Citations for
1RMDN3, VAPB
The VAPB-PTPIP51 endoplasmic reticulum-mitochondria tethering proteins are present in neuronal synapses and regulate synaptic activity
Gómez-Suaga P, Pérez-Nievas BG, Glennon EB, Lau DHW, Paillusson S, Mórotz GM, Calě T, Pizzo P, Noble W, Miller CCJ.
Acta Neuropathol Commun. Mar 6;7(1):35. doi: 10.1186/s40478-019-0688-4 2019
2RMDN3, VAPB
ER-mitochondria signaling regulates autophagy
Gomez-Suaga P, Paillusson S, Miller CCJ
Autophagy Jul 3;13(7):1250-1251. doi: 10.1080/15548627.2017.1317913. Epub 2017 May 26. 2017
3RMDN3, VAPB
The ER-Mitochondria Tethering Complex VAPB-PTPIP51 Regulates Autophagy
Gomez-Suaga P, Paillusson S, Stoica R, Noble W, Hanger DP, Miller CCJ.
Curr Biol. Feb 6;27(3):371-385. doi: 10.1016/j.cub.2016.12.038. Epub 2017 Jan 26 2017
4COL4A3BP, OSBP, VAPA, VAPB
CARTS biogenesis requires VAP-lipid transfer protein complexes functioning at the endoplasmic reticulum-Golgi interface.
Wakana Y, Kotake R, Oyama N, Murate M, Kobayashi T, Arasaki K, Inoue H, Tagaya M.
Mol Biol Cell 26(25):4686-99. doi: 10.1091/mbc.E15-08-0599. 2015
5ASNA1, FAF1, VAPB
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 12:39. doi: 10.1186/1741-7007-12-39. 2014
6RAB3GAP1, VAPB
VAP-B binds to Rab3GAP1 at the ER: its implication in nuclear envelope formation through the ER-Golgi intermediate compartment.
Hantan D, Yamamoto Y, Sakisaka T.
Kobe J Med Sci 60(3):E48-56. 2014
7VAPA, VAPB
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 12:39. doi: 10.1186/1741-7007-12-39. 2014
8ALS8, VAPB
Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis.
Kabashi E, El Oussini H, Bercier V, Gros-Louis F, Valdmanis PN, McDearmid J, Mejier IA, Dion PA, Dupre N, Hollinger D, Sinniger J, Dirrig-Grosch S, Camu W, Meininger V, Loeffler JP, René F, Drapeau P, Rouleau GA, Dupuis L.
Hum Mol Genet 22(12):2350-60. doi: 10.1093/hmg/ddt080. Epub 2013 Feb 26. 2013
9VAPB, YIF1A
The ALS8 protein VAPB interacts with the ER-Golgi recycling protein YIF1A and regulates membrane delivery into dendrites.
Kuijpers M, Yu KL, Teuling E, Akhmanova A, Jaarsma D, Hoogenraad CC.
EMBO J. Jul 17;32(14):2056-72. doi: 10.1038/emboj.2013.131. Epub 2013 Jun 4 2013
10VAPB
VAMP-associated protein B (VAPB) promotes breast tumor growth by modulation of Akt activity.
Rao M, Song W, Jiang A, Shyr Y, Lev S, Greenstein D, Brantley-Sieders D, Chen J.
PLoS One 7(10):e46281. doi: 10.1371/journal.pone.0046281. Epub 2012 Oct 1. 2012
11ALS8, ALSFTD1, C9orf72, VAPB
VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient.
van Blitterswijk M, van Es MA, Koppers M, van Rheenen W, Medic J, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH.
Neurobiol Aging 33(12):2950.e1-4. doi: 10.1016/j.neurobiolaging.2012.07.004. Epub 2012 Aug 9. 2012
12ALS8, VAPB
A mutation in VAPB that causes amyotrophic lateral sclerosis also causes a nuclear envelope defect.
Tran D, Chalhoub A, Schooley A, Zhang W, Ngsee JK.
J Cell Sci 125(Pt 12):2831-6. doi: 10.1242/jcs.102111. Epub 2012 Mar 27. 2012
13RMDN3, VAPB
VAPB interacts with the mitochondrial protein PTPIP51 to regulate calcium homeostasis
De Vos KJ, Mórotz GM, Stoica R, Tudor EL, Lau KF, Ackerley S, Warley A, Shaw CE, Miller CC.
