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...

ADAS-viewer: web-based application for integrative analysis of multi-omics data in Alzheimer’s disease

NPJ systems biology and applications, 2021-03, Vol.7 (1), p.18-18, Article 18

2021

Volltextzugriff (PDF)

Alternative Splicing Regulation of Low-Frequency Genetic Variants in Exon 2 of TREM2 in Alzheimer’s Disease by Splicing-Based Aggregation

International journal of molecular sciences, 2021-09, Vol.22 (18), p.9865

2021

Volltextzugriff (PDF)

Analysis of unmapped regions associated with long deletions in Korean whole genome sequences based on short read data

Genomics & informatics, 2019, Vol.17 (4), p.40.1-40.9

2019

Volltextzugriff (PDF)

Analysis of unmapped regions associated with long deletions in Korean whole genome sequences based on short read data

Genomics & Informatics, 2019, 17(4), , pp.40-40

2019

Volltextzugriff (PDF)

Association Analysis of SLC6A20 Polymorphisms With Hirschsprung Disease

Journal of pediatric gastroenterology and nutrition, 2016-01, Vol.62 (1), p.64-70

2016

Volltextzugriff (PDF)

Association of an APBA3 Missense Variant with Risk of Premature Ovarian Failure in the Korean Female Population

Journal of personalized medicine, 2020-10, Vol.10 (4), p.193

2020

Volltextzugriff (PDF)

Association of RANBP1 Haplotype With Smooth Pursuit Eue Movement Abnormality

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011, Vol.156 (1), p.67-71

2011

Volltextzugriff (PDF)

Association of RANBP1 haplotype with smooth pursuit eye movement abnormality

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-01, Vol.156B (1), p.67-71

2011

Volltextzugriff (PDF)

Association study of polymorphisms in interferon-γ receptor genes with the risk of pulmonary tuberculosis

Molecular medicine reports, 2015-07, Vol.12 (1), p.1568-1578

2015

Volltextzugriff (PDF)

Body Height Effect on Brain Volumes in Youth Decreases in Old Age in Koreans

Interdisciplinary bio central, 2011-08, Vol.3 (3), p.1-5

Koh, InSong

2011

Volltextzugriff (PDF)

Body size effect on brain volume in Korean youth

Neuroreport, 2005-12, Vol.16 (18), p.2029-2032

2005

Volltextzugriff (PDF)

Brain Region-Dependent Alternative Splicing of Alzheimer Disease (AD)-Risk Genes Is Associated With Neuropathological Features in AD

International neurourology journal, 2022-11, Vol.26 (Suppl 2), p.S126-136

2022

Volltextzugriff (PDF)

Brain regional alternative splicing and clinical traits in Alzheimer’s disease

Alzheimer's & dementia, 2023-06, Vol.19 (S1), p.n/a

2023

Volltextzugriff (PDF)

Cancer-specific functional profiling in microsatellite-unstable (MSI) colon and endometrial cancers using combined differentially expressed genes and biclustering analysis

Medicine (Baltimore), 2023-05, Vol.102 (19), p.e33647-e33647

2023

Volltextzugriff (PDF)

Comparative Statistic Module (CSM) for Significant Gene Selection

Genomics & Informatics, 2004, 2(4), , pp.180-183

2004

Volltextzugriff (PDF)

Contribution of the OBSCN nonsynonymous variants to aspirin exacerbated respiratory disease susceptibility in Korean population

DNA and cell biology, 2012-06, Vol.31 (6), p.1001-1009

2012

Volltextzugriff (PDF)

Deciphering the human microbiome using next-generation sequencing data and bioinformatics approaches

Methods (San Diego, Calif.), 2015-06, Vol.79-80, p.52-59

2015

Volltextzugriff (PDF)

Differential Expression Profiling of Long Noncoding RNA and mRNA during Osteoblast Differentiation in Mouse

International journal of genomics, 2018-01, Vol.2018 (2018), p.1-13

2018

Volltextzugriff (PDF)

Diplotyper: diplotype-based association analysis

BMC medical genomics, 2013, Vol.6 Suppl 2 (Suppl 2), p.S5-S5, Article S5

2013

Volltextzugriff (PDF)

Epistasis between SNPs in genes involved in lipoprotein metabolism influences high- and low-density lipoprotein cholesterol levels

Genes & Genomics, 2014, 36(6), , pp.809-817

2014

Volltextzugriff (PDF)

