UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 677

Sortiert nach

Reliable Low-Density DNA Array Based on Allele-Specific Probes for Detection of 118 Mutations Causing Familial Hypercholesterolemia

Clinical chemistry (Baltimore, Md.), 2005-07, Vol.51 (7), p.1137-1144

2005

Link zum Volltext

Verfügbarkeit prüfen

Can we predict top-level sports performance in power vs endurance events? A genetic approach

Scandinavian journal of medicine & science in sports, 2011-08, Vol.21 (4), p.570-579

2011

Link zum Volltext

Verfügbarkeit prüfen

A new tool based on next generation sequencing for an efficient and rapid diagnosis of familial hypercholesterolemia

Atherosclerosis, 2014-08, Vol.235 (2), p.e57-e57

2014

Link zum Volltext

Verfügbarkeit prüfen

The C677T polymorphism in the MTHFR gene is associated with the toxicity of methotrexate in a Spanish rheumatoid arthritis population

Scandinavian journal of rheumatology, 2012-02, Vol.41 (1), p.10-14

2012

Link zum Volltext

Verfügbarkeit prüfen

Validation of a ce marked tool (seqpro lipo rs) based on next generation sequencing for diagnosis of familial hypercholesterolemia

Atherosclerosis, 2014-08, Vol.235 (2), p.e57-e58

2014

Link zum Volltext

Verfügbarkeit prüfen

Improved prediction of knee osteoarthritis progression by genetic polymorphisms. Arthrotest study results

Osteoarthritis and cartilage, 2014-04, Vol.22, p.S236-S236

2014

Link zum Volltext

Verfügbarkeit prüfen

THU0211 Genetic Polymorphisms Can Predict Knee Osteoarthritis Progression. Results from the Arthrotest Multicenter Association Study

Annals of the rheumatic diseases, 2014-06, Vol.73 (Suppl 2), p.254-255

2014

Link zum Volltext

Verfügbarkeit prüfen

AB0857 Single nucleotide polymorphisms associated with non response to anti-TNF-alpha treatment in ankylosing spondylitis patients. Data from regisponser

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.687-687

2013

Link zum Volltext

Verfügbarkeit prüfen

(4) Routine diagnosis of familial hypercholesterolemia with next generation sequencing

Atherosclerosis, 2012-08, Vol.223 (2), p.528-529

2012

Link zum Volltext

Verfügbarkeit prüfen

Haplotype analyses, mechanism and evolution of common double mutants in the human LDL receptor gene

Molecular genetics and genomics : MGG, 2010-06, Vol.283 (6), p.565-574

2010

Link zum Volltext

Verfügbarkeit prüfen

A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia

Journal of medical genetics, 2003-03, Vol.40 (3), p.163-168

2003

Link zum Volltext

Verfügbarkeit prüfen

Genetic Correlations of Brain Lesion Distribution in Multiple Sclerosis: An Exploratory Study

American journal of neuroradiology : AJNR, 2011-04, Vol.32 (4), p.695-703

2011

Link zum Volltext

Verfügbarkeit prüfen

Toward Personalized Medicine in Renal Transplantation

Transplantation proceedings, 2010-10, Vol.42 (8), p.2864-2867

2010

Link zum Volltext

Verfügbarkeit prüfen

Intussusception: US findings with pathologic correlation--the crescent-in-doughnut sign

Radiology, 1996-06, Vol.199 (3), p.688

1996

Link zum Volltext

Verfügbarkeit prüfen

Multicomponent Domino Processes Based on the Organocatalytic Generation of Conjugated Acetylides: Efficient Synthetic Manifolds for Diversity-Oriented Molecular Construction

Chemistry : a European journal, 2005-06, Vol.11 (12), p.3502-3510

2005

Link zum Volltext

Verfügbarkeit prüfen

Imaging markers of small vessel disease and brain frailty, and outcomes in acute stroke

Neurology, 2020-02, Vol.94 (5), p.e439

2020

Link zum Volltext

Verfügbarkeit prüfen

Autour de j’aimerais dire : de l’approche polyphonique à l’ethos

Çédille revista de estudios franceses, 2023 (23), p.91-105

TEJEDOR DE FELIPE, Didier

2023

Link zum Volltext

Verfügbarkeit prüfen

A Diversity-Oriented Strategy for the Construction of Tetrasubstituted Pyrroles via Coupled Domino Processes

