9. Longitudinal transcriptomic analysis of altered pathways in a CHMP2B Waegaert R; Dirrig-Grosch S; Parisot F; Keime C; Henriques A; Loeffler JP; René F Neurobiol Dis; 2020 Mar; 136():104710. PubMed ID: 31837425 [TBL] [Abstract][Full Text] [Related]
10. A transgenic mouse expressing CHMP2Bintron5 mutant in neurons develops histological and behavioural features of amyotrophic lateral sclerosis and frontotemporal dementia. Vernay A; Therreau L; Blot B; Risson V; Dirrig-Grosch S; Waegaert R; Lequeu T; Sellal F; Schaeffer L; Sadoul R; Loeffler JP; René F Hum Mol Genet; 2016 Aug; 25(15):3341-3360. PubMed ID: 27329763 [TBL] [Abstract][Full Text] [Related]
12. Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations. Urwin H; Authier A; Nielsen JE; Metcalf D; Powell C; Froud K; Malcolm DS; Holm I; Johannsen P; Brown J; Fisher EM; van der Zee J; Bruyland M; ; Van Broeckhoven C; Collinge J; Brandner S; Futter C; Isaacs AM Hum Mol Genet; 2010 Jun; 19(11):2228-38. PubMed ID: 20223751 [TBL] [Abstract][Full Text] [Related]
13. Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutation. Clayton EL; Mancuso R; Nielsen TT; Mizielinska S; Holmes H; Powell N; Norona F; Larsen JO; Milioto C; Wilson KM; Lythgoe MF; Ourselin S; Nielsen JE; Johannsen P; Holm I; Collinge J; ; Oliver PL; Gomez-Nicola D; Isaacs AM Hum Mol Genet; 2017 Mar; 26(5):873-887. PubMed ID: 28093491 [TBL] [Abstract][Full Text] [Related]
14. Alteration of the Neuromuscular Junction and Modifications of Muscle Metabolism in Response to Neuron-Restricted Expression of the CHMP2B Waegaert R; Dirrig-Grosch S; Liu H; Boutry M; Luan P; Loeffler JP; René F Biomolecules; 2022 Mar; 12(4):. PubMed ID: 35454086 [TBL] [Abstract][Full Text] [Related]
15. Expression of mutant CHMP2B, an ESCRT-III component involved in frontotemporal dementia, causes eye deformities due to Notch misregulation in Drosophila. Cheruiyot A; Lee JA; Gao FB; Ahmad ST FASEB J; 2014 Feb; 28(2):667-75. PubMed ID: 24158394 [TBL] [Abstract][Full Text] [Related]
17. Expression of a human variant of CHMP2B linked to neurodegeneration in Drosophila external sensory organs leads to cell fate transformations associated with increased Notch activity. Wilson C; Kavaler J; Ahmad ST Dev Neurobiol; 2020 Mar; 80(3-4):85-97. PubMed ID: 31587468 [TBL] [Abstract][Full Text] [Related]
18. The enhanced association between mutant CHMP2B and spastin is a novel pathological link between frontotemporal dementia and hereditary spastic paraplegias. Chen Y; Krishnan G; Parsi S; Pons M; Nikolaki V; Cao L; Xu Z; Gao FB Acta Neuropathol Commun; 2022 Nov; 10(1):169. PubMed ID: 36414997 [TBL] [Abstract][Full Text] [Related]
19. Rab8, POSH, and TAK1 regulate synaptic growth in a Drosophila model of frontotemporal dementia. West RJ; Lu Y; Marie B; Gao FB; Sweeney ST J Cell Biol; 2015 Mar; 208(7):931-47. PubMed ID: 25800055 [TBL] [Abstract][Full Text] [Related]
20. Molecular Genetics of Frontotemporal Dementia Elucidated by Vandal SE; Zheng X; Ahmad ST Int J Mol Sci; 2018 Jun; 19(6):. PubMed ID: 29890743 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]