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 Differentially Expressed Genes in the Substantia Nigra in Parkinson's Disease Supports Phenotype-Specific Transcriptome Changes

Frontiers in neuroscience, 2020-12, Vol.14, p.596105-596105

2020

Volltextzugriff (PDF)

Global Analysis of the Human RNA Degradome Reveals Widespread Decapped and Endonucleolytic Cleaved Transcripts

International journal of molecular sciences, 2020-09, Vol.21 (18), p.6452

2020

Volltextzugriff (PDF)

RelCurator: a text mining-based curation system for extracting gene–phenotype relationships specific to neurodegenerative disorders

Genes & Genomics, 2023, 45(8), , pp.1025-1036

2023

Volltextzugriff (PDF)

Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease

Journal Of Movement Disorders, 2022, 15(2), , pp.132-139

2022

Volltextzugriff (PDF)

The Korea‐Vietnam trade and the bilateral exchange rate: Asymmetric evidence from commodity trade data

Australian economic papers, 2023-03, Vol.62 (1), p.124-148

2023

Volltextzugriff (PDF)

The burden of rare damaging variants in hereditary atypical parkinsonism genes is increased in patients with Parkinson’s disease

Neurobiology of aging, 2021-04, Vol.100, p.118.e5-118.e13

2021

Volltextzugriff (PDF)

Extraction of Informative Genes from Multiple Microarray Data Integrated by Rank-Based Approach

IEICE Transactions on Information and Systems, 2011/04/01, Vol.E94.D(4), pp.841-854

2011

Volltextzugriff (PDF)

2314-PUB: No Clinical Factors, Except Baseline HbA1c, Can Predict Glycemic Response to Dulaglutide: Real-World Data in Korean Patients

Diabetes (New York, N.Y.), 2019-06, Vol.68 (Supplement_1)

2019

Volltextzugriff (PDF)

1247-P: Mildly Elevated Triglyceride Levels Are Associated with Increased Risk for Major Adverse Cardiovascular Events in Statin-Naïve Rheumatoid Arthritis Patients—A Nationwide Cohort Study

Diabetes (New York, N.Y.), 2023-06, Vol.72 (Supplement_1), p.1

2023

Volltextzugriff (PDF)

The Protein-Protein Interaction Network of Hereditary Parkinsonism Genes Is a Hierarchical Scale-Free Network

Yonsei Medical Journal, 2022, 63(8), , pp.724-734

2022

Volltextzugriff (PDF)

Synthesis and Reactivity of a Mononuclear Manganese(II) Complex Having Pseudo-Seven Coordination Environment

Bulletin of the Korean Chemical Society, 2009, 30(3), , pp.679-682

2009

Volltextzugriff (PDF)

GAAP: A Genome Assembly + Annotation Pipeline

BioMed research international, 2019, Vol.2019 (2019), p.1-12

2019

Volltextzugriff (PDF)

Effect of polygenic load on striatal dopaminergic deterioration in Parkinson disease

Neurology, 2019-08, Vol.93 (7), p.e665

2019

Volltextzugriff (PDF)

A Case of Endobronchial Osteochondromatous Hamartoma Removed Using Flexible Bronchoscopy

Archivos de bronconeumología (English ed.), 2012-11, Vol.48 (11), p.427-428

2012

Volltextzugriff (PDF)

A computational method for detecting copy number variations using scale-space filtering

BMC bioinformatics, 2013-02, Vol.14 (1), p.57-57, Article 57

2013

Volltextzugriff (PDF)

PhenGenVar: A User-Friendly Genetic Variant Detection and Visualization Tool for Precision Medicine

Journal of personalized medicine, 2022-06, Vol.12 (6), p.959

2022

Volltextzugriff (PDF)

Comparing Montreal Cognitive Assessment Performance in Parkinson’s Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning

Journal of movement disorders, 2024-04, Vol.17 (2), p.171-180

2024

Volltextzugriff (PDF)

ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data

BioMed research international, 2017-01, Vol.2017 (2017), p.1-11

2017

Volltextzugriff (PDF)

Dysregulation of the causative genes for hereditary parkinsonism in the midbrain in Parkinson's disease

Movement disorders, 2017-08, Vol.32 (8), p.1211-1220

2017

Volltextzugriff (PDF)

