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...

Multi-Axis 3D Printing Defect Detecting by Machine Vision with Convolutional Neural Networks

Experimental techniques (Westport, Conn.), 2023-06, Vol.47 (3), p.619-631

2023

Volltextzugriff (PDF)

Efficacy and safety of combination therapy with vildagliptin and metformin versus metformin uptitration in Chinese patients with type 2 diabetes inadequately controlled with metformin monotherapy: a randomized, open-label, prospective study (VISION)

Diabetes, obesity & metabolism, 2016-08, Vol.18 (8), p.775-782

2016

Volltextzugriff (PDF)

Ferroelectric properties and microstructures of Nd2O3-doped Bi4Ti3O12 ceramics

Physica status solidi. A, Applied research, 2003-12, Vol.200 (2), p.446-450

2003

Volltextzugriff (PDF)

Self-assembly and photovoltaic properties of multilayer films based on partially doped polyaniline and poly(4-carboxyphenyl)acetylene

Journal of polymer science. Part A, Polymer chemistry, 2004-07, Vol.42 (13), p.3224-3229

2004

Volltextzugriff (PDF)

A genetic coding variant rs72474224 in GJB2 is associated with clinical features of psoriasis vulgaris in a Chinese Han population

Tissue antigens, 2015-08, Vol.86 (2), p.134-138

2015

Volltextzugriff (PDF)

Three novel mutations in GPNMB in two pedigrees with amyloidosis cutis dyschromica

The British journal of dermatology, 2019, Vol.181 (6), p.1327-1329

2019

Volltextzugriff (PDF)

Tumor necrosis factor prevents alendronate‐induced osteoclast apoptosis in vivo by stimulating Bcl‐xL expression through Ets‐2

Arthritis and rheumatism, 2005-09, Vol.52 (9), p.2708-2718

2005

Volltextzugriff (PDF)

Synthesis and characterization of highly random copolymer of ϵ-caprolactone and D,L-lactide using rare earth catalyst

Journal of polymer science. Part A, Polymer chemistry, 1996-07, Vol.34 (9), p.1799-1805

1996

Volltextzugriff (PDF)

Surface modification of poly (D,L-lactic acid) with chitosan and its effects on the culture of osteoblasts in vitro

Journal of biomedical materials research, 2002-06, Vol.60 (3), p.398-404

2002

Volltextzugriff (PDF)

Ferroelectric properties and microstructures of Nd(2)O(3)-doped Bi(4)Ti(3)O(12) ceramics

Physica status solidi. A, Applied research, 2003-12, Vol.200 (2), p.446-450

2003

Volltextzugriff (PDF)

A rare RECQL4 indel mutation in a Chinese patient with Rothmund-Thomson syndrome

Journal of the European Academy of Dermatology and Venereology : JEADV, 2016, Vol.30 (11), p.e159-e161

2016

Volltextzugriff (PDF)

Gene diagnosis and prenatal genetic diagnosis of a case of dystrophic epidermolysis bullosa family caused by gonadosomatic mosaicism for the COL7A1 mutation p.Gly2043Arg in the pregnant mother

Journal of the European Academy of Dermatology and Venereology : JEADV, 2016, Vol.30 (9), p.1627-1629

2016

Volltextzugriff (PDF)

Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novel KITLG mutation

The British journal of dermatology, 2016, Vol.175 (6), p.1369-1371

2016

Volltextzugriff (PDF)

Improvement of the functions of osteoblasts seeded on modified poly(D,L-lactic acid) with poly(aspartic acid)

Journal of biomedical materials research, 2002-11, Vol.62 (2), p.283-291

2002

Volltextzugriff (PDF)

Synthesis and Superconducting Properties of the Ca1−xNaxLaBaCu3Oy System

Physica status solidi. A, Applied research, 1996-06, Vol.155 (2), p.467-472

1996

Volltextzugriff (PDF)

A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature

American journal of medical genetics, 2002-11, Vol.113 (1), p.29-39

2002

Volltextzugriff (PDF)

Genome-wide linkage and exome sequencing analyses identify an initiation codon mutation of KRT5 in a unique Chinese family with generalized Dowling-Degos disease

The British journal of dermatology, 2016, Vol.174 (3), p.663-666

2016

Volltextzugriff (PDF)

Polymorphic microsatellite markers in the Zhikong scallop Chlamys farreri

Molecular ecology notes, 2006-03, Vol.6 (1), p.127-129

2006

Volltextzugriff (PDF)

ChemInform Abstract: Experimental Study of the Isothermal Section of the Ho-Fe-Cr System at 873 K

ChemInform, 2011-03, Vol.42 (11), p.no-no

2011

Volltextzugriff (PDF)

