UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Two Years of COVID: The Journey to Discover a New Disease

COVID, 2024-01, Vol.4 (1), p.85-86

Novelli, Giuseppe

2024

Link zum Volltext

Verfügbarkeit prüfen

HLA allele frequencies and susceptibility to COVID‐19 in a group of 99 Italian patients

HLA, 2020-11, Vol.96 (5), p.610-614

2020

Link zum Volltext

Verfügbarkeit prüfen

Genetic variants of the human host influencing the coronavirus-associated phenotypes (SARS, MERS and COVID-19): rapid systematic review and field synopsis

Human genomics, 2020-09, Vol.14 (1), p.30-30, Article 30

2020

Link zum Volltext

Verfügbarkeit prüfen

MEFV Gene Variant Alleles in Normal Population of Northwest of Iran, Which Is Near to Mediterranean Sea

Genetics research international, 2019, Vol.2019, p.6418759-4

2019

Link zum Volltext

Verfügbarkeit prüfen

Genetic polymorphisms associated with susceptibility to COVID-19 disease and severity: A systematic review and meta-analysis

PloS one, 2022-07, Vol.17 (7), p.e0270627-e0270627

2022

Link zum Volltext

Verfügbarkeit prüfen

Analysis of Mutation Rate of 17 Y-Chromosome Short Tandem Repeats Loci Using Tanzanian Father-Son Paired Samples

Genetics research international, 2018-01, Vol.2018, p.8090469-5

2018

Link zum Volltext

Verfügbarkeit prüfen

Genetics: A Starting Point for the Prevention and the Treatment of Obesity

Nutrients, 2023-06, Vol.15 (12), p.2782

2023

Link zum Volltext

Verfügbarkeit prüfen

A focus on the spread of the delta variant of SARS-CoV-2 in India

The Indian Journal of Medical Research, 2021-05, Vol.153 (5-6), p.537-541

2021

Link zum Volltext

Verfügbarkeit prüfen

COVID-19 and Genetic Variants of Protein Involved in the SARS-CoV-2 Entry into the Host Cells

Genes, 2020-08, Vol.11 (9), p.1010

2020

Link zum Volltext

Verfügbarkeit prüfen

Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery

Human genomics, 2020-06, Vol.14 (1), p.1-25, Article 25

2020

Link zum Volltext

Verfügbarkeit prüfen

Cell-free DNA analysis in healthy individuals by next-generation sequencing: a proof of concept and technical validation study

Cell death & disease, 2019-07, Vol.10 (7), p.534-11, Article 534

2019

Link zum Volltext

Verfügbarkeit prüfen

COVID-19 and Molecular Genetics

Genes, 2022-04, Vol.13 (4), p.676

2022

Link zum Volltext

Verfügbarkeit prüfen

Influence of CYP2C9 and VKORC1 on patient response to warfarin: a systematic review and meta-analysis

PloS one, 2012-08, Vol.7 (8), p.e44064

2012

Link zum Volltext

Verfügbarkeit prüfen

An integrated clinical and genetic model for predicting risk of severe COVID-19: A population-based case-control study

PloS one, 2021-02, Vol.16 (2), p.e0247205-e0247205

2021

Link zum Volltext

Verfügbarkeit prüfen

Analysis of ACE2 genetic variants in 131 Italian SARS-CoV-2-positive patients

Human genomics, 2020-09, Vol.14 (1), p.29-6, Article 29

2020

Link zum Volltext

Verfügbarkeit prüfen

Sex difference for the risk of amputation in diabetic patients: A systematic review and meta-analysis

PloS one, 2021-03, Vol.16 (3), p.e0243797-e0243797

2021

Link zum Volltext

Verfügbarkeit prüfen

COVID-19 2022 update: transition of the pandemic to the endemic phase

Human genomics, 2022-06, Vol.16 (1), p.19-19, Article 19

2022

Link zum Volltext

Verfügbarkeit prüfen

Decoding type 2 diabetes mellitus genetic risk variants in Pakistani Pashtun ethnic population using the nascent whole exome sequencing and MassARRAY genotyping: A case-control association study

PloS one, 2023-01, Vol.18 (1), p.e0281070-e0281070

2023

Link zum Volltext

Verfügbarkeit prüfen

MicroRNA 217 Modulates Endothelial Cell Senescence via Silent Information Regulator 1

