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0034655131
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WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3–24.1, a region frequently affected in breast cancer
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Characterizing WW domain interactions of tumor suppressor WWOX reveals its association with multiprotein networks
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WWOX at the crossroads of cancer, metabolic syndrome related traits and CNS pathologies
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Aldaz CM,Ferguson BW,Abba MC.WWOX at the crossroads of cancer, metabolic syndrome related traits and CNS pathologies.Biochim Biophys Acta. 2014;1846:188-200
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WW domain-containing oxidoreductase’s role in myriad cancers: clinical significance and future implications
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Gardenswartz A,Aqeilan RI.WW domain-containing oxidoreductase’s role in myriad cancers: clinical significance and future implications.Exp Biol Med. 2014;239:253-63
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Gene mapping and expression analysis of 16q loss of heterozygosity identifies WWOX and CYLD as being important in determining clinical outcome in mulitiple myeloma
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Jenner MW,Leone PE,Walker BA,Ross FM,Johnson DC,Gonzalez D,Chiecchio L,Dachs Cabanas E,Dagrada GP,Nightingale M,Protheroe RK,Stockley D,Else M,Dickens NJ,Cross NC,Davies FE,Morgan GJ.Gene mapping and expression analysis of 16q loss of heterozygosity identifies WWOX and CYLD as being important in determining clinical outcome in mulitiple myeloma.Blood. 2007;110:3291-300
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Common chromosomal fragile site gene WWOX in metabolic disorders and tumors
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The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation
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Mallaret M,Synofzik M,Lee J,Sagum CA,Mahajnah M,Sharkia R,Drouot N,Renaud M,Klein FA,Anheim M,Tranchant C,Mignot C,Mandel JL,Bedford M,Bauer P,Salih MA,Schüle R,Schöls L,Aldaz CM,Koenig M.The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.Brain. 2014;137:411-9
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The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration
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Abdel-Salam G,Thoenes M,Afifi HH,Korber F,Swan D,Bolz HJ.The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration.Orphanet J Rare Dis. 2014;9:12-12
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Expression of WW domain-containing oxidoreductase WOX1 in the developing murine nervous system
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Chen ST,Chuang JI,Wang JP,Tsai MS,Li H,Chang NS.Expression of WW domain-containing oxidoreductase WOX1 in the developing murine nervous system.Neuroscience. 2004;124:831-9
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Signaling from membrane receptors to tumor suppressor WW domain-containing oxidoreductase
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Chang JY,He RY,Lin HP,Hsu LJ,Lai FJ,Hong Q,Chen SJ,Chang NS.Signaling from membrane receptors to tumor suppressor WW domain-containing oxidoreductase.Exp Biol Med. 2010;235:796-804
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A spontaneous mutation of the Wwox gene and audiogenic seizures in rats with lethal dwarfism and epilepsy
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Hyaluronidase induction of a WW domain containing oxidoreductase that enhances tumor necrosis factor cytotoxicity
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Chang NS,Pratt N,Heath J,Schiltz L,Sleve D,Carey GB,Zevotek N.Hyaluronidase induction of a WW domain containing oxidoreductase that enhances tumor necrosis factor cytotoxicity.J Biol Chem. 2001;276:3361-70
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WWOX-mediated apopotosis in A549 cells mainly involves the mitochondrial pathway
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Zhang P,Jia R,Ying L,Liu B,Qian G,Fan X,Ge S.WWOX-mediated apopotosis in A549 cells mainly involves the mitochondrial pathway.Mol Med Rep. 2012;6:121-4
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WW domain-containing oxidoreductase promotes neuronal differentiation via negative regulation of glycogen synthase kinase 3ß
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Wang HY,Juo LI,Lin YT,Hsiao M,Lin JT,Tsai CH,Tzeng YH,Chuang YC,Chang NS,Yang CN,Lu PJ.WW domain-containing oxidoreductase promotes neuronal differentiation via negative regulation of glycogen synthase kinase 3ß.Cell Death Differ. 2012;19:1049-59
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MPP+− induced neuronal death in rats involves tyrosine 33 phosphorylation of WW domain-containing oxidoreductase WOX1
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Lo CP,Hsu LJ,Li MY,Hsu SY,Chuang JI,Tsai MS,Lin SR,Chang NS,Chen ST.MPP+− induced neuronal death in rats involves tyrosine 33 phosphorylation of WW domain-containing oxidoreductase WOX1.Eur J Neurosci. 2008;27:1634-46
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