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...

Toward optimal detection of the common prenatal aneuploidies by quantitative fluorescent-polymerase chain reaction: comparison of two commercial assays

Genetic testing and molecular biomarkers, 2012-08, Vol.16 (8), p.943-947

2012

Volltextzugriff (PDF)

An HFE Intronic Variant Promotes Misdiagnosis of Hereditary Hemochromatosis

American journal of human genetics, 1999-09, Vol.65 (3), p.924-926

1999

Volltextzugriff (PDF)

The development of RAPD and microsatellite markers in lodgepole pine (Pinus contorta var. latifolia)

Genome, 1998, Vol.41 (6), p.797-805

1998

Volltextzugriff (PDF)

Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids

American journal of human genetics, 2012-05, Vol.90 (5), p.809-820

2012

Volltextzugriff (PDF)

The maize methylome influences mRNA splice sites and reveals widespread paramutation-like switches guided by small RNA

Genome research, 2013-10, Vol.23 (10), p.1651-1662

2013

Volltextzugriff (PDF)

Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans

PLoS genetics, 2011-06, Vol.7 (6), p.e1002150

2011

Volltextzugriff (PDF)

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

PLoS genetics, 2013-02, Vol.9 (2), p.e1003266-e1003266

2013

Volltextzugriff (PDF)

Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1

Genes & development, 2014-10, Vol.28 (19), p.2090-2102

2014

Volltextzugriff (PDF)

The trans-ancestral genomic architecture of glycemic traits

Nature genetics, 2021-06, Vol.53 (6), p.840-860

2021

Volltextzugriff (PDF)

Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathy

Human molecular genetics, 2014-05, Vol.23 (9), p.2353-2363

2014

Volltextzugriff (PDF)

A generalizable pre-clinical research approach for orphan disease therapy

Orphanet journal of rare diseases, 2012-06, Vol.7 (1), p.39-39, Article 39

2012

Volltextzugriff (PDF)

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature genetics, 2014-11, Vol.46 (11), p.1173-1186

2014

Volltextzugriff (PDF)

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

Nature genetics, 2010-12, Vol.42 (12), p.1068-1076

2010

Volltextzugriff (PDF)

Discovery and refinement of loci associated with lipid levels

Nature genetics, 2013-11, Vol.45 (11), p.1274-1283

2013

Volltextzugriff (PDF)

Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation

Human molecular genetics, 2015-12, Vol.24 (24), p.6958-6974

2015

Volltextzugriff (PDF)

The RNA-binding protein Rbfox1 regulates splicing required for skeletal muscle structure and function

Human molecular genetics, 2015-04, Vol.24 (8), p.2360-2374

2015

Volltextzugriff (PDF)

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

Nature genetics, 2016-10, Vol.48 (10), p.1171-1184

2016

Volltextzugriff (PDF)

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

Nature genetics, 2017-03, Vol.49 (3), p.403-415

2017

Volltextzugriff (PDF)

NALP3 inflammasome upregulation and CASP1 cleavage of the glucocorticoid receptor cause glucocorticoid resistance in leukemia cells

Nature genetics, 2015-06, Vol.47 (6), p.607-614

2015

Volltextzugriff (PDF)

Common variants associated with plasma triglycerides and risk for coronary artery disease

Nature genetics, 2013-11, Vol.45 (11), p.1345-1352

2013

Volltextzugriff (PDF)

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

PLoS genetics, 2015-10, Vol.11 (10), p.e1005378

2015

Volltextzugriff (PDF)

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

Nature genetics, 2020-05, Vol.52 (5), p.494-504

2020

Volltextzugriff (PDF)

Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death

Nature genetics, 2000-02, Vol.24 (2), p.175-179

2000

Volltextzugriff (PDF)

1 – 25 von 54

Suche als RSS-Feed

Aktive Filter

KollektionTaylor & Francis

ThemaGenetics & Heredity

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(53)
Mit Volltextzugriff
(28)

Publikationsform

Artikel
(54)

Sprache

Englisch
(54)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Toward optimal detection of the common prenatal aneuploidies by quantitative fluorescent-polymerase chain reaction: comparison of two commercial assays

An HFE Intronic Variant Promotes Misdiagnosis of Hereditary Hemochromatosis

The development of RAPD and microsatellite markers in lodgepole pine (Pinus contorta var. latifolia)

Genetic Adaptation of Fatty-Acid Metabolism: A Human-Specific Haplotype Increasing the Biosynthesis of Long-Chain Omega-3 and Omega-6 Fatty Acids

The maize methylome influences mRNA splice sites and reveals widespread paramutation-like switches guided by small RNA

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1

The trans-ancestral genomic architecture of glycemic traits

Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathy

A generalizable pre-clinical research approach for orphan disease therapy

Defining the role of common variation in the genomic and biological architecture of adult human height

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

Discovery and refinement of loci associated with lipid levels

The Knockout Mouse Project

Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation

The RNA-binding protein Rbfox1 regulates splicing required for skeletal muscle structure and function

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

NALP3 inflammasome upregulation and CASP1 cleavage of the glucocorticoid receptor cause glucocorticoid resistance in leukemia cells

Common variants associated with plasma triglycerides and risk for coronary artery disease

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death

Aktive Filter

Suchergebnisse filtern