about
Genetic and epigenetic regulation of intestinal fibrosisEpigenetic Editing: On the Verge of Reprogramming Gene Expression at WillGenome-wide methylation analysis of a large population sample shows neurological pathways involvement in chronic widespread musculoskeletal pain.Genetic Loci and Novel Discrimination Measures Associated with Blood Pressure Variation in African Americans Living in Tallahassee.Early hypermethylation of hepatic Igfbp2 results in its reduced expression preceding fatty liver in mice.Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.DNA methylation-based variation between human populations.When chromatin organisation floats astray: the Srcap gene and Floating-Harbor syndrome.Single-cell genome-wide studies give new insight into nongenetic cell-to-cell variability in animals.Genotypic Context and Epistasis in Individuals and Populations.Towards DNA methylation detection using biosensors.Nutrients and the microenvironment to feed a T cell army.Immune disease-associated variants in gene enhancers point to BET epigenetic mechanisms for therapeutic intervention.The resolution of ambiguity as the basis for life: A cellular bridge between Western reductionism and Eastern holism.Review article: next-generation transformative advances in the pathogenesis and management of autoimmune hepatitis.Epigenetics in the Primary Biliary Cholangitis and Primary Sclerosing Cholangitis.Epigenetic Regulation of the Protein Translation Machinery.The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseasesThe Future of CRISPR Applications in the Lab, the Clinic and Society.Genetic and epigenetic epidemiology of chronic widespread pain.Early-life adversity and long-term neurobehavioral outcomes: epigenome as a bridge?Hypomethylation of CYP2E1 and DUSP22 promoters associated with disease activity and erosive disease among rheumatoid arthritis patients.Grandmaternal smoking increases asthma risk in grandchildren: A nationwide Swedish cohort.Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes.Type 1 diabetes genome-wide association studies: not to be lost in translation.Cartilage repair by mesenchymal stem cells: Clinical trial update and perspectives.SNP-Based Heritability Estimates of Common and Specific Variance in Self- and Informant-Reported Neuroticism Scales.BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues.Gestational exposure to chlordecone promotes transgenerational changes in the murine reproductive system of males.Disentangling associations between DNA methylation and blood lipids: a Mendelian randomization approachEpigenetics, heritability and longitudinal analysis
P2860
Q26740553-DD1EB0C2-A633-4C1E-A7D2-9F35090FFE9AQ28080188-E6783944-2762-4514-AE82-CB3E0BA9CC04Q33669877-824F53B0-CCCF-4B16-9E42-0C79B05A8C41Q36230385-7D118ECA-CED8-4730-9D4F-9C9A468E3187Q37530239-9E224A68-48F6-4B58-96B3-1E6680AFD272Q38797075-AB8A9AAA-444E-41D8-9488-61323E7532EAQ38798399-86AA8F74-486A-4F8B-BE12-09FF6FC38A18Q38840545-4D067E7E-23D6-4335-9545-9C0C36BED6FBQ38895607-E2DBD654-4C4D-4AB3-9603-8FCD96A917DBQ38897737-B4A28D18-557F-4BB0-8E4A-4507058A72C1Q38972400-37DB8841-6538-4FBB-8D0F-B9F7984B894AQ38974085-E4608677-09A5-4578-ADDD-38701096BFBFQ39031414-43BBCD67-0C0C-496C-8EE3-1C10B54F1595Q39458071-6C2FD454-FBDE-4331-88D2-0832585ABB16Q40044046-3B78818B-0D12-41F0-81E4-433D8EAE0BA2Q41361892-BD305580-0C51-4BDA-87A1-16878A93D7C2Q41813295-628DC533-C2E3-40D7-8AE6-7FB40E66913DQ42280727-F94E4FF6-45DF-4836-AED9-CA115172FBB2Q46262974-FAD0BACC-A12A-49B3-AAF0-6AB84C20C2CEQ47126487-363C49B0-3FE6-4B7E-B49B-64206233C05FQ47138080-C80B68DD-213A-4768-998B-66E01563D1F7Q47183251-F62A44CD-1A78-4620-AED5-F2302E74F686Q47682027-F25ABA58-EEF2-4944-AF02-73867AE47766Q48370906-1036CB4D-42DB-49D0-9D08-5AFE2CDD351EQ49200841-57477014-623E-4155-AE23-4D62023F71CCQ52584243-AE209F0C-0BD6-47A1-AE96-061E9A28EB83Q52776796-8AC9F65B-1BB9-428B-BB7B-ABC1531F061CQ55105895-891A1AC7-B1AD-4568-ACD5-A059E6D0567EQ55710805-C382BE72-F62A-476E-9CC0-C8E0D4F11288Q57074250-6B301716-B83F-48EA-B69D-E08CC43954D0Q57156070-9C484B52-6776-44C9-A612-E1D835D9B17C
P2860
description
2015 nî lūn-bûn
@nan
2015 թուականին հրատարակուած գիտական յօդուած
@hyw
2015 թվականին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Epigenetic inheritance and the missing heritability
@ast
Epigenetic inheritance and the missing heritability
@en
Epigenetic inheritance and the missing heritability
@nl
type
label
Epigenetic inheritance and the missing heritability
@ast
Epigenetic inheritance and the missing heritability
@en
Epigenetic inheritance and the missing heritability
@nl
prefLabel
Epigenetic inheritance and the missing heritability
@ast
Epigenetic inheritance and the missing heritability
@en
Epigenetic inheritance and the missing heritability
@nl
P2860
P50
P3181
P1433
P1476
Epigenetic inheritance and the missing heritability
@en
P2093
Valeria Relli
P2860
P2888
P3181
P356
10.1186/S40246-015-0041-3
P407
P577
2015-01-01T00:00:00Z
2015-07-28T00:00:00Z
P5875
P6179
1028262096