CRELD1基因在汉族完全型房室间隔缺损患儿心肌组织表达情况的初步分析(4)
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[16]Maslen CL,Babcock D,Robinson SW,et al.CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defect in down syndrome[J].Am J Med Genet A,2006,140(22):2501-2505.
[17]Zatyka M,Priestley M,Ladusans EJ,et al.Analysis of CRELD1 as a candidate 3p25 atrioventicular septal defect locus (AVSD2)[J].Clin Genet,2005,67(6):526-528.
[18]Sarkozy A,Esposito G,Conti E,et al.CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects[J].Am J Med Genet A,2005,139(3):236-238.
[19]Posch MG,Perrot A,Schmitt K,et al.Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects [J].Am J Med Genet A,2008,146A(2):251-253.
[20]Lincoln J, Alfieri CM, Yutzey KE.BMP and FGF regulatory pathways control cell lineage diversification of heart valve precursor cells [J].Dev Biol,2006,292(2):292-302.
[21]Iwamoto R,Mekada E.ErbB and HB-EGF signaling in heart development and function[J].Cell Struct Funct,2006,31(1):1-14.
[22]Yoshioka K,Matsuda F,Takakura K,et al.Determination of genes involved in the process of implantation:Application of Gene Chip to scan 6500 genes[J].Biochem Biophys Res,2000,272(2):531-538.
[23]Patel ZM,Gawde HM,Khatkhatay MI.22q11 microdeletion studies in the heart tissue of an abortus involving a familial form of congenital heart disease[J].J Clin Lab Anal,2006,20(4):160-163.
[24]Miertus J,Amoroso A.Microarray-based genetics of cardiac malformations[J].Ital Heart J,2001,2(8):565-567.
[25]Kaynak B,von Heydebreck A,Mebus S.Genome-wide array analysis of normal and malformed human hearts[J].Circulation,2003,107:2467.
[26]Sharma HS,Peters TH,Moorhouse MJ.DNA microarray analysis for human congenital heart disease[J].Cell Biochem Biophys,2006,44(1):1-9.
[16]Maslen CL,Babcock D,Robinson SW,et al.CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defect in down syndrome[J].Am J Med Genet A,2006,140(22):2501-2505.
[17]Zatyka M,Priestley M,Ladusans EJ,et al.Analysis of CRELD1 as a candidate 3p25 atrioventicular septal defect locus (AVSD2)[J].Clin Genet,2005,67(6):526-528.
[18]Sarkozy A,Esposito G,Conti E,et al.CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects[J].Am J Med Genet A,2005,139(3):236-238.
[19]Posch MG,Perrot A,Schmitt K,et al.Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects [J].Am J Med Genet A,2008,146A(2):251-253.
[20]Lincoln J, Alfieri CM, Yutzey KE.BMP and FGF regulatory pathways control cell lineage diversification of heart valve precursor cells [J].Dev Biol,2006,292(2):292-302.
[21]Iwamoto R,Mekada E.ErbB and HB-EGF signaling in heart development and function[J].Cell Struct Funct,2006,31(1):1-14.
[22]Yoshioka K,Matsuda F,Takakura K,et al.Determination of genes involved in the process of implantation:Application of Gene Chip to scan 6500 genes[J].Biochem Biophys Res,2000,272(2):531-538.
[23]Patel ZM,Gawde HM,Khatkhatay MI.22q11 microdeletion studies in the heart tissue of an abortus involving a familial form of congenital heart disease[J].J Clin Lab Anal,2006,20(4):160-163.
[24]Miertus J,Amoroso A.Microarray-based genetics of cardiac malformations[J].Ital Heart J,2001,2(8):565-567.
[25]Kaynak B,von Heydebreck A,Mebus S.Genome-wide array analysis of normal and malformed human hearts[J].Circulation,2003,107:2467.
[26]Sharma HS,Peters TH,Moorhouse MJ.DNA microarray analysis for human congenital heart disease[J].Cell Biochem Biophys,2006,44(1):1-9.
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