Hum Mol Genet. Mar 15;21(6):1299-311. doi: 10.1093/hmg/ddr559. Epub 2011 Nov 30. 2012
14VAPA, VAPB
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 404(2):605-9. Epub 2010 Dec 7. 2011
15ALS8, VAPB
Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients.
Mitne-Neto M, Machado-Costa M, Marchetto MC, Bengtson MH, Joazeiro CA, Tsuda H, Bellen HJ, Silva HC, Oliveira AS, Lazar M, Muotri AR, Zatz M.
Hum Mol Genet 20(18):3642-52. doi: 10.1093/hmg/ddr284. Epub 2011 Jun 17. 2011
16ALS8, VAPB
Novel splice variants of the amyotrophic lateral sclerosis-associated gene VAPB expressed in human tissues.
Nachreiner T, Esser M, Tenten V, Troost D, Weis J, Krüttgen A.
Biochem Biophys Res Commun 394(3):703-8. Epub 2010 Mar 17. 2010
17ALS1, ALS10, ALS6, ALS8, ALS9, ANG, FUS, SOD1, TARDBP, VAPB
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
Millecamps S, Salachas F, Cazeneuve C, Gordon P, Bricka B, Camuzat A, Guillot-Noël L, Russaouen O, Bruneteau G, Pradat PF, Le Forestier N, Vandenberghe N, Danel-Brunaud V, Guy N, Thauvin-Robinet C, Lacomblez L, Couratier P, Hannequin D, Seilhean D, Le Ber I, Corcia P, Camu W, Brice A, Rouleau G, LeGuern E, Meininger V.
J Med Genet 47(8):554-60. Epub 2010 Jun 24.PMID: 20577002 2010
18ALS8, VAPB
Characterization of the properties of a novel mutation in VAPB in familial amyotrophic lateral sclerosis.
Chen HJ, Anagnostou G, Chai A, Withers J, Morris A, Adhikaree J, Pennetta G, de Belleroche JS.
J Biol Chem 285(51):40266-81. Epub 2010 Oct 12. 2010
19VAPB, ALS8, VAPA
hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular junction.
Chai A, Withers J, Koh YH, Parry K, Bao H, Zhang B, Budnik V, Pennetta G.
Hum Mol Genet 17(2):266-80. Epub 2007 Oct 18. 2008
20VAPA, VAPB
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 17(11):1517-26. Epub 2008 Feb 8. 2008
21ALS8, VAPB
The amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors.
Tsuda H, Han SM, Yang Y, Tong C, Lin YQ, Mohan K, Haueter C, Zoghbi A, Harati Y, Kwan J, Miller MA, Bellen HJ.
Cell 133(6):963-77. 2008
22VAPB
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 Jr.
Neurology 70(14):1179-85. Epub 2008 Mar 5. 2008
23VAPA, VAPB
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 27(36):9801-15. 2007
24VAPB, ALS8
Characterization of amyotrophic lateral sclerosis-linked P56S mutation of vesicle-associated membrane protein-associated protein B (VAPB/ALS8).
Kanekura K, Nishimoto I, Aiso S, Matsuoka M.
J Biol Chem 281(40):30223-33. Epub 2006 Aug 4. 2006
25VAPA, VAPB
Human VAP-B is involved in hepatitis C virus replication through interaction with NS5A and NS5B.
Hamamoto I, Nishimura Y, Okamoto T, Aizaki H, Liu M, Mori Y, Abe T, Suzuki T, Lai MM, Miyamura T, Moriishi K, Matsuura Y.
J Virol 79(21):13473-82. 2005
26VAPB, ALS8, SMAPA
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis.
Nishimura AL, Mitne-Neto M, Silva HC, Richieri-Costa A, Middleton S, Cascio D, Kok F, Oliveira JR, Gillingwater T, Webb J, Skehel P, Zatz M.
Am J Hum Genet 75(5):822-31. Epub 2004 Sep 15. 2004
27VAPA, VAPB
Molecular cloning and characterization of mammalian homologues of vesicle-associated membrane protein-associated (VAMP-associated) proteins.
Nishimura Y, Hayashi M, Inada H, Tanaka T.
Biochem Biophys Res Commun 254(1):21-6. 1999
28SMAPA, VAPB
Autosomal dominant late adult spinal muscular atrophy, type Finkel.
Richieri-Costa A, Rogatko A, Levisky R, Finkel N, Frota-Pessoa O.
Am J Med Genet 9(2):119-28. 1981