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...

Comparative method evaluation for size and size-distribution analysis of gold nanoparticles

Journal of separation science, 2013-09, Vol.36 (17), p.2952-2961

2013

Volltextzugriff (PDF)

Fabrication and bonding of thiol-ene-based microfluidic devices

Journal of micromechanics and microengineering, 2013-03, Vol.23 (3), p.37002-7

2013

Volltextzugriff (PDF)

Rapid and sensitive drug metabolism studies by SU-8 microchip capillary electrophoresis-electrospray ionization mass spectrometry

Journal of Chromatography A, 2011-02, Vol.1218 (5), p.739-745

2011

Volltextzugriff (PDF)

Preparation of some 10, 10 -dimethyltricyclo(7.1.1.0(2,7))undecenones and 9,9 -dimethyltricyclo(6.1.1.0(2,6))-decenones from 2-pinene and 2(10)-pinene

Kopsa-Moilanen, Vieno Maria

1993

Volltextzugriff (PDF)

Serum Amyloid A as a Marker of Persistent Inflammation and an Indicator of Cardiovascular and Renal Involvement in Patients with Rheumatoid Arthritis

Mediators of Inflammation, 2014-01, Vol.2014 (8), p.65-71

2014

Volltextzugriff (PDF)

Light scattering by airborne ice crystals – An inventory of atmospheric halos

Journal of quantitative spectroscopy & radiative transfer, 2022-11, Vol.290, p.108313, Article 108313

2022

Volltextzugriff (PDF)

Determination of strewn fields for meteorite falls

Monthly notices of the Royal Astronomical Society, 2021-05, Vol.503 (3), p.3337-3350

2021

Volltextzugriff (PDF)

How threats inform conservation planning-A systematic review protocol

PloS one, 2022-05, Vol.17 (5), p.e0269107-e0269107

2022

Volltextzugriff (PDF)

Expression of Annexin-A1 and Galectin-1 Anti-Inflammatory Proteins and mRNA in Chronic Gastritis and Gastric Cancer

Mediators of Inflammation, 2013-01, Vol.2013 (2013), p.201-211-018

2013

Volltextzugriff (PDF)

Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases

Neuropediatrics, 2018-08, Vol.49 (4), p.256-261

2018

Volltextzugriff (PDF)

Brain MRI findings in paediatric genetic disorders associated with white matter abnormalities

Developmental medicine and child neurology, 2024-07

2024

Volltextzugriff (PDF)

Response to: Comment on ＂Serum Amyloid A as a Marker of Persistent Inflammation and an Indicator of Cardiovascular and Renal Involvement in Patients with Rheumatoid Arthritis

Mediators of Inflammation, 2015-01, Vol.2015 (2015), p.843-843-387

2015

Volltextzugriff (PDF)

Autism Spectrum Disorders According to DSM-IV-TR and Comparison With DSM-5 Draft Criteria: An Epidemiological Study

Journal of the American Academy of Child and Adolescent Psychiatry, 2011-06, Vol.50 (6), p.583-592.e11

2011

Volltextzugriff (PDF)

FEM-based time-reversal enhanced ultrasonic cleaning

Ultrasonics sonochemistry, 2021-11, Vol.79, p.105798-105798, Article 105798

2021

Volltextzugriff (PDF)

Integrating biodiversity, ecosystem services and socio-economic data to identify priority areas and landowners for conservation actions at the national scale

Biological conservation, 2017-02, Vol.206, p.56-64

2017

Volltextzugriff (PDF)

The co‐occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific

Aging cell, 2014-06, Vol.13 (3), p.401-407

2014

Volltextzugriff (PDF)

Epidemiological, clinical, and genetic characteristics of paediatric genetic white matter disorders in Northern Finland

Developmental medicine and child neurology, 2021-09, Vol.63 (9), p.1066-1074

2021

Volltextzugriff (PDF)

Inhibition of Let‐7 microRNA attenuates myocardial remodeling and improves cardiac function postinfarction in mice

Pharmacology research & perspectives, 2014-08, Vol.2 (4), p.e00056-n/a

2014

Volltextzugriff (PDF)

Clinical and genetic characteristics and natural history of Finnish families with familial exudative vitreoretinopathy due to pathogenic FZD4 variants

