Michael S. Kobor mainly investigates Genetics, DNA methylation, Molecular biology, Epigenetics and CpG site. His Genetics research incorporates elements of Life expectancy, Mortality rate, Incidence and Hispanic paradox. His DNA methylation research is under the purview of Gene.
His research in Molecular biology intersects with topics in Cell biology, RNA polymerase II, X-inactivation, Transcription factor II D and RNA polymerase II holoenzyme. Michael S. Kobor combines subjects such as Developmental psychology, Epigenesis, Pediatrics and C-reactive protein with his study of Epigenetics. In his work, Concordance, Whole blood and Computational biology is strongly intertwined with Methylation, which is a subfield of CpG site.
His primary areas of investigation include DNA methylation, Epigenetics, Genetics, Methylation and Gene. His DNA methylation study combines topics from a wide range of disciplines, such as Internal medicine, Computational biology and Immunology. Michael S. Kobor has researched Epigenetics in several fields, including Gene expression, Bioinformatics, Epigenomics, Human genetics and Epigenome.
His work in Genetics addresses issues such as Cell biology, which are connected to fields such as Molecular biology. His biological study spans a wide range of topics, including Whole blood and Differentially methylated regions. Michael S. Kobor usually deals with Saccharomyces cerevisiae and limits it to topics linked to Transcription factor and RNA polymerase II and Transcription.
Michael S. Kobor mainly focuses on DNA methylation, Epigenetics, Gene, CpG site and dNaM. DNA methylation is a subfield of Genetics that he explores. His Epigenetics research is multidisciplinary, relying on both Methylation, Clinical psychology, Physiology, Cohort and Epigenome.
His Gene research is multidisciplinary, incorporating elements of DNA and Cell biology. His research investigates the connection with dNaM and areas like Bioinformatics which intersect with concerns in Gestational age. As part of one scientific family, Michael S. Kobor deals mainly with the area of Genome, narrowing it down to issues related to the Socioeconomic status, and often Young adult.
Michael S. Kobor spends much of his time researching DNA methylation, Epigenetics, CpG site, Gene and dNaM. His DNA methylation research integrates issues from Oncology, Genome, Internal medicine, Socioeconomic status and Computational biology. Michael S. Kobor interconnects Methylation, Young adult, Biomarker, Physiology and Cohort in the investigation of issues within Epigenetics.
The CpG site study combines topics in areas such as Database normalization, Normalization, Multivariate statistics and Linear regression. Gene is a subfield of Genetics that he studies. His work on Whole genome sequencing, Untranslated region and Allele as part of general Genetics study is frequently linked to Glutaminase, bridging the gap between disciplines.
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Low early-life social class leaves a biological residue manifested by decreased glucocorticoid and increased proinflammatory signaling
Gregory E. Miller;Edith Chen;Alexandra K. Fok;Hope Walker.
Proceedings of the National Academy of Sciences of the United States of America (2009)
A Protein Complex Containing the Conserved Swi2/Snf2-Related ATPase Swr1p Deposits Histone Variant H2A.Z into Euchromatin
Michael. S Kobor;Shivkumar Venkatasubrahmanyam;Marc D Meneghini;Jennifer W Gin.
PLOS Biology (2004)
RNA polymerase II elongation factors of Saccharomyces cerevisiae: a targeted proteomics approach.
Nevan J. Krogan;Minkyu Kim;Seong Hoon Ahn;Guoqing Zhong.
Molecular and Cellular Biology (2002)
Opposing effects of Ctk1 kinase and Fcp1 phosphatase at Ser 2 of the RNA polymerase II C-terminal domain
Eun-Jung Cho;Michael S. Kobor;Minkyu Kim;Jack Greenblatt.
Genes & Development (2001)
DNA methylation and healthy human aging
Meaghan J. Jones;Sarah J. Goodman;Michael S. Kobor.
Aging Cell (2015)
Epigenetic Vestiges of Early Developmental Adversity: Childhood Stress Exposure and DNA Methylation in Adolescence.
Marilyn J. Essex;W. Thomas Boyce;Clyde Hertzman;Lucia L. Lam.
Child Development (2013)
Additional annotation enhances potential for biologically-relevant analysis of the Illumina Infinium HumanMethylation450 BeadChip array
E Magda Price;E Magda Price;Allison M Cotton;Lucia L Lam;Pau Farré.
Epigenetics & Chromatin (2013)
Factors underlying variable DNA methylation in a human community cohort
Lucia L. Lam;Eldon Emberly;Hunter B. Fraser;Sarah M. Neumann.
Proceedings of the National Academy of Sciences of the United States of America (2012)
Social stress up-regulates inflammatory gene expression in the leukocyte transcriptome via β-adrenergic induction of myelopoiesis
Nicole D Powell;Erica Kate Sloan;Michael T Bailey;Jesusa Mg Arevalo.
Proceedings of the National Academy of Sciences of the United States of America (2013)
An epigenetic clock analysis of race/ethnicity, sex, and coronary heart disease
Steve Horvath;Michael Gurven;Morgan E. Levine;Benjamin C. Trumble.
Genome Biology (2016)
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