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Volumn 11, Issue 5, 2016, Pages

Genome-wide DNA methylation analysis and epigenetic variations associated with Congenital Aortic Valve Stenosis (AVS)

Author keywords

[No Author keywords available]

Indexed keywords

LOW DENSITY LIPOPROTEIN RECEPTOR;

EID: 84968911245     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0154010     Document Type: Article
Times cited : (43)

References (51)
  • 1
    • 84868466125 scopus 로고    scopus 로고
    • Prevalence, timing of diagnosis and mortality of newborns with congenital heart defects: A population-based study
    • PMID: 22888161
    • Khoshnood B, Lelong N, Houyel L, Thieulin AC, Jouannic JM, Magnier S, et al. Prevalence, timing of diagnosis and mortality of newborns with congenital heart defects: a population-based study. Heart. 2012; 98(22):1667-73. doi: 10.1136/heartjnl-2012-302543 PMID: 22888161.
    • (2012) Heart , vol.98 , Issue.22 , pp. 1667-1673
    • Khoshnood, B.1    Lelong, N.2    Houyel, L.3    Thieulin, A.C.4    Jouannic, J.M.5    Magnier, S.6
  • 2
    • 56049102822 scopus 로고    scopus 로고
    • Prevalence of congenital heart defects in metropolitan Atlanta, 1998-2005
    • PMID: 18657826; PubMed Central PMCID: PMC2613036
    • Reller MD, Strickland MJ, Riehle-Colarusso T, Mahle WT, Correa A. Prevalence of congenital heart defects in metropolitan Atlanta, 1998-2005. The Journal of pediatrics. 2008; 153(6):807-13. doi: 10.1016/j.jpeds.2008.05.059 PMID: 18657826; PubMed Central PMCID: PMC2613036.
    • (2008) The Journal of Pediatrics , vol.153 , Issue.6 , pp. 807-813
    • Reller, M.D.1    Strickland, M.J.2    Riehle-Colarusso, T.3    Mahle, W.T.4    Correa, A.5
  • 3
    • 0034444407 scopus 로고    scopus 로고
    • Epidemiology of cardiovascular malformations: Prevalence and risk factors
    • PMID: 11376444
    • Loffredo CA. Epidemiology of cardiovascular malformations: prevalence and risk factors. American journal of medical genetics. 2000; 97(4):319-25. PMID: 11376444.
    • (2000) American Journal of Medical Genetics , vol.97 , Issue.4 , pp. 319-325
    • Loffredo, C.A.1
  • 4
    • 14044262240 scopus 로고    scopus 로고
    • Frequency by decades of unicuspid, bicuspid, and tricuspid aortic valves in adults having isolated aortic valve replacement for aortic stenosis, with or without associated aortic regurgitation
    • PMID: 15710758
    • Roberts WC, Ko JM. Frequency by decades of unicuspid, bicuspid, and tricuspid aortic valves in adults having isolated aortic valve replacement for aortic stenosis, with or without associated aortic regurgitation. Circulation. 2005; 111(7):920-5. doi: 10.1161/01.CIR.0000155623.48408.C5 PMID: 15710758.
    • (2005) Circulation , vol.111 , Issue.7 , pp. 920-925
    • Roberts, W.C.1    Ko, J.M.2
  • 5
    • 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: Endorsed by the American Academy of Pediatrics
    • PMID: 17519398
    • Pierpont ME, Basson CT, Benson DW Jr., Gelb BD, Giglia TM, Goldmuntz E, et al. 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. 2007; 115(23):3015-38. doi: 10.1161/CIRCULATIONAHA.106.183056 PMID: 17519398.
    • (2007) Circulation , vol.115 , Issue.23 , pp. 3015-3038
    • Pierpont, M.E.1    Basson, C.T.2    Benson, D.W.3    Gelb, B.D.4    Giglia, T.M.5    Goldmuntz, E.6
  • 6
    • 0031022393 scopus 로고    scopus 로고
    • Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis
    • PMID: 9002679
    • Sheffield VC, Pierpont ME, Nishimura D, Beck JS, Burns TL, Berg MA, et al. Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis. Human molecular genetics. 1997; 6(1):117-21. PMID: 9002679.
