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...

High Glucose Induces the Loss of Retinal Pericytes Partly via NLRP3-Caspase-1-GSDMD-Mediated Pyroptosis

BioMed research international, 2020, Vol.2020 (2020), p.1-12

2020

Volltextzugriff (PDF)

The MicroRNA Family Both in Normal Development and in Different Diseases: The miR-17-92 Cluster

BioMed research international, 2019-01, Vol.2019 (2019), p.1-11

2019

Volltextzugriff (PDF)

Whole-Exome Sequencing Identifies a Novel TRPM4 Mutation in a Chinese Family with Atrioventricular Block

BioMed research international, 2021, Vol.2021, p.9247541-6

2021

Volltextzugriff (PDF)

A Genetic Variant in GPR126 Causing a Decreased Inclusion of Exon 6 Is Associated with Cartilage Development in Adolescent Idiopathic Scoliosis Population

BioMed research international, 2019-01, Vol.2019 (2019), p.1-8

2019

Volltextzugriff (PDF)

Impact of Matrix Metalloproteinase 9 on COPD Development in Polish Patients: Genetic Polymorphism, Protein Level, and Their Relationship with Lung Function

BioMed research international, 2018-01, Vol.2018 (2018), p.1-11

2018

Volltextzugriff (PDF)

Vitamin D Receptor Gene Polymorphisms and Autoimmune Thyroiditis: Are They Associated with Disease Occurrence and Its Features?

BioMed research international, 2019, Vol.2019 (2019), p.1-9

2019

Volltextzugriff (PDF)

Associations between Inflammatory Cytokine Gene Polymorphisms and Susceptibilities to Intracranial Aneurysm in Chinese Population

BioMed research international, 2021, Vol.2021, p.8865601-9

2021

Volltextzugriff (PDF)

A Novel BBS9 Mutation Identified via Whole-Exome Sequencing in a Chinese Family with Bardet-Biedl Syndrome

BioMed research international, 2021, Vol.2021, p.4514967-5

2021

Volltextzugriff (PDF)

The Novel Compound Heterozygous Mutations of ECEL1 Identified in a Family with Distal Arthrogryposis Type 5D

BioMed research international, 2020, Vol.2020 (2020), p.1-6

2020

Volltextzugriff (PDF)

Whole-Exome Sequencing Identified a Novel Homozygous Frameshift Mutation of HPS3 in a Consanguineous Family with Hermansky-Pudlak Syndrome

BioMed research international, 2021, Vol.2021, p.4535349-7

2021

Volltextzugriff (PDF)

Association between VEGF Gene Polymorphisms and the Susceptibility to Lung Cancer: An Updated Meta-Analysis

BioMed research international, 2018-01, Vol.2018 (2018), p.1-16

2018

Volltextzugriff (PDF)

Ethnicity-Stratified Analysis of the Association between TNF-α Genetic Polymorphisms and Acute Kidney Injury: A Systematic Review and Meta-Analysis

BioMed research international, 2020, Vol.2020 (2020), p.1-8

2020

Volltextzugriff (PDF)

Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution

BioMed research international, 2019, Vol.2019 (2019), p.1-9

2019

Volltextzugriff (PDF)

Genetic Polymorphisms of IL1B, IL6, and TNFα in a Chinese Han Population with Pulmonary Tuberculosis

BioMed research international, 2018-01, Vol.2018 (2018), p.1-10

2018

Volltextzugriff (PDF)

Association of EPAS1 and PPARA Gene Polymorphisms with High-Altitude Headache in Chinese Han Population

BioMed research international, 2020, Vol.2020 (2020), p.1-11

2020

Volltextzugriff (PDF)

Association of rs2910164 Polymorphism in miRNA-146 and rs3746444 Polymorphism in miRNA-499 with Inflammatory Arthritis: A Meta-Analysis

BioMed research international, 2019-01, Vol.2019 (2019), p.1-9

2019

Volltextzugriff (PDF)

Rare Mutations in AHDC1 in Patients with Obstructive Sleep Apnea

BioMed research international, 2019, Vol.2019 (2019), p.1-7

2019

Volltextzugriff (PDF)

Methylation Changes of Primary Tumors, Monolayer, and Spheroid Tissue Culture Environments in Malignant Melanoma and Breast Carcinoma

BioMed research international, 2019-01, Vol.2019 (2019), p.1-9

2019

Volltextzugriff (PDF)

Biological Pathways of Long-Term Visit-to-Visit Blood Pressure Variability in the American Population: Cardiovascular Health Study and Women’s Health Initiatives

BioMed research international, 2020, Vol.2020 (2020), p.1-7

2020

Volltextzugriff (PDF)

Validation of Reference Genes for Gene Expression Normalization in RAW264.7 Cells under Different Conditions

BioMed research international, 2019-01, Vol.2019 (2019), p.1-9

2019

Volltextzugriff (PDF)

Rs4846049 Polymorphism at the 3′-UTR of MTHFR Gene: Association with Susceptibility to Childhood Acute Lymphoblastic Leukemia

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

2019

Volltextzugriff (PDF)

