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...

Osteogenesis imperfecta

The Lancet (British edition), 2016-04, Vol.387 (10028), p.1657-1671

2016

Volltextzugriff (PDF)

New perspectives on osteogenesis imperfecta

Nature reviews. Endocrinology, 2011-09, Vol.7 (9), p.540-557

2011

Volltextzugriff (PDF)

Outer Membrane Vesicles (OMVs) as Biomedical Tools and Their Relevance as Immune-Modulating Agents against H. pylori Infections: Current Status and Future Prospects

International journal of molecular sciences, 2023-05, Vol.24 (10), p.8542

2023

Volltextzugriff (PDF)

Appendage Regeneration in Vertebrates: What Makes This Possible?

Cells (Basel, Switzerland), 2021-01, Vol.10 (2), p.242

2021

Volltextzugriff (PDF)

Zebrafish: A Resourceful Vertebrate Model to Investigate Skeletal Disorders

Frontiers in endocrinology (Lausanne), 2020-07, Vol.11, p.489

2020

Volltextzugriff (PDF)

4-PBA ameliorates cellular homeostasis in fibroblasts from osteogenesis imperfecta patients by enhancing autophagy and stimulating protein secretion

Biochimica et biophysica acta. Molecular basis of disease, 2018-05, Vol.1864 (5), p.1642-1652

2018

Volltextzugriff (PDF)

Dissecting the phenotypic variability of osteogenesis imperfecta

Disease models & mechanisms, 2022-05, Vol.15 (5)

2022

Volltextzugriff (PDF)

The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta

Human molecular genetics, 2017-08, Vol.26 (15), p.2897-2911

2017

Volltextzugriff (PDF)

Severely Impaired Bone Material Quality in Chihuahua Zebrafish Resembles Classical Dominant Human Osteogenesis Imperfecta

Journal of bone and mineral research, 2018-08, Vol.33 (8), p.1489-1499

2018

Volltextzugriff (PDF)

Knocking out TMEM38B in human foetal osteoblasts hFOB 1.19 by CRISPR/Cas9: A model for recessive OI type XIV

PloS one, 2021-09, Vol.16 (9), p.e0257254-e0257254

2021

Volltextzugriff (PDF)

Editorial: Molecular Mechanisms of Heritable Connective Tissue Disorders

Frontiers in genetics, 2022-04, Vol.13, p.866665-866665

2022

Volltextzugriff (PDF)

Phenotypic Characterization of Immortalized Chondrocytes from a Desbuquois Dysplasia Type 1 Mouse Model: A Tool for Studying Defects in Glycosaminoglycan Biosynthesis

International journal of molecular sciences, 2021-09, Vol.22 (17), p.9304

2021

Volltextzugriff (PDF)

Intracellular and Extracellular Markers of Lethality in Osteogenesis Imperfecta: A Quantitative Proteomic Approach

International journal of molecular sciences, 