| 1 | CFC1
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| Cripto-1 modulates macrophage cytokine secretion and phagocytic activity via NF-κB signaling.
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| Zhang DM, Bao YL, Yu CL, Wang YM, Song ZB.
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| Immunol Res 64(1):104-14.
2016
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| 2 | CFC1, HTX2
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| Duplication and deletion of CFC1 associated with heterotaxy syndrome.
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| Cao R, Long F, Wang L, Xu Y, Guo Y, Li F, Chen S, Sun K, Xu R.
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| DNA Cell Biol 34(2):101-6. doi: 10.1089/dna.2014.2616.
2015
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| 3 | CFC1, GDF1, NODAL
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| Nodal·Gdf1 heterodimers with bound prodomains enable serum-independent nodal signaling and endoderm differentiation.
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| Fuerer C, Nostro MC, Constam DB.
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| J Biol Chem 289(25):17854-71. doi: 10.1074/jbc.M114.550301.
2014
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| 4 | CFC1
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| CFC1 mutations in Chinese children with congenital heart disease.
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| Wang B, Wang J, Liu S, Han X, Xie X, Tao Y, Yan J, Ma X.
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| Int J Cardiol 146(1):86-8. doi: 10.1016/j.ijcard.2009.07.034.
2011
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| 5 | CFC1, TDGF1
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| Functional redundancy of EGF-CFC genes in epiblast and extraembryonic patterning during early mouse embryogenesis.
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| Chu J, Shen MM.
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| Dev Biol 342(1):63-73. doi: 10.1016/j.ydbio.2010.03.009.
2010
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| 6 | CFC1, CSX, DORV
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| Double outlet right ventricle: aetiologies and associations.
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| Obler D, Juraszek AL, Smoot LB, Natowicz MR.
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| J Med Genet 45(8):481-97. Epub 2008 May 2. Review. 2008
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| 7 | CFC1
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| Characterization of the glycosylphosphatidylinositol-anchor signal sequence of human Cryptic with a hydrophilic extension.
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| Watanabe K, Nagaoka T, Strizzi L, Mancino M, Gonzales M, Bianco C, Salomon DS.
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| Biochim Biophys Acta 1778(12):2671-81. doi: 10.1016/j.bbamem.2008.09.011.
2008
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| 8 | CFC1
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| CFC1 gene involvement in biliary atresia with polysplenia syndrome.
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| Davit-Spraul A, Baussan C, Hermeziu B, Bernard O, Jacquemin E.
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| J Pediatr Gastroenterol Nutr 46(1):111-2.
2008
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| 9 | CFC1, HSPA5, TDGF1
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| GRP78 and Cripto form a complex at the cell surface and collaborate to inhibit transforming growth factor beta signaling and enhance cell growth.
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| Shani G, Fischer WH, Justice NJ, Kelber JA, Vale W, Gray PC.
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| Mol Cell Biol 28(2):666-77.
2008
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| 10 | CFC1
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| Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart disease.
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| Ozcelik C, Bit-Avragim N, Panek A, Gaio U, Geier C, Lange PE, Dietz R, Posch MG, Perrot A, Stiller B.
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| Pediatr Cardiol 27(6):695-8.
2006
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| 11 | CFC1, NS1, COSTS
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| Exclusion of PTPN11 mutations in Costello syndrome: further evidence for distinct genetic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes.
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| Tartaglia M, Cotter PD, Zampino G, Gelb BD, Rauen KA.
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| Clin Genet 63(5):423-6. 2003
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| 12 | CFC1, DORV
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| CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle.
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| Goldmuntz E, Bamford R, Karkera JD, dela Cruz J, Roessler E, Muenke M.
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| Am J Hum Genet 70(3):776-80. 2002
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| 13 | CFC1, HTX2
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| Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects.
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| Bamford RN, Roessler E, Burdine RD, Saplakoglu U, dela Cruz J, Splitt M, Towbin J, Bowers P, Marino B, Schier AF, Shen MM, Muenke M, Casey B.
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| Nat Genet 26(3):365-9. 2000
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| 14 | CFC1
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| The EGF-CFC gene family in vertebrate development.
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| Shen MM, Schier AF.
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| Trends Genet 16(7):303-9. Review. 2000
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| 15 | CFC1
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| Neurologic and gastrointestinal dysfunction in cardio-facio-cutaneous syndrome: identification of a severe phenotype.
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| Grebe TA, Clericuzio C.
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| Am J Med Genet 95(2):135-43. 2000
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| 16 | CFC1
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| A differential display strategy identifies Cryptic, a novel EGF-related gene expressed in the axial and lateral mesoderm during mouse gastrulation.
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| Shen MM, Wang H, Leder P.
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| Development 124(2):429-42. 1997
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