    • (1997) Human Molecular Genetics , vol.6 , Issue.1 , pp. 117-121
    • Sheffield, V.C.1    Pierpont, M.E.2    Nishimura, D.3    Beck, J.S.4    Burns, T.L.5    Berg, M.A.6
  • 7
    • 77956313143 scopus 로고    scopus 로고
    • Consanguinity mapping of congenital heart disease in a South Indian population
    • PMID: 20422016; PubMed Central PMCID: PMC2858208
    • McGregor TL, Misri A, Bartlett J, Orabona G, Friedman RD, Sexton D, et al. Consanguinity mapping of congenital heart disease in a South Indian population. PloS one. 2010; 5(4):e10286. doi: 10.1371/journal.pone.0010286 PMID: 20422016; PubMed Central PMCID: PMC2858208.
    • (2010) PloS One , vol.5 , Issue.4
    • McGregor, T.L.1    Misri, A.2    Bartlett, J.3    Orabona, G.4    Friedman, R.D.5    Sexton, D.6
  • 8
    • 0014515851 scopus 로고
    • Possible X-linked congenital heart disease
    • PMID: 5787314
    • Monteleone PL, Fagan LF. Possible X-linked congenital heart disease. Circulation. 1969; 39(5):611-4. PMID: 5787314.
    • (1969) Circulation , vol.39 , Issue.5 , pp. 611-614
    • Monteleone, P.L.1    Fagan, L.F.2
  • 10
    • 84885383754 scopus 로고    scopus 로고
    • Nongenetic risk factors and congenital heart defects
    • PMID: 23963188
    • Patel SS, Burns TL. Nongenetic risk factors and congenital heart defects. Pediatric cardiology. 2013; 34(7):1535-55. doi: 10.1007/s00246-013-0775-4 PMID: 23963188.
    • (2013) Pediatric Cardiology , vol.34 , Issue.7 , pp. 1535-1555
    • Patel, S.S.1    Burns, T.L.2
  • 11
    • 33644853792 scopus 로고    scopus 로고
    • Familial aggregation of calcific aortic valve stenosis in the western part of France
    • PMID: 16461814
    • Probst V, Le Scouarnec S, Legendre A, Jousseaume V, Jaafar P, Nguyen JM, et al. Familial aggregation of calcific aortic valve stenosis in the western part of France. Circulation. 2006; 113(6):856-60. doi: 10.1161/CIRCULATIONAHA.105.569467 PMID: 16461814.
    • (2006) Circulation , vol.113 , Issue.6 , pp. 856-860
    • Probst, V.1    Le Scouarnec, S.2    Legendre, A.3    Jousseaume, V.4    Jaafar, P.5    Nguyen, J.M.6
  • 12
    • 12744280946 scopus 로고    scopus 로고
    • Heterogeneous geographic distribution of patients with aortic valve stenosis: Arguments for new aetiological hypothesis
    • PMID: 15657257; PubMed Central PMCID: PMC1768671
    • Le Gal G, Bertault V, Bezon E, Cornily JC, Barra JA, Blanc JJ. Heterogeneous geographic distribution of patients with aortic valve stenosis: arguments for new aetiological hypothesis. Heart. 2005; 91(2):247-9. doi: 10.1136/hrt.2004.037093 PMID: 15657257; PubMed Central PMCID: PMC1768671.
    • (2005) Heart , vol.91 , Issue.2 , pp. 247-249
    • Le Gal, G.1    Bertault, V.2    Bezon, E.3    Cornily, J.C.4    Barra, J.A.5    Blanc, J.J.6
  • 14
    • 23944467475 scopus 로고    scopus 로고
    • Epidemiology of noncomplex left ventricular outflow tract obstruction malformations (aortic valve stenosis, coarctation of the aorta, hypoplastic left heart syndrome) in Texas, 1999-2001
    • PMID: 16007587; PubMed Central PMCID: PMC1361303
    • McBride KL, Marengo L, Canfield M, Langlois P, Fixler D, Belmont JW. Epidemiology of noncomplex left ventricular outflow tract obstruction malformations (aortic valve stenosis, coarctation of the aorta, hypoplastic left heart syndrome) in Texas, 1999-2001. Birth defects research Part A, Clinical and molecular teratology. 2005; 73(8):555-61. doi: 10.1002/bdra.20169 PMID: 16007587; PubMed Central PMCID: PMC1361303.
