Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood.
暂无分享,去创建一个
Dvir Aran | Michael Rosenberg | Benjamin Glaser | B. Glaser | Y. Friedlander | D. Aran | J. Kark | E. Levy-Lahad | A. Hellman | Jeremy D Kark | Julio Wainstein | Ephrat Levy-Lahad | Yechiel Friedlander | G. Toperoff | Michael Rosenberg | Tatyana Dubnikov | Batel Nissan | J. Wainstein | Asaf Hellman | Gidon Toperoff | Tatyana Dubnikov | Batel Nissan | Dvir Aran | Gidon Toperoff
[1] F. Watt,et al. Cytosine methylation prevents binding to DNA of a HeLa cell transcription factor required for optimal expression of the adenovirus major late promoter. , 1988, Genes & development.
[2] Ayellet V. Segrè,et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis , 2010, Nature Genetics.
[3] Ian M. Morison,et al. Integrated Genetic and Epigenetic Analysis Identifies Haplotype-Specific Methylation in the FTO Type 2 Diabetes and Obesity Susceptibility Locus , 2010, PloS one.
[4] A. Chess,et al. Extensive sequence-influenced DNA methylation polymorphism in the human genome , 2010, Epigenetics & Chromatin.
[5] D. Aran,et al. Replication timing-related and gene body-specific methylation of active human genes. , 2011, Human molecular genetics.
[6] I. Weissman,et al. Pioneer factor interactions and unmethylated CpG dinucleotides mark silent tissue-specific enhancers in embryonic stem cells , 2007, Proceedings of the National Academy of Sciences.
[7] H. Cedar,et al. Linking DNA methylation and histone modification: patterns and paradigms , 2009, Nature Reviews Genetics.
[8] E. Flemington,et al. CpG methylation as a mechanism for the regulation of E2F activity. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[9] D. Balding,et al. Epigenome-wide association studies for common human diseases , 2011, Nature Reviews Genetics.
[10] R. T. Lie,et al. FTO, Type 2 Diabetes, and Weight Gain Throughout Adult Life , 2011, Diabetes.
[11] B. Tycko,et al. Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation , 2008, Nature Genetics.
[12] T. Mikkelsen,et al. Genome-wide maps of chromatin state in pluripotent and lineage-committed cells , 2007, Nature.
[13] R. Plomin,et al. Allelic skewing of DNA methylation is widespread across the genome. , 2010, American journal of human genetics.
[14] C. Gieger,et al. Variants of the PPARG, IGF2BP2, CDKAL1, HHEX, and TCF7L2 Genes Confer Risk of Type 2 Diabetes Independently of BMI in the German KORA Studies , 2008, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.
[15] R. Plomin,et al. DNA methylation profiling using bisulfite-based epityping of pooled genomic DNA. , 2010, Methods.
[16] D. Siscovick,et al. Birth weight of offspring, maternal pre-pregnancy characteristics, and mortality of mothers: the Jerusalem perinatal study cohort. , 2009, Annals of epidemiology.
[17] Madeleine P. Ball,et al. Corrigendum: Targeted and genome-scale strategies reveal gene-body methylation signatures in human cells , 2009, Nature Biotechnology.
[18] M. Jarvelin,et al. A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity , 2007, Science.
[19] Mark I McCarthy,et al. Type 2 diabetes: new genes, new understanding. , 2008, Trends in genetics : TIG.
[20] Ugo Boggi,et al. Apoptotic, regenerative, and immune-related signaling in human islets from type 2 diabetes individuals. , 2009, Journal of proteome research.
[21] R. Plomin,et al. Bisulfite-based epityping on pooled genomic DNA provides an accurate estimate of average group DNA methylation , 2009, Epigenetics & Chromatin.
[22] Andrew P Feinberg,et al. An integrated epigenetic and genetic approach to common human disease. , 2004, Trends in genetics : TIG.
[23] D. Altshuler,et al. A map of human genome variation from population-scale sequencing , 2010, Nature.
[24] G. Prendergast,et al. Methylation-sensitive sequence-specific DNA binding by the c-Myc basic region. , 1991, Science.
[25] A. Verhoeven,et al. Glucose increases hepatic lipase expression in HepG2 liver cells through upregulation of upstream stimulatory factors 1 and 2 , 2008, Diabetologia.
[26] M. Bonke,et al. Chromatin "Prepattern" and Histone Modifiers in a Fate Choice for Liver and Pancreas , 2011 .
[27] G. Luc,et al. Taq1B CETP polymorphism, plasma CETP, lipoproteins, apolipoproteins and sex differences in a Jewish population sample characterized by low HDL-cholesterol. , 2000, Atherosclerosis.
[28] M. Esteller,et al. Epigenetic modifications and human disease , 2010, Nature Biotechnology.
[29] Mark I. McCarthy,et al. Assessing the Combined Impact of 18 Common Genetic Variants of Modest Effect Sizes on Type 2 Diabetes Risk , 2008, Diabetes.
[30] Albert Jeltsch,et al. BISMA - Fast and accurate bisulfite sequencing data analysis of individual clones from unique and repetitive sequences , 2010, BMC Bioinformatics.
[31] A. Mortazavi,et al. Genome-Wide Mapping of in Vivo Protein-DNA Interactions , 2007, Science.
[32] Daniel F. Gudbjartsson,et al. Parental origin of sequence variants associated with complex diseases , 2009, Nature.
[33] Arturas Petronis,et al. Epigenetics as a unifying principle in the aetiology of complex traits and diseases , 2010, Nature.
[34] Hei Sook Sul,et al. A Role of DNA-PK for the Metabolic Gene Regulation in Response to Insulin , 2009, Cell.
[35] Holger Karas,et al. TRANSFAC: a database on transcription factors and their DNA binding sites , 1996, Nucleic Acids Res..
[36] S. Vaulont,et al. Differential Roles of Upstream Stimulatory Factors 1 and 2 in the Transcriptional Response of Liver Genes to Glucose* , 1998, The Journal of Biological Chemistry.
[37] Zhaohui S. Qin,et al. A second generation human haplotype map of over 3.1 million SNPs , 2007, Nature.
[38] J. Bressler,et al. Risk of Type 2 Diabetes and Obesity Is Differentially Associated with Variation in FTO in Whites and African-Americans in the ARIC Study , 2010, PloS one.
[39] J. Eeckhoute,et al. Epigenetic switch involved in activation of pioneer factor FOXA1-dependent enhancers. , 2011, Genome research.
[40] P. Jacques,et al. Plasma Homocysteine and Parental Myocardial Infarction in Young Adults in Jerusalem , 2002, Circulation.
[41] Jonathan Schug,et al. The Nucleosome Map of the Mammalian Liver , 2011, Nature Structural &Molecular Biology.
[42] Lee E. Edsall,et al. Human DNA methylomes at base resolution show widespread epigenomic differences , 2009, Nature.
[43] Ina Ruck,et al. USA , 1969, The Lancet.
[44] John D. Storey,et al. Statistical significance for genomewide studies , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[45] A. Chess,et al. Gene Body-Specific Methylation on the Active X Chromosome , 2007, Science.
[46] Y. Benjamini,et al. Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .