UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 68

Sortiert nach

A text-mining analysis of the human phenome

European journal of human genetics : EJHG, 2006-05, Vol.14 (5), p.535-542

2006

Volltextzugriff (PDF)

Genome-Wide Pattern of TCF7L2/TCF4 Chromatin Occupancy in Colorectal Cancer Cells

Molecular and Cellular Biology, 2008-04, Vol.28 (8), p.2732-2744

2008

Volltextzugriff (PDF)

Characterization of genome-wide p53-binding sites upon stress response

Nucleic acids research, 2008-06, Vol.36 (11), p.3639

2008

Volltextzugriff (PDF)

Dynamic histone H3 epigenome marking during the intraerythrocytic cycle of Plasmodium falciparum

Proceedings of the National Academy of Sciences - PNAS, 2009-06, Vol.106 (24), p.9655-9660

2009

Volltextzugriff (PDF)

MetiTree: a web application to organize and process high-resolution multi-stage mass spectrometry metabolomics data

Bioinformatics (Oxford, England), 2012-10, Vol.28 (20), p.2707-2709

2012

Volltextzugriff (PDF)

ODoSE: a webserver for genome-wide calculation of adaptive divergence in prokaryotes

PloS one, 2013-05, Vol.8 (5), p.e62447-e62447

2013

Volltextzugriff (PDF)

ChIP-Seq of ERα and RNA polymerase II defines genes differentially responding to ligands

The EMBO journal, 2009-05, Vol.28 (10), p.1418-1428

2009

Volltextzugriff (PDF)

Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon

Human genetics, 2003-08, Vol.113 (3), p.268-275

2003

Volltextzugriff (PDF)

From syndrome families to functional genomics

Nature reviews. Genetics, 2004-07, Vol.5 (7), p.545-551

2004

Volltextzugriff (PDF)

Modulating crossover positioning by introducing large structural changes in chromosomes

BMC genomics, 2015-02, Vol.16 (1), p.89-89, Article 89

2015

Volltextzugriff (PDF)

Bioinformatics methods for identifying candidate disease genes

Human genomics, 2006-06, Vol.2 (6), p.429-432

2006

Volltextzugriff (PDF)

Computational disease gene identification: a concert of methods prioritizes type 2 diabetes and obesity candidate genes

Nucleic acids research, 2006-01, Vol.34 (10), p.3067

2006

Volltextzugriff (PDF)

A new web-based data mining tool for the identification of candidate genes for human genetic disorders

European journal of human genetics : EJHG, 2003-01, Vol.11 (1), p.57-63

2003

Volltextzugriff (PDF)

Autosomal Dominant Rhegmatogenous Retinal Detachment Associated with an Arg453Ter Mutation in the COL2A1 Gene

Investigative ophthalmology & visual science, 2003-09, Vol.44 (9), p.4035-4043

2003

Volltextzugriff (PDF)

ABCR unites what ophthalmologists divide(s)

Ophthalmic genetics, 1998, Vol.19 (3), p.117-122

1998

Volltextzugriff (PDF)

Isolation and Mapping of Novel Candidate Genes for Retinal Disorders Using Suppression Subtractive Hybridization

Genomics (San Diego, Calif.), 1999-06, Vol.58 (3), p.240-249

1999

Volltextzugriff (PDF)

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Nature genetics, 1999-10, Vol.23 (2), p.217-221

1999

Volltextzugriff (PDF)

The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease

American journal of human genetics, 1999-04, Vol.64 (4), p.1024-1035

1999

Volltextzugriff (PDF)

MetIDB: A Publicly Accessible Database of Predicted and Experimental 1 H NMR Spectra of Flavonoids

Analytical chemistry (Washington), 2013-09, Vol.85 (18), p.8700-8707

2013

Volltextzugriff (PDF)

Genomic structure and assessment of the retinally expressed RFamide-related peptide gene in dominant cystoid macular dystrophy

Molecular vision, 2002-03, Vol.8, p.67-71

2002

Volltextzugriff (PDF)

MetIDB: A Publicly Accessible Database of Predicted and Experimental 1H NMR Spectra of Flavonoids

Analytical chemistry (Washington), 2013-09, Vol.85 (18), p.8700-8707

2013

Volltextzugriff (PDF)

ChIP-Seq of ER[alpha] and RNA polymerase II defines genes differentially responding to ligands

The EMBO journal, 2009-05, Vol.28 (10), p.1418

2009

Volltextzugriff (PDF)

PathoVA: A visual analytics tool for pathology diagnosis and reporting

2017 IEEE Workshop on Visual Analytics in Healthcare (VAHC), 2017, p.77-83

2017

Volltextzugriff (PDF)

ChIP-Seq of ERalpha and RNA polymerase II defines genes differentially responding to ligands

The EMBO journal, 2009-05, Vol.28 (10), p.1418

2009

Volltextzugriff (PDF)

1 – 25 von 68

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(64)
Mit Volltextzugriff
(57)

Publikationsform

Sprache

Englisch
(68)
Japanisch
(9)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

A text-mining analysis of the human phenome

Genome-Wide Pattern of TCF7L2/TCF4 Chromatin Occupancy in Colorectal Cancer Cells

Characterization of genome-wide p53-binding sites upon stress response

Dynamic histone H3 epigenome marking during the intraerythrocytic cycle of Plasmodium falciparum

MetiTree: a web application to organize and process high-resolution multi-stage mass spectrometry metabolomics data

ODoSE: a webserver for genome-wide calculation of adaptive divergence in prokaryotes

ChIP-Seq of ERα and RNA polymerase II defines genes differentially responding to ligands

Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon

From syndrome families to functional genomics

Modulating crossover positioning by introducing large structural changes in chromosomes

Bioinformatics methods for identifying candidate disease genes

Computational disease gene identification: a concert of methods prioritizes type 2 diabetes and obesity candidate genes

iAnn: an event sharing platform for the life sciences

A new web-based data mining tool for the identification of candidate genes for human genetic disorders

Autosomal Dominant Rhegmatogenous Retinal Detachment Associated with an Arg453Ter Mutation in the COL2A1 Gene

ABCR unites what ophthalmologists divide(s)

Isolation and Mapping of Novel Candidate Genes for Retinal Disorders Using Suppression Subtractive Hybridization

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease

MetIDB: A Publicly Accessible Database of Predicted and Experimental 1 H NMR Spectra of Flavonoids

Genomic structure and assessment of the retinally expressed RFamide-related peptide gene in dominant cystoid macular dystrophy

MetIDB: A Publicly Accessible Database of Predicted and Experimental 1H NMR Spectra of Flavonoids

ChIP-Seq of ER[alpha] and RNA polymerase II defines genes differentially responding to ligands

PathoVA: A visual analytics tool for pathology diagnosis and reporting

ChIP-Seq of ERalpha and RNA polymerase II defines genes differentially responding to ligands

Suchergebnisse filtern