    • (2005) Birth Defects Research Part A, Clinical and Molecular Teratology , vol.73 , Issue.8 , pp. 555-561
    • McBride, K.L.1    Marengo, L.2    Canfield, M.3    Langlois, P.4    Fixler, D.5    Belmont, J.W.6
  • 15
    • 84893701427 scopus 로고    scopus 로고
    • Risk factors in the origin of congenital left-ventricular outflow-tract obstruction defects of the heart: A population-based case-control study
    • PMID: 23843102
    • Csaky-Szunyogh M, Vereczkey A, Kosa Z, Gerencser B, Czeizel AE. Risk factors in the origin of congenital left-ventricular outflow-tract obstruction defects of the heart: a population-based case-control study. Pediatric cardiology. 2014; 35(1):108-20. doi: 10.1007/s00246-013-0749-6 PMID: 23843102.
    • (2014) Pediatric Cardiology , vol.35 , Issue.1 , pp. 108-120
    • Csaky-Szunyogh, M.1    Vereczkey, A.2    Kosa, Z.3    Gerencser, B.4    Czeizel, A.E.5
  • 16
    • 0004130447 scopus 로고    scopus 로고
    • A practical guide to fetal echocardiography
    • Second edition 2010: LippincottWilliams and Wilkins Philadelphia, PA
    • Abuhamad A, Chaoui RC. A practical guide to fetal echocardiography. Normal and abnormal hearts. Second edition 2010: LippincottWilliams and Wilkins Philadelphia, PA. 2010.
    • (2010) Normal and Abnormal Hearts
    • Abuhamad, A.1    Chaoui, R.C.2
  • 17
    • 84968709306 scopus 로고    scopus 로고
    • Elevated hsa-miR-99a levels in maternal plasma may indicate congenital heart defects
    • PMID: 26623032; PubMed Central PMCID: PMC4660590
    • Kehler L, Biro O, Lazar L, Rigo J Jr., Nagy B. Elevated hsa-miR-99a levels in maternal plasma may indicate congenital heart defects. Biomed Rep. 2015; 3(6):869-73. doi: 10.3892/br.2015.510 PMID: 26623032; PubMed Central PMCID: PMC4660590.
    • (2015) Biomed Rep. , vol.3 , Issue.6 , pp. 869-873
    • Kehler, L.1    Biro, O.2    Lazar, L.3    Rigo, J.4    Nagy, B.5
  • 18
    • 10044224512 scopus 로고    scopus 로고
    • Hungarian cohort-controlled trial of periconceptional multivitamin supplementation shows a reduction in certain congenital abnormalities
    • PMID: 15523663
    • Czeizel AE, Dobo M, Vargha P. Hungarian cohort-controlled trial of periconceptional multivitamin supplementation shows a reduction in certain congenital abnormalities. Birth defects research Part A, Clinical and molecular teratology. 2004; 70(11):853-61. doi: 10.1002/bdra.20086 PMID: 15523663.
    • (2004) Birth Defects Research Part A, Clinical and Molecular Teratology , vol.70 , Issue.11 , pp. 853-861
    • Czeizel, A.E.1    Dobo, M.2    Vargha, P.3
  • 22
    • 84886943157 scopus 로고    scopus 로고
    • Newborn screening for congenital heart defects: A systematic review and cost-effectiveness analysis
    • PMID: 16297355
    • Knowles R, Griebsch I, Dezateux C, Brown J, Bull C, Wren C. Newborn screening for congenital heart defects: a systematic review and cost-effectiveness analysis. Health technology assessment. 2005; 9(44):1-152, iii-iv. PMID: 16297355.
