553 related articles for article (PubMed ID: 28404863)
61. Microglial Progranulin: Involvement in Alzheimer's Disease and Neurodegenerative Diseases.
Mendsaikhan A; Tooyama I; Walker DG
Cells; 2019 Mar; 8(3):. PubMed ID: 30862089
[TBL] [Abstract][Full Text] [Related]
62. Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal Dementia.
Guven G; Bilgic B; Tufekcioglu Z; Erginel Unaltuna N; Hanagasi H; Gurvit H; Singleton A; Hardy J; Emre M; Gulec C; Bras J; Guerreiro R; Lohmann E
J Alzheimers Dis; 2019; 67(1):159-167. PubMed ID: 30475763
[TBL] [Abstract][Full Text] [Related]
63. Neuronal ceroid lipofuscinosis type-11 in an adolescent.
Kamate M; Detroja M; Hattiholi V
Brain Dev; 2019 Jun; 41(6):542-545. PubMed ID: 30922528
[TBL] [Abstract][Full Text] [Related]
64. Epigenetic modulation through BET bromodomain inhibitors as a novel therapeutic strategy for progranulin-deficient frontotemporal dementia.
Rosenthal ZC; Fass DM; Payne NC; She A; Patnaik D; Hennig KM; Tesla R; Werthmann GC; Guhl C; Reis SA; Wang X; Chen Y; Placzek M; Williams NS; Hooker J; Herz J; Mazitschek R; Haggarty SJ
Sci Rep; 2024 Apr; 14(1):9064. PubMed ID: 38643236
[TBL] [Abstract][Full Text] [Related]
65. Progranulin Insufficiency Affects Lysosomal Homeostasis in Retinal Pigment Epithelium.
Takahashi K; Nakamura S; Shimazawa M; Hara H
In Vivo; 2022; 36(2):610-617. PubMed ID: 35241513
[TBL] [Abstract][Full Text] [Related]
66. Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation.
Bruni AC; Momeni P; Bernardi L; Tomaino C; Frangipane F; Elder J; Kawarai T; Sato C; Pradella S; Wakutani Y; Anfossi M; Gallo M; Geracitano S; Costanzo A; Smirne N; Curcio SA; Mirabelli M; Puccio G; Colao R; Maletta RG; Kertesz A; St George-Hyslop P; Hardy J; Rogaeva E
Neurology; 2007 Jul; 69(2):140-7. PubMed ID: 17620546
[TBL] [Abstract][Full Text] [Related]
67. Lysosomal Dysfunction and Other Pathomechanisms in FTLD: Evidence from Progranulin Genetics and Biology.
Zhou X; Kukar T; Rademakers R
Adv Exp Med Biol; 2021; 1281():219-242. PubMed ID: 33433878
[TBL] [Abstract][Full Text] [Related]
68. Progranulin haploinsufficiency causes biphasic social dominance abnormalities in the tube test.
Arrant AE; Filiano AJ; Warmus BA; Hall AM; Roberson ED
Genes Brain Behav; 2016 Jul; 15(6):588-603. PubMed ID: 27213486
[TBL] [Abstract][Full Text] [Related]
69. Progranulin deficiency promotes neuroinflammation and neuron loss following toxin-induced injury.
Martens LH; Zhang J; Barmada SJ; Zhou P; Kamiya S; Sun B; Min SW; Gan L; Finkbeiner S; Huang EJ; Farese RV
J Clin Invest; 2012 Nov; 122(11):3955-9. PubMed ID: 23041626
[TBL] [Abstract][Full Text] [Related]
70. hiPSC-derived GRN-deficient astrocytes delay spiking activity of developing neurons.
Lee C; Frew J; Weilinger NL; Wendt S; Cai W; Sorrentino S; Wu X; MacVicar BA; Willerth SM; Nygaard HB
Neurobiol Dis; 2023 Jun; 181():106124. PubMed ID: 37054899
[TBL] [Abstract][Full Text] [Related]
71. Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency.
