UB Paderborn / Katalog / Suche / in CDI

1 – 14 von 14

Sortiert nach

A magnetically controlled multi-winding sub-compensated active harmonic isolator

2024 IEEE 10th International Power Electronics and Motion Control Conference (IPEMC2024-ECCE Asia), 2024, p.3748-3752

2024

Volltextzugriff (PDF)

Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

Human genetics, 2013-03, Vol.132 (3), p.285-292

2013

Volltextzugriff (PDF)

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

Genetics in medicine, 2020-12, Vol.22 (12), p.2020-2028

2020

Volltextzugriff (PDF)

A highly efficient transcriptome-based biosynthesis of non-ethanol chemicals in Crabtree negative Saccharomyces cerevisiae

Biotechnology for biofuels and bioproducts, 2023-03, Vol.16 (1), p.37-37, Article 37

2023

Volltextzugriff (PDF)

Genome-wide microRNA expression profiling in idiopathic non-obstructive azoospermia: significant up-regulation of miR-141, miR-429 and miR-7-1-3p

Human reproduction (Oxford), 2013-07, Vol.28 (7), p.1827-1836

2013

Volltextzugriff (PDF)

Porous CaP/silk composite scaffolds to repair femur defects in an osteoporotic model

Journal of materials science. Materials in medicine, 2013-08, Vol.24 (8), p.1963-1975

2013

Volltextzugriff (PDF)

Learnable Color Image Zero-Watermarking Based on Feature Comparison

Neural Information Processing, p.472-483

Volltextzugriff (PDF)

Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia

Journal of medical genetics, 2014-03, Vol.51 (3), p.197-202

2014

Volltextzugriff (PDF)

Neuregulin 1 genetic variation and anterior cingulum integrity in patients with schizophrenia and healthy controls

Journal of psychiatry & neuroscience, 2009-05, Vol.34 (3), p.181-186

2009

Volltextzugriff (PDF)

Comprehensive pathway-based analysis identifies associations of BCL2, GNAO1 and CHD2 with non-obstructive azoospermia risk

Human reproduction (Oxford), 2014-04, Vol.29 (4), p.860-866

2014

Volltextzugriff (PDF)

Design Charts for Reinforced Slopes with Turning Corner

Proceedings of GeoShanghai 2018 International Conference: Ground Improvement and Geosynthetics, p.297-306

Volltextzugriff (PDF)

Research on CO2 Laser Frequency Stabilization by Adjusting Grating Angle

Proceedings of the 5th International Conference on Electrical Engineering and Automatic Control, 2016, Vol.367, p.513-519

2016

Volltextzugriff (PDF)

1 – 14 von 14

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(11)
Mit Volltextzugriff
(13)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(13)
Life Sciences & Biomedicine
(9)
Humans
(8)
Male
(7)
Genetics & Heredity
(5)
Technology
(5)
Female
(4)
Hernias
(4)
Hernias, Diaphragmatic, Congenital - Genetics
(4)
Engineering
(3)
Genetic Aspects
(3)
Genetic Variation
(3)
Genomes
(3)
Genotype
(3)
Infant, Newborn
(3)
Mutation, Missense
(3)
Sequence Analysis, Dna
(3)
Animals
(2)
Azoospermia - Genetics
(2)
Biological And Medical Sciences
(2)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

A magnetically controlled multi-winding sub-compensated active harmonic isolator

De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

A highly efficient transcriptome-based biosynthesis of non-ethanol chemicals in Crabtree negative Saccharomyces cerevisiae

Genome-wide microRNA expression profiling in idiopathic non-obstructive azoospermia: significant up-regulation of miR-141, miR-429 and miR-7-1-3p

Porous CaP/silk composite scaffolds to repair femur defects in an osteoporotic model

Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene

Learnable Color Image Zero-Watermarking Based on Feature Comparison

Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia

Neuregulin 1 genetic variation and anterior cingulum integrity in patients with schizophrenia and healthy controls

Comprehensive pathway-based analysis identifies associations of BCL2, GNAO1 and CHD2 with non-obstructive azoospermia risk

Design Charts for Reinforced Slopes with Turning Corner

Research on CO2 Laser Frequency Stabilization by Adjusting Grating Angle

Suchergebnisse filtern