    • (2005) Health Technology Assessment , vol.9 , Issue.44
    • Knowles, R.1    Griebsch, I.2    Dezateux, C.3    Brown, J.4    Bull, C.5    Wren, C.6
  • 23
    • 84874940399 scopus 로고    scopus 로고
    • The use of DNA from archival dried blood spots with the Infinium HumanMethylation450 array
    • PMID: 23497093; PubMed Central PMCID: PMC3610215
    • Joo JE, Wong EM, Baglietto L, Jung CH, Tsimiklis H, Park DJ, et al. The use of DNA from archival dried blood spots with the Infinium HumanMethylation450 array. BMC Biotechnol. 2013; 13:23. doi: 10.1186/1472-6750-13-23 PMID: 23497093; PubMed Central PMCID: PMC3610215.
    • (2013) BMC Biotechnol , vol.13 , pp. 23
    • Joo, J.E.1    Wong, E.M.2    Baglietto, L.3    Jung, C.H.4    Tsimiklis, H.5    Park, D.J.6
  • 24
    • 55949107158 scopus 로고    scopus 로고
    • Archived Guthrie blood spots as a novel source for quantitative DNA methylation analysis
    • 8 passim PMID: 18855769
    • Wong N, Morley R, Saffery R, Craig J. Archived Guthrie blood spots as a novel source for quantitative DNA methylation analysis. Biotechniques. 2008; 45(4):423-4, 6, 8 passim. doi: 10.2144/000112945 PMID: 18855769.
    • (2008) Biotechniques , vol.45 , Issue.4
    • Wong, N.1    Morley, R.2    Saffery, R.3    Craig, J.4
  • 25
    • 84896327297 scopus 로고    scopus 로고
    • Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes
    • PMID: 24501229; PubMed Central PMCID: PMC3963529
    • Docherty LE, Rezwan FI, Poole RL, Jagoe H, Lake H, Lockett GA, et al. Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes. Journal of medical genetics. 2014; 51(4):229-38. doi: 10.1136/jmedgenet-2013-102116 PMID: 24501229; PubMed Central PMCID: PMC3963529.
    • (2014) Journal of Medical Genetics , vol.51 , Issue.4 , pp. 229-238
    • Docherty, L.E.1    Rezwan, F.I.2    Poole, R.L.3    Jagoe, H.4    Lake, H.5    Lockett, G.A.6
  • 26
    • 84867159872 scopus 로고    scopus 로고
    • Measuring the methylome in clinical samples: Improved processing of the Infinium Human Methylation450 BeadChip Array
    • PMID: 22964528; PubMed Central PMCID: PMC3469459
    • Pan H, Chen L, Dogra S, Teh AL, Tan JH, Lim YI, et al. Measuring the methylome in clinical samples: improved processing of the Infinium Human Methylation450 BeadChip Array. Epigenetics: official journal of the DNA Methylation Society. 2012; 7(10):1173-87. doi: 10.4161/epi.22102 PMID: 22964528; PubMed Central PMCID: PMC3469459.
    • (2012) Epigenetics: Official Journal of the DNA Methylation Society , vol.7 , Issue.10 , pp. 1173-1187
    • Pan, H.1    Chen, L.2    Dogra, S.3    Teh, A.L.4    Tan, J.H.5    Lim, Y.I.6
  • 27
    • 84873576566 scopus 로고    scopus 로고
    • Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis
    • PMID: 23334450; PubMed Central PMCID: PMCPMC3598632
    • Liu Y, Aryee MJ, Padyukov L, Fallin MD, Hesselberg E, Runarsson A, et al. Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis. Nat Biotechnol. 2013; 31(2):142-7. doi: 10.1038/nbt.2487 PMID: 23334450; PubMed Central PMCID: PMCPMC3598632.
    • (2013) Nat Biotechnol. , vol.31 , Issue.2 , pp. 142-147
    • Liu, Y.1    Aryee, M.J.2    Padyukov, L.3    Fallin, M.D.4    Hesselberg, E.5    Runarsson, A.6
  • 28
    • 84874353239 scopus 로고    scopus 로고
    • Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray
    • PMID: 23314698; PubMed Central PMCID: PMCPMC3592906
    • Chen YA, Lemire M, Choufani S, Butcher DT, Grafodatskaya D, Zanke BW, et al. Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray. Epigenetics. 2013; 8(2):203-9. doi: 10.4161/epi.23470 PMID: 23314698; PubMed Central PMCID: PMCPMC3592906.
