254 related articles for article (PubMed ID: 36131016)
1. CLN3 is required for the clearance of glycerophosphodiesters from lysosomes.
Laqtom NN; Dong W; Medoh UN; Cangelosi AL; Dharamdasani V; Chan SH; Kunchok T; Lewis CA; Heinze I; Tang R; Grimm C; Dang Do AN; Porter FD; Ori A; Sabatini DM; Abu-Remaileh M
Nature; 2022 Sep; 609(7929):1005-1011. PubMed ID: 36131016
[TBL] [Abstract][Full Text] [Related]
2. Glycerophosphodiesters inhibit lysosomal phospholipid catabolism in Batten disease.
Nyame K; Hims A; Aburous A; Laqtom NN; Dong W; Medoh UN; Heiby JC; Xiong J; Ori A; Abu-Remaileh M
Mol Cell; 2024 Apr; 84(7):1354-1364.e9. PubMed ID: 38447580
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. The CLN3 gene and protein: What we know.
Mirza M; Vainshtein A; DiRonza A; Chandrachud U; Haslett LJ; Palmieri M; Storch S; Groh J; Dobzinski N; Napolitano G; Schmidtke C; Kerkovich DM
Mol Genet Genomic Med; 2019 Dec; 7(12):e859. PubMed ID: 31568712
[TBL] [Abstract][Full Text] [Related]
5. Defective lysosomal arginine transport in juvenile Batten disease.
Ramirez-Montealegre D; Pearce DA
Hum Mol Genet; 2005 Dec; 14(23):3759-73. PubMed ID: 16251196
[TBL] [Abstract][Full Text] [Related]
6. Loss of the Batten disease gene CLN3 prevents exit from the TGN of the mannose 6-phosphate receptor.
Metcalf DJ; Calvi AA; Seaman MNj; Mitchison HM; Cutler DF
Traffic; 2008 Nov; 9(11):1905-14. PubMed ID: 18817525
[TBL] [Abstract][Full Text] [Related]
7. Neuronal genetic rescue normalizes brain network dynamics in a lysosomal storage disorder despite persistent storage accumulation.
Ahrens-Nicklas RC; Tecedor L; Hall AF; Kane O; Chung RJ; Lysenko E; Marsh ED; Stein CS; Davidson BL
Mol Ther; 2022 Jul; 30(7):2464-2473. PubMed ID: 35395398
[TBL] [Abstract][Full Text] [Related]
8. Partial correction of the CNS lysosomal storage defect in a mouse model of juvenile neuronal ceroid lipofuscinosis by neonatal CNS administration of an adeno-associated virus serotype rh.10 vector expressing the human CLN3 gene.
Sondhi D; Scott EC; Chen A; Hackett NR; Wong AM; Kubiak A; Nelvagal HR; Pearse Y; Cotman SL; Cooper JD; Crystal RG
Hum Gene Ther; 2014 Mar; 25(3):223-39. PubMed ID: 24372003
[TBL] [Abstract][Full Text] [Related]
9. Role of the Lysosomal Membrane Protein, CLN3, in the Regulation of Cathepsin D Activity.
Cárcel-Trullols J; Kovács AD; Pearce DA
J Cell Biochem; 2017 Nov; 118(11):3883-3890. PubMed ID: 28390177
[TBL] [Abstract][Full Text] [Related]
10. Loss of the batten disease protein CLN3 leads to mis-trafficking of M6PR and defective autophagic-lysosomal reformation.
Calcagni' A; Staiano L; Zampelli N; Minopoli N; Herz NJ; Di Tullio G; Huynh T; Monfregola J; Esposito A; Cirillo C; Bajic A; Zahabiyon M; Curnock R; Polishchuk E; Parkitny L; Medina DL; Pastore N; Cullen PJ; Parenti G; De Matteis MA; Grumati P; Ballabio A
Nat Commun; 2023 Jul; 14(1):3911. PubMed ID: 37400440
[TBL] [Abstract][Full Text] [Related]
11. Loss of CLN3, the gene mutated in juvenile neuronal ceroid lipofuscinosis, leads to metabolic impairment and autophagy induction in retinal pigment epithelium.