Evers BM; Rodriguez-Navas C; Tesla RJ; Prange-Kiel J; Wasser CR; Yoo KS; McDonald J; Cenik B; Ravenscroft TA; Plattner F; Rademakers R; Yu G; White CL; Herz J
Cell Rep; 2017 Sep; 20(11):2565-2574. PubMed ID: 28903038
[TBL] [Abstract][Full Text] [Related]
72. Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage.
Smith KR; Damiano J; Franceschetti S; Carpenter S; Canafoglia L; Morbin M; Rossi G; Pareyson D; Mole SE; Staropoli JF; Sims KB; Lewis J; Lin WL; Dickson DW; Dahl HH; Bahlo M; Berkovic SF
Am J Hum Genet; 2012 Jun; 90(6):1102-7. PubMed ID: 22608501
[TBL] [Abstract][Full Text] [Related]
73. Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia.
Wilke C; Gillardon F; Deuschle C; Hobert MA; Jansen IE; Metzger FG; Heutink P; Gasser T; Maetzler W; Blauwendraat C; Synofzik M
Neurodegener Dis; 2017; 17(2-3):83-88. PubMed ID: 27760429
[TBL] [Abstract][Full Text] [Related]
74. Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog.
Hirz M; Drögemüller M; Schänzer A; Jagannathan V; Dietschi E; Goebel HH; Hecht W; Laubner S; Schmidt MJ; Steffen F; Hilbe M; Köhler K; Drögemüller C; Herden C
Mol Genet Metab; 2017 Mar; 120(3):269-277. PubMed ID: 28024876
[TBL] [Abstract][Full Text] [Related]
75. Neurovascular dysfunction in GRN-associated frontotemporal dementia identified by single-nucleus RNA sequencing of human cerebral cortex.
Gerrits E; Giannini LAA; Brouwer N; Melhem S; Seilhean D; Le Ber I; ; Kamermans A; Kooij G; de Vries HE; Boddeke EWGM; Seelaar H; van Swieten JC; Eggen BJL
Nat Neurosci; 2022 Aug; 25(8):1034-1048. PubMed ID: 35879464
[TBL] [Abstract][Full Text] [Related]
76. Intrafamilial clinical phenotypic heterogeneity with progranulin gene p.Glu498fs mutation.
Larner AJ
J Neurol Sci; 2012 May; 316(1-2):189-90. PubMed ID: 22280948
[TBL] [Abstract][Full Text] [Related]
77. Progranulin mutations result in impaired processing of prosaposin and reduced glucocerebrosidase activity.
Valdez C; Ysselstein D; Young TJ; Zheng J; Krainc D
Hum Mol Genet; 2020 Mar; 29(5):716-726. PubMed ID: 31600775
[TBL] [Abstract][Full Text] [Related]
78. Loss of Progranulin Results in Increased Pan-Cathepsin Activity and Reduced LAMP1 Lysosomal Protein.
Anderson A; Tansey MG
bioRxiv; 2023 Jul; ():. PubMed ID: 37503267
[TBL] [Abstract][Full Text] [Related]
79. Murine knockin model for progranulin-deficient frontotemporal dementia with nonsense-mediated mRNA decay.
Nguyen AD; Nguyen TA; Zhang J; Devireddy S; Zhou P; Karydas AM; Xu X; Miller BL; Rigo F; Ferguson SM; Huang EJ; Walther TC; Farese RV
Proc Natl Acad Sci U S A; 2018 Mar; 115(12):E2849-E2858. PubMed ID: 29511098
[TBL] [Abstract][Full Text] [Related]
80. Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.
Janssens J; Philtjens S; Kleinberger G; Van Mossevelde S; van der Zee J; Cacace R; Engelborghs S; Sieben A; Banzhaf-Strathmann J; Dillen L; Merlin C; Cuijt I; Robberecht C; Schmid B; Santens P; Ivanoiu A; Vandenbulcke M; Vandenberghe R; Cras P; De Deyn PP; Martin JJ; Maudsley S; Haass C; Cruts M; Van Broeckhoven C;
Acta Neuropathol Commun; 2015 Nov; 3():68. PubMed ID: 26555887
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
