UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 184

Sortiert nach

Experimental investigation of electroplated CBN wheel with phyllotactic pattern part I: cylindrical-face grinding performance

International journal of advanced manufacturing technology, 2021-12, Vol.117 (11-12), p.3681-3691

2021

Link zum Volltext

Verfügbarkeit prüfen

Expression- and splicing-based multi-tissue transcriptome-wide association studies identified multiple genes for breast cancer by estrogen-receptor status

Breast cancer research : BCR, 2024-03, Vol.26 (1), p.51-51, Article 51

2024

Link zum Volltext

Verfügbarkeit prüfen

Formation mechanism and morphology prediction of CFRP chips

International journal of advanced manufacturing technology, 2021-07, Vol.115 (1-2), p.165-177

2021

Link zum Volltext

Verfügbarkeit prüfen

Comprehensive association analysis of nine candidate genes with serum 25-hydroxy vitamin D levels among healthy Caucasian subjects

Human genetics, 2010-11, Vol.128 (5), p.549-556

2010

Link zum Volltext

Verfügbarkeit prüfen

Trans-ethnic predicted expression genome-wide association analysis identifies a gene for estrogen receptor-negative breast cancer

PLoS genetics, 2017-09, Vol.13 (9), p.e1006727-e1006727

2017

Link zum Volltext

Verfügbarkeit prüfen

Resveratrol modulates angiogenesis through the GSK3β/β-catenin/TCF-dependent pathway in human endothelial cells

Biochemical pharmacology, 2010-11, Vol.80 (9), p.1386-1395

2010

Link zum Volltext

Verfügbarkeit prüfen

Characterization of Nuclear Localization Signal in the N Terminus of CUL4B and Its Essential Role in Cyclin E Degradation and Cell Cycle Progression

The Journal of biological chemistry, 2009-11, Vol.284 (48), p.33320-33332

2009

Link zum Volltext

Verfügbarkeit prüfen

Rare variant association testing by adaptive combination of P-values

PloS one, 2014-01, Vol.9 (1), p.e85728-e85728

2014

Link zum Volltext

Verfügbarkeit prüfen

Plasma metabolites and lipids associate with kidney function and kidney volume in hypertensive ADPKD patients early in the disease course

BMC nephrology, 2019-02, Vol.20 (1), p.66-66, Article 66

2019

Link zum Volltext

Verfügbarkeit prüfen

A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42)

American journal of human genetics, 2008-12, Vol.83 (6), p.752-759

2008

Link zum Volltext

Verfügbarkeit prüfen

Mutation in CUL4B, Which Encodes a Member of Cullin-RING Ubiquitin Ligase Complex, Causes X-Linked Mental Retardation

American journal of human genetics, 2007-03, Vol.80 (3), p.561-566

2007

Link zum Volltext

Verfügbarkeit prüfen

WHSC1L1 drives cell cycle progression through transcriptional regulation of CDC6 and CDK2 in squamous cell carcinoma of the head and neck

Oncotarget, 2016-07, Vol.7 (27), p.42527-42538

2016

Link zum Volltext

Verfügbarkeit prüfen

Association study between vitamin D receptor gene polymorphisms and asthma in the Chinese Han population: a case-control study

BMC medical genetics, 2009-07, Vol.10 (1), p.71-71, Article 71

2009

Link zum Volltext

Verfügbarkeit prüfen

Discrimination of benign from malignant breast lesions in dense breasts with model-based analysis of regions-of-interest using directional diffusion-weighted images

BMC medical imaging, 2020-06, Vol.20 (1), p.1-61, Article 61

2020

Link zum Volltext

Verfügbarkeit prüfen

O11: Defining the pleiotropic GATA2 deficiency phenotype for the development of ACMG-AMP variant curation rules for GATA2

Genetics in Medicine Open, 2023, Vol.1 (1), p.100055, Article 100055

2023

Link zum Volltext

Verfügbarkeit prüfen

Novel strategy for disease risk prediction incorporating predicted gene expression and DNA methylation data: a multi‐phased study of prostate cancer

Cancer communications (London, England), 2021-12, Vol.41 (12), p.1387-1397

2021

Link zum Volltext

Verfügbarkeit prüfen

Pharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the Genetics of Lipid-Lowering Drugs and Diet Network study

Pharmacogenetics and genomics, 2009-02, Vol.19 (2), p.161-169

2009

Link zum Volltext

Verfügbarkeit prüfen

Apolipoprotein B genetic variants modify the response to fenofibrate: a GOLDN study[S]

Journal of lipid research, 2010-11, Vol.51 (11), p.3316-3323

2010

Link zum Volltext

Verfügbarkeit prüfen

MethylPCA: a toolkit to control for confounders in methylome-wide association studies