    • (2013) Epigenetics , vol.8 , Issue.2 , pp. 203-209
    • Chen, Y.A.1    Lemire, M.2    Choufani, S.3    Butcher, D.T.4    Grafodatskaya, D.5    Zanke, B.W.6
  • 29
    • 84884592505 scopus 로고    scopus 로고
    • Review of processing and analysis methods for DNA methylation array data
    • PMID: 23982603; PubMed Central PMCID: PMC3777004
    • Wilhelm-Benartzi CS, Koestler DC, Karagas MR, Flanagan JM, Christensen BC, Kelsey KT, et al. Review of processing and analysis methods for DNA methylation array data. Br J Cancer. 2013; 109(6):1394-402. doi: 10.1038/bjc.2013.496 PMID: 23982603; PubMed Central PMCID: PMC3777004.
    • (2013) Br J Cancer , vol.109 , Issue.6 , pp. 1394-1402
    • Wilhelm-Benartzi, C.S.1    Koestler, D.C.2    Karagas, M.R.3    Flanagan, J.M.4    Christensen, B.C.5    Kelsey, K.T.6
  • 30
    • 84961168013 scopus 로고    scopus 로고
    • Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: Implications for comparative population studies
    • PMID: 26607064; PubMed Central PMCID: PMC4659175
    • Daca-Roszak P, Pfeifer A, Zebracka-Gala J, Rusinek D, Szybinska A, Jarzab B, et al. Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: implications for comparative population studies. BMC Genomics. 2015; 16(1):1003. doi: 10.1186/s12864-015-2202-0 PMID: 26607064; PubMed Central PMCID: PMC4659175.
    • (2015) BMC Genomics , vol.16 , Issue.1 , pp. 1003
    • Daca-Roszak, P.1    Pfeifer, A.2    Zebracka-Gala, J.3    Rusinek, D.4    Szybinska, A.5    Jarzab, B.6
  • 31
    • 84966342666 scopus 로고    scopus 로고
    • ComplexHeatmap: Making Complex Heatmaps
    • Gu. Z. ComplexHeatmap: Making Complex Heatmaps. R package version 1.6.0. https://githubcom/jokergoo/ComplexHeatmap.2015.
    • (2015) R Package Version 1.6.0
    • Gu, Z.1
  • 32
    • 84940368260 scopus 로고    scopus 로고
    • Genome-wide DNA methylation analysis in dermal fibroblasts from patients with diffuse and limited systemic sclerosis reveals common and subset-specific DNA methylation aberrancies
    • PMID: 24812288
    • Altorok N, Tsou PS, Coit P, Khanna D, Sawalha AH. Genome-wide DNA methylation analysis in dermal fibroblasts from patients with diffuse and limited systemic sclerosis reveals common and subset-specific DNA methylation aberrancies. Annals of the rheumatic diseases. 2014. doi: 10.1136/annrheumdis-2014-205303 PMID: 24812288.
    • (2014) Annals of the Rheumatic Diseases
    • Altorok, N.1    Tsou, P.S.2    Coit, P.3    Khanna, D.4    Sawalha, A.H.5
  • 33
    • 0001677717 scopus 로고
    • Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
    • Benjamini Y, Hochberg Y. Controlling the False Discovery Rate: a Practical and Powerful Approach to Multiple Testing. J R Statist Soc B. 1995; 57:289-300.
    • (1995) J R Statist Soc B , vol.57 , pp. 289-300
    • Benjamini, Y.1    Hochberg, Y.2
  • 34
    • 61449172037 scopus 로고    scopus 로고
    • Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
    • PMID: 19131956
    • Huang da W, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nature protocols. 2009; 4(1):44-57. doi: 10.1038/nprot.2008.211 PMID: 19131956.
