| 1 | SH3PXD2A, SH3PXD2B
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| The role of Tks adaptor proteins in invadopodia formation, growth and metastasis of melanoma.
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| Iizuka S, Abdullah C, Buschman MD, Diaz B, Courtneidge SA.
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| Oncotarget ncotarget. 2016 Oct 27. doi: 10.18632/oncotarget.12954. [Epub ahead of print]
2016
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| 2 | FTHS, SH3PXD2B
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| The scaffold protein Tks4 is required for the differentiation of mesenchymal stromal cells (MSCs) into adipogenic and osteogenic lineages.
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| Dülk M, Kudlik G, Fekete A, Ernszt D, Kvell K, Pongrácz JE, Merő BL, Szeder B, Radnai L, Geiszt M, Csécsy DE, Kovács T, Uher F, Lányi Á, Vas V, Buday L.
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| Sci Rep 6:34280. doi: 10.1038/srep34280.
2016
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| 3 | FTHS, SH3PXD2B
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| Accumulation of the PX domain mutant Frank-ter Haar syndrome protein Tks4 in aggresomes.
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| Ádám C, Fekete A, Bőgel G, Németh Z, Tőkési N, Ovádi J, Liliom K, Pesti S, Geiszt M, Buday L.
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| Cell Commun Signal 13:33. doi: 10.1186/s12964-015-0108-8.
2015
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| 4 | FTHS, SH3PXD2B
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| Expression, purification and preliminary crystallographic studies of the C-terminal SH3 domain of human Tks4.
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| Huang Y, Qian H, Wang X, Cheng Z, Ren J, Zhao W, Xie Y.
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| Acta Crystallogr F Struct Biol Commun 70(Pt 3):343-6. doi: 10.1107/S2053230X14001952.
2014
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| 5 | FTHS, SH3PXD2B
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| Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome.
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| Wilson GR, Sunley J, Smith KR, Pope K, Bromhead CJ, Fitzpatrick E, Di Rocco M, van Steensel M, Coman DJ, Leventer RJ, Delatycki MB, Amor DJ, Bahlo M, Lockhart PJ.
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| Eur J Hum Genet 22(6):741-7. doi: 10.1038/ejhg.2013.229.
2014
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| 6 | SH3PXD2B
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| Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucoma.
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| Mao M, Solivan-Timpe F, Roos BR, Mullins RF, Oetting TA, Kwon YH, Brzeskiewicz PM, Stone EM, Alward WL, Anderson MG, Fingert JH.
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| Mol Vis 18:705-13.
2012
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| 7 | SH3PXD2A, SH3PXD2B
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| Cell migration and invasion in human disease: the Tks adaptor proteins.
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| Courtneidge SA.
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| Biochem Soc Trans 40(1):129-32. doi: 10.1042/BST20110685. Review.
2012
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| 8 | CTTN, SH3PXD2B, SRC
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| The homolog of the five SH3-domain protein (HOFI/SH3PXD2B) regulates lamellipodia formation and cell spreading.
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| Lányi Á, Baráth M, Péterfi Z, Bogel G, Orient A, Simon T, Petrovszki E, Kis-Tóth K, Sirokmány G, Rajnavölgyi É, Terhorst C, Buday L, Geiszt M.
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| PLoS One 6(8):e23653. doi: 10.1371/journal.pone.0023653.
2011
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| 9 | NOXA1, SH3PXD2A, SH3PXD2B
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| Direct interaction between Tks proteins and the N-terminal proline-rich region (PRR) of NoxA1 mediates Nox1-dependent ROS generation.
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| Gianni D, DerMardirossian C, Bokoch GM.
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| Eur J Cell Biol 90(2-3):164-71. doi: 10.1016/j.ejcb.2010.05.007.
2011
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| 10 | FTHS, SH3PXD2B
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| Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar Syndrome.
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| Iqbal Z, Cejudo-Martin P, de Brouwer A, van der Zwaag B, Ruiz-Lozano P, Scimia MC, Lindsey JD, Weinreb R, Albrecht B, Megarbane A, Alanay Y, Ben-Neriah Z, Amenduni M, Artuso R, Veltman JA, van Beusekom E, Oudakker A, Millán JL, Hennekam R, Hamel B, Courtneidge SA, van Bokhoven H.
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| Am J Hum Genet 86(2):254-61. Epub 2010 Feb 4.PMID: 20137777 2010
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| 11 | SH3PXD2B
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| The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development.
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| Mao M, Thedens DR, Chang B, Harris BS, Zheng QY, Johnson KR, Donahue LR, Anderson MG.
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| Mamm Genome 20(8):462-75. Epub 2009 Aug 8.PMID: 19669234 2009
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| 12 | SH3PXD2B
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| The novel adaptor protein Tks4 (SH3PXD2B) is required for functional podosome formation.
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| Buschman MD, Bromann PA, Cejudo-Martin P, Wen F, Pass I, Courtneidge SA.
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| Mol Biol Cell 20(5):1302-11. Epub 2009 Jan 14.PMID: 19144821 2009
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| 13 | SH3PXD2B
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| A novel gene, fad49, plays a crucial role in the immediate early stage of adipocyte differentiation via involvement in mitotic clonal expansion.
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| Hishida T, Eguchi T, Osada S, Nishizuka M, Imagawa M.
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| FEBS J 275(22):5576-88.PMID: 18959745 2008
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| 14 | ALPK3, ARHGAP21, ARHGAP28, ASH1L, BOD1L, CASKIN1, CDH6, CGN, CHD7, COG1, CPSF2, CRAMP1L, DNAH1, EBF4, EIF2AK1, EIF2AK4, FAM135A, FAM63A, FBXO41, FBXO42, FGD6, FRMD4A, G2E3, HACE1, HEATR5B, HOMEZ, IBTK, IFT80, IGSF9, JMJD1C, KCNT1, KIAA1109, KIAA1328, KIAA1377, KIAA1383, KIAA1407, KIAA1430, KIF17, KLF17, KLHDC5, KLHL11, KLHL12, KLHL13, KLHL14, KLHL15, KLHL8, KLHL9, LRP2BP, LRRC7, MARCH4, MIB1, MRTFA, N4BP2, NFIA, NUFIP2, PCDH10, PDCD6IP, PDP2, PTCHD2, RBM27, RCOR3, RGAG1, RIC1, ROBO2, RPAP1, SEMA6A, SH3PXD2B, SIPA1L2, STAMBPL1, STARD9, TSR1, TULP4, TXNDC16, UPF2, WDFY1, WDR11, WDR35, ZMYM6, ZNF391, ZNF395, ZNF398, ZNF471, ZNF687, ZNFX1
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| Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro.
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| Nagase T, Kikuno R, Ishikawa KI, Hirosawa M, Ohara O.
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| DNA Res 7(1):65-73. 2000
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