Citations for
1CMT1C, LITAF
Phenotypic spectrum of Charcot-Marie-Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patients.
Guimarães-Costa R, Iancu Ferfoglia R, Leonard-Louis S, Ziegler F, Magy L, Fournier E, Dubourg O, Bouche P, Maisonobe T, Lacour A, Moerman A, Latour P, Stojkovic T.
Eur J Neurol 24(3):530-538. doi: 10.1111/ene.13239. 2017
2CDIP1, LITAF
The Charcot Marie Tooth disease protein LITAF is a zinc-binding monotopic membrane protein.
Qin W, Wunderley L, Barrett AL, High S, Woodman PG.
Biochem J 473(21):3965-3978. Epub 2016 Aug 31. 2016
3CMT1C, LITAF
Dysregulated Inflammatory Signaling upon Charcot-Marie-Tooth Type 1C Mutation of SIMPLE Protein.
Li W, Zhu H, Zhao X, Brancho D, Liang Y, Zou Y, Bennett C, Chow CW.
Mol Cell Biol 35(14):2464-78. 2015
4CHST11, LITAF, ROR2, RREB1, SPATA5, TWIST1
Genome-wide Twist1 occupancy in endocardial cushion cells, embryonic limb buds, and peripheral nerve sheath tumor cells.
Lee MP, Ratner N, Yutzey KE.
BMC Genomics 15:821. doi: 10.1186/1471-2164-15-821. 2014
5CMT1C, LITAF
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease.
Ciotti P, Luigetti M, Geroldi A, Capponi S, Pezzini I, Gulli R, Pazzaglia C, Padua L, Massa R, Mandich P, Bellone E.
J Neurol Sci 343(1-2):183-6. doi: 10.1016/j.jns.2014.05.029. Epub 2014 May 22. 2014
6CMT1C, LITAF
LITAF mutations associated with Charcot-Marie-Tooth disease 1C show mislocalization from the late endosome/lysosome to the mitochondria.
Lacerda AF, Hartjes E, Brunetti CR.
PLoS One 9(7):e103454. doi: 10.1371/journal.pone.0103454. eCollection 2014. 2014
7BCL6, LITAF
LITAF, a BCL6 target gene, regulates autophagy in mature B-cell lymphomas.
Bertolo C, Roa S, Sagardoy A, Mena-Varas M, Robles EF, Martinez-Ferrandis JI, Sagaert X, Tousseyn T, Orta A, Lossos IS, Amar S, Natkunam Y, Briones J, Melnick A, Malumbres R, Martinez-Climent JA.
Br J Haematol 162(5):621-30. doi: 10.1111/bjh.12440. Epub 2013 Jun 25. 2013
8CMT1C, LITAF
Mutation of SIMPLE in Charcot-Marie-Tooth 1C alters production of exosomes.
Zhu H, Guariglia S, Yu RY, Li W, Brancho D, Peinado H, Lyden D, Salzer J, Bennett C, Chow CW.
Mol Biol Cell 24(11):1619-37, S1-3. doi: 10.1091/mbc.E12-07-0544. Epub 2013 Apr 10. 2013
9CMT1C, HGS, LITAF, STAM, TSG101
Charcot-Marie-Tooth disease-linked protein SIMPLE functions with the ESCRT machinery in endosomal trafficking.
Lee SM, Chin LS, Li L.
J Cell Biol 199(5):799-816. doi: 10.1083/jcb.201204137. Epub 2012 Nov 19. 2012
10LITAF
LITAF (SIMPLE) regulates Wallerian degeneration after injury but is not essential for peripheral nerve development and maintenance: implications for Charcot-Marie-Tooth disease.
Somandin C, Gerber D, Pereira JA, Horn M, Suter U.
Glia 60(10):1518-28. doi: 10.1002/glia.22371. Epub 2012 Jun 21. 2012
11LITAF, STAT6
Novel regulation of CCL2 gene expression by murine LITAF and STAT6B.
Tang X, Yang Y, Amar S.
PLoS One 6(9):e25083. Epub 2011 Sep 28. 2011
12LITAF
LITAF mediation of increased TNF-α secretion from inflamed colonic lamina propria macrophages.
Bushell KN, Leeman SE, Gillespie E, Gower AC, Reed KL, Stucchi AF, Becker JM, Amar S.
PLoS One 6(9):e25849. Epub 2011 Sep 30. 2011
13ITCH, LITAF
SIMPLE/LITAF expression induces the translocation of the ubiquitin ligase itch towards the lysosomal compartments.
Eaton HE, Desrochers G, Drory SB, Metcalf J, Angers A, Brunetti CR.
PLoS One 6(2):e16873. 2011
14LITAF, TNFSF15
LITAF and TNFSF15, two downstream targets of AMPK, exert inhibitory effects on tumor growth.
Zhou J, Yang Z, Tsuji T, Gong J, Xie J, Chen C, Li W, Amar S, Luo Z.
Oncogene 30(16):1892-900. Epub 2011 Jan 10. 2011
15CMT1C, LITAF
Mutations associated with Charcot-Marie-Tooth disease cause SIMPLE protein mislocalization and degradation by the proteasome and aggresome-autophagy pathways.
Lee SM, Olzmann JA, Chin LS, Li L.
J Cell Sci 124(Pt 19):3319-31. doi: 10.1242/jcs.087114. Epub 2011 Sep 6. 2011
16CMT1C, LITAF
Clinical characterization and genetic analysis of a possible novel type of dominant Charcot-Marie-Tooth disease.
Lee YC, Lee TC, Lin KP, Lin MW, Chang MH, Soong BW.
Neuromuscul Disord 20(8):534-9. 2010
17GJB1, CMTX1, LITAF, CMT1C
Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE.
Beauvais K, Furby A, Latour P.
Neuromuscul Disord 16(1):14-8. Epub 2005 Dec 20. 2006
18CMT1C, LITAF
Mutation frequency for Charcot-Marie-Tooth disease type 1 in the Chinese population is similar to that in the global ethnic patients.
Song S, Zhang Y, Chen B, Zhang Y, Wang M, Wang Y, Yan M, Zou J, Huang Y, Zhong N.
Genet Med 8(8):532-5. 2006
19LITAF, CMT1C
SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutations.
Latour P, Gonnaud PM, Ollagnon E, Chan V, Perelman S, Stojkovic T, Stoll C, Vial C, Ziegler F, Vandenberghe A, Maire I.
J Peripher Nerv Syst 11(2):148-55. 2006
20CMT1C, LITAF
SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation.
Saifi GM, Szigeti K, Wiszniewski W, Shy ME, Krajewski K, Hausmanowa-Petrusewicz I, Kochanski A, Reeser S, Mancias P, Butler I, Lupski JR.
Hum Mutat 25(4):372-83. 2005
21LITAF, PMP22, CMT1A, CMT1C, CMT1E
Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease.
Meggouh F, de Visser M, Arts WF, De Coo RI, van Schaik IN, Baas F.
Ann Neurol 57(4):589-91. 2005
22CMT1C, LITAF
Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C.
Street VA, Bennett CL, Goldy JD, Shirk AJ, Kleopa KA, Tempel BL, Lipe HP, Scherer SS, Bird TD, Chance PF.
Neurology 60(1):22-6. 2003
23LITAF, TNF
Identification and functional characterization of a novel binding site on TNF-alpha promoter.
Tang X, Fenton MJ, Amar S.
Proc Natl Acad Sci U S A 100(7):4096-101. Epub 2003 Mar 24. 2003