    • (2009) Nature Protocols , vol.4 , Issue.1 , pp. 44-57
    • Huang Da, W.1    Sherman, B.T.2    Lempicki, R.A.3
  • 35
    • 58549112996 scopus 로고    scopus 로고
    • Bioinformatics enrichment tools: Paths toward the comprehensive functional analysis of large gene lists
    • PMID: 19033363; PubMed Central PMCID: PMC2615629
    • Huang da W, Sherman BT, Lempicki RA. Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists. Nucleic acids research. 2009; 37(1):1-13. doi: 10.1093/nar/gkn923 PMID: 19033363; PubMed Central PMCID: PMC2615629.
    • (2009) Nucleic Acids Research , vol.37 , Issue.1 , pp. 1-13
    • Huang Da, W.1    Sherman, B.T.2    Lempicki, R.A.3
  • 36
    • 84893160260 scopus 로고    scopus 로고
    • Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot
    • PMID: 24479926; PubMed Central PMCID: PMC3915623
    • Sheng W, Qian Y, Zhang P, Wu Y, Wang H, Ma X, et al. Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot. Journal of translational medicine. 2014; 12:31. doi: 10.1186/1479-5876-12-31 PMID: 24479926; PubMed Central PMCID: PMC3915623.
    • (2014) Journal of Translational Medicine , vol.12 , pp. 31
    • Sheng, W.1    Qian, Y.2    Zhang, P.3    Wu, Y.4    Wang, H.5    Ma, X.6
  • 37
    • 4444261091 scopus 로고    scopus 로고
    • Familial hypercholesterolemia, peripheral arterial disease, and stroke: A HuGE minireview
    • PMID: 15321839
    • Hutter CM, Austin MA, Humphries SE. Familial hypercholesterolemia, peripheral arterial disease, and stroke: a HuGE minireview. Am J Epidemiol. 2004; 160(5):430-5. doi: 10.1093/aje/kwh238 PMID: 15321839.
    • (2004) Am J Epidemiol. , vol.160 , Issue.5 , pp. 430-435
    • Hutter, C.M.1    Austin, M.A.2    Humphries, S.E.3
  • 38
    • 4444328790 scopus 로고    scopus 로고
    • Familial hypercholesterolemia and coronary heart disease: A HuGE association review
    • PMID: 15321838
    • Austin MA, Hutter CM, Zimmern RL, Humphries SE. Familial hypercholesterolemia and coronary heart disease: a HuGE association review. Am J Epidemiol. 2004; 160(5):421-9. doi: 10.1093/aje/kwh237 PMID: 15321838.
    • (2004) Am J Epidemiol. , vol.160 , Issue.5 , pp. 421-429
    • Austin, M.A.1    Hutter, C.M.2    Zimmern, R.L.3    Humphries, S.E.4
  • 39
    • 61349121385 scopus 로고    scopus 로고
    • Hypercholesterolemia association with aortic stenosis of various etiologies
    • PMID: 19267822
    • Rabus MB, Kayalar N, Sareyyupoglu B, Erkin A, Kirali K, Yakut C. Hypercholesterolemia association with aortic stenosis of various etiologies. J Card Surg. 2009; 24(2):146-50. doi: 10.1111/j.1540-8191.2009.00814.x PMID: 19267822.
    • (2009) J Card Surg. , vol.24 , Issue.2 , pp. 146-150
    • Rabus, M.B.1    Kayalar, N.2    Sareyyupoglu, B.3    Erkin, A.4    Kirali, K.5    Yakut, C.6
  • 40
    • 0035158955 scopus 로고    scopus 로고
    • Association between calcific aortic stenosis and hypercholesterolemia: Is there a need for a randomized controlled trial of cholesterol-lowering therapy?
    • PMID: 11195607
    • Chui MC, Newby DE, Panarelli M, Bloomfield P, Boon NA. Association between calcific aortic stenosis and hypercholesterolemia: is there a need for a randomized controlled trial of cholesterol-lowering therapy? Clin Cardiol. 2001; 24(1):52-5. PMID: 11195607.
