Year |
Citation |
Score |
2014 |
Baulac S, Lenk GM, Dufresnois B, Ouled Amar Bencheikh B, Couarch P, Renard J, Larson PA, Ferguson CJ, Noé E, Poirier K, Hubans C, Ferreira S, Guerrini R, Ouazzani R, El Hachimi KH, et al. Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria. Neurology. 82: 1068-75. PMID 24598713 DOI: 10.1212/Wnl.0000000000000241 |
0.436 |
|
2012 |
Zhang Y, McCartney AJ, Zolov SN, Ferguson CJ, Meisler MH, Sutton MA, Weisman LS. Modulation of synaptic function by VAC14, a protein that regulates the phosphoinositides PI(3,5)Pâ‚‚ and PI(5)P. The Embo Journal. 31: 3442-56. PMID 22842785 DOI: 10.1038/Emboj.2012.200 |
0.509 |
|
2012 |
Ferguson CJ, Lenk GM, Jones JM, Grant AE, Winters JJ, Dowling JJ, Giger RJ, Meisler MH. Neuronal expression of Fig4 is both necessary and sufficient to prevent spongiform neurodegeneration. Human Molecular Genetics. 21: 3525-34. PMID 22581779 DOI: 10.1093/Hmg/Dds179 |
0.526 |
|
2011 |
Winters JJ, Ferguson CJ, Lenk GM, Giger-Mateeva VI, Shrager P, Meisler MH, Giger RJ. Congenital CNS hypomyelination in the Fig4 null mouse is rescued by neuronal expression of the PI(3,5)P(2) phosphatase Fig4. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 17736-51. PMID 22131434 DOI: 10.1523/Jneurosci.1482-11.2011 |
0.514 |
|
2011 |
Nicholson G, Lenk GM, Reddel SW, Grant AE, Towne CF, Ferguson CJ, Simpson E, Scheuerle A, Yasick M, Hoffman S, Blouin R, Brandt C, Coppola G, Biesecker LG, Batish SD, et al. Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)Pâ‚‚ phosphatase FIG4. Brain : a Journal of Neurology. 134: 1959-71. PMID 21705420 DOI: 10.1093/Brain/Awr148 |
0.512 |
|
2011 |
Lenk GM, Ferguson CJ, Chow CY, Jin N, Jones JM, Grant AE, Zolov SN, Winters JJ, Giger RJ, Dowling JJ, Weisman LS, Meisler MH. Pathogenic mechanism of the FIG4 mutation responsible for Charcot-Marie-Tooth disease CMT4J. Plos Genetics. 7: e1002104. PMID 21655088 DOI: 10.1371/Journal.Pgen.1002104 |
0.512 |
|
2010 |
Ferguson CJ, Lenk GM, Meisler MH. PtdIns(3,5)P2 and autophagy in mouse models of neurodegeneration. Autophagy. 6: 170-1. PMID 20009544 DOI: 10.4161/Auto.6.1.10626 |
0.511 |
|
2009 |
Ferguson CJ, Lenk GM, Meisler MH. Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2. Human Molecular Genetics. 18: 4868-78. PMID 19793721 DOI: 10.1093/Hmg/Ddp460 |
0.557 |
|
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