| 1 | WNT10A
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| WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness.
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| Cuellar-Partida G, Springelkamp H, Lucas SE, Yazar S, Hewitt AW, Iglesias AI, Montgomery GW, Martin NG, Pennell CE, van Leeuwen EM, Verhoeven VJ, Hofman A, Uitterlinden AG, Ramdas WD, Wolfs RC, Vingerling JR, Brown MA, Mills RA, Craig JE, Klaver CC, van Duijn CM, Burdon KP, MacGregor S, Mackey DA.
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| Hum Mol Genet 24(17):5060-8. doi: 10.1093/hmg/ddv211. Epub 2015 Jun 5.
2015
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| 2 | WNT10A
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| WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma.
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| Long A, Giroux V, Whelan KA, Hamilton KE, Tétreault MP, Tanaka K, Lee JS, Klein-Szanto AJ, Nakagawa H, Rustgi AK.
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| Carcinogenesis 36(5):598-606. doi: 10.1093/carcin/bgv025. Epub 2015 Mar 20.
2015
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| 3 | STHAG4, WNT10A
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| WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.
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| Arzoo PS, Klar J, Bergendal B, Norderyd J, Dahl N.
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| Am J Med Genet A 164A(2):353-9. doi: 10.1002/ajmg.a.36243. Epub 2013 Nov 25.
2014
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| 4 | WNT10A
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| Role of WNT10A-expressing kidney fibroblasts in acute interstitial nephritis.
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| Kuma A, Yamada S, Wang KY, Kitamura N, Yamaguchi T, Iwai Y, Izumi H, Tamura M, Otsuji Y, Kohno K.
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| PLoS One 9(7):e103240. doi: 10.1371/journal.pone.0103240. eCollection 2014.
2014
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| 5 | STHAG4, WNT10A
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| A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
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| Abdalla EM, Mostowska A, Jagodziński PP, Dwidar K, Ismail SR.
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| Arch Oral Biol 59(7):722-8. doi: 10.1016/j.archoralbio.2014.04.004. Epub 2014 Apr 19.
2014
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| 6 | STHAG4, WNT10A
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| WNT10A variants are associated with non-syndromic tooth agenesis in the general population.
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| Song S, Zhao R, He H, Zhang J, Feng H, Lin L.
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| Hum Genet 133(1):117-24. doi: 10.1007/s00439-013-1360-x. Epub 2013 Sep 17.
2014
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| 7 | WNT10A
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| Down-regulation of Wnt10a affects odontogenesis and proliferation in mesenchymal cells.
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| Liu Y, Han D, Wang L, Feng H.
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| Biochem Biophys Res Commun 434(4):717-21. doi: 10.1016/j.bbrc.2013.03.088. Epub 2013 Apr 18.
2013
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| 8 | STHAG4, WNT10A
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| Mutations in WNT10A are present in more than half of isolated hypodontia cases.
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| van den Boogaard MJ, Créton M, Bronkhorst Y, van der Hout A, Hennekam E, Lindhout D, Cune M, Ploos van Amstel HK.
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| J Med Genet 49(5):327-31. doi: 10.1136/jmedgenet-2012-100750.
2012
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| 9 | WNT10A, WNT10B, WNT6
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| Wnt6, Wnt10a and Wnt10b inhibit adipogenesis and stimulate osteoblastogenesis through a β-catenin-dependent mechanism.
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| Cawthorn WP, Bree AJ, Yao Y, Du B, Hemati N, Martinez-Santibañez G, MacDougald OA.
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| Bone 50(2):477-89. doi: 10.1016/j.bone.2011.08.010. Epub 2011 Aug 18.
2012
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| 10 | ED12, ED3, EDA, EDAR, EDARADD, HEDAD, OODD, WNT10A
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| Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.
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| Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Bal E, Chassaing N, Vincent MC, Viot G, Clauss F, Manière MC, Toupenay S, Le Merrer M, Lyonnet S, Cormier-Daire V, Amiel J, Faivre L, de Prost Y, Munnich A, Bonnefont JP, Bodemer C, Smahi A.
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| Hum Mutat 32(1):70-2. 2011
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| 11 | STHAG4, WNT10A
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| WNT10A and isolated hypodontia.
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| Kantaputra P, Sripathomsawat W.
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| Am J Med Genet A 155A(5):1119-22. doi: 10.1002/ajmg.a.33840. Epub 2011 Apr 11.
2011
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| 12 | SSPS, WNT10A
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| Intra-familial variability of ectodermal defects associated with WNT10A mutations.
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| Wedgeworth EK, Nagy N, White JM, Pembroke AC, McGrath JA.
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| Acta Derm Venereol 91(3):346-7. doi: 10.2340/00015555-1028. No abstract available.
2011
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| 13 | SSPS, WNT10A
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| WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.
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| Bohring A, Stamm T, Spaich C, Haase C, Spree K, Hehr U, Hoffmann M, Ledig S, Sel S, Wieacker P, Röpke A.
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| Am J Hum Genet 85(1):97-105. Epub 2009 Jun 25.
2009
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| 14 | OODD, WNT10A
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| WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.
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| Nawaz S, Klar J, Wajid M, Aslam M, Tariq M, Schuster J, Baig SM, Dahl N.
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| Eur J Hum Genet 17(12):1600-5. Epub 2009 May 27.PMID: 19471313 2009
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| 15 | WNT10A, OODD
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| Mutation in WNT10A Is Associated with an Autosomal Recessive Ectodermal Dysplasia: The Odonto-onycho-dermal Dysplasia.
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| Adaimy L, Chouery E, Megarbane H, Mroueh S, Delague V, Nicolas E, Belguith H, de Mazancourt P, Megarbane A.
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| Am J Hum Genet 81(4):821-8. Epub 2007 Aug 9. 2007
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| 16 | DSPP, WNT10A
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| Wnt10a regulates dentin sialophosphoprotein mRNA expression and possibly links odontoblast differentiation and tooth morphogenesis.
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| Yamashiro T, Zheng L, Shitaku Y, Saito M, Tsubakimoto T, Takada K, Takano-Yamamoto T, Thesleff I.
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| Differentiation 75(5):452-62. Epub 2007 Feb 5.
2007
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| 17 | WNT1, WNT10A, WNT10B, WNT6
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| WNT10A and WNT6, clustered in human chromosome 2q35 region with head-to-tail manner, are strongly coexpressed in SW480 cells.
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| Kirikoshi H, Sekihara H, Katoh M.
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| Biochem Biophys Res Commun 283(4):798-805. 2001
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