BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

509 related articles for article (PubMed ID: 35252181)

  • 1. Autophagy in the Neuronal Ceroid Lipofuscinoses (Batten Disease).
    Kim WD; Wilson-Smillie MLDM; Thanabalasingam A; Lefrancois S; Cotman SL; Huber RJ
    Front Cell Dev Biol; 2022; 10():812728. PubMed ID: 35252181
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Recent insights into the networking of CLN genes and proteins in mammalian cells.
    Huber RJ
    J Neurochem; 2023 Jun; 165(5):643-659. PubMed ID: 37022340
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetics of the neuronal ceroid lipofuscinoses (Batten disease).
    Mole SE; Cotman SL
    Biochim Biophys Acta; 2015 Oct; 1852(10 Pt B):2237-41. PubMed ID: 26026925
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Emerging new roles of the lysosome and neuronal ceroid lipofuscinoses.
    Mukherjee AB; Appu AP; Sadhukhan T; Casey S; Mondal A; Zhang Z; Bagh MB
    Mol Neurodegener; 2019 Jan; 14(1):4. PubMed ID: 30651094
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Moving towards a new era of genomics in the neuronal ceroid lipofuscinoses.
    Butz ES; Chandrachud U; Mole SE; Cotman SL
    Biochim Biophys Acta Mol Basis Dis; 2020 Sep; 1866(9):165571. PubMed ID: 31678159
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Genetic Basis of Phenotypic Heterogeneity in the Neuronal Ceroid Lipofuscinoses.
    Gardner E; Mole SE
    Front Neurol; 2021; 12():754045. PubMed ID: 34733232
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Abnormal triaging of misfolded proteins by adult neuronal ceroid lipofuscinosis-associated DNAJC5/CSPα mutants causes lipofuscin accumulation.
    Lee J; Xu Y; Saidi L; Xu M; Zinsmaier K; Ye Y
    Autophagy; 2023 Jan; 19(1):204-223. PubMed ID: 35506243
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The conserved cellular roles of CLN proteins: Novel insights from Dictyostelium discoideum.
    Remtulla AAN; Huber RJ
    Eur J Cell Biol; 2023 Jun; 102(2):151305. PubMed ID: 36917916
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic basis and phenotypic correlations of the neuronal ceroid lipofusinoses.
    Warrier V; Vieira M; Mole SE
    Biochim Biophys Acta; 2013 Nov; 1832(11):1827-30. PubMed ID: 23542453
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cln3-mutations underlying juvenile neuronal ceroid lipofuscinosis cause significantly reduced levels of Palmitoyl-protein thioesterases-1 (Ppt1)-protein and Ppt1-enzyme activity in the lysosome.
    Appu AP; Bagh MB; Sadhukhan T; Mondal A; Casey S; Mukherjee AB
    J Inherit Metab Dis; 2019 Sep; 42(5):944-954. PubMed ID: 31025705
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Enzyme replacement therapy with recombinant pro-CTSD (cathepsin D) corrects defective proteolysis and autophagy in neuronal ceroid lipofuscinosis.
    Marques ARA; Di Spiezio A; Thießen N; Schmidt L; Grötzinger J; Lüllmann-Rauch R; Damme M; Storck SE; Pietrzik CU; Fogh J; Bär J; Mikhaylova M; Glatzel M; Bassal M; Bartsch U; Saftig P
    Autophagy; 2020 May; 16(5):811-825. PubMed ID: 31282275
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Altered protein secretion in Batten disease.
    Huber RJ
    Dis Model Mech; 2021 Dec; 14(12):. PubMed ID: 34870700
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lysosomal dysfunction, autophagic defects, and CLN5 accumulation underlie the pathogenesis of KCTD7-mutated neuronal ceroid lipofuscinoses.
    Wang Y; Wang H; Wang C
    Autophagy; 2023 Jun; 19(6):1876-1878. PubMed ID: 36368077
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular networking in the neuronal ceroid lipofuscinoses: insights from mammalian models and the social amoeba Dictyostelium discoideum.
    Huber RJ
    J Biomed Sci; 2020 May; 27(1):64. PubMed ID: 32430003
    [TBL] [Abstract][Full Text] [Related]  

  • 15. You say lipofuscin, we say ceroid: defining autofluorescent storage material.
    Seehafer SS; Pearce DA
    Neurobiol Aging; 2006 Apr; 27(4):576-88. PubMed ID: 16455164
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A lysosomal enigma CLN5 and its significance in understanding neuronal ceroid lipofuscinosis.
    Basak I; Wicky HE; McDonald KO; Xu JB; Palmer JE; Best HL; Lefrancois S; Lee SY; Schoderboeck L; Hughes SM
    Cell Mol Life Sci; 2021 May; 78(10):4735-4763. PubMed ID: 33792748
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pathogenesis and therapies for infantile neuronal ceroid lipofuscinosis (infantile CLN1 disease).
    Hawkins-Salsbury JA; Cooper JD; Sands MS
    Biochim Biophys Acta; 2013 Nov; 1832(11):1906-9. PubMed ID: 23747979
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Bioinformatic perspectives in the neuronal ceroid lipofuscinoses.
    Kmoch S; Stránecký V; Emes RD; Mitchison HM
    Biochim Biophys Acta; 2013 Nov; 1832(11):1831-41. PubMed ID: 23274885
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Glial Dysfunction and Its Contribution to the Pathogenesis of the Neuronal Ceroid Lipofuscinoses.
    Takahashi K; Nelvagal HR; Lange J; Cooper JD
    Front Neurol; 2022; 13():886567. PubMed ID: 35444603
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neuronal ceroid lipofuscinosis associated with an MFSD8 mutation in Chihuahuas.
    Ashwini A; D'Angelo A; Yamato O; Giordano C; Cagnotti G; Harcourt-Brown T; Mhlanga-Mutangadura T; Guo J; Johnson GS; Katz ML
    Mol Genet Metab; 2016 Aug; 118(4):326-32. PubMed ID: 27211611
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 26.