A novel mutation in the COL7A1 gene results in a unique phenotype of epidermolysis bullosa pruriginosa

Journal of the European Academy of Dermatology and Venereology : JEADV, 2016, Vol.30 (3), p.535-536

2016

Volltextzugriff (PDF)

A recurrent mutation in the APCDD1 gene responsible for hereditary hypotrichosis simplex in a large Chinese family

The British journal of dermatology, 2012, Vol.167 (4), p.952-954

2012

Volltextzugriff (PDF)

3-(2-Chlorobenzyl)-2-thioxoperhydropyrimidin-4-one

Acta crystallographica. Section E, Structure reports online, 2004-06, Vol.60 (6), p.o943-o945

2004

Volltextzugriff (PDF)

2‐(2,4‐Dichlorophenoxy)‐N‐(4,6‐dimethoxypyrimidin‐2‐yl)propionamide

Acta crystallographica. Section E, Structure reports online, 2006-03, Vol.62 (3), p.o1028-o1029

2006

Volltextzugriff (PDF)

Support Vector Machine-based QSPR for the Prediction of Van der Waals' Constants

QSAR & combinatorial science, 2005-03, Vol.24 (2), p.227-239

2005

Volltextzugriff (PDF)

Characterization of HLA-B5516, -B1313, -B9512, and -DRB11457 alleles identified in a southwest Chinese population

Tissue antigens, 2006-10, Vol.68 (4), p.339-343

2006

Volltextzugriff (PDF)

1 – 25 von 47

Suche als RSS-Feed

Aktive Filter

Nur zeigenGeprüft (Peer-Review)

KollektionWiley Online Library

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Mit Volltextzugriff
(41)

Publikationsform

Sprache

Englisch
(47)
Japanisch
(2)

Erscheinungsjahr

n.n

Kollektion

3 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Multi-Axis 3D Printing Defect Detecting by Machine Vision with Convolutional Neural Networks

Efficacy and safety of combination therapy with vildagliptin and metformin versus metformin uptitration in Chinese patients with type 2 diabetes inadequately controlled with metformin monotherapy: a randomized, open-label, prospective study (VISION)

Ferroelectric properties and microstructures of Nd2O3-doped Bi4Ti3O12 ceramics

Self-assembly and photovoltaic properties of multilayer films based on partially doped polyaniline and poly(4-carboxyphenyl)acetylene

A genetic coding variant rs72474224 in GJB2 is associated with clinical features of psoriasis vulgaris in a Chinese Han population

Three novel mutations in GPNMB in two pedigrees with amyloidosis cutis dyschromica

Tumor necrosis factor prevents alendronate‐induced osteoclast apoptosis in vivo by stimulating Bcl‐xL expression through Ets‐2

Synthesis and characterization of highly random copolymer of ϵ-caprolactone and D,L-lactide using rare earth catalyst

Surface modification of poly (D,L-lactic acid) with chitosan and its effects on the culture of osteoblasts in vitro

Ferroelectric properties and microstructures of Nd(2)O(3)-doped Bi(4)Ti(3)O(12) ceramics

A rare RECQL4 indel mutation in a Chinese patient with Rothmund-Thomson syndrome

Gene diagnosis and prenatal genetic diagnosis of a case of dystrophic epidermolysis bullosa family caused by gonadosomatic mosaicism for the COL7A1 mutation p.Gly2043Arg in the pregnant mother

Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novel KITLG mutation

Improvement of the functions of osteoblasts seeded on modified poly(D,L-lactic acid) with poly(aspartic acid)

Synthesis and Superconducting Properties of the Ca1−xNaxLaBaCu3Oy System

A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature

Genome-wide linkage and exome sequencing analyses identify an initiation codon mutation of KRT5 in a unique Chinese family with generalized Dowling-Degos disease

Polymorphic microsatellite markers in the Zhikong scallop Chlamys farreri

ChemInform Abstract: Experimental Study of the Isothermal Section of the Ho-Fe-Cr System at 873 K

A novel mutation in the COL7A1 gene results in a unique phenotype of epidermolysis bullosa pruriginosa

A recurrent mutation in the APCDD1 gene responsible for hereditary hypotrichosis simplex in a large Chinese family

3-(2-Chlorobenzyl)-2-thioxoperhydropyrimidin-4-one

2‐(2,4‐Dichlorophenoxy)‐N‐(4,6‐dimethoxypyrimidin‐2‐yl)propionamide

Support Vector Machine-based QSPR for the Prediction of Van der Waals' Constants

Characterization of HLA-B5516, -B1313, -B9512, and -DRB11457 alleles identified in a southwest Chinese population

Aktive Filter

Suchergebnisse filtern