BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 38763444)

  • 1. Targeting autophagy impairment improves the phenotype of a novel CLN8 zebrafish model.
    Marchese M; Bernardi S; Ogi A; Licitra R; Silvi G; Mero S; Galatolo D; Gammaldi N; Doccini S; Ratto GM; Rapposelli S; Neuhauss SCF; Zang J; Rocchiccioli S; Michelucci E; Ceccherini E; Santorelli FM
    Neurobiol Dis; 2024 Jul; 197():106536. PubMed ID: 38763444
    [TBL] [Abstract][Full Text] [Related]  

  • 2. CLN8 is an endoplasmic reticulum cargo receptor that regulates lysosome biogenesis.
    di Ronza A; Bajaj L; Sharma J; Sanagasetti D; Lotfi P; Adamski CJ; Collette J; Palmieri M; Amawi A; Popp L; Chang KT; Meschini MC; Leung HE; Segatori L; Simonati A; Sifers RN; Santorelli FM; Sardiello M
    Nat Cell Biol; 2018 Dec; 20(12):1370-1377. PubMed ID: 30397314
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Localization of wild-type and mutant neuronal ceroid lipofuscinosis CLN8 proteins in non-neuronal and neuronal cells.
    Lonka L; Salonen T; Siintola E; Kopra O; Lehesjoki AE; Jalanko A
    J Neurosci Res; 2004 Jun; 76(6):862-71. PubMed ID: 15160397
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Progress towards understanding disease mechanisms in small vertebrate models of neuronal ceroid lipofuscinosis.
    Cooper JD; Russell C; Mitchison HM
    Biochim Biophys Acta; 2006 Oct; 1762(10):873-89. PubMed ID: 17023146
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The neuronal ceroid lipofuscinosis-related protein CLN8 regulates endo-lysosomal dynamics and dendritic morphology.
    Pesaola F; Quassollo G; Venier AC; De Paul AL; Noher I; Bisbal M
    Biol Cell; 2021 Oct; 113(10):419-437. PubMed ID: 34021618
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital CLN8 disease of neuronal ceroid lipofuscinosis: a novel phenotype.
    Pesaola F; Kohan R; Cismondi IA; Guelbert N; Pons P; Oller-Ramirez AM; Noher de Halac I
    Rev Neurol; 2019 Feb; 68(4):155-159. PubMed ID: 30741402
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Galactolipid deficiency in the early pathogenesis of neuronal ceroid lipofuscinosis model Cln8mnd : implications to delayed myelination and oligodendrocyte maturation.
    Kuronen M; Hermansson M; Manninen O; Zech I; Talvitie M; Laitinen T; Gröhn O; Somerharju P; Eckhardt M; Cooper JD; Lehesjoki AE; Lahtinen U; Kopra O
    Neuropathol Appl Neurobiol; 2012 Aug; 38(5):471-86. PubMed ID: 22044361
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum.
    Lonka L; Kyttälä A; Ranta S; Jalanko A; Lehesjoki AE
    Hum Mol Genet; 2000 Jul; 9(11):1691-7. PubMed ID: 10861296
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A CLN8 nonsense mutation in the whole genome sequence of a mixed breed dog with neuronal ceroid lipofuscinosis and Australian Shepherd ancestry.
    Guo J; Johnson GS; Brown HA; Provencher ML; da Costa RC; Mhlanga-Mutangadura T; Taylor JF; Schnabel RD; O'Brien DP; Katz ML
    Mol Genet Metab; 2014 Aug; 112(4):302-9. PubMed ID: 24953404
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identifying protein partners of CLN8, an ER-resident protein involved in neuronal ceroid lipofuscinosis.
    Passantino R; Cascio C; Deidda I; Galizzi G; Russo D; Spedale G; Guarneri P
    Biochim Biophys Acta; 2013 Mar; 1833(3):529-40. PubMed ID: 23142642
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. CLN8 Mutations Presenting with a Phenotypic Continuum of Neuronal Ceroid Lipofuscinosis-Literature Review and Case Report.
    Badura-Stronka M; Winczewska-Wiktor A; Pietrzak A; Hirschfeld AS; Zemojtel T; Wołyńska K; Bednarek-Rajewska K; Seget-Dubaniewicz M; Matheisel A; Latos-Bielenska A; Steinborn B
    Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34201538
    [TBL] [Abstract][Full Text] [Related]  

  • 13. AAV9 Gene Therapy Increases Lifespan and Treats Pathological and Behavioral Abnormalities in a Mouse Model of CLN8-Batten Disease.
    Johnson TB; White KA; Brudvig JJ; Cain JT; Langin L; Pratt MA; Booth CD; Timm DJ; Davis SS; Meyerink B; Likhite S; Meyer K; Weimer JM
    Mol Ther; 2021 Jan; 29(1):162-175. PubMed ID: 33010819
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Different early ER-stress responses in the CLN8(mnd) mouse model of neuronal ceroid lipofuscinosis.
    Galizzi G; Russo D; Deidda I; Cascio C; Passantino R; Guarneri R; Bigini P; Mennini T; Drago G; Guarneri P
    Neurosci Lett; 2011 Jan; 488(3):258-62. PubMed ID: 21094208
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel mutation of the CLN8 gene: is there a Mediterranean phenotype?
    Zelnik N; Mahajna M; Iancu TC; Sharony R; Zeigler M
    Pediatr Neurol; 2007 Jun; 36(6):411-3. PubMed ID: 17560505
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Selective spatiotemporal patterns of glial activation and neuron loss in the sensory thalamocortical pathways of neuronal ceroid lipofuscinosis 8 mice.
    Kuronen M; Lehesjoki AE; Jalanko A; Cooper JD; Kopra O
    Neurobiol Dis; 2012 Sep; 47(3):444-57. PubMed ID: 22569358
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the Mediterranean.
    Cannelli N; Cassandrini D; Bertini E; Striano P; Fusco L; Gaggero R; Specchio N; Biancheri R; Vigevano F; Bruno C; Simonati A; Zara F; Santorelli FM
    Neurogenetics; 2006 May; 7(2):111-7. PubMed ID: 16570191
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deficient mitochondrial Ca(2+) buffering in the Cln8(mnd) mouse model of neuronal ceroid lipofuscinosis.
    Kolikova J; Afzalov R; Surin A; Lehesjoki AE; Khiroug L
    Cell Calcium; 2011 Dec; 50(6):491-501. PubMed ID: 21917311
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neuronal ceroid lipofuscinosis related ER membrane protein CLN8 regulates PP2A activity and ceramide levels.
    Adhikari B; De Silva B; Molina JA; Allen A; Peck SH; Lee SY
    Biochim Biophys Acta Mol Basis Dis; 2019 Feb; 1865(2):322-328. PubMed ID: 30453012
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel missense mutation in CLN8 in late infantile neuronal ceroid lipofuscinosis: The first report of a CLN8 mutation in Japan.
    Katata Y; Uematsu M; Sato H; Suzuki S; Nakayama T; Kubota Y; Kobayashi T; Hino-Fukuyo N; Saitsu H; Kure S
    Brain Dev; 2016 Mar; 38(3):341-5. PubMed ID: 26443629
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.