329 related articles for article (PubMed ID: 33764426)
1. Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking.
Sanderson LE; Lanko K; Alsagob M; Almass R; Al-Ahmadi N; Najafi M; Al-Muhaizea MA; Alzaidan H; AlDhalaan H; Perenthaler E; van der Linde HC; Nikoncuk A; Kühn NA; Antony D; Owaidah TM; Raskin S; Vieira LGDR; Mombach R; Ahangari N; Silveira TRD; Ameziane N; Rolfs A; Alharbi A; Sabbagh RM; AlAhmadi K; Alawam B; Ghebeh H; AlHargan A; Albader AA; Binhumaid FS; Goljan E; Monies D; Mustafa OM; Aldosary M; AlBakheet A; Alyounes B; Almutairi F; Al-Odaib A; Aksoy DB; Basak AN; Palvadeau R; Trabzuni D; Rosenfeld JA; Karimiani EG; Meyer BF; Karakas B; Al-Mohanna F; Arold ST; Colak D; Maroofian R; Houlden H; Bertoli-Avella AM; Schmidts M; Barakat TS; van Ham TJ; Kaya N
Brain; 2021 Apr; 144(3):769-780. PubMed ID: 33764426
[TBL] [Abstract][Full Text] [Related]
2. Loss-of-Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities.
Steel D; Zech M; Zhao C; Barwick KES; Burke D; Demailly D; Kumar KR; Zorzi G; Nardocci N; Kaiyrzhanov R; Wagner M; Iuso A; Berutti R; Škorvánek M; Necpál J; Davis R; Wiethoff S; Mankad K; Sudhakar S; Ferrini A; Sharma S; Kamsteeg EJ; Tijssen MA; Verschuuren C; van Egmond ME; Flowers JM; McEntagart M; Tucci A; Coubes P; Bustos BI; Gonzalez-Latapi P; Tisch S; Darveniza P; Gorman KM; Peall KJ; Bötzel K; Koch JC; Kmieć T; Plecko B; Boesch S; Haslinger B; Jech R; Garavaglia B; Wood N; Houlden H; Gissen P; Lubbe SJ; Sue CM; Cif L; Mencacci NE; Anderson G; Kurian MA; Winkelmann J;
Ann Neurol; 2020 Nov; 88(5):867-877. PubMed ID: 32808683
[TBL] [Abstract][Full Text] [Related]
3. Distinct sets of tethering complexes, SNARE complexes, and Rab GTPases mediate membrane fusion at the vacuole in Arabidopsis.
Takemoto K; Ebine K; Askani JC; Krüger F; Gonzalez ZA; Ito E; Goh T; Schumacher K; Nakano A; Ueda T
Proc Natl Acad Sci U S A; 2018 Mar; 115(10):E2457-E2466. PubMed ID: 29463724
[TBL] [Abstract][Full Text] [Related]
4. VPS18 recruits VPS41 to the human HOPS complex via a RING-RING interaction.
Hunter MR; Scourfield EJ; Emmott E; Graham SC
Biochem J; 2017 Oct; 474(21):3615-3626. PubMed ID: 28931724
[TBL] [Abstract][Full Text] [Related]
5. Recruitment of VPS33A to HOPS by VPS16 Is Required for Lysosome Fusion with Endosomes and Autophagosomes.
Wartosch L; Günesdogan U; Graham SC; Luzio JP
Traffic; 2015 Jul; 16(7):727-42. PubMed ID: 25783203
[TBL] [Abstract][Full Text] [Related]
6. Arabidopsis HOPS subunit VPS41 carries out plant-specific roles in vacuolar transport and vegetative growth.
Jiang D; He Y; Zhou X; Cao Z; Pang L; Zhong S; Jiang L; Li R
Plant Physiol; 2022 Jun; 189(3):1416-1434. PubMed ID: 35417008
[TBL] [Abstract][Full Text] [Related]
7. Homozygous missense VPS16 variant is associated with a novel disease, resembling mucopolysaccharidosis-plus syndrome in two siblings.
Yıldız Y; Koşukcu C; Aygün D; Akçaboy M; Öztek Çelebi FZ; Taşcı Yıldız Y; Şahin G; Aytekin C; Yüksel D; Lay İ; Özgül RK; Dursun A
Clin Genet; 2021 Sep; 100(3):308-317. PubMed ID: 34013567
[TBL] [Abstract][Full Text] [Related]
8. Phosphoinositides control the localization of HOPS subunit VPS41, which together with VPS33 mediates vacuole fusion in plants.
