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...

State-level benefits of energy efficiency

Energy policy, 2007-07, Vol.35 (7), p.3665-3674

2007

Volltextzugriff (PDF)

The remarkable journey of one female individual with ornithine transcarbamylase deficiency diagnosed post‐mortem

JIMD reports, 2023-05, Vol.64 (3), p.233-237

2023

Volltextzugriff (PDF)

Point mutations regarded as missense mutations cause splicing defects in the factor XI gene

Journal of thrombosis and haemostasis, 2011-10, Vol.9 (10), p.1977-1984

2011

Volltextzugriff (PDF)

Prospective diagnosis of MT-ATP6-related mitochondrial disease by newborn screening

Molecular genetics and metabolism, 2021-09, Vol.134 (1-2), p.37-42

2021

Volltextzugriff (PDF)

Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews

Journal of thrombosis and haemostasis, 2013-04, Vol.11 (4), p.724-730

2013

Volltextzugriff (PDF)

Natural history of the oldest known females with mucopolysaccharidosis type IVA (Morquio A syndrome)

American journal of medical genetics. Part A, 2020-06, Vol.182 (6), p.1491-1495

2020

Volltextzugriff (PDF)

A de novo hexokinase 1 (HK1) variant presenting as Boucher–Neuhäuser syndrome

American journal of medical genetics. Part A, 2023-02, Vol.191 (2), p.624-629

2023

Volltextzugriff (PDF)

A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency

Journal of thrombosis and haemostasis, 2004-06, Vol.2 (6), p.918-924

2004

Volltextzugriff (PDF)

Time dependent protection of amifostine from renal and hematopoietic cisplatin induced toxicity

Life sciences (1973), 2005-03, Vol.76 (16), p.1825-1834

2005

Volltextzugriff (PDF)

Aragonite crystalline matrix as an instructive microenvironment for neural development

Journal of tissue engineering and regenerative medicine, 2008-12, Vol.2 (8), p.463-471

2008

Volltextzugriff (PDF)

Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patients

Journal of thrombosis and haemostasis, 2006-08, Vol.4 (8), p.1730-1737

2006

Volltextzugriff (PDF)

Explaining the Performance of Mature Municipal Solid Waste Recycling Programs

Journal of environmental planning and management, 2005-09, Vol.48 (5), p.627-650

2005

Volltextzugriff (PDF)

Triggered C-reactive protein (CRP) concentrations and the CRP gene −717A>G polymorphism in acute stroke or transient ischemic attack

European journal of neurology, 2007-03, Vol.14 (3), p.315-320

2007

Volltextzugriff (PDF)

An assessment of waste issues associated with the production of new, lightweight, fuel-efficient vehicles

Journal of cleaner production, 2003-11, Vol.11 (7), p.753-765

2003

Volltextzugriff (PDF)

The human platelet αIIb gene is not closely linked to its integrin partner β3

Blood, 1999-09, Vol.94 (6), p.2039-2047

1999

Volltextzugriff (PDF)

Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish population

Journal of medical genetics, 2005-05, Vol.42 (5), p.e30-e30

2005

Volltextzugriff (PDF)

Evaluating knowledge benefits of automotive lightweighting materials R&D projects

Evaluation and program planning, 2009-08, Vol.32 (3), p.300-309

2009

Volltextzugriff (PDF)

The Making of Black Metropolis

The Annals of the American Academy of Political and Social Science, 2004-09, Vol.595 (1), p.168-175

Peretz, Henri

2004

Volltextzugriff (PDF)

Glanzmann thrombasthenia: new insights from an historical perspective

Seminars in hematology, 1994-10, Vol.31 (4), p.301-311

1994

Volltextzugriff (PDF)

Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene

Blood, 2002-04, Vol.99 (7), p.2448-2454

2002

Volltextzugriff (PDF)

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

Blood, 1998-08, Vol.92 (4), p.1119-1124

1998

Volltextzugriff (PDF)

Polymorphic markers in the XDH gene as diagnostic tools for typing classical xanthinuria

Advances in experimental medicine and biology, 2000, Vol.486, p.83

2000

Volltextzugriff (PDF)

Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure-function correlations of α IIb β 3 integrin ( ITGA2B, ITGB3 )

Human mutation, 2006-04, Vol.27 (4), p.359-369

2006

Volltextzugriff (PDF)

Application of economic evaluation techniques to automotive lightweighting materials research and development projects

Research evaluation, 2008-06, Vol.17 (2), p.133-148

2008

Volltextzugriff (PDF)

Improved method for genotyping apolipoprotein E polymorphisms by a PCR-based assay simultaneously utilizing two distinct restriction enzymes

Clinical chemistry (Baltimore, Md.), 1997-09, Vol.43 (9), p.1657-1659

1997

Volltextzugriff (PDF)

1 – 25 von 513

Suche als RSS-Feed

Aktive Filter

PublikationsformBücher

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(429)
Mit Volltextzugriff
(388)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

State-level benefits of energy efficiency

The remarkable journey of one female individual with ornithine transcarbamylase deficiency diagnosed post‐mortem

Point mutations regarded as missense mutations cause splicing defects in the factor XI gene

Prospective diagnosis of MT-ATP6-related mitochondrial disease by newborn screening

Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews

Natural history of the oldest known females with mucopolysaccharidosis type IVA (Morquio A syndrome)

A de novo hexokinase 1 (HK1) variant presenting as Boucher–Neuhäuser syndrome

A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency

Time dependent protection of amifostine from renal and hematopoietic cisplatin induced toxicity

Aragonite crystalline matrix as an instructive microenvironment for neural development

Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patients

Explaining the Performance of Mature Municipal Solid Waste Recycling Programs

Triggered C-reactive protein (CRP) concentrations and the CRP gene −717A>G polymorphism in acute stroke or transient ischemic attack

An assessment of waste issues associated with the production of new, lightweight, fuel-efficient vehicles

The human platelet αIIb gene is not closely linked to its integrin partner β3

Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish population

Evaluating knowledge benefits of automotive lightweighting materials R&D projects

The Making of Black Metropolis

Glanzmann thrombasthenia: new insights from an historical perspective

Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

Polymorphic markers in the XDH gene as diagnostic tools for typing classical xanthinuria

Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure-function correlations of α IIb β 3 integrin ( ITGA2B, ITGB3 )

Application of economic evaluation techniques to automotive lightweighting materials research and development projects

Improved method for genotyping apolipoprotein E polymorphisms by a PCR-based assay simultaneously utilizing two distinct restriction enzymes

Aktive Filter

Suchergebnisse filtern