PubMed (OMIM) for id: 9217

Year	Number of Results
1965	1
1968	1
1969	1
1971	1
1978	1
1981	1
1990	1
1991	1
1992	1
1999	1
2004	2
2005	1
2006	1
2007	3
2008	2
2010	2
2011	1
2012	2
2013	2
2014	1
2015	1
2017	1
2024	0

1

Peroxisomal ACBD4 interacts with VAPB and promotes ER-peroxisome associations.

Costello JL, Castro IG, Schrader TA, Islinger M, Schrader M. Costello JL, et al. Cell Cycle. 2017 Jun 3;16(11):1039-1045. doi: 10.1080/15384101.2017.1314422. Epub 2017 May 2. Cell Cycle. 2017. PMID: 28463579 Free PMC article.

2

Vapb/Amyotrophic lateral sclerosis 8 knock-in mice display slowly progressive motor behavior defects accompanying ER stress and autophagic response.

Larroquette F, Seto L, Gaub PL, Kamal B, Wallis D, Larivière R, Vallée J, Robitaille R, Tsuda H. Larroquette F, et al. Hum Mol Genet. 2015 Nov 15;24(22):6515-29. doi: 10.1093/hmg/ddv360. Epub 2015 Sep 11. Hum Mol Genet. 2015. PMID: 26362257 Free PMC article.

3

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. Moustaqim-Barrette A, et al. Hum Mol Genet. 2014 Apr 15;23(8):1975-89. doi: 10.1093/hmg/ddt594. Epub 2013 Nov 23. Hum Mol Genet. 2014. PMID: 24271015 Free PMC article.

4

Amyotrophic lateral sclerosis-related VAPB P56S mutation differentially affects the function and survival of corticospinal and spinal motor neurons.

Aliaga L, Lai C, Yu J, Chub N, Shim H, Sun L, Xie C, Yang WJ, Lin X, O'Donovan MJ, Cai H. Aliaga L, et al. Hum Mol Genet. 2013 Nov 1;22(21):4293-305. doi: 10.1093/hmg/ddt279. Epub 2013 Jun 13. Hum Mol Genet. 2013. PMID: 23771029 Free PMC article.

5

Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria.

Mórotz GM, De Vos KJ, Vagnoni A, Ackerley S, Shaw CE, Miller CC. Mórotz GM, et al. Hum Mol Genet. 2012 May 1;21(9):1979-88. doi: 10.1093/hmg/dds011. Epub 2012 Jan 17. Hum Mol Genet. 2012. PMID: 22258555 Free PMC article.

6

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. De Vos KJ, et al. Hum Mol Genet. 2012 Mar 15;21(6):1299-311. doi: 10.1093/hmg/ddr559. Epub 2011 Nov 30. Hum Mol Genet. 2012. PMID: 22131369 Free PMC article.

7

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. Chen HJ, et al. J Biol Chem. 2010 Dec 17;285(51):40266-81. doi: 10.1074/jbc.M110.161398. Epub 2010 Oct 12. J Biol Chem. 2010. PMID: 20940299 Free PMC article.

8

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. Millecamps S, et al. J Med Genet. 2010 Aug;47(8):554-60. doi: 10.1136/jmg.2010.077180. Epub 2010 Jun 24. J Med Genet. 2010. PMID: 20577002 Free article.

9

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. Landers JE, et al. Neurology. 2008 Apr 1;70(14):1179-85. doi: 10.1212/01.wnl.0000289760.85237.4e. Epub 2008 Mar 5. Neurology. 2008. PMID: 18322265

10

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. Chai A, et al. Hum Mol Genet. 2008 Jan 15;17(2):266-80. doi: 10.1093/hmg/ddm303. Epub 2007 Oct 18. Hum Mol Genet. 2008. PMID: 17947296 Free PMC article.

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