Single Nucleotide Polymorphisms in Selected Genes in Inflammatory Bowel Disease

BioMed research international, 2018-01, Vol.2018 (2018), p.1-5

2018

Volltextzugriff (PDF)

Molecular Evolutionary Analysis of the HCRTR Gene Family in Vertebrates

BioMed research international, 2018-01, Vol.2018 (2018), p.1-9

2018

Volltextzugriff (PDF)

Factors Affecting Quality and Safety of Fresh-Cut Produce

Critical reviews in food science and nutrition, 2012-07, Vol.52 (7), p.595-610

2012

Volltextzugriff (PDF)

Comprehensive Validation of Snapback Primer-Based Melting Curve Analysis to Detect Nucleotide Variation in the Codon 12 and 13 of KRAS Gene

BioMed research international, 2018-01, Vol.2018 (2018), p.1-13

2018

Volltextzugriff (PDF)

1 – 25 von 1.002

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(766)
Mit Volltextzugriff
(721)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

2 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

MEDLINE
(410)
IngentaConnect
(408)
EZB Electronic Journals Library
(350)
Journals@Ovid Full Text
(272)
Elsevier ScienceDirect Journals Complete
(175)
IngentaConnect Journals
(146)
SpringerLink
(131)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(111)
Single Journals
(103)
Wiley Blackwell Single Titles
(102)
Oxford journals
(86)
Oxford Journals 2020 Medicine
(78)
Wiley Online Library
(74)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(63)
Taylor & Francis Online
(39)
Taylor & Francis
(36)
Taylor & Francis Journals
(35)
Ebook Central Perpetual and DDA
(33)
eBooks on EBSCOhost
(30)
IEEE Xplore
(21)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(4)
... seit 90 Tagen
(15)

Menü

Weitere Dienste

Einstellungen

High Glucose Induces the Loss of Retinal Pericytes Partly via NLRP3-Caspase-1-GSDMD-Mediated Pyroptosis

The MicroRNA Family Both in Normal Development and in Different Diseases: The miR-17-92 Cluster

Whole-Exome Sequencing Identifies a Novel TRPM4 Mutation in a Chinese Family with Atrioventricular Block

A Genetic Variant in GPR126 Causing a Decreased Inclusion of Exon 6 Is Associated with Cartilage Development in Adolescent Idiopathic Scoliosis Population

Impact of Matrix Metalloproteinase 9 on COPD Development in Polish Patients: Genetic Polymorphism, Protein Level, and Their Relationship with Lung Function

Vitamin D Receptor Gene Polymorphisms and Autoimmune Thyroiditis: Are They Associated with Disease Occurrence and Its Features?

Associations between Inflammatory Cytokine Gene Polymorphisms and Susceptibilities to Intracranial Aneurysm in Chinese Population

A Novel BBS9 Mutation Identified via Whole-Exome Sequencing in a Chinese Family with Bardet-Biedl Syndrome

The Novel Compound Heterozygous Mutations of ECEL1 Identified in a Family with Distal Arthrogryposis Type 5D

Whole-Exome Sequencing Identified a Novel Homozygous Frameshift Mutation of HPS3 in a Consanguineous Family with Hermansky-Pudlak Syndrome

Association between VEGF Gene Polymorphisms and the Susceptibility to Lung Cancer: An Updated Meta-Analysis

Ethnicity-Stratified Analysis of the Association between TNF-α Genetic Polymorphisms and Acute Kidney Injury: A Systematic Review and Meta-Analysis

Analysis of the UGT1A1 Genotype in Hyperbilirubinemia Patients: Differences in Allele Frequency and Distribution

Genetic Polymorphisms of IL1B, IL6, and TNFα in a Chinese Han Population with Pulmonary Tuberculosis

Association of EPAS1 and PPARA Gene Polymorphisms with High-Altitude Headache in Chinese Han Population

Association of rs2910164 Polymorphism in miRNA-146 and rs3746444 Polymorphism in miRNA-499 with Inflammatory Arthritis: A Meta-Analysis

Rare Mutations in AHDC1 in Patients with Obstructive Sleep Apnea

Methylation Changes of Primary Tumors, Monolayer, and Spheroid Tissue Culture Environments in Malignant Melanoma and Breast Carcinoma

Biological Pathways of Long-Term Visit-to-Visit Blood Pressure Variability in the American Population: Cardiovascular Health Study and Women’s Health Initiatives

Validation of Reference Genes for Gene Expression Normalization in RAW264.7 Cells under Different Conditions

Rs4846049 Polymorphism at the 3′-UTR of MTHFR Gene: Association with Susceptibility to Childhood Acute Lymphoblastic Leukemia

Single Nucleotide Polymorphisms in Selected Genes in Inflammatory Bowel Disease

Molecular Evolutionary Analysis of the HCRTR Gene Family in Vertebrates

Factors Affecting Quality and Safety of Fresh-Cut Produce

Comprehensive Validation of Snapback Primer-Based Melting Curve Analysis to Detect Nucleotide Variation in the Codon 12 and 13 of KRAS Gene

Suchergebnisse filtern