Journal of the American Chemical Society, 2004-07, Vol.126 (27), p.8390-8391

2004

Link zum Volltext

Verfügbarkeit prüfen

Congenital and acquired anomalies of the portal venous system

Radiographics, 2002-01, Vol.22 (1), p.141

2002

Link zum Volltext

Verfügbarkeit prüfen

Apolipoprotein E genotype is not associated with cardiovascular disease in heterozygous subjects with familial hypercholesterolemia

The American heart journal, 2003-06, Vol.145 (6), p.999-1005

2003

Link zum Volltext

Verfügbarkeit prüfen

W14.393 A DNA microarray for the detection of 154 mutations causing familial hypercholesterolemia

Atherosclerosis, 2004-04, Vol.5 (1), p.91

TEJEDOR, D

2004

Link zum Volltext

Verfügbarkeit prüfen

An Unprecedented, Tandem Aldol−Grob Reaction Sequence

Journal of organic chemistry, 1998-09, Vol.63 (19), p.6438-6439

1998

Link zum Volltext

Verfügbarkeit prüfen

Genetic polymorphisms inside and outside the MHC improve prediction of AS radiographic severity in addition to clinical variables

Rheumatology (Oxford, England), 2012-08, Vol.51 (8), p.1471-1478

2012

Link zum Volltext

Verfügbarkeit prüfen

A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular disease

Human mutation, 2002-12, Vol.20 (6), p.477-477

2002

Link zum Volltext

Verfügbarkeit prüfen

Intussusception in children: current concepts in diagnosis and enema reduction

Radiographics, 1999-03, Vol.19 (2), p.299

1999

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 677

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(574)
Mit Volltextzugriff
(599)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

4 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(8)

Menü

Weitere Dienste

Einstellungen

Reliable Low-Density DNA Array Based on Allele-Specific Probes for Detection of 118 Mutations Causing Familial Hypercholesterolemia

Can we predict top-level sports performance in power vs endurance events? A genetic approach

A new tool based on next generation sequencing for an efficient and rapid diagnosis of familial hypercholesterolemia

The C677T polymorphism in the MTHFR gene is associated with the toxicity of methotrexate in a Spanish rheumatoid arthritis population

Validation of a ce marked tool (seqpro lipo rs) based on next generation sequencing for diagnosis of familial hypercholesterolemia

Improved prediction of knee osteoarthritis progression by genetic polymorphisms. Arthrotest study results

THU0211 Genetic Polymorphisms Can Predict Knee Osteoarthritis Progression. Results from the Arthrotest Multicenter Association Study

AB0857 Single nucleotide polymorphisms associated with non response to anti-TNF-alpha treatment in ankylosing spondylitis patients. Data from regisponser

(4) Routine diagnosis of familial hypercholesterolemia with next generation sequencing

Haplotype analyses, mechanism and evolution of common double mutants in the human LDL receptor gene

A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia

Genetic Correlations of Brain Lesion Distribution in Multiple Sclerosis: An Exploratory Study

Toward Personalized Medicine in Renal Transplantation

Intussusception: US findings with pathologic correlation--the crescent-in-doughnut sign

Multicomponent Domino Processes Based on the Organocatalytic Generation of Conjugated Acetylides: Efficient Synthetic Manifolds for Diversity-Oriented Molecular Construction

Imaging markers of small vessel disease and brain frailty, and outcomes in acute stroke

Autour de j’aimerais dire : de l’approche polyphonique à l’ethos

A Diversity-Oriented Strategy for the Construction of Tetrasubstituted Pyrroles via Coupled Domino Processes

Congenital and acquired anomalies of the portal venous system

Apolipoprotein E genotype is not associated with cardiovascular disease in heterozygous subjects with familial hypercholesterolemia

W14.393 A DNA microarray for the detection of 154 mutations causing familial hypercholesterolemia

An Unprecedented, Tandem Aldol−Grob Reaction Sequence

Genetic polymorphisms inside and outside the MHC improve prediction of AS radiographic severity in addition to clinical variables

A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular disease

Intussusception in children: current concepts in diagnosis and enema reduction

Suchergebnisse filtern