UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

A single-cell atlas of chromatin accessibility in the human genome

Cell, 2021-11, Vol.184 (24), p.5985-6001.e19

2021

Volltextzugriff (PDF)

Detection of human adaptation during the past 2000 years

Science (American Association for the Advancement of Science), 2016-11, Vol.354 (6313), p.760-764

2016

Volltextzugriff (PDF)

The miRNA profile of human pancreatic islets and beta-cells and relationship to type 2 diabetes pathogenesis

PloS one, 2013-01, Vol.8 (1), p.e55272-e55272

2013

Volltextzugriff (PDF)

The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease

PLoS genetics, 2015-04, Vol.11 (4), p.e1005165-e1005165

2015

Volltextzugriff (PDF)

Single-cell chromatin accessibility identifies pancreatic islet cell type- and state-specific regulatory programs of diabetes risk

Nature genetics, 2021-04, Vol.53 (4), p.455-466

2021

Volltextzugriff (PDF)

Leveraging type 1 diabetes human genetic and genomic data in the T1D knowledge portal

PLoS biology, 2023-08, Vol.21 (8), p.e3002233-e3002233

2023

Volltextzugriff (PDF)

Transcript Expression Data from Human Islets Links Regulatory Signals from Genome-Wide Association Studies for Type 2 Diabetes and Glycemic Traits to Their Downstream Effectors

PLoS genetics, 2015-12, Vol.11 (12), p.e1005694-e1005694

2015

Volltextzugriff (PDF)

Characterizing cis-regulatory elements using single-cell epigenomics

Nature reviews. Genetics, 2023-01, Vol.24 (1), p.21-43

2023

Volltextzugriff (PDF)

Common DNA sequence variation influences 3-dimensional conformation of the human genome

Genome Biology, 2019-11, Vol.20 (1), p.255-25, Article 255

2019

Volltextzugriff (PDF)

A map of open chromatin in human pancreatic islets

Nature genetics, 2010-03, Vol.42 (3), p.255-259

2010

Volltextzugriff (PDF)

Pancreatic islet chromatin accessibility and conformation reveals distal enhancer networks of type 2 diabetes risk

Nature communications, 2019-05, Vol.10 (1), p.2078-2078, Article 2078

2019

Volltextzugriff (PDF)

Sequence logic at enhancers governs a dual mechanism of endodermal organ fate induction by FOXA pioneer factors

Nature communications, 2021-11, Vol.12 (1), p.6636-6636, Article 6636

2021

Volltextzugriff (PDF)

Identification of a regulatory variant that binds FOXA1 and FOXA2 at the CDC123/CAMK1D type 2 diabetes GWAS locus

PLoS genetics, 2014-09, Vol.10 (9), p.e1004633

2014

Volltextzugriff (PDF)

Glucocorticoid signaling in pancreatic islets modulates gene regulatory programs and genetic risk of type 2 diabetes

PLoS genetics, 2021-05, Vol.17 (5), p.e1009531

2021

Volltextzugriff (PDF)

Mapping genetic effects on cell type-specific chromatin accessibility and annotating complex immune trait variants using single nucleus ATAC-seq in peripheral blood

PLoS genetics, 2023-06, Vol.19 (6), p.e1010759-e1010759

2023

Volltextzugriff (PDF)

Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci

eLife, 2018-02, Vol.7

2018

Volltextzugriff (PDF)

Lipid-induced epigenomic changes in human macrophages identify a coronary artery disease-associated variant that regulates PPAP2B Expression through Altered C/EBP-beta binding

PLoS genetics, 2015-04, Vol.11 (4), p.e1005061-e1005061

2015

Volltextzugriff (PDF)

Interpreting non-coding disease-associated human variants using single-cell epigenomics

Nature reviews. Genetics, 2023-08, Vol.24 (8), p.516-534

2023

Volltextzugriff (PDF)

Nutrient regulation of the islet epigenome controls adaptive insulin secretion

The Journal of clinical investigation, 2023-04, Vol.133 (8), p.1-15

2023

Volltextzugriff (PDF)

Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data

Genome medicine, 2019-03, Vol.11 (1), p.19-19, Article 19

2019

Volltextzugriff (PDF)

Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol

American journal of human genetics, 2015-12, Vol.97 (6), p.801-815

2015

Volltextzugriff (PDF)

138-OR: Characterization and Prediction of Genetic Risk of T1D in Individuals without HLA-DR3 or HLA-DR4

Diabetes (New York, N.Y.), 2023-06, Vol.72 (Supplement_1), p.1

2023

Volltextzugriff (PDF)

Pancreatic progenitor epigenome maps prioritize type 2 diabetes risk genes with roles in development

eLife, 2021-02, Vol.10

2021

Volltextzugriff (PDF)

1 – 25 von 95

Suche als RSS-Feed

Aktive Filter

KollektioneBooks on EBSCOhost

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(93)
Mit Volltextzugriff
(68)

Publikationsform

Artikel
(95)

Sprache

Englisch
(95)
Japanisch
(18)

Erscheinungsjahr

n.n

Thema

Science & Technology
(63)
Humans
(56)
Life Sciences & Biomedicine
(49)
Genomes
(38)
Diabetes
(36)
Gene Expression
(32)
Genetics & Heredity
(29)
Diabetes Mellitus
(25)
Diabetes Mellitus, Type 2 - Genetics
(25)
Genome-Wide Association Study
(24)
Chromatin
(22)
Genes
(18)
Genome-Wide Association Studies
(16)
Pancreas
(16)
Female
(15)
Genetic Aspects
(15)
Genetic Variation
(15)
Genomics
(15)
Male
(15)
Genetics
(14)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Plos Genetics
(15)
Diabetes
(13)
Nature Genetics
(9)
Nature
(8)
American Journal Of Human Genetics
(4)
Nature Communications
(4)
Elife
(3)
Human Molecular Genetics
(3)
Human Molecular Genetics Online/human Molecular Genetics
(3)
Bioinformatics
(2)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

A single-cell atlas of chromatin accessibility in the human genome

Detection of human adaptation during the past 2000 years

The miRNA profile of human pancreatic islets and beta-cells and relationship to type 2 diabetes pathogenesis

The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease

Single-cell chromatin accessibility identifies pancreatic islet cell type- and state-specific regulatory programs of diabetes risk

Leveraging type 1 diabetes human genetic and genomic data in the T1D knowledge portal

Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants

Transcript Expression Data from Human Islets Links Regulatory Signals from Genome-Wide Association Studies for Type 2 Diabetes and Glycemic Traits to Their Downstream Effectors

Single-cell multiomic profiling of human lungs reveals cell-type-specific and age-dynamic control of SARS-CoV2 host genes

Characterizing cis-regulatory elements using single-cell epigenomics

Common DNA sequence variation influences 3-dimensional conformation of the human genome

A map of open chromatin in human pancreatic islets

Pancreatic islet chromatin accessibility and conformation reveals distal enhancer networks of type 2 diabetes risk

Sequence logic at enhancers governs a dual mechanism of endodermal organ fate induction by FOXA pioneer factors

Identification of a regulatory variant that binds FOXA1 and FOXA2 at the CDC123/CAMK1D type 2 diabetes GWAS locus

Glucocorticoid signaling in pancreatic islets modulates gene regulatory programs and genetic risk of type 2 diabetes

Mapping genetic effects on cell type-specific chromatin accessibility and annotating complex immune trait variants using single nucleus ATAC-seq in peripheral blood

Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci

Lipid-induced epigenomic changes in human macrophages identify a coronary artery disease-associated variant that regulates PPAP2B Expression through Altered C/EBP-beta binding

Interpreting non-coding disease-associated human variants using single-cell epigenomics

Nutrient regulation of the islet epigenome controls adaptive insulin secretion

Developing a network view of type 2 diabetes risk pathways through integration of genetic, genomic and functional data

Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol

138-OR: Characterization and Prediction of Genetic Risk of T1D in Individuals without HLA-DR3 or HLA-DR4

Pancreatic progenitor epigenome maps prioritize type 2 diabetes risk genes with roles in development

Aktive Filter

Suchergebnisse filtern