262 related articles for article (PubMed ID: 23350547)
41. Adaptations of energy metabolism associated with increased levels of mitochondrial cholesterol in Niemann-Pick type C1-deficient cells.
Kennedy BE; Madreiter CT; Vishnu N; Malli R; Graier WF; Karten B
J Biol Chem; 2014 Jun; 289(23):16278-89. PubMed ID: 24790103
[TBL] [Abstract][Full Text] [Related]
42. Niemann-Pick type C disease: importance of N-glycosylation sites for function and cellular location of the NPC2 protein.
Chikh K; Vey S; Simonot C; Vanier MT; Millat G
Mol Genet Metab; 2004 Nov; 83(3):220-30. PubMed ID: 15542393
[TBL] [Abstract][Full Text] [Related]
43. FTY720/fingolimod increases NPC1 and NPC2 expression and reduces cholesterol and sphingolipid accumulation in Niemann-Pick type C mutant fibroblasts.
Newton J; Hait NC; Maceyka M; Colaco A; Maczis M; Wassif CA; Cougnoux A; Porter FD; Milstien S; Platt N; Platt FM; Spiegel S
FASEB J; 2017 Apr; 31(4):1719-1730. PubMed ID: 28082351
[TBL] [Abstract][Full Text] [Related]
44. Intracellular cholesterol trafficking is dependent upon NPC2 interaction with lysobisphosphatidic acid.
McCauliff LA; Langan A; Li R; Ilnytska O; Bose D; Waghalter M; Lai K; Kahn PC; Storch J
Elife; 2019 Oct; 8():. PubMed ID: 31580258
[TBL] [Abstract][Full Text] [Related]
45. Structural Basis of Low-pH-Dependent Lysosomal Cholesterol Egress by NPC1 and NPC2.
Qian H; Wu X; Du X; Yao X; Zhao X; Lee J; Yang H; Yan N
Cell; 2020 Jul; 182(1):98-111.e18. PubMed ID: 32544384
[TBL] [Abstract][Full Text] [Related]
46. NPC1 late endosomes contain elevated levels of non-esterified ('free') fatty acids and an abnormally glycosylated form of the NPC2 protein.
Chen FW; Gordon RE; Ioannou YA
Biochem J; 2005 Sep; 390(Pt 2):549-61. PubMed ID: 15896196
[TBL] [Abstract][Full Text] [Related]
47. Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C disease.
Chen J; Soni RK; Xu Y; Simoes S; Liang FX; DeFreitas L; Hwang R; Montesinos J; Lee JH; Area-Gomez E; Nandakumar R; Vardarajan B; Marquer C
EBioMedicine; 2023 Jun; 92():104628. PubMed ID: 37245481
[TBL] [Abstract][Full Text] [Related]
48. Mechanism of cholesterol transfer from the Niemann-Pick type C2 protein to model membranes supports a role in lysosomal cholesterol transport.
Cheruku SR; Xu Z; Dutia R; Lobel P; Storch J
J Biol Chem; 2006 Oct; 281(42):31594-604. PubMed ID: 16606609
[TBL] [Abstract][Full Text] [Related]
49. Sterols and intracellular vesicular trafficking: lessons from the study of NPC1.
Strauss JF; Liu P; Christenson LK; Watari H
Steroids; 2002 Nov; 67(12):947-51. PubMed ID: 12398991
[TBL] [Abstract][Full Text] [Related]
50. Niemann-Pick type C disease: molecular mechanisms and potential therapeutic approaches.
Rosenbaum AI; Maxfield FR
J Neurochem; 2011 Mar; 116(5):789-95. PubMed ID: 20807315
[TBL] [Abstract][Full Text] [Related]
51. Simulations of NPC1(NTD):NPC2 Protein Complex Reveal Cholesterol Transfer Pathways.
Hodošček M; Elghobashi-Meinhardt N
Int J Mol Sci; 2018 Sep; 19(9):. PubMed ID: 30181526
[TBL] [Abstract][Full Text] [Related]
52. Regulation of sterol transport between membranes and NPC2.
Xu Z; Farver W; Kodukula S; Storch J
Biochemistry; 2008 Oct; 47(42):11134-43. PubMed ID: 18823126
[TBL] [Abstract][Full Text] [Related]
53. Defective endocytic trafficking of NPC1 and NPC2 underlying infantile Niemann-Pick type C disease.
Blom TS; Linder MD; Snow K; Pihko H; Hess MW; Jokitalo E; Veckman V; Syvänen AC; Ikonen E
Hum Mol Genet; 2003 Feb; 12(3):257-72. PubMed ID: 12554680
[TBL] [Abstract][Full Text] [Related]
54. Sterol-modulated glycolipid sorting occurs in niemann-pick C1 late endosomes.
Zhang M; Dwyer NK; Neufeld EB; Love DC; Cooney A; Comly M; Patel S; Watari H; Strauss JF; Pentchev PG; Hanover JA; Blanchette-Mackie EJ
J Biol Chem; 2001 Feb; 276(5):3417-25. PubMed ID: 11032830
[TBL] [Abstract][Full Text] [Related]
55. Impaired dynamics of the late endosome/lysosome compartment in human Niemann-Pick type C skin fibroblasts carrying mutation in NPC1 gene.
Sztolsztener ME; Dobrzyn A; Pikula S; Tylki-Szymanska A; Bandorowicz-Pikula J
Mol Biosyst; 2012 Apr; 8(4):1197-205. PubMed ID: 22286891
[TBL] [Abstract][Full Text] [Related]
56. Niemann-Pick Type C2 protein contributes to the transport of endosomal cholesterol to mitochondria without interacting with NPC1.
Kennedy BE; Charman M; Karten B
J Lipid Res; 2012 Dec; 53(12):2632-42. PubMed ID: 22962690
[TBL] [Abstract][Full Text] [Related]
57. Endocytosis of beta-cyclodextrins is responsible for cholesterol reduction in Niemann-Pick type C mutant cells.
Rosenbaum AI; Zhang G; Warren JD; Maxfield FR
Proc Natl Acad Sci U S A; 2010 Mar; 107(12):5477-82. PubMed ID: 20212119
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. Characterization of the Niemann-Pick C pathway in alveolar type II cells and lamellar bodies of the lung.
Roszell BR; Tao JQ; Yu KJ; Huang S; Bates SR
Am J Physiol Lung Cell Mol Physiol; 2012 May; 302(9):L919-32. PubMed ID: 22367786
[TBL] [Abstract][Full Text] [Related]
60. Flux of fatty acids through NPC1 lysosomes.
Passeggio J; Liscum L
J Biol Chem; 2005 Mar; 280(11):10333-9. PubMed ID: 15632139
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