Brillada C; Zheng J; Krüger F; Rovira-Diaz E; Askani JC; Schumacher K; Rojas-Pierce M
Proc Natl Acad Sci U S A; 2018 Aug; 115(35):E8305-E8314. PubMed ID: 30104351
[TBL] [Abstract][Full Text] [Related]
9. Neurodegenerative VPS41 variants inhibit HOPS function and mTORC1-dependent TFEB/TFE3 regulation.
van der Welle REN; Jobling R; Burns C; Sanza P; van der Beek JA; Fasano A; Chen L; Zwartkruis FJ; Zwakenberg S; Griffin EF; Ten Brink C; Veenendaal T; Liv N; van Ravenswaaij-Arts CMA; Lemmink HH; Pfundt R; Blaser S; Sepulveda C; Lozano AM; Yoon G; Santiago-Sim T; Asensio CS; Caldwell GA; Caldwell KA; Chitayat D; Klumperman J
EMBO Mol Med; 2021 May; 13(5):e13258. PubMed ID: 33851776
[TBL] [Abstract][Full Text] [Related]
10. Impairment of autophagosome-lysosome fusion in the buff mutant mice with the VPS33A(D251E) mutation.
Zhen Y; Li W
Autophagy; 2015; 11(9):1608-22. PubMed ID: 26259518
[TBL] [Abstract][Full Text] [Related]
11. The hookup model of the HOPS complex in autophagosome-lysosome fusion.
Zhang S; Li L; Liu X; Zhong Q
Autophagy; 2024 Mar; 20(3):714-715. PubMed ID: 38083843
[TBL] [Abstract][Full Text] [Related]
12. Interaction of the HOPS complex with Syntaxin 17 mediates autophagosome clearance in Drosophila.
Takáts S; Pircs K; Nagy P; Varga Á; Kárpáti M; Hegedűs K; Kramer H; Kovács AL; Sass M; Juhász G
Mol Biol Cell; 2014 Apr; 25(8):1338-54. PubMed ID: 24554766
[TBL] [Abstract][Full Text] [Related]
13. Molecular architecture of the multisubunit homotypic fusion and vacuole protein sorting (HOPS) tethering complex.
Bröcker C; Kuhlee A; Gatsogiannis C; Balderhaar HJ; Hönscher C; Engelbrecht-Vandré S; Ungermann C; Raunser S
Proc Natl Acad Sci U S A; 2012 Feb; 109(6):1991-6. PubMed ID: 22308417
[TBL] [Abstract][Full Text] [Related]
14. [Prokaryotic expression, protein purification and functional verification of human homotypic fusion and vacuole protein sorting complex subunit].
Chen Y; Guo R; Huang S; Song D; Liu R
Sheng Wu Gong Cheng Xue Bao; 2020 Jan; 36(1):133-142. PubMed ID: 32072788
[TBL] [Abstract][Full Text] [Related]
15. RILP interacts with HOPS complex via VPS41 subunit to regulate endocytic trafficking.
Lin X; Yang T; Wang S; Wang Z; Yun Y; Sun L; Zhou Y; Xu X; Akazawa C; Hong W; Wang T
Sci Rep; 2014 Dec; 4():7282. PubMed ID: 25445562
[TBL] [Abstract][Full Text] [Related]
16. HOPS-associated neurological disorders (HOPSANDs): linking endolysosomal dysfunction to the pathogenesis of dystonia.
Monfrini E; Zech M; Steel D; Kurian MA; Winkelmann J; Di Fonzo A
Brain; 2021 Oct; 144(9):2610-2615. PubMed ID: 33871597
[TBL] [Abstract][Full Text] [Related]
17. Bi-allelic VPS16 variants limit HOPS/CORVET levels and cause a mucopolysaccharidosis-like disease.
Sofou K; Meier K; Sanderson LE; Kaminski D; Montoliu-Gaya L; Samuelsson E; Blomqvist M; Agholme L; Gärtner J; Mühlhausen C; Darin N; Barakat TS; Schlotawa L; van Ham T; Asin Cayuela J; Sterky FH
EMBO Mol Med; 2021 May; 13(5):e13376. PubMed ID: 33938619
[TBL] [Abstract][Full Text] [Related]
18. CORVET-specific subunit levels determine the balance between HOPS/CORVET endosomal tethering complexes.
Sőth Á; Molnár M; Lőrincz P; Simon-Vecsei Z; Juhász G
Sci Rep; 2024 May; 14(1):10146. PubMed ID: 38698024
[TBL] [Abstract][Full Text] [Related]
19. A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects.
Zhang J; Lachance V; Schaffner A; Li X; Fedick A; Kaye LE; Liao J; Rosenfeld J; Yachelevich N; Chu ML; Mitchell WG; Boles RG; Moran E; Tokita M; Gorman E; Bagley K; Zhang W; Xia F; Leduc M; Yang Y; Eng C; Wong LJ; Schiffmann R; Diaz GA; Kornreich R; Thummel R; Wasserstein M; Yue Z; Edelmann L
PLoS Genet; 2016 Apr; 12(4):e1005848. PubMed ID: 27120463
[TBL] [Abstract][Full Text] [Related]
20. MiniCORVET is a Vps8-containing early endosomal tether in Drosophila.
Lőrincz P; Lakatos Z; Varga Á; Maruzs T; Simon-Vecsei Z; Darula Z; Benkő P; Csordás G; Lippai M; Andó I; Hegedűs K; Medzihradszky KF; Takáts S; Juhász G
Elife; 2016 Jun; 5():. PubMed ID: 27253064
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