BMC bioinformatics, 2013-03, Vol.14 (1), p.74-74, Article 74

2013

Link zum Volltext

Verfügbarkeit prüfen

Tinnitus management with percutaneous osseointegrated auditory implants for unilateral sensorineural hearing loss

American journal of otolaryngology, 2015-11, Vol.36 (6), p.810-813

2015

Link zum Volltext

Verfügbarkeit prüfen

Serum withdrawal up‐regulates human SIRT1 gene expression in a p53‐dependent manner

Journal of cellular and molecular medicine, 2009-10, Vol.13 (10), p.4176-4184

2009

Link zum Volltext

Verfügbarkeit prüfen

The SCARB1 gene is associated with lipid response to dietary and pharmacological interventions

Journal of human genetics, 2008-08, Vol.53 (8), p.709-717

2008

Link zum Volltext

Verfügbarkeit prüfen

Multi-tissue transcriptome-wide association studies identified 235 genes for intrinsic subtypes of breast cancer

JNCI : Journal of the National Cancer Institute, 2024-07, Vol.116 (7), p.1105-1115

2024

Link zum Volltext

Verfügbarkeit prüfen

A rapid conditional enumeration haplotyping method in pedigrees

Genetics selection evolution (Paris), 2008-01, Vol.40 (1), p.25-36, Article 25

2008

Link zum Volltext

Verfügbarkeit prüfen

RETRACTED: Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells

Experimental cell research, 2009-10, Vol.315 (17), p.2953-2962

2009

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 184

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(165)
Mit Volltextzugriff
(168)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(127)
Life Sciences & Biomedicine
(102)
Humans
(74)
Genetics & Heredity
(35)
Female
(34)
Male
(24)
Animals
(23)
Polymorphism, Single Nucleotide
(21)
Physical Sciences
(19)
Technology
(18)
Adult
(16)
Computer Simulation
(15)
Genome-Wide Association Study
(15)
Models, Genetic
(15)
Oncology
(15)
Genetic Predisposition To Disease
(14)
Genetics
(13)
Linkage Disequilibrium
(13)
Mathematical & Computational Biology
(13)
Algorithms
(12)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Experimental investigation of electroplated CBN wheel with phyllotactic pattern part I: cylindrical-face grinding performance

Expression- and splicing-based multi-tissue transcriptome-wide association studies identified multiple genes for breast cancer by estrogen-receptor status

Formation mechanism and morphology prediction of CFRP chips

Comprehensive association analysis of nine candidate genes with serum 25-hydroxy vitamin D levels among healthy Caucasian subjects

Trans-ethnic predicted expression genome-wide association analysis identifies a gene for estrogen receptor-negative breast cancer

Resveratrol modulates angiogenesis through the GSK3β/β-catenin/TCF-dependent pathway in human endothelial cells

Characterization of Nuclear Localization Signal in the N Terminus of CUL4B and Its Essential Role in Cyclin E Degradation and Cell Cycle Progression

Rare variant association testing by adaptive combination of P-values

Plasma metabolites and lipids associate with kidney function and kidney volume in hypertensive ADPKD patients early in the disease course

A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42)

Mutation in CUL4B, Which Encodes a Member of Cullin-RING Ubiquitin Ligase Complex, Causes X-Linked Mental Retardation

WHSC1L1 drives cell cycle progression through transcriptional regulation of CDC6 and CDK2 in squamous cell carcinoma of the head and neck

Association study between vitamin D receptor gene polymorphisms and asthma in the Chinese Han population: a case-control study

Discrimination of benign from malignant breast lesions in dense breasts with model-based analysis of regions-of-interest using directional diffusion-weighted images

O11: Defining the pleiotropic GATA2 deficiency phenotype for the development of ACMG-AMP variant curation rules for GATA2

Novel strategy for disease risk prediction incorporating predicted gene expression and DNA methylation data: a multi‐phased study of prostate cancer

Pharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the Genetics of Lipid-Lowering Drugs and Diet Network study

Apolipoprotein B genetic variants modify the response to fenofibrate: a GOLDN study[S]

MethylPCA: a toolkit to control for confounders in methylome-wide association studies

Tinnitus management with percutaneous osseointegrated auditory implants for unilateral sensorineural hearing loss

Serum withdrawal up‐regulates human SIRT1 gene expression in a p53‐dependent manner

The SCARB1 gene is associated with lipid response to dietary and pharmacological interventions

Multi-tissue transcriptome-wide association studies identified 235 genes for intrinsic subtypes of breast cancer

A rapid conditional enumeration haplotyping method in pedigrees

RETRACTED: Resveratrol augments the canonical Wnt signaling pathway in promoting osteoblastic differentiation of multipotent mesenchymal cells

Suchergebnisse filtern