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...

Breast cancer risk–associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression

Nature genetics, 2012-11, Vol.44 (11), p.1191-1198

2012

Volltextzugriff (PDF)

ZNF143 provides sequence specificity to secure chromatin interactions at gene promoters

Nature communications, 2015-02, Vol.6 (1), Article 6186

2015

Volltextzugriff (PDF)

The HDL proteome in acute coronary syndromes shifts to an inflammatory profile

Biochimica et biophysica acta, 2012-03, Vol.1821 (3), p.405-415

2012

Volltextzugriff (PDF)

3D genomic analysis reveals novel enhancer-hijacking caused by complex structural alterations that drive oncogene overexpression

Nature communications, 2024-07, Vol.15 (1), p.6130-15, Article 6130

2024

Volltextzugriff (PDF)

Integrative functional genomics identifies an enhancer looping to the SOX9 gene disrupted by the 17q24.3 prostate cancer risk locus

Genome research, 2012-08, Vol.22 (8), p.1437-1446

2012

Volltextzugriff (PDF)

Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study

Scientific reports, 2016-01, Vol.6 (1), p.18672-18672, Article 18672

2016

Volltextzugriff (PDF)

A predominant enhancer co-amplified with the SOX2 oncogene is necessary and sufficient for its expression in squamous cancer

Nature communications, 2021-12, Vol.12 (1), p.7139-7139, Article 7139

2021

Volltextzugriff (PDF)

Noncoding somatic and inherited single-nucleotide variants converge to promote ESR1 expression in breast cancer

Nature genetics, 2016-10, Vol.48 (10), p.1260-1266

2016

Volltextzugriff (PDF)

Genetic Variants of FTO Influence Adiposity, Insulin Sensitivity, Leptin Levels, and Resting Metabolic Rate in the Quebec Family Study

Diabetes (New York, N.Y.), 2008-04, Vol.57 (4), p.1147-1150

2008

Volltextzugriff (PDF)

Soluble factors in malignant ascites promote the metastatic adhesion of gastric adenocarcinoma cells

Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2023, Vol.26 (1), p.55-68

2023

Volltextzugriff (PDF)

To bind or not to bind: Cistromic reprogramming in prostate cancer

Frontiers in oncology, 2022-09, Vol.12, p.963007-963007

2022

Volltextzugriff (PDF)

The effect of chromosome 9p21 variants on cardiovascular disease may be modified by dietary intake: evidence from a case/control and a prospective study

PLoS medicine, 2011-10, Vol.8 (10), p.e1001106

2011

Volltextzugriff (PDF)

The Transcriptional Repressor Polycomb Group Factor 6, PCGF6, Negatively Regulates Dendritic Cell Activation and Promotes Quiescence

Cell reports (Cambridge), 2016-08, Vol.16 (7), p.1829-1837

2016

Volltextzugriff (PDF)

Enhancer alterations in cancer: a source for a cell identity crisis

Genome medicine, 2014-09, Vol.6 (9), p.77-77, Article 77

2014

Volltextzugriff (PDF)

Laying a solid foundation for Manhattan – ‘setting the functional basis for the post-GWAS era’

Trends in genetics, 2014-04, Vol.30 (4), p.140-149

2014

Volltextzugriff (PDF)

Pre-neoplastic epigenetic disruption of transcriptional enhancers in chronic inflammation

Oncotarget, 2016-03, Vol.7 (13), p.15772-15786

2016

Volltextzugriff (PDF)

C3D: a tool to predict 3D genomic interactions between cis-regulatory elements

Bioinformatics, 2019-03, Vol.35 (5), p.877-879

2019

Volltextzugriff (PDF)

Modulation of long noncoding RNAs by risk SNPs underlying genetic predispositions to prostate cancer

Nature genetics, 2016-10, Vol.48 (10), p.1142-1150

2016

Volltextzugriff (PDF)

Chromatin Looping Shapes KLF5-Dependent Transcriptional Programs in Human Epithelial Cancers

Cancer research (Chicago, Ill.), 2020-12, Vol.80 (24), p.5464-5477

2020

Volltextzugriff (PDF)

Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma

Nature (London), 2019-10, Vol.574 (7780), p.707-711

2019

Volltextzugriff (PDF)

HiChIP-Based Epigenomic Footprinting Identifies a Promoter Variant of UXS1 That Confers Genetic Susceptibility to Gastroesophageal Cancer

Cancer research (Chicago, Ill.), 2024-07, Vol.84 (14), p.2377-2389

2024

Volltextzugriff (PDF)

Common Polymorphisms in the Promoter of the Visfatin Gene (PBEF1) Influence Plasma Insulin Levels in a French-Canadian Population

Diabetes (New York, N.Y.), 2006-10, Vol.55 (10), p.2896-2902

2006

Volltextzugriff (PDF)

ABC: a tool to identify SNVs causing allele-specific transcription factor binding from ChIP-Seq experiments

Bioinformatics, 2015-09, Vol.31 (18), p.3057-3059

2015

Volltextzugriff (PDF)

BioID identifies novel c-MYC interacting partners in cultured cells and xenograft tumors

Journal of proteomics, 2015-04, Vol.118, p.95-111

2015

Volltextzugriff (PDF)

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

PloS one, 2008-10, Vol.3 (10), p.e3583-e3583

2008

Volltextzugriff (PDF)

1 – 25 von 49

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(48)
Mit Volltextzugriff
(35)

Publikationsform

Artikel
(49)

Sprache

Englisch
(49)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Nature Genetics
(7)
Nature Communications
(6)
Diabetes Care
(5)
Cancer Research
(4)
Bioinformatics
(2)
Diabetes
(2)
European Journal Of Human Genetics
(2)
European Journal Of Human Genetics : Ejhg
(2)
Nature
(2)
Plos Medicine
(2)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Breast cancer risk–associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression

ZNF143 provides sequence specificity to secure chromatin interactions at gene promoters

The HDL proteome in acute coronary syndromes shifts to an inflammatory profile

3D genomic analysis reveals novel enhancer-hijacking caused by complex structural alterations that drive oncogene overexpression

Integrative functional genomics identifies an enhancer looping to the SOX9 gene disrupted by the 17q24.3 prostate cancer risk locus

Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study

A predominant enhancer co-amplified with the SOX2 oncogene is necessary and sufficient for its expression in squamous cancer

Noncoding somatic and inherited single-nucleotide variants converge to promote ESR1 expression in breast cancer

Genetic Variants of FTO Influence Adiposity, Insulin Sensitivity, Leptin Levels, and Resting Metabolic Rate in the Quebec Family Study

Soluble factors in malignant ascites promote the metastatic adhesion of gastric adenocarcinoma cells

To bind or not to bind: Cistromic reprogramming in prostate cancer

The effect of chromosome 9p21 variants on cardiovascular disease may be modified by dietary intake: evidence from a case/control and a prospective study

The Transcriptional Repressor Polycomb Group Factor 6, PCGF6, Negatively Regulates Dendritic Cell Activation and Promotes Quiescence

Enhancer alterations in cancer: a source for a cell identity crisis

Laying a solid foundation for Manhattan – ‘setting the functional basis for the post-GWAS era’

Pre-neoplastic epigenetic disruption of transcriptional enhancers in chronic inflammation

C3D: a tool to predict 3D genomic interactions between cis-regulatory elements

Modulation of long noncoding RNAs by risk SNPs underlying genetic predispositions to prostate cancer

Chromatin Looping Shapes KLF5-Dependent Transcriptional Programs in Human Epithelial Cancers

Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma

HiChIP-Based Epigenomic Footprinting Identifies a Promoter Variant of UXS1 That Confers Genetic Susceptibility to Gastroesophageal Cancer

Common Polymorphisms in the Promoter of the Visfatin Gene (PBEF1) Influence Plasma Insulin Levels in a French-Canadian Population

ABC: a tool to identify SNVs causing allele-specific transcription factor binding from ChIP-Seq experiments

BioID identifies novel c-MYC interacting partners in cultured cells and xenograft tumors

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

Suchergebnisse filtern