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...

Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization

Nature genetics, 2013-08, Vol.45 (8), p.902-906

2013

Volltextzugriff (PDF)

Impaired spatial learning and suppression of sharp wave ripples by cholinergic activation at the goal location

eLife, 2021-04, Vol.10

2021

Volltextzugriff (PDF)

A gene-based test of association using canonical correlation analysis

Bioinformatics (Oxford, England), 2012-03, Vol.28 (6), p.845-850

2012

Volltextzugriff (PDF)

The functional role of sequentially neuromodulated synaptic plasticity in behavioural learning

PLoS computational biology, 2021-06, Vol.17 (6), p.e1009017-e1009017

2021

Volltextzugriff (PDF)

Differential vulnerability of hippocampal CA3-CA1 synapses to Aβ

Acta neuropathologica communications, 2022-04, Vol.10 (1), p.45-45, Article 45

2022

Volltextzugriff (PDF)

Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system development

PLoS genetics, 2021-08, Vol.17 (8), p.e1009698-e1009698

2021

Volltextzugriff (PDF)

Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese

Human molecular genetics, 2012-03, Vol.21 (5), p.1184-1189

2012

Volltextzugriff (PDF)

General and Sex-Specific Effects of Vitamin D Against Atrial Fibrillation and Young-Onset Ischemic Stroke: A Mendelian Randomization Series

Journal of Clinical Biochemistry and Nutrition, 2024, pp.24-79

2024

Volltextzugriff (PDF)

High-sensitivity troponin I and B-type natriuretic peptide biomarkers for prediction of cardiovascular events in patients with coronary artery disease with and without diabetes mellitus

Cardiovascular diabetology, 2019-12, Vol.18 (1), p.171-171, Article 171

2019

Volltextzugriff (PDF)

Persistent barrage firing in cortical interneurons can be induced in vivo and may be important for the suppression of epileptiform activity

Frontiers in cellular neuroscience, 2014-03, Vol.8, p.76-76

2014

Volltextzugriff (PDF)

Biliary atresia

Nature reviews. Disease primers, 2024-07, Vol.10 (1), p.47, Article 47

2024

Volltextzugriff (PDF)

A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits

PloS one, 2012-02, Vol.7 (2), p.e31489

2012

Volltextzugriff (PDF)

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

BMC medical genomics, 2016-12, Vol.9 (1), p.75-75, Article 75

2016

Volltextzugriff (PDF)

A structural split in the human genome

PloS one, 2007-07, Vol.2 (7), p.e603-e603

2007

Volltextzugriff (PDF)

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study

JAMA oncology, 2017-05, Vol.3 (5), p.636

2017

Volltextzugriff (PDF)

Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population

PloS one, 2010-06, Vol.5 (6), p.e10918-e10918

2010

Volltextzugriff (PDF)

Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism

BMC medical genetics, 2015-07, Vol.16 (1), p.49-49, Article 49

2015

Volltextzugriff (PDF)

Mendelian Randomization Focused Analysis of Vitamin D on the Secondary Prevention of Ischemic Stroke

Stroke (1970), 2021-12, Vol.52 (12), p.3926-3937

2021

Volltextzugriff (PDF)

An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population

Human molecular genetics, 2021-05, Vol.30 (9), p.836-842

2021

Volltextzugriff (PDF)

Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese

Nature communications, 2015-12, Vol.6 (1), p.10206-10206, Article 10206

2015

Volltextzugriff (PDF)

Age-Biomarkers-Clinical Risk Factors for Prediction of Cardiovascular Events in Patients With Coronary Artery Disease

Arteriosclerosis, thrombosis, and vascular biology, 2018-10, Vol.38 (10), p.2519-2527

2018

Volltextzugriff (PDF)

Coverage and diagnostic yield of Whole Exome Sequencing for the Evaluation of Cases with Dilated and Hypertrophic Cardiomyopathy

Scientific reports, 2018-07, Vol.8 (1), p.10846-7, Article 10846

2018

Volltextzugriff (PDF)

Genetic Regulation of Pigment Epithelium-Derived Factor (PEDF): An Exome-Chip Association Analysis in Chinese Subjects With Type 2 Diabetes

Diabetes (New York, N.Y.), 2019-01, Vol.68 (1), p.198-206

2019

Volltextzugriff (PDF)

De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca

Human molecular genetics, 2018-01, Vol.27 (2), p.351-358

2018

Volltextzugriff (PDF)

1 – 25 von 279

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(231)
Mit Volltextzugriff
(227)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(279)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(179)
Life Sciences & Biomedicine
(143)
Humans
(99)
Female
(63)
Male
(56)
Genetics & Heredity
(33)
Middle Aged
(33)
Adult
(32)
Genomes
(31)
Animals
(28)
Genome-Wide Association Study
(25)
Science & Technology - Other Topics
(25)
Biochemistry & Molecular Biology
(21)
Multidisciplinary Sciences
(21)
Mutation
(21)
Patients
(21)
Medicine
(20)
Polymorphism, Single Nucleotide
(20)
Aged
(19)
Oncology
(19)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization

Impaired spatial learning and suppression of sharp wave ripples by cholinergic activation at the goal location

A gene-based test of association using canonical correlation analysis

The functional role of sequentially neuromodulated synaptic plasticity in behavioural learning

Differential vulnerability of hippocampal CA3-CA1 synapses to Aβ

Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system development

Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese

General and Sex-Specific Effects of Vitamin D Against Atrial Fibrillation and Young-Onset Ischemic Stroke: A Mendelian Randomization Series

High-sensitivity troponin I and B-type natriuretic peptide biomarkers for prediction of cardiovascular events in patients with coronary artery disease with and without diabetes mellitus

Persistent barrage firing in cortical interneurons can be induced in vivo and may be important for the suppression of epileptiform activity

Biliary atresia

A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

A structural split in the human genome

Genome-wide copy number variation study in anorectal malformations

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study

Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population

Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism

Mendelian Randomization Focused Analysis of Vitamin D on the Secondary Prevention of Ischemic Stroke

An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population

Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese

Age-Biomarkers-Clinical Risk Factors for Prediction of Cardiovascular Events in Patients With Coronary Artery Disease

Coverage and diagnostic yield of Whole Exome Sequencing for the Evaluation of Cases with Dilated and Hypertrophic Cardiomyopathy

Genetic Regulation of Pigment Epithelium-Derived Factor (PEDF): An Exome-Chip Association Analysis in Chinese Subjects With Type 2 Diabetes

De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca

Suchergebnisse filtern