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Journal of Translational Medicine, ISSN 1479-5876, 01/2019, Volume 17, Issue 1, pp. 15 - 16
Journal Article
Experimental Hematology, ISSN 0301-472X, 08/2018, Volume 64, pp. S85 - S86
Journal Article
2016, Translational Epigenetics Series, ISBN 9780128004968
Web Resource
2016, Translational epigenetics series, ISBN 9780128001400, 329
Epigenomics in Health and Disease discusses the next generation sequencing technologies shaping our current knowledge with regards to the role of epigenetics... 
Epigenetics | Biology, life sciences | Developmental genetics | Embryology, Human
eBook
Aging Cell, ISSN 1474-9718, 04/2017, Volume 16, Issue 2, pp. 293 - 303
Aging is associated with a progressive loss of the CD28 costimulatory molecule in CD4 super(+) lymphocytes (CD28 super(null) T cells), which is accompanied by... 
Journal Article
Discovery medicine, ISSN 1539-6509, 2010, Volume 10, Issue 52, pp. 225 - 233
Aging is one of the most challenging and unresolved problems in biology owing to its highly complex nature. Public interest in aging has increased not only... 
Animals | Aging - genetics | Epigenesis, Genetic - genetics | Models, Biological | Humans | MEDICINE, RESEARCH & EXPERIMENTAL
Journal Article
Journal Article
Journal of Applied Physiology, ISSN 8750-7587, 03/2012, Volume 112, Issue 6, pp. 1085 - 1085
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 5/2013, Volume 70, Issue 9, pp. 1543 - 1573
Epigenetic mechanisms play an important role in gene regulation during development. DNA methylation, which is probably the most important and best-studied... 
Life Sciences | Biochemistry, general | Life Sciences, general | Disease | Epigenetics | Mutation | Biomedicine general | Cell Biology | SYSTEMIC-LUPUS-ERYTHEMATOSUS | RUBINSTEIN-TAYBI-SYNDROME | BIOCHEMISTRY & MOLECULAR BIOLOGY | S-ADENOSYLMETHIONINE SYNTHETASE | CPG-BINDING-PROTEIN | XNP/ATR-X GENE | METHIONINE ADENOSYLTRANSFERASE 1A | CELL BIOLOGY | FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY | COFFIN-LOWRY-SYNDROME | SINGLE NUCLEOTIDE POLYMORPHISM | GLYCINE N-METHYLTRANSFERASE | Coffin-Lowry Syndrome - genetics | Neoplasms - metabolism | Epigenesis, Genetic | Humans | Lupus Erythematosus, Systemic - metabolism | Muscular Dystrophy, Facioscapulohumeral - genetics | alpha-Thalassemia - metabolism | DNA Methylation | Mental Retardation, X-Linked - genetics | Rubinstein-Taybi Syndrome - genetics | Neoplasms - genetics | Sotos Syndrome - metabolism | Coffin-Lowry Syndrome - metabolism | alpha-Thalassemia - genetics | Muscular Dystrophy, Facioscapulohumeral - metabolism | Sotos Syndrome - genetics | DNA Modification Methylases - metabolism | Cockayne Syndrome - metabolism | DNA - metabolism | Rubinstein-Taybi Syndrome - metabolism | DNA - genetics | Rett Syndrome - metabolism | DNA Modification Methylases - genetics | Animals | Histones - genetics | CHARGE Syndrome - metabolism | Lupus Erythematosus, Systemic - genetics | Cockayne Syndrome - genetics | CHARGE Syndrome - genetics | Histones - metabolism | Rett Syndrome - genetics | Mental Retardation, X-Linked - metabolism | Liver cancer | Gene mutations | Genes | Transferases | Immunodeficiency | Physiological aspects | Methylation | Glycine | Mental illness | S-adenosylmethionine | CHARGE syndrome
Journal Article