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A Yeast Genomic Screen to Identify Effectors of Kir2.1 Plasma Membrane Residence

Kolb, A. (2013) · D-Scholarship@Pitt (University of Pittsburgh)

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Frontotemporal Dementia Linked to Chromosome 3 in Saccharomyces cerevisiae

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Frontotemporal Dementia, Chromosome 3-Linked

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Neuronal Differentiation of Cartilage-derived Stem Cells In Vitro and their Delivery to the Spinal Cord in a Mouse Model of ALS Using MRI-guided Focused Ultrasound

Shah, K. (2020) · TSpace (University of Toronto)

Premature termination codon readthrough restores progranulin expression in preclinical models of frontotemporal dementia and neuronal ceroid lipofuscinosis

Frew, J. (2021) · cIRcle (University of British Columbia) · doi:10.14288/1.0396548

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Johannsen, P., Eskildsen, S. F., Nielsen, J. E., Isaacs, A. M., Zeidler, D., & Østergaard, L. (2008) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2008.05.131

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HD-PTP/PTPN23 hypomorphic mice display lipodystrophyPreprint

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Analysis of Adult Hippocampal Neurogenesis in Neurodegenerative disease

HAN, G. (2022) · Cronfa (Swansea University) · doi:10.23889/suthesis.62147

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Neuronal Deletion of Tumor Susceptibility Gene 101 (Tsg101) Causes Rapid Apoptotic Loss of Hippocampal CA3 Neurons

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Genetics of Frontotemporal Dementia: an updated overview

Ghanim, M. A., Abuawad, M., Alqub, M., Dwikat, M., Alkhaldi, S., & Rabaya, D. (2024) · Palestinian medical and pharmaceutical journal/Palestinian medical & pharmaceutical journal · doi:10.59049/2790-0231.10.1.2273

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Autophagy and tau in Niemann-Pick type C disease

Pacheco, C. D. (2008) · Deep Blue (University of Michigan)

Additional file 4 of 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. C., Nikolaki, V., Cao, L., Xu, Z., & Gao, F. (2022) · Figshare · doi:10.6084/m9.figshare.21621923

Additional file 3 of Network analysis of the progranulin-deficient mouse brain proteome reveals pathogenic mechanisms shared in human frontotemporal dementia caused by GRN mutations

Huang, M., Modeste, E. S., Dammer, E., Merino, P., Taylor, G., Duong, D. M., Deng, Q., Holler, C. J., Gearing, M., Dickson, D. W., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13064301

Additional file 1 of 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. C., Nikolaki, V., Cao, L., Xu, Z., & Gao, F. (2022) · Figshare · doi:10.6084/m9.figshare.21621914

Additional file 2 of Network analysis of the progranulin-deficient mouse brain proteome reveals pathogenic mechanisms shared in human frontotemporal dementia caused by GRN mutations

Huang, M., Modeste, E. S., Dammer, E., Merino, P., Taylor, G., Duong, D. M., Deng, Q., Holler, C. J., Gearing, M., Dickson, D. W., et al. (2020) · Figshare · doi:10.6084/m9.figshare.13064298

Additional file 3 of 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. C., Nikolaki, V., Cao, L., Xu, Z., & Gao, F. (2022) · Figshare · doi:10.6084/m9.figshare.21621920

Additional file 2 of The ESCRT-III protein VPS4, but not CHMP4B or CHMP2B, is pathologically increased in familial and sporadic ALS neuronal nuclei

Coyne, A. N., & Rothstein, J. D. (2021) · Figshare · doi:10.6084/m9.figshare.15020774

Additional file 2 of 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. C., Nikolaki, V., Cao, L., Xu, Z., & Gao, F. (2022) · Figshare · doi:10.6084/m9.figshare.21621917

Rôle d'HDAC6 et de VCP dans la réponse au stress thermique. Implications dans l'IBMPFD

Pernet, L. (2014) · theses.fr (ABES) · doi:10.70675/47616bc9zd164z44b3z889cze4a70ebf46b9

Comportement et dégénérescence frontotemporale : apport de la cohorte nantaise, développement de l'échelle DAPHNE et données neuropsychologiques

Boutoleau‐Bretonnière, C. (2015) · theses.fr (ABES) · doi:10.70675/85cf2bf3zce07z46cbzb836zf9cda8e7cde4

Conditional truncation of the FUS protein in mice : a new animal model of the ALS/FTD continuum

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Modeling C9ORF72 loss-of-function : a knockdown mouse model

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Inhibition of ESCRT-III activates alternative pathways for protein degradation and secretion

Fujiwara, M., Sakai, R., Takahashi, M., Matsumoto, G., Hashimoto, T., & Kabuta, T. (2026) · Neurochemistry International · doi:10.1016/j.neuint.2026.106153

Régulation de la voie autophagique par la Gigaxonine E3-ligase, et implication dans les maladies neurodégénératives

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Mechanical properties and function of CHMP2B in the ESCRT membrane remodelling and scission pathway

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Etude du continuum mécanistique et physiopathologique entre la Sclérose Latérale Amyotrophique et la Démence FrontoTemporale

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Étude de la composante neuroinflammatoire dans les DFT/SLA

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Mutations in the ESCRTIII endosomal complex protein CHMP2B associate with frontotemporal dementia

Skibinski, G. (2005) · OpenGrey (Institut de l'Information Scientifique et Technique)

Frontotemporal dementia: an endosomal problem?

Bradbury, J. (2005) · The Lancet Neurology · doi:10.1016/s1474-4422(05)70160-5

P3–155: Mutation in the endosomal ESCRT111–complex in frontotemporal dementia

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A novel splice‐site mutation in CHMP2B associated with frontotemporal dementia: The first report from China and literature review

Li, C., Wen, Y., Zhao, M., Wang, Y., Li, P., Wang, L., & Wang, S. H. (2023) · Molecular Genetics & Genomic Medicine · doi:10.1002/mgg3.2222 · Cited by 3

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