    • (2001) Clin Cardiol. , vol.24 , Issue.1 , pp. 52-55
    • Chui, M.C.1    Newby, D.E.2    Panarelli, M.3    Bloomfield, P.4    Boon, N.A.5
  • 41
    • 84968713606 scopus 로고    scopus 로고
    • Functional analysis of Dusp27, a novel target gene of the JAK1/STAT1 pathway
    • Thesis (PhD) - Hong Kong University of Science and Technology
    • Li Y. Functional analysis of Dusp27, a novel target gene of the JAK1/STAT1 pathway, in myogenesis. Thesis (PhD) - Hong Kong University of Science and Technology,. 2011.
    • (2011) Myogenesis
    • Li, Y.1
  • 42
    • 84860788246 scopus 로고    scopus 로고
    • Exome analysis of a family with pleiotropic congenital heart disease
    • PMID: 22337856; PubMed Central PMCID: PMC3329568
    • Arrington CB, Bleyl SB, Matsunami N, Bonnell GD, Otterud BE, Nielsen DC, et al. Exome analysis of a family with pleiotropic congenital heart disease. Circ Cardiovasc Genet. 2012; 5(2):175-82. doi: 10.1161/CIRCGENETICS.111.961797 PMID: 22337856; PubMed Central PMCID: PMC3329568.
    • (2012) Circ Cardiovasc Genet. , vol.5 , Issue.2 , pp. 175-182
    • Arrington, C.B.1    Bleyl, S.B.2    Matsunami, N.3    Bonnell, G.D.4    Otterud, B.E.5    Nielsen, D.C.6
  • 43
    • 84895032730 scopus 로고    scopus 로고
    • Evaluation of links between high-density lipoprotein genetics, functionality, and aortic valve stenosis risk in humans
    • PMID: 24334872
    • Arsenault BJ, Dube MP, Brodeur MR, de Oliveira Moraes AB, Lavoie V, Kernaleguen AE, et al. Evaluation of links between high-density lipoprotein genetics, functionality, and aortic valve stenosis risk in humans. Arterioscler Thromb Vasc Biol. 2014; 34(2):457-62. doi: 10.1161/ATVBAHA.113.302730 PMID: 24334872.
    • (2014) Arterioscler Thromb Vasc Biol. , vol.34 , Issue.2 , pp. 457-462
    • Arsenault, B.J.1    Dube, M.P.2    Brodeur, M.R.3    De Oliveira Moraes, A.B.4    Lavoie, V.5    Kernaleguen, A.E.6
  • 44
    • 3943083323 scopus 로고    scopus 로고
    • Association of APOA5 gene single nucleotide polymorphism with levels of lipids and coronary heart disease in Chinese
    • PMID: 15300628
    • Liu HK, Wang CT, Zhang SZ, Xiao CY, Li XF, Zhang KL, et al. [Association of APOA5 gene single nucleotide polymorphism with levels of lipids and coronary heart disease in Chinese]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004; 21(4):335-8. PMID: 15300628.
    • (2004) Zhonghua Yi Xue Yi Chuan Xue Za Zhi , vol.21 , Issue.4 , pp. 335-338
    • Liu, H.K.1    Wang, C.T.2    Zhang, S.Z.3    Xiao, C.Y.4    Li, X.F.5    Zhang, K.L.6
  • 45
    • 55149083476 scopus 로고    scopus 로고
    • APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia
    • PMID: 18779834
    • Wang J, Ban MR, Kennedy BA, Anand S, Yusuf S, Huff MW, et al. APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia. Nat Clin Pract Cardiovasc Med. 2008; 5(11):730-7. doi: 10.1038/ncpcardio1326 PMID: 18779834.
    • (2008) Nat Clin Pract Cardiovasc Med. , vol.5 , Issue.11 , pp. 730-737
    • Wang, J.1    Ban, M.R.2    Kennedy, B.A.3    Anand, S.4    Yusuf, S.5    Huff, M.W.6
  • 46
    • 33645103550 scopus 로고    scopus 로고
    • Sequence variations in PCSK9, low LDL, and protection against coronary heart disease
    • PMID: 16554528
    • Cohen JC, Boerwinkle E, Mosley TH Jr., Hobbs HH. Sequence variations in PCSK9, low LDL, and protection against coronary heart disease. N Engl J Med. 2006; 354(12):1264-72. doi: 10.1056/ NEJMoa054013 PMID: 16554528.