Erratum to: Lack of Associations of Neuregulin 1 Variations with Schizophrenia and Smooth Pursuit Eye Movement Abnormality in a Korean Population

Journal of molecular neuroscience, 2012-03, Vol.46 (3), p.688-688

2012

Volltextzugriff (PDF)

Exome sequencing and subsequent association studies identify five amino acid-altering variants influencing human height

Human genetics, 2012-03, Vol.131 (3), p.471-478

2012

Volltextzugriff (PDF)

Exome sequencing identified five novel USH2A variants in Korean patients with retinitis pigmentosa

Ophthalmic genetics, 2023-04, Vol.44 (2), p.163-170

2023

Volltextzugriff (PDF)

Exome sequencing identified five novel USH2A variants in Korean patients with retinitis pigmentosa

Ophthalmic Genetics, 2023, Vol.44 (2), p.163-170

2023

Volltextzugriff (PDF)

Exome sequencing identifies KIAA1377 and C5orf42 as susceptibility genes for monomelic amyotrophy

Neuromuscular disorders : NMD, 2012-05, Vol.22 (5), p.394-400

2012

Volltextzugriff (PDF)

1 – 25 von 67

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(64)
Mit Volltextzugriff
(63)

Publikationsform

Artikel
(66)
Berichte
(1)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(46)
Life Sciences & Biomedicine
(40)
Humans
(29)
Female
(20)
Male
(18)
Adult
(14)
Biochemistry & Molecular Biology
(11)
Genomes
(11)
Middle Aged
(11)
Single Nucleotide Polymorphism
(10)
Genetics & Heredity
(9)
Polymorphism, Single Nucleotide
(9)
Single-Nucleotide Polymorphism
(9)
Aged
(8)
Biological And Medical Sciences
(8)
Genes
(8)
Genetic Predisposition To Disease
(8)
Young Adult
(8)
Asian Continental Ancestry Group - Genetics
(7)
Haplotypes
(7)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

ADAS-viewer: web-based application for integrative analysis of multi-omics data in Alzheimer’s disease

Alternative Splicing Regulation of Low-Frequency Genetic Variants in Exon 2 of TREM2 in Alzheimer’s Disease by Splicing-Based Aggregation

Analysis of unmapped regions associated with long deletions in Korean whole genome sequences based on short read data

Analysis of unmapped regions associated with long deletions in Korean whole genome sequences based on short read data

Association Analysis of SLC6A20 Polymorphisms With Hirschsprung Disease

Association of an APBA3 Missense Variant with Risk of Premature Ovarian Failure in the Korean Female Population

Association of RANBP1 Haplotype With Smooth Pursuit Eue Movement Abnormality

Association of RANBP1 haplotype with smooth pursuit eye movement abnormality

Association study of polymorphisms in interferon-γ receptor genes with the risk of pulmonary tuberculosis

Body Height Effect on Brain Volumes in Youth Decreases in Old Age in Koreans

Body size effect on brain volume in Korean youth

Brain Region-Dependent Alternative Splicing of Alzheimer Disease (AD)-Risk Genes Is Associated With Neuropathological Features in AD

Brain regional alternative splicing and clinical traits in Alzheimer’s disease

Cancer-specific functional profiling in microsatellite-unstable (MSI) colon and endometrial cancers using combined differentially expressed genes and biclustering analysis

Comparative Statistic Module (CSM) for Significant Gene Selection

Contribution of the OBSCN nonsynonymous variants to aspirin exacerbated respiratory disease susceptibility in Korean population

Deciphering the human microbiome using next-generation sequencing data and bioinformatics approaches

Differential Expression Profiling of Long Noncoding RNA and mRNA during Osteoblast Differentiation in Mouse

Diplotyper: diplotype-based association analysis

Epistasis between SNPs in genes involved in lipoprotein metabolism influences high- and low-density lipoprotein cholesterol levels

Erratum to: Lack of Associations of Neuregulin 1 Variations with Schizophrenia and Smooth Pursuit Eye Movement Abnormality in a Korean Population

Exome sequencing and subsequent association studies identify five amino acid-altering variants influencing human height

Exome sequencing identified five novel USH2A variants in Korean patients with retinitis pigmentosa

Exome sequencing identified five novel USH2A variants in Korean patients with retinitis pigmentosa

Exome sequencing identifies KIAA1377 and C5orf42 as susceptibility genes for monomelic amyotrophy

Suchergebnisse filtern