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Volumn 15, Issue 7-8, 2011, Pages 483-487

A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CELL ADHESION MOLECULE; CYSTEINE; EPIDERMAL GROWTH FACTOR; PROTEIN CRELD1; UNCLASSIFIED DRUG;

EID: 79960449197     PISSN: 19450265     EISSN: 19450257     Source Type: Journal    
DOI: 10.1089/gtmb.2010.0246     Document Type: Article
Times cited : (15)

References (25)
  • 1
    • 39749191367 scopus 로고    scopus 로고
    • The developmental genetics of congenital heart disease
    • DOI 10.1038/nature06801, PII NATURE06801
    • Bruneau BG (2008) The developmental genetics of congenital heart disease. Nature 451:943-948. (Pubitemid 351301750)
    • (2008) Nature , vol.451 , Issue.7181 , pp. 943-948
    • Bruneau, B.G.1
  • 2
    • 77955984188 scopus 로고    scopus 로고
    • A novel mutation in GATA4 gene associated with dominant inherited familial atrial septal defect
    • Chen Y, Han Z, Yan W, et al. (2010) A novel mutation in GATA4 gene associated with dominant inherited familial atrial septal defect. J Thorac Cardiovasc Surg 140:684-687.
    • (2010) J Thorac Cardiovasc Surg , vol.140 , pp. 684-687
    • Chen, Y.1    Han, Z.2    Yan, W.3
  • 3
    • 79960450982 scopus 로고    scopus 로고
    • Analysis and homology modeling of proteins derived from NKX2.5 non-synonymous single nucleotide polymorphisms involved in congenital heart disease
    • Dinesh SM, Karunakar P, Amruthavalli C, et al. (2010a) Analysis and homology modeling of proteins derived from NKX2.5 non-synonymous single nucleotide polymorphisms involved in congenital heart disease. Nature Sci 8:27-38.
    • (2010) Nature Sci , vol.8 , pp. 27-38
    • Dinesh, S.M.1    Karunakar, P.2    Amruthavalli, C.3
  • 4
    • 79960454266 scopus 로고    scopus 로고
    • The most frequent c.239A>G SNP of NKX2.5 is not involved in congenital heart disease
    • Dinesh SM, Kusuma L, Ramachandra NB (2010b) The most frequent c.239A>G SNP of NKX2.5 is not involved in congenital heart disease. NY Sci J 3:43-47.
    • (2010) NY Sci J , vol.3 , pp. 43-47
    • Dinesh, S.M.1    Kusuma, L.2    Ramachandra, N.B.3
  • 6
    • 62149117229 scopus 로고    scopus 로고
    • Investigation of somatic NKX2-5 mutations in congenital heart disease
    • Draus Jr JM, Hauck MA, Goetsch M, et al. (2009) Investigation of somatic NKX2-5 mutations in congenital heart disease. J Med Genet 46:115-122.
    • (2009) J Med Genet , vol.46 , pp. 115-122
    • Draus Jr., J.M.1    Hauck, M.A.2    Goetsch, M.3
  • 9
    • 58249143935 scopus 로고    scopus 로고
    • Can recent insights into cardiac development improve our understanding of congenitally malformed hearts?
    • Horsthuis T, Christoffels VM, Anderson RH, et al. (2009) Can recent insights into cardiac development improve our understanding of congenitally malformed hearts? Clin Anat 22:4-20.
    • (2009) Clin Anat , vol.22 , pp. 4-20
    • Horsthuis, T.1    Christoffels, V.M.2    Anderson, R.H.3
  • 10
    • 42249105030 scopus 로고    scopus 로고
    • Genes in congenital heart disease: Atrioventricular valve formation
    • Joziasse IC, van de Smagt JJ, Smith K, et al. (2008) Genes in congenital heart disease: atrioventricular valve formation. Basic Res Cardiol 103:216-227.
    • (2008) Basic Res Cardiol , vol.103 , pp. 216-227
    • Joziasse, I.C.1    Van De Smagt, J.J.2    Smith, K.3
  • 11
    • 35348847064 scopus 로고    scopus 로고
    • SNP genotyping: Technologies and biomedical applications
    • DOI 10.1146/annurev.bioeng.9.060906.152037
    • Kim S, Misra A (2007) SNP genotyping: technologies and bio-medical applications. Annu Rev Biomed Eng 9:289-320. (Pubitemid 350246659)