    • (2006) N Engl J Med. , vol.354 , Issue.12 , pp. 1264-1272
    • Cohen, J.C.1    Boerwinkle, E.2    Mosley, T.H.3    Hobbs, H.H.4
  • 47
    • 79959497037 scopus 로고    scopus 로고
    • Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene
    • PMID: 21626672
    • Click ES, Cox B, Olson SB, Grompe M, Akkari Y, Moreau LA, et al. Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene. Am J Med Genet A. 2011; 155A(7):1673-9. doi: 10.1002/ajmg.a.34024 PMID: 21626672.
    • (2011) Am J Med Genet A , vol.155 A , Issue.7 , pp. 1673-1679
    • Click, E.S.1    Cox, B.2    Olson, S.B.3    Grompe, M.4    Akkari, Y.5    Moreau, L.A.6
  • 48
    • 73949139581 scopus 로고    scopus 로고
    • Detailed molecular and clinical characterization of three patients with 21q deletions
    • PMID: 19863549
    • Lindstrand A, Malmgren H, Sahlen S, Schoumans J, Nordgren A, Ergander U, et al. Detailed molecular and clinical characterization of three patients with 21q deletions. Clin Genet. 2010; 77(2):145-54. doi: 10.1111/j.1399-0004.2009.01289.x PMID: 19863549.
    • (2010) Clin Genet. , vol.77 , Issue.2 , pp. 145-154
    • Lindstrand, A.1    Malmgren, H.2    Sahlen, S.3    Schoumans, J.4    Nordgren, A.5    Ergander, U.6
  • 49
    • 6344277918 scopus 로고    scopus 로고
    • Essential role for mitochondrial thioredoxin reductase in hematopoiesis, heart development, and heart function
    • PMID: 15485910; PubMed Central PMCID: PMC522221
    • Conrad M, Jakupoglu C, Moreno SG, Lippl S, Banjac A, Schneider M, et al. Essential role for mitochondrial thioredoxin reductase in hematopoiesis, heart development, and heart function. Mol Cell Biol. 2004; 24(21):9414-23. doi: 10.1128/MCB.24.21.9414-9423.2004 PMID: 15485910; PubMed Central PMCID: PMC522221.
    • (2004) Mol Cell Biol. , vol.24 , Issue.21 , pp. 9414-9423
    • Conrad, M.1    Jakupoglu, C.2    Moreno, S.G.3    Lippl, S.4    Banjac, A.5    Schneider, M.6
  • 50
    • 0035514706 scopus 로고    scopus 로고
    • Chromosomal microdeletions: Dissecting del22q11 syndrome
    • PMID: 11715041
    • Lindsay EA. Chromosomal microdeletions: dissecting del22q11 syndrome. Nat Rev Genet. 2001; 2(11):858-68. doi: 10.1038/35098574 PMID: 11715041.
    • (2001) Nat Rev Genet. , vol.2 , Issue.11 , pp. 858-868
    • Lindsay, E.A.1
  • 51
    • 84894337731 scopus 로고    scopus 로고
    • Helicase-like transcription factor (Hltf) regulates G2/M transition, Wt1/Gata4/Hif-1a cardiac transcription networks, and collagen biogenesis
    • PMID: 24278285; PubMed Central PMCID: PMC3835564
    • Helmer RA, Martinez-Zaguilan R, Dertien JS, Fulford C, Foreman O, Peiris V, et al. Helicase-like transcription factor (Hltf) regulates G2/M transition, Wt1/Gata4/Hif-1a cardiac transcription networks, and collagen biogenesis. PLoS One. 2013; 8(11):e80461. doi: 10.1371/journal.pone.0080461 PMID: 24278285; PubMed Central PMCID: PMC3835564.
    • (2013) PLoS One , vol.8 , Issue.11
    • Helmer, R.A.1    Martinez-Zaguilan, R.2    Dertien, J.S.3    Fulford, C.4    Foreman, O.5    Peiris, V.6


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