Acta ophthalmologica (Oxford, England), 2024-05

2024

Volltextzugriff (PDF)

Anti‐rheumatic medication and salivary MMP‐8, a biomarker for periodontal disease

Oral diseases, 2018-11, Vol.24 (8), p.1562-1571

2018

Volltextzugriff (PDF)

Clinical and Genetic Characteristics of Finnish Patients with Autosomal Recessive and Dominant Non-Syndromic Hearing Loss Due to Pathogenic TMC1 Variants

Journal of clinical medicine, 2022-03, Vol.11 (7), p.1837

2022

Volltextzugriff (PDF)

Early Detection, Diagnosis and Intervention Services for Young Children with Autism Spectrum Disorder in the European Union (ASDEU): Family and Professional Perspectives

Journal of autism and developmental disorders, 2020-09, Vol.50 (9), p.3380-3394

2020

Volltextzugriff (PDF)

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

Journal of allergy and clinical immunology, 2010-02, Vol.125 (2), p.424-432.e8

2010

Volltextzugriff (PDF)

ECRIN – CESSDA strategies for cross metadata mappings in selected areas between life sciences and social sciences and humanities

Open research Europe, 2023, Vol.3, p.180-180

2023

Volltextzugriff (PDF)

ECRIN - CESSDA strategies for cross metadata mappings in selected areas between life sciences and social sciences and humanities

Open research Europe, 2023, Vol.3, p.180

2023

Volltextzugriff (PDF)

1 – 25 von 65

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(62)
Mit Volltextzugriff
(58)

Publikationsform

Sprache

Englisch
(65)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Comparative method evaluation for size and size-distribution analysis of gold nanoparticles

Fabrication and bonding of thiol-ene-based microfluidic devices

Rapid and sensitive drug metabolism studies by SU-8 microchip capillary electrophoresis-electrospray ionization mass spectrometry

Preparation of some 10, 10 -dimethyltricyclo(7.1.1.0(2,7))undecenones and 9,9 -dimethyltricyclo(6.1.1.0(2,6))-decenones from 2-pinene and 2(10)-pinene

Serum Amyloid A as a Marker of Persistent Inflammation and an Indicator of Cardiovascular and Renal Involvement in Patients with Rheumatoid Arthritis

Light scattering by airborne ice crystals – An inventory of atmospheric halos

Determination of strewn fields for meteorite falls

How threats inform conservation planning-A systematic review protocol

Expression of Annexin-A1 and Galectin-1 Anti-Inflammatory Proteins and mRNA in Chronic Gastritis and Gastric Cancer

Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases

Brain MRI findings in paediatric genetic disorders associated with white matter abnormalities

Response to: Comment on ＂Serum Amyloid A as a Marker of Persistent Inflammation and an Indicator of Cardiovascular and Renal Involvement in Patients with Rheumatoid Arthritis

Autism Spectrum Disorders According to DSM-IV-TR and Comparison With DSM-5 Draft Criteria: An Epidemiological Study

FEM-based time-reversal enhanced ultrasonic cleaning

Integrating biodiversity, ecosystem services and socio-economic data to identify priority areas and landowners for conservation actions at the national scale

The co‐occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific

Epidemiological, clinical, and genetic characteristics of paediatric genetic white matter disorders in Northern Finland

Inhibition of Let‐7 microRNA attenuates myocardial remodeling and improves cardiac function postinfarction in mice

Clinical and genetic characteristics and natural history of Finnish families with familial exudative vitreoretinopathy due to pathogenic FZD4 variants

Anti‐rheumatic medication and salivary MMP‐8, a biomarker for periodontal disease

Clinical and Genetic Characteristics of Finnish Patients with Autosomal Recessive and Dominant Non-Syndromic Hearing Loss Due to Pathogenic TMC1 Variants

Early Detection, Diagnosis and Intervention Services for Young Children with Autism Spectrum Disorder in the European Union (ASDEU): Family and Professional Perspectives

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

ECRIN – CESSDA strategies for cross metadata mappings in selected areas between life sciences and social sciences and humanities

ECRIN - CESSDA strategies for cross metadata mappings in selected areas between life sciences and social sciences and humanities

Suchergebnisse filtern