Circulation (New York, N.Y.), 2009-10, Vol.120 (15), p.1524-1532

2009

Link zum Volltext

Verfügbarkeit prüfen

Non-invasive prenatal diagnosis of single gene disorders with enhanced relative haplotype dosage analysis for diagnostic implementation

PloS one, 2023-04, Vol.18 (4), p.e0280976-e0280976

2023

Link zum Volltext

Verfügbarkeit prüfen

The Qatari population’s genetic structure and gene flow as revealed by the Y chromosome

PloS one, 2023-09, Vol.18 (9), p.e0290844-e0290844

2023

Link zum Volltext

Verfügbarkeit prüfen

Rare CIDEC coding variants enriched in age-related macular degeneration patients with small low-luminance deficit cause lipid droplet and fat storage defects

PloS one, 2023-04, Vol.18 (4), p.e0280484-e0280484

2023

Link zum Volltext

Verfügbarkeit prüfen

Genetic polymorphisms associated with psoriasis and development of psoriatic arthritis in patients with psoriasis

PloS one, 2018-02, Vol.13 (2), p.e0192010-e0192010

2018

Link zum Volltext

Verfügbarkeit prüfen

Medicalizing risk: How experts and consumers manage uncertainty in genetic health testing

PloS one, 2022-08, Vol.17 (8), p.e0270430-e0270430

2022

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 911

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(839)
Mit Volltextzugriff
(829)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(720)
Life Sciences & Biomedicine
(600)
Humans
(567)
Female
(265)
Male
(257)
Genetics & Heredity
(192)
Adult
(155)
Mutation
(132)
Biological And Medical Sciences
(130)
Middle Aged
(129)
Science & Technology - Other Topics
(121)
Multidisciplinary Sciences
(119)
Medical Sciences
(117)
Genes
(111)
Animals
(106)
Genetic Aspects
(98)
Genetics
(94)
Medicine
(85)
Aged
(84)
Biochemistry & Molecular Biology
(84)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(11)

Menü

Weitere Dienste

Einstellungen

Two Years of COVID: The Journey to Discover a New Disease

HLA allele frequencies and susceptibility to COVID‐19 in a group of 99 Italian patients

Genetic variants of the human host influencing the coronavirus-associated phenotypes (SARS, MERS and COVID-19): rapid systematic review and field synopsis

MEFV Gene Variant Alleles in Normal Population of Northwest of Iran, Which Is Near to Mediterranean Sea

Genetic polymorphisms associated with susceptibility to COVID-19 disease and severity: A systematic review and meta-analysis

Analysis of Mutation Rate of 17 Y-Chromosome Short Tandem Repeats Loci Using Tanzanian Father-Son Paired Samples

Genetics: A Starting Point for the Prevention and the Treatment of Obesity

A focus on the spread of the delta variant of SARS-CoV-2 in India

COVID-19 and Genetic Variants of Protein Involved in the SARS-CoV-2 Entry into the Host Cells

Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery

Cell-free DNA analysis in healthy individuals by next-generation sequencing: a proof of concept and technical validation study

COVID-19 and Molecular Genetics

Influence of CYP2C9 and VKORC1 on patient response to warfarin: a systematic review and meta-analysis

An integrated clinical and genetic model for predicting risk of severe COVID-19: A population-based case-control study

Analysis of ACE2 genetic variants in 131 Italian SARS-CoV-2-positive patients

Sex difference for the risk of amputation in diabetic patients: A systematic review and meta-analysis

COVID-19 2022 update: transition of the pandemic to the endemic phase

Decoding type 2 diabetes mellitus genetic risk variants in Pakistani Pashtun ethnic population using the nascent whole exome sequencing and MassARRAY genotyping: A case-control association study

MicroRNA 217 Modulates Endothelial Cell Senescence via Silent Information Regulator 1

Non-invasive prenatal diagnosis of single gene disorders with enhanced relative haplotype dosage analysis for diagnostic implementation

The Qatari population’s genetic structure and gene flow as revealed by the Y chromosome

Rare CIDEC coding variants enriched in age-related macular degeneration patients with small low-luminance deficit cause lipid droplet and fat storage defects

Genetic polymorphisms associated with psoriasis and development of psoriatic arthritis in patients with psoriasis

Medicalizing risk: How experts and consumers manage uncertainty in genetic health testing

Inhibition of HECT E3 ligases as potential therapy for COVID-19

Suchergebnisse filtern