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23. Sequestosome 1 Is Part of the Interaction Network of VAPB. James C; Lenz C; Urlaub H; Kehlenbach RH Int J Mol Sci; 2021 Dec; 22(24):. PubMed ID: 34948065 [TBL] [Abstract][Full Text] [Related]
24. ALS-Linked VapB P56S Mutation Alters Neuronal Mitochondrial Turnover at the Synapse. Wong HC; Lang AE; Stein C; Drerup CM J Neurosci; 2024 Aug; 44(35):. PubMed ID: 39054069 [TBL] [Abstract][Full Text] [Related]
25. Motor neuron disease-associated mutant vesicle-associated membrane protein-associated protein (VAP) B recruits wild-type VAPs into endoplasmic reticulum-derived tubular aggregates. Teuling E; Ahmed S; Haasdijk E; Demmers J; Steinmetz MO; Akhmanova A; Jaarsma D; Hoogenraad CC J Neurosci; 2007 Sep; 27(36):9801-15. PubMed ID: 17804640 [TBL] [Abstract][Full Text] [Related]
26. Accumulation of wildtype and ALS-linked mutated VAPB impairs activity of the proteasome. Moumen A; Virard I; Raoul C PLoS One; 2011; 6(10):e26066. PubMed ID: 21998752 [TBL] [Abstract][Full Text] [Related]
27. VAPB interacts with and modulates the activity of ATF6. Gkogkas C; Middleton S; Kremer AM; Wardrope C; Hannah M; Gillingwater TH; Skehel P Hum Mol Genet; 2008 Jun; 17(11):1517-26. PubMed ID: 18263603 [TBL] [Abstract][Full Text] [Related]
28. FFAT rescues VAPA-mediated inhibition of ER-to-Golgi transport and VAPB-mediated ER aggregation. Prosser DC; Tran D; Gougeon PY; Verly C; Ngsee JK J Cell Sci; 2008 Sep; 121(Pt 18):3052-61. PubMed ID: 18713837 [TBL] [Abstract][Full Text] [Related]
29. Expression of vesicle-associated membrane-protein-associated protein B cleavage products in peripheral blood leukocytes and cerebrospinal fluid of patients with sporadic amyotrophic lateral sclerosis. Deidda I; Galizzi G; Passantino R; Cascio C; Russo D; Colletti T; La Bella V; Guarneri P Eur J Neurol; 2014 Mar; 21(3):478-85. PubMed ID: 24372953 [TBL] [Abstract][Full Text] [Related]
31. Atypical familial amyotrophic lateral sclerosis with initial symptoms of pain or tremor in a Chinese family harboring VAPB-P56S mutation. Di L; Chen H; Da Y; Wang S; Shen XM J Neurol; 2016 Feb; 263(2):263-268. PubMed ID: 26566915 [TBL] [Abstract][Full Text] [Related]
32. Human VAPA and the yeast VAP Scs2p with an altered proline distribution can phenocopy amyotrophic lateral sclerosis-associated VAPB(P56S). Nakamichi S; Yamanaka K; Suzuki M; Watanabe T; Kagiwada S Biochem Biophys Res Commun; 2011 Jan; 404(2):605-9. PubMed ID: 21144830 [TBL] [Abstract][Full Text] [Related]
33. VAMP associated proteins are required for autophagic and lysosomal degradation by promoting a PtdIns4P-mediated endosomal pathway. Mao D; Lin G; Tepe B; Zuo Z; Tan KL; Senturk M; Zhang S; Arenkiel BR; Sardiello M; Bellen HJ Autophagy; 2019 Jul; 15(7):1214-1233. PubMed ID: 30741620 [TBL] [Abstract][Full Text] [Related]
34. Mitigating Motor Neuronal Loss in C. elegans Model of ALS8. Zhang W; Colavita A; Ngsee JK Sci Rep; 2017 Sep; 7(1):11582. PubMed ID: 28912432 [TBL] [Abstract][Full Text] [Related]
35. VAPB/ALS8 interacts with FFAT-like proteins including the p97 cofactor FAF1 and the ASNA1 ATPase. Baron Y; Pedrioli PG; Tyagi K; Johnson C; Wood NT; Fountaine D; Wightman M; Alexandru G BMC Biol; 2014 May; 12():39. PubMed ID: 24885147 [TBL] [Abstract][Full Text] [Related]
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37. New VAPB deletion variant and exclusion of VAPB mutations in familial ALS. Landers JE; Leclerc AL; Shi L; Virkud A; Cho T; Maxwell MM; Henry AF; Polak M; Glass JD; Kwiatkowski TJ; Al-Chalabi A; Shaw CE; Leigh PN; Rodriguez-Leyza I; McKenna-Yasek D; Sapp PC; Brown RH Neurology; 2008 Apr; 70(14):1179-85. PubMed ID: 18322265 [TBL] [Abstract][Full Text] [Related]
38. The amyotrophic lateral sclerosis 8 protein, VAP, is required for ER protein quality control. Moustaqim-Barrette A; Lin YQ; Pradhan S; Neely GG; Bellen HJ; Tsuda H Hum Mol Genet; 2014 Apr; 23(8):1975-89. PubMed ID: 24271015 [TBL] [Abstract][Full Text] [Related]
39. The ALS8-associated mutant VAPB(P56S) is resistant to proteolysis in neurons. Gkogkas C; Wardrope C; Hannah M; Skehel P J Neurochem; 2011 Apr; 117(2):286-94. PubMed ID: 21275991 [TBL] [Abstract][Full Text] [Related]
40. Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues. Watanabe M; Dykes-Hoberg M; Culotta VC; Price DL; Wong PC; Rothstein JD Neurobiol Dis; 2001 Dec; 8(6):933-41. PubMed ID: 11741389 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]