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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

220 related articles for article (PubMed ID: 31587468)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 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. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Expression of mutant CHMP2B linked to neurodegeneration in humans disrupts circadian rhythms in
    Lee D; Zheng X; Shigemori K; Krasniak C; Bin Liu J; Tang C; Kavaler J; Ahmad ST
    FASEB Bioadv; 2019 Aug; 1(8):511-520. PubMed ID: 32123847
    [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. Loss- and gain-of-function analyses of vacuolar protein sorting 2 in Notch signaling of Drosophila melanogaster.
    Aoyama N; Yamakawa T; Sasamura T; Yoshida Y; Ohori M; Okubo H; Iida E; Sasaki N; Ueda R; Matsuno K
    Genes Genet Syst; 2013; 88(1):45-57. PubMed ID: 23676709
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Monitoring notch/delta endosomal trafficking and signaling in Drosophila.
    Loubéry S; González-Gaitán M
    Methods Enzymol; 2014; 534():301-21. PubMed ID: 24359961
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Frontotemporal dementia caused by CHMP2B mutations.
    Isaacs AM; Johannsen P; Holm I; Nielsen JE;
    Curr Alzheimer Res; 2011 May; 8(3):246-51. PubMed ID: 21222599
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prospero and Pax2 combinatorially control neural cell fate decisions by modulating Ras- and Notch-dependent signaling.
    Charlton-Perkins M; Whitaker SL; Fei Y; Xie B; Li-Kroeger D; Gebelein B; Cook T
    Neural Dev; 2011 May; 6():20. PubMed ID: 21539742
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lessons learned from CHMP2B, implications for frontotemporal dementia and amyotrophic lateral sclerosis.
    Ugbode C; West RJH
    Neurobiol Dis; 2021 Jan; 147():105144. PubMed ID: 33144171
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.