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 *

759 related articles for article (PubMed ID: 32522631)

  • 41. Laboratory diagnosis of the Niemann-Pick type C disease: an inherited neurodegenerative disorder of cholesterol metabolism.
    Sitarska D; Ługowska A
    Metab Brain Dis; 2019 Oct; 34(5):1253-1260. PubMed ID: 31197681
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. Apolipoprotein D-mediated preservation of lysosomal function promotes cell survival and delays motor impairment in Niemann-Pick type A disease.
    Pascua-Maestro R; Corraliza-Gomez M; Fadrique-Rojo C; Ledesma MD; Schuchman EH; Sanchez D; Ganfornina MD
    Neurobiol Dis; 2020 Oct; 144():105046. PubMed ID: 32798728
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Enrichment of NPC1-deficient cells with the lipid LBPA stimulates autophagy, improves lysosomal function, and reduces cholesterol storage.
    Ilnytska O; Lai K; Gorshkov K; Schultz ML; Tran BN; Jeziorek M; Kunkel TJ; Azaria RD; McLoughlin HS; Waghalter M; Xu Y; Schlame M; Altan-Bonnet N; Zheng W; Lieberman AP; Dobrowolski R; Storch J
    J Biol Chem; 2021 Jul; 297(1):100813. PubMed ID: 34023384
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Lipidomic Analysis Reveals Altered Fatty Acid Metabolism in the Liver of the Symptomatic Niemann-Pick, Type C1 Mouse Model.
    Pergande MR; Serna-Perez F; Mohsin SB; Hanek J; Cologna SM
    Proteomics; 2019 Sep; 19(18):e1800285. PubMed ID: 31394590
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 2-Hydroxypropyl-gamma-cyclodextrin overcomes NPC1 deficiency by enhancing lysosome-ER association and autophagy.
    Singhal A; Krystofiak ES; Jerome WG; Song B
    Sci Rep; 2020 May; 10(1):8663. PubMed ID: 32457374
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The role of Niemann-Pick type C2 in zebrafish embryonic development.
    Tseng WC; Johnson Escauriza AJ; Tsai-Morris CH; Feldman B; Dale RK; Wassif CA; Porter FD
    Development; 2021 Apr; 148(7):. PubMed ID: 33722902
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Hydroxypropyl-beta and -gamma cyclodextrins rescue cholesterol accumulation in Niemann-Pick C1 mutant cell via lysosome-associated membrane protein 1.
    Singhal A; Szente L; Hildreth JEK; Song B
    Cell Death Dis; 2018 Oct; 9(10):1019. PubMed ID: 30282967
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Myelin Defects in Niemann-Pick Type C Disease: Mechanisms and Possible Therapeutic Perspectives.
    Bernardo A; De Nuccio C; Visentin S; Martire A; Minghetti L; Popoli P; Ferrante A
    Int J Mol Sci; 2021 Aug; 22(16):. PubMed ID: 34445564
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Reversal of Pathologic Lipid Accumulation in NPC1-Deficient Neurons by Drug-Promoted Release of LAMP1-Coated Lamellar Inclusions.
    Demais V; Barthélémy A; Perraut M; Ungerer N; Keime C; Reibel S; Pfrieger FW
    J Neurosci; 2016 Jul; 36(30):8012-25. PubMed ID: 27466344
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Lipid-induced lysosomal damage after demyelination corrupts microglia protective function in lysosomal storage disorders.
    Gabandé-Rodríguez E; Pérez-Cañamás A; Soto-Huelin B; Mitroi DN; Sánchez-Redondo S; Martínez-Sáez E; Venero C; Peinado H; Ledesma MD
    EMBO J; 2019 Jan; 38(2):. PubMed ID: 30530526
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. Metabolomic Studies of Lipid Storage Disorders, with Special Reference to Niemann-Pick Type C Disease: A Critical Review with Future Perspectives.
    Percival BC; Gibson M; Wilson PB; Platt FM; Grootveld M
    Int J Mol Sci; 2020 Apr; 21(7):. PubMed ID: 32260582
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Improvement in lipid and protein trafficking in Niemann-Pick C1 cells by correction of a secondary enzyme defect.
    Devlin C; Pipalia NH; Liao X; Schuchman EH; Maxfield FR; Tabas I
    Traffic; 2010 May; 11(5):601-15. PubMed ID: 20412078
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Identification and characterization of protein interactions with the major Niemann-Pick type C disease protein in yeast reveals pathways of therapeutic potential.
    Hammond N; Snider J; Stagljar I; Mitchell K; Lagutin K; Jessulat M; Babu M; Teesdale-Spittle PH; Sheridan JP; Sturley SL; Munkacsi AB
    Genetics; 2023 Aug; 225(1):. PubMed ID: 37440478
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Lipids regulate the hydrolysis of membrane bound glucosylceramide by lysosomal β-glucocerebrosidase.
    Abdul-Hammed M; Breiden B; Schwarzmann G; Sandhoff K
    J Lipid Res; 2017 Mar; 58(3):563-577. PubMed ID: 28126847
    [TBL] [Abstract][Full Text] [Related]  

  • 57. An "exacerbate-reverse" strategy in yeast identifies histone deacetylase inhibition as a correction for cholesterol and sphingolipid transport defects in human Niemann-Pick type C disease.
    Munkacsi AB; Chen FW; Brinkman MA; Higaki K; Gutiérrez GD; Chaudhari J; Layer JV; Tong A; Bard M; Boone C; Ioannou YA; Sturley SL
    J Biol Chem; 2011 Jul; 286(27):23842-51. PubMed ID: 21489983
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Clinical and Molecular Features of Early Infantile Niemann Pick Type C Disease.
    Seker Yilmaz B; Baruteau J; Rahim AA; Gissen P
    Int J Mol Sci; 2020 Jul; 21(14):. PubMed ID: 32709131
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Niemann-Pick disease type C: analysis of 7 patients.
    Xiong H; Bao XH; Zhang YH; Xu YN; Qin J; Shi HP; Wu XR
    World J Pediatr; 2012 Feb; 8(1):61-6. PubMed ID: 21633862
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Genetic and pharmacological evidence implicates cathepsins in Niemann-Pick C cerebellar degeneration.
    Chung C; Puthanveetil P; Ory DS; Lieberman AP
    Hum Mol Genet; 2016 Apr; 25(7):1434-46. PubMed ID: 26908626
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 38.