Zhong Y; Mohan K; Liu J; Al-Attar A; Lin P; Flight RM; Sun Q; Warmoes MO; Deshpande RR; Liu H; Jung KS; Mitov MI; Lin N; Butterfield DA; Lu S; Liu J; Moseley HNB; Fan TWM; Kleinman ME; Wang QJ
Biochim Biophys Acta Mol Basis Dis; 2020 Oct; 1866(10):165883. PubMed ID: 32592935
[TBL] [Abstract][Full Text] [Related]
12. Increased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissue.
Pohl S; Mitchison HM; Kohlschütter A; van Diggelen O; Braulke T; Storch S
J Neurochem; 2007 Dec; 103(6):2177-88. PubMed ID: 17868323
[TBL] [Abstract][Full Text] [Related]
13. Converging roles of PSENEN/PEN2 and CLN3 in the autophagy-lysosome system.
Klein M; Kaleem A; Oetjen S; Wünkhaus D; Binkle L; Schilling S; Gjorgjieva M; Scholz R; Gruber-Schoffnegger D; Storch S; Kins S; Drewes G; Hoffmeister-Ullerich S; Kuhl D; Hermey G
Autophagy; 2022 Sep; 18(9):2068-2085. PubMed ID: 34964690
[TBL] [Abstract][Full Text] [Related]
14. A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis.
Kitzmüller C; Haines RL; Codlin S; Cutler DF; Mole SE
Hum Mol Genet; 2008 Jan; 17(2):303-12. PubMed ID: 17947292
[TBL] [Abstract][Full Text] [Related]
15. CLN3, at the crossroads of endocytic trafficking.
Cotman SL; Lefrancois S
Neurosci Lett; 2021 Sep; 762():136117. PubMed ID: 34274435
[TBL] [Abstract][Full Text] [Related]
16. CLN3 deficiency leads to neurological and metabolic perturbations during early development.
Heins-Marroquin U; Singh RR; Perathoner S; Gavotto F; Merino Ruiz C; Patraskaki M; Gomez-Giro G; Kleine Borgmann F; Meyer M; Carpentier A; Warmoes MO; Jäger C; Mittelbronn M; Schwamborn JC; Cordero-Maldonado ML; Crawford AD; Schymanski EL; Linster CL
Life Sci Alliance; 2024 Mar; 7(3):. PubMed ID: 38195117
[TBL] [Abstract][Full Text] [Related]
17. Revisiting the neuronal localization and trafficking of CLN3 in juvenile neuronal ceroid lipofuscinosis.
Oetjen S; Kuhl D; Hermey G
J Neurochem; 2016 Nov; 139(3):456-470. PubMed ID: 27453211
[TBL] [Abstract][Full Text] [Related]
18. Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments.
Uusi-Rauva K; Kyttälä A; van der Kant R; Vesa J; Tanhuanpää K; Neefjes J; Olkkonen VM; Jalanko A
Cell Mol Life Sci; 2012 Jun; 69(12):2075-89. PubMed ID: 22261744
[TBL] [Abstract][Full Text] [Related]
19. Deletion of the Caenorhabditis elegans homologues of the CLN3 gene, involved in human juvenile neuronal ceroid lipofuscinosis, causes a mild progeric phenotype.
de Voer G; van der Bent P; Rodrigues AJ; van Ommen GJ; Peters DJ; Taschner PE
J Inherit Metab Dis; 2005; 28(6):1065-80. PubMed ID: 16435200
[TBL] [Abstract][Full Text] [Related]
20. Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse models.
Chan CH; Mitchison HM; Pearce DA
Hum Mol Genet; 2008 Nov; 17(21):3332-9. PubMed ID: 18678598
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