WebPORD: a web-based pipeline of RNA degradome

International journal of data mining and bioinformatics, 2019, Vol.22 (3), p.216

2019

Volltextzugriff (PDF)

Draft Genome of Toxocara canis, a Pathogen Responsible for Visceral Larva Migrans

Korean journal of parasitology, 2016-12, Vol.54 (6), p.751-758

2016

Volltextzugriff (PDF)

WebPORD: a web-based pipeline of RNA degradome

International journal of data mining and bioinformatics, 2019, Vol.22 (3), p.216

2019

Volltextzugriff (PDF)

An efficient noise reduction method for copy number variations detection from whole exome sequencing data

2016 International Conference on High Performance Computing & Simulation (HPCS), 2016, p.1027-1028

2016

Volltextzugriff (PDF)

Detection of copy number variation using scale space filtering

2011 Annual International Conference of the IEEE Engineering in Medicine and Biology Society, 2011, Vol.2011, p.5555-5558

2011

Volltextzugriff (PDF)

Shape-based retrieval of CNV regions in read coverage data

International journal of data mining and bioinformatics, 2014, Vol.9 (3), p.254

2014

Volltextzugriff (PDF)

1 – 25 von 59

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(44)
Mit Volltextzugriff
(43)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(34)
Life Sciences & Biomedicine
(26)
Humans
(14)
Genomics
(8)
Original
(8)
Genomes
(7)
Technology
(7)
Gene Expression
(6)
Animals
(5)
Biochemistry & Molecular Biology
(5)
General & Internal Medicine
(5)
Medicine, General & Internal
(5)
Neurosciences & Neurology
(5)
Parkinson’s Disease
(5)
Algorithms
(4)
Bioinformatics
(4)
Biotechnology & Applied Microbiology
(4)
Computer Science
(4)
Genes
(4)
Aged
(3)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Meta-Analysis of Differentially Expressed Genes in the Substantia Nigra in Parkinson's Disease Supports Phenotype-Specific Transcriptome Changes

Global Analysis of the Human RNA Degradome Reveals Widespread Decapped and Endonucleolytic Cleaved Transcripts

RelCurator: a text mining-based curation system for extracting gene–phenotype relationships specific to neurodegenerative disorders

Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease

The Korea‐Vietnam trade and the bilateral exchange rate: Asymmetric evidence from commodity trade data

The burden of rare damaging variants in hereditary atypical parkinsonism genes is increased in patients with Parkinson’s disease

Extraction of Informative Genes from Multiple Microarray Data Integrated by Rank-Based Approach

2314-PUB: No Clinical Factors, Except Baseline HbA1c, Can Predict Glycemic Response to Dulaglutide: Real-World Data in Korean Patients

1247-P: Mildly Elevated Triglyceride Levels Are Associated with Increased Risk for Major Adverse Cardiovascular Events in Statin-Naïve Rheumatoid Arthritis Patients—A Nationwide Cohort Study

The Protein-Protein Interaction Network of Hereditary Parkinsonism Genes Is a Hierarchical Scale-Free Network

Synthesis and Reactivity of a Mononuclear Manganese(II) Complex Having Pseudo-Seven Coordination Environment

GAAP: A Genome Assembly + Annotation Pipeline

Effect of polygenic load on striatal dopaminergic deterioration in Parkinson disease

A Case of Endobronchial Osteochondromatous Hamartoma Removed Using Flexible Bronchoscopy

A computational method for detecting copy number variations using scale-space filtering

PhenGenVar: A User-Friendly Genetic Variant Detection and Visualization Tool for Precision Medicine

Comparing Montreal Cognitive Assessment Performance in Parkinson’s Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning

ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data

Dysregulation of the causative genes for hereditary parkinsonism in the midbrain in Parkinson's disease

WebPORD: a web-based pipeline of RNA degradome

Draft Genome of Toxocara canis, a Pathogen Responsible for Visceral Larva Migrans

WebPORD: a web-based pipeline of RNA degradome

An efficient noise reduction method for copy number variations detection from whole exome sequencing data

Detection of copy number variation using scale space filtering

Shape-based retrieval of CNV regions in read coverage data

Suchergebnisse filtern