UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 97

Sortiert nach

Polygenic scores via penalized regression on summary statistics

Genetic epidemiology, 2017-09, Vol.41 (6), p.469-480

2017

Link zum Volltext

Verfügbarkeit prüfen

Identification of long non-protein coding RNAs in chicken skeletal muscle using next generation sequencing

Genomics (San Diego, Calif.), 2012-05, Vol.99 (5), p.292-298

2012

Link zum Volltext

Verfügbarkeit prüfen

Co-occurring protein phosphorylation are functionally associated

PLoS computational biology, 2017-05, Vol.13 (5), p.e1005502-e1005502

2017

Link zum Volltext

Verfügbarkeit prüfen

Interactive effect of nitrogen addition and throughfall reduction decreases soil aggregate stability through reducing biological binding agents

Forest ecology and management, 2019-08, Vol.445, p.13-19

2019

Link zum Volltext

Verfügbarkeit prüfen

Phase separation as a possible mechanism for dosage sensitivity

Genome Biology, 2024-01, Vol.25 (1), p.17-17, Article 17

2024

Link zum Volltext

Verfügbarkeit prüfen

Nitrogen addition decreases soil aggregation but enhances soil organic carbon stability in a temperate forest

Geoderma, 2022-11, Vol.426, p.116112, Article 116112

2022

Link zum Volltext

Verfügbarkeit prüfen

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

Nature genetics, 2011-06, Vol.43 (6), p.531-538

2011

Link zum Volltext

Verfügbarkeit prüfen

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

Genetics in medicine, 2020-12, Vol.22 (12), p.2020-2028

2020

Link zum Volltext

Verfügbarkeit prüfen

Environmental Regulation, Promotion Pressure of Officials, and Enterprise Environmental Protection Investment

Frontiers in public health, 2021-08, Vol.9, p.724351-724351

2021

Link zum Volltext

Verfügbarkeit prüfen

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches

Journal of human genetics, 2014-11, Vol.59 (11), p.599-607

2014

Link zum Volltext

Verfügbarkeit prüfen

A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population

Neurobiology of aging, 2018-08, Vol.68, p.160.e1-160.e7

2018

Link zum Volltext

Verfügbarkeit prüfen

Soil water response to rainfall in a dune-interdune landscape in Horqin Sand Land, northern China

Soil and water research, 2019-01, Vol.14 (4), p.229-239

2019

Link zum Volltext

Verfügbarkeit prüfen

Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density

Frontiers in genetics, 2018-08, Vol.9, p.267-267

2018

Link zum Volltext

Verfügbarkeit prüfen

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family

Clinica chimica acta, 2012-07, Vol.413 (13-14), p.1049-1052

2012

Link zum Volltext

Verfügbarkeit prüfen

Identification and Characterization of Human snoRNA Core Promoters

Genomics (San Diego, Calif.), 2010-07, Vol.96 (1), p.50-56

2010

Link zum Volltext

Verfügbarkeit prüfen

Polymorphisms at 16p13 are associated with systemic lupus erythematosus in the Chinese population

Journal of medical genetics, 2011-01, Vol.48 (1), p.69-72

2011

Link zum Volltext

Verfügbarkeit prüfen

A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population

Circulation. Cardiovascular genetics, 2011-12, Vol.4 (6), p.687

2011

Link zum Volltext

Verfügbarkeit prüfen

Recent ultra-rare inherited variants implicate new autism candidate risk genes

Nature genetics, 2021-08, Vol.53 (8), p.1125-1134

2021

Link zum Volltext

Verfügbarkeit prüfen

A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway

Molecular human reproduction, 2016-09, Vol.22 (9), p.669-678

2016

Link zum Volltext

Verfügbarkeit prüfen

Systematic Characterization and Prediction of Post-Translational Modification Cross-Talk

Molecular & cellular proteomics, 2015-03, Vol.14 (3), p.761-770

2015

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations

American journal of human genetics, 2013-09, Vol.93 (3), p.545-554

2013

Link zum Volltext

Verfügbarkeit prüfen

Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene

American journal of human genetics, 2021-10, Vol.108 (10), p.1964-1980

2021

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 97

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(89)
Mit Volltextzugriff
(91)

Publikationsform

Sprache

Englisch
(97)
Japanisch
(10)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Polygenic scores via penalized regression on summary statistics

Identification of long non-protein coding RNAs in chicken skeletal muscle using next generation sequencing

Co-occurring protein phosphorylation are functionally associated

Interactive effect of nitrogen addition and throughfall reduction decreases soil aggregate stability through reducing biological binding agents

Phase separation as a possible mechanism for dosage sensitivity

Nitrogen addition decreases soil aggregation but enhances soil organic carbon stability in a temperate forest

De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

Environmental Regulation, Promotion Pressure of Officials, and Enterprise Environmental Protection Investment

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches

A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population

Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Soil water response to rainfall in a dune-interdune landscape in Horqin Sand Land, northern China

Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family

Identification and Characterization of Human snoRNA Core Promoters

Polymorphisms at 16p13 are associated with systemic lupus erythematosus in the Chinese population

A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population

Recent ultra-rare inherited variants implicate new autism candidate risk genes

A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway

Systematic Characterization and Prediction of Post-Translational Modification Cross-Talk

Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations

Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Suchergebnisse filtern