233 related articles for article (PubMed ID: 37400440)
1. 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]
2. 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]
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. 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]
5. Lysosomal proteome analysis reveals that CLN3-defective cells have multiple enzyme deficiencies associated with changes in intracellular trafficking.
Schmidtke C; Tiede S; Thelen M; Käkelä R; Jabs S; Makrypidi G; Sylvester M; Schweizer M; Braren I; Brocke-Ahmadinejad N; Cotman SL; Schulz A; Gieselmann V; Braulke T
J Biol Chem; 2019 Jun; 294(24):9592-9604. PubMed ID: 31040178
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. CLN3, the protein associated with batten disease: structure, function and localization.
Phillips SN; Benedict JW; Weimer JM; Pearce DA
J Neurosci Res; 2005 Mar; 79(5):573-83. PubMed ID: 15657902
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. Unbiased Cell-based Screening in a Neuronal Cell Model of Batten Disease Highlights an Interaction between Ca2+ Homeostasis, Autophagy, and CLN3 Protein Function.
Chandrachud U; Walker MW; Simas AM; Heetveld S; Petcherski A; Klein M; Oh H; Wolf P; Zhao WN; Norton S; Haggarty SJ; Lloyd-Evans E; Cotman SL
J Biol Chem; 2015 Jun; 290(23):14361-80. PubMed ID: 25878248
[TBL] [Abstract][Full Text] [Related]
14. Lysosomal alterations and decreased electrophysiological activity in CLN3 disease patient-derived cortical neurons.
Chear S; Perry S; Wilson R; Bindoff A; Talbot J; Ware TL; Grubman A; Vickers JC; Pébay A; Ruddle JB; King AE; Hewitt AW; Cook AL
Dis Model Mech; 2022 Dec; 15(12):. PubMed ID: 36453132
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Interconnections of CLN3, Hook1 and Rab proteins link Batten disease to defects in the endocytic pathway.
Luiro K; Yliannala K; Ahtiainen L; Maunu H; Järvelä I; Kyttälä A; Jalanko A
Hum Mol Genet; 2004 Dec; 13(23):3017-27. PubMed ID: 15471887
[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. Localization and processing of CLN3, the protein associated to Batten disease: where is it and what does it do?
Pearce DA
J Neurosci Res; 2000 Jan; 59(1):19-23. PubMed ID: 10658181
[TBL] [Abstract][Full Text] [Related]
19. Photoreceptor phagosome processing defects and disturbed autophagy in retinal pigment epithelium of Cln3Δex1-6 mice modelling juvenile neuronal ceroid lipofuscinosis (Batten disease).
Wavre-Shapton ST; Calvi AA; Turmaine M; Seabra MC; Cutler DF; Futter CE; Mitchison HM
Hum Mol Genet; 2015 Dec; 24(24):7060-74. PubMed ID: 26450516
[TBL] [Abstract][Full Text] [Related]
20. CLN3 regulates endosomal function by modulating Rab7A-effector interactions.
Yasa S; Modica G; Sauvageau E; Kaleem A; Hermey G; Lefrancois S
J Cell Sci; 2020 Mar; 133(6):. PubMed ID: 32034082
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
