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...

Extracellular Regulation of BMP Signaling in Vertebrates: A Cocktail of Modulators

Developmental Biology, 2002-10, Vol.250 (2), p.231-250

2002

Volltextzugriff (PDF)

Diarylquinolines Are Bactericidal for Dormant Mycobacteria as a Result of Disturbed ATP Homeostasis

The Journal of biological chemistry, 2008-09, Vol.283 (37), p.25273-25280

2008

Volltextzugriff (PDF)

Novel Antibiotics Targeting Respiratory ATP Synthesis in Gram-Positive Pathogenic Bacteria

Antimicrobial Agents and Chemotherapy, 2012-08, Vol.56 (8), p.4131-4139

2012

Volltextzugriff (PDF)

The Binding Between Sclerostin and LRP5 is Altered by DKK1 and by High-Bone Mass LRP5 Mutations

Calcified tissue international, 2008-06, Vol.82 (6), p.445-453

2008

Volltextzugriff (PDF)

The Genetics of Low-Density Lipoprotein Receptor-Related Protein 5 in Bone: A Story of Extremes

Endocrinology (Philadelphia), 2007-06, Vol.148 (6), p.2622-2629

2007

Volltextzugriff (PDF)

Essentiality of FASII pathway for Staphylococcus aureus

Nature (London), 2010-01, Vol.463 (7279), p.E3-E3

2010

Volltextzugriff (PDF)

Van Buchem Disease (Hyperostosis Corticalis Generalisata) Maps to Chromosome 17q12-q21

American journal of human genetics, 1998-02, Vol.62 (2), p.391-399

1998

Volltextzugriff (PDF)

Minireview : The genetics of low-density Lipoprotein receptor-related protein 5 in bone: A story of extremes

Endocrinology (Philadelphia), 2007-06, Vol.148 (6), p.2622-2629

2007

Volltextzugriff (PDF)

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)

Human molecular genetics, 2001-03, Vol.10 (5), p.537-543

2001

Volltextzugriff (PDF)

Design, Synthesis, and Biological Evaluation of Novel Indoles Targeting the Influenza PB2 Cap Binding Region

Journal of medicinal chemistry, 2019-11, Vol.62 (21), p.9680-9690

2019

Volltextzugriff (PDF)

New Anti-Tuberculosis Drugs in Clinical Development: An Overview

Current bioactive compounds, 2009-06, Vol.5 (2), p.137-154

2009

Volltextzugriff (PDF)

Recurrent Sclerosing Dysplasia of Bone: Report of a Case

Journal of oral and maxillofacial surgery, 2008-11, Vol.66 (11), p.2372-2374

2008

Volltextzugriff (PDF)

Novel LRP5 Missense Mutation in a Patient With a High Bone Mass Phenotype Results in Decreased DKK1‐Mediated Inhibition of Wnt Signaling

Journal of bone and mineral research, 2007-05, Vol.22 (5), p.708-716

2007

Volltextzugriff (PDF)

A generalized skeletal hyperostosis in two siblings caused by a novel mutation in the SOST gene

Bone (New York, N.Y.), 2005-06, Vol.36 (6), p.943-947

2005

Volltextzugriff (PDF)

Common Genetic Variation in the DKK1 Gene is Associated with Hip Axis Length but not with Bone Mineral Density and Bone Turnover Markers in Young Adult Men: Results from the Odense Androgen Study

Calcified tissue international, 2010-04, Vol.86 (4), p.271-281

2010

Volltextzugriff (PDF)

Patients with Van Buchem Disease, an Osteosclerotic Genetic Disease, Have Elevated Bone Formation Markers, Higher Bone Density, and Greater Derived Polar Moment of Inertia than Normal

The journal of clinical endocrinology and metabolism, 2003-12, Vol.88 (12), p.5778-5783

2003

Volltextzugriff (PDF)

An Autosomal Dominant High Bone Mass Phenotype in Association With Craniosynostosis in an Extended Family Is Caused by an LRP5 Missense Mutation

Journal of bone and mineral research, 2005-07, Vol.20 (7), p.1254-1260

2005

Volltextzugriff (PDF)

Essentiality of FASII pathway for Staphylococcus aureus/Brinster et al. reply

Nature (London), 2010-01, Vol.463 (7279), p.E3

2010

Volltextzugriff (PDF)

Genetic analysis and effect of triiodothyronine and prednisone trial on bone turnover in a patient with craniotubular hyperostosis

Bone (New York, N.Y.), 2008-08, Vol.43 (2), p.405-409

2008

Volltextzugriff (PDF)

Missense Mutations in LRP5 Are Not a Common Cause of Idiopathic Osteoporosis in Adult Men