    • (2007) Annual Review of Biomedical Engineering , vol.9 , pp. 289-320
    • Kim, S.1    Misra, A.2
  • 12
    • 64149083449 scopus 로고    scopus 로고
    • Advances in molecular genetics of congenital heart disease
    • Marín-García J (2009) Advances in molecular genetics of congenital heart disease. Rev Esp Cardiol 62:242-245.
    • (2009) Rev Esp Cardiol , vol.62 , pp. 242-245
    • Marín-García, J.1
  • 13
    • 33750594384 scopus 로고    scopus 로고
    • CRELD1 mutations contribute to the occurrence of cardiac atrioven-tricular septal defects in down syndrome
    • Maslen CL, Babcock D, Robinson SW, et al. (2006) CRELD1 mutations contribute to the occurrence of cardiac atrioven-tricular septal defects in down syndrome. Am J of Med Genet A 9999: 1-5.
    • (2006) Am J of Med Genet A , vol.9999 , pp. 1-5
    • Maslen, C.L.1    Babcock, D.2    Robinson, S.W.3
  • 14
    • 34250305402 scopus 로고    scopus 로고
    • Genetic basis for congenital heart defects: Current knowledge - A scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young
    • DOI 10.1161/CIRCULATIONAHA.106.183056, PII 0000301720070612000017
    • Pierpont ME, Basson CT, Benson DW Jr, et al. (2007) American Heart Association congenital cardiac defects committee, council on cardiovascular disease in the young. Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, council on cardiovascular disease in the young: endorsed by the American Academy of Pediatrics. Circulation 115:3015-3038. (Pubitemid 46912107)
    • (2007) Circulation , vol.115 , Issue.23 , pp. 3015-3038
    • Pierpont, M.E.1    Basson, C.T.2    Benson Jr., D.W.3    Gelb, B.D.4    Giglia, T.M.5    Goldmuntz, E.6    McGee, G.7    Sable, C.A.8    Srivastava, D.9    Webb, C.L.10
  • 15
    • 37849053289 scopus 로고    scopus 로고
    • Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects
    • Posch MG, Perrot A, Schmitt K, et al. (2008) Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects. Am J Med Genet A 146:251-253.
    • (2008) Am J Med Genet A , vol.146 , pp. 251-253
    • Posch, M.G.1    Perrot, A.2    Schmitt, K.3
  • 17
    • 7244238119 scopus 로고    scopus 로고
    • TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts
    • Reamon-Buettner SM, Borlak J (2004) TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts. Human Mut 24:104.
    • (2004) Human Mut , vol.24 , pp. 104
    • Reamon-Buettner, S.M.1    Borlak, J.2
  • 22
    • 33745140823 scopus 로고    scopus 로고
    • Prevalence of congenital heart diseases in Mysore
    • Smitha R, Karat SC, Narayanappa D, et al. (2006) Prevalence of congenital heart diseases in Mysore. Ind J Hum Genet 12: 12-17.
    • (2006) Ind J Hum Genet , vol.12 , pp. 12-17
    • Smitha, R.1    Karat, S.C.2    Narayanappa, D.3
  • 23
    • 77956291376 scopus 로고    scopus 로고
    • Common variation in ISL1 confers genetic susceptibility for human congenital heart disease
    • Stevens KN, Hakonarson H, Kim CE, et al. (2010) Common variation in ISL1 confers genetic susceptibility for human congenital heart disease. PLoS ONE 5: e10855.
    • (2010) PLoS ONE , vol.5
    • Stevens, K.N.1    Hakonarson, H.2    Kim, C.E.3
  • 24
    • 70649088948 scopus 로고    scopus 로고
    • Genetic variation in CYP27B1 is associated with congestive heart failure in patient with hypertension
    • Wilke RA, Simpson RU, Mukesh BN, et al. (2009) Genetic variation in CYP27B1 is associated with congestive heart failure in patient with hypertension. Pharmacology 10:1789-1797.
    • (2009) Pharmacology , vol.10 , pp. 1789-1797
    • Wilke, R.A.1    Simpson, R.U.2    Mukesh, B.N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.