125 related articles for article (PubMed ID: 38183651)
21. Normalization of cholesterol homeostasis by 2-hydroxypropyl-β-cyclodextrin in neurons and glia from Niemann-Pick C1 (NPC1)-deficient mice.
Peake KB; Vance JE
J Biol Chem; 2012 Mar; 287(12):9290-8. PubMed ID: 22277650
[TBL] [Abstract][Full Text] [Related]
22. Niemann-Pick Type C Disease Reveals a Link between Lysosomal Cholesterol and PtdIns(4,5)P
Vivas O; Tiscione SA; Dixon RE; Ory DS; Dickson EJ
Cell Rep; 2019 May; 27(9):2636-2648.e4. PubMed ID: 31141688
[TBL] [Abstract][Full Text] [Related]
23. In vitro evaluation of 2-hydroxyalkylated β-cyclodextrins as potential therapeutic agents for Niemann-Pick Type C disease.
Kondo Y; Tokumaru H; Ishitsuka Y; Matsumoto T; Taguchi M; Motoyama K; Higashi T; Arima H; Matsuo M; Higaki K; Ohno K; Irie T
Mol Genet Metab; 2016 Jul; 118(3):214-219. PubMed ID: 27184436
[TBL] [Abstract][Full Text] [Related]
24. ER-lysosome contacts enable cholesterol sensing by mTORC1 and drive aberrant growth signalling in Niemann-Pick type C.
Lim CY; Davis OB; Shin HR; Zhang J; Berdan CA; Jiang X; Counihan JL; Ory DS; Nomura DK; Zoncu R
Nat Cell Biol; 2019 Oct; 21(10):1206-1218. PubMed ID: 31548609
[TBL] [Abstract][Full Text] [Related]
25. The Niemann-Pick C proteins and trafficking of cholesterol through the late endosomal/lysosomal system.
Garver WS; Heidenreich RA
Curr Mol Med; 2002 Aug; 2(5):485-505. PubMed ID: 12125814
[TBL] [Abstract][Full Text] [Related]
26. Iron Limitation Restores Autophagy and Increases Lifespan in the Yeast Model of Niemann-Pick Type C1.
Martins TS; Costa RS; Vilaça R; Lemos C; Teixeira V; Pereira C; Costa V
Int J Mol Sci; 2023 Mar; 24(7):. PubMed ID: 37047194
[TBL] [Abstract][Full Text] [Related]
27. Genistein Activates Transcription Factor EB and Corrects Niemann-Pick C Phenotype.
Argüello G; Balboa E; Tapia PJ; Castro J; Yañez MJ; Mattar P; Pulgar R; Zanlungo S
Int J Mol Sci; 2021 Apr; 22(8):. PubMed ID: 33921734
[TBL] [Abstract][Full Text] [Related]
28. Cyclodextrin overcomes deficient lysosome-to-endoplasmic reticulum transport of cholesterol in Niemann-Pick type C cells.
Abi-Mosleh L; Infante RE; Radhakrishnan A; Goldstein JL; Brown MS
Proc Natl Acad Sci U S A; 2009 Nov; 106(46):19316-21. PubMed ID: 19884502
[TBL] [Abstract][Full Text] [Related]
29. Endosomal/lysosomal processing of gangliosides affects neuronal cholesterol sequestration in Niemann-Pick disease type C.
Zhou S; Davidson C; McGlynn R; Stephney G; Dobrenis K; Vanier MT; Walkley SU
Am J Pathol; 2011 Aug; 179(2):890-902. PubMed ID: 21708114
[TBL] [Abstract][Full Text] [Related]
30. Histone deacetylase inhibitors correct the cholesterol storage defect in most Niemann-Pick C1 mutant cells.
Pipalia NH; Subramanian K; Mao S; Ralph H; Hutt DM; Scott SM; Balch WE; Maxfield FR
J Lipid Res; 2017 Apr; 58(4):695-708. PubMed ID: 28193631
[TBL] [Abstract][Full Text] [Related]
31. Quantitative Analysis of the Proteome Response to the Histone Deacetylase Inhibitor (HDACi) Vorinostat in Niemann-Pick Type C1 disease.
Subramanian K; Rauniyar N; Lavalleé-Adam M; Yates JR; Balch WE
Mol Cell Proteomics; 2017 Nov; 16(11):1938-1957. PubMed ID: 28860124
[TBL] [Abstract][Full Text] [Related]
32. Trehalose enhances mitochondria deficits in human NPC1 mutant fibroblasts but disrupts mouse Purkinje cell dendritic growth ex vivo.
MacLeod CM; Yousufzai FAK; Spencer LT; Kim S; Rivera-Rosario LA; Barrera ZD; Walsh L; Krummenacher C; Carone B; Soto I
PLoS One; 2023; 18(11):e0294312. PubMed ID: 38033125
[TBL] [Abstract][Full Text] [Related]
33. The Niemann-Pick type diseases - A synopsis of inborn errors in sphingolipid and cholesterol metabolism.
Pfrieger FW
Prog Lipid Res; 2023 Apr; 90():101225. PubMed ID: 37003582
[TBL] [Abstract][Full Text] [Related]
34. Correction of Niemann-Pick type C1 trafficking and activity with the histone deacetylase inhibitor valproic acid.
Subramanian K; Hutt DM; Scott SM; Gupta V; Mao S; Balch WE
J Biol Chem; 2020 Jun; 295(23):8017-8035. PubMed ID: 32354745
[TBL] [Abstract][Full Text] [Related]
35. Histone deacetylase inhibitor treatment dramatically reduces cholesterol accumulation in Niemann-Pick type C1 mutant human fibroblasts.
Pipalia NH; Cosner CC; Huang A; Chatterjee A; Bourbon P; Farley N; Helquist P; Wiest O; Maxfield FR
Proc Natl Acad Sci U S A; 2011 Apr; 108(14):5620-5. PubMed ID: 21436030
[TBL] [Abstract][Full Text] [Related]
36. Exosome secretion ameliorates lysosomal storage of cholesterol in Niemann-Pick type C disease.
Strauss K; Goebel C; Runz H; Möbius W; Weiss S; Feussner I; Simons M; Schneider A
J Biol Chem; 2010 Aug; 285(34):26279-88. PubMed ID: 20554533
[TBL] [Abstract][Full Text] [Related]
37. Lysosomal vitamin E accumulation in Niemann-Pick type C disease.
Yévenes LF; Klein A; Castro JF; Marín T; Leal N; Leighton F; Alvarez AR; Zanlungo S
Biochim Biophys Acta; 2012 Feb; 1822(2):150-60. PubMed ID: 22120593
[TBL] [Abstract][Full Text] [Related]
38. GCase and LIMP2 Abnormalities in the Liver of Niemann Pick Type C Mice.
van der Lienden MJC; Aten J; Marques ARA; Waas ISE; Larsen PWB; Claessen N; van der Wel NN; Ottenhoff R; van Eijk M; Aerts JMFG
Int J Mol Sci; 2021 Mar; 22(5):. PubMed ID: 33802460
[TBL] [Abstract][Full Text] [Related]
39. [Annexins in Niemann-Pick type C disease].
Buszewska ME; Strzelecka-Kiliszek A; Tylki-Szymańska A; Bandorowicz-Pikuła J
Postepy Biochem; 2007; 53(2):169-73. PubMed ID: 17969878
[TBL] [Abstract][Full Text] [Related]
40. A human iPSC-derived inducible neuronal model of Niemann-Pick disease, type C1.
Prabhu AV; Kang I; De Pace R; Wassif CA; Fujiwara H; Kell P; Jiang X; Ory DS; Bonifacino JS; Ward ME; Porter FD
BMC Biol; 2021 Oct; 19(1):218. PubMed ID: 34592985
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