Journal of bone and mineral research, 2005-11, Vol.20 (11), p.1951-1959

2005

Volltextzugriff (PDF)

Localization of the Gene for Sclerosteosis to the van Buchem Disease–Gene Region on Chromosome 17q12–q21

American journal of human genetics, 1999-06, Vol.64 (6), p.1661-1669

1999

Volltextzugriff (PDF)

Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity

Journal of bone and mineral research, 1998-06, Vol.13 (6), p.911-917

1998

Volltextzugriff (PDF)

Positional Cloning of a Gene Involved in Hereditary Multiple Exostoses

Human molecular genetics, 1996-10, Vol.5 (10), p.1547-1557

1996

Volltextzugriff (PDF)

A known SOST gene mutation causes sclerosteosis in a familial and an isolated case from Brazilian origin

Genetic testing, 2008-12, Vol.12 (4), p.475-479

2008

Volltextzugriff (PDF)

Molecular and radiological diagnosis of sclerosing bone dysplasias

European journal of radiology, 2001-12, Vol.40 (3), p.198-207

2001

Volltextzugriff (PDF)

1 – 25 von 34

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(32)
Mit Volltextzugriff
(31)

Publikationsform

Artikel
(33)
Dissertationen
(1)

Sprache

Englisch
(34)

Erscheinungsjahr

n.n

Thema

Science & Technology
(27)
Humans
(26)
Life Sciences & Biomedicine
(26)
Biological And Medical Sciences
(20)
Medical Sciences
(16)
Male
(15)
Female
(14)
Pedigree
(11)
Adult
(10)
Endocrinology & Metabolism
(10)
Genetics & Heredity
(9)
Diseases Of The Osteoarticular System
(8)
Chromosome Mapping
(7)
Bone Density
(6)
Fundamental And Applied Biological Sciences. Psychology
(6)
Genetic Markers
(6)
Radiography
(6)
Amino Acid Sequence
(5)
Ldl-Receptor Related Proteins - Genetics
(5)
Low Density Lipoprotein Receptor-Related Protein-5
(5)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Extracellular Regulation of BMP Signaling in Vertebrates: A Cocktail of Modulators

Diarylquinolines Are Bactericidal for Dormant Mycobacteria as a Result of Disturbed ATP Homeostasis

Novel Antibiotics Targeting Respiratory ATP Synthesis in Gram-Positive Pathogenic Bacteria

The Binding Between Sclerostin and LRP5 is Altered by DKK1 and by High-Bone Mass LRP5 Mutations

The Genetics of Low-Density Lipoprotein Receptor-Related Protein 5 in Bone: A Story of Extremes

Essentiality of FASII pathway for Staphylococcus aureus

Van Buchem Disease (Hyperostosis Corticalis Generalisata) Maps to Chromosome 17q12-q21

Minireview : The genetics of low-density Lipoprotein receptor-related protein 5 in bone: A story of extremes

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)

Design, Synthesis, and Biological Evaluation of Novel Indoles Targeting the Influenza PB2 Cap Binding Region

New Anti-Tuberculosis Drugs in Clinical Development: An Overview

Recurrent Sclerosing Dysplasia of Bone: Report of a Case

Novel LRP5 Missense Mutation in a Patient With a High Bone Mass Phenotype Results in Decreased DKK1‐Mediated Inhibition of Wnt Signaling

A generalized skeletal hyperostosis in two siblings caused by a novel mutation in the SOST gene

Common Genetic Variation in the DKK1 Gene is Associated with Hip Axis Length but not with Bone Mineral Density and Bone Turnover Markers in Young Adult Men: Results from the Odense Androgen Study

Patients with Van Buchem Disease, an Osteosclerotic Genetic Disease, Have Elevated Bone Formation Markers, Higher Bone Density, and Greater Derived Polar Moment of Inertia than Normal

An Autosomal Dominant High Bone Mass Phenotype in Association With Craniosynostosis in an Extended Family Is Caused by an LRP5 Missense Mutation

Essentiality of FASII pathway for Staphylococcus aureus/Brinster et al. reply

Genetic analysis and effect of triiodothyronine and prednisone trial on bone turnover in a patient with craniotubular hyperostosis

Missense Mutations in LRP5 Are Not a Common Cause of Idiopathic Osteoporosis in Adult Men

Localization of the Gene for Sclerosteosis to the van Buchem Disease–Gene Region on Chromosome 17q12–q21

Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity

Positional Cloning of a Gene Involved in Hereditary Multiple Exostoses

A known SOST gene mutation causes sclerosteosis in a familial and an isolated case from Brazilian origin

Molecular and radiological diagnosis of sclerosing bone dysplasias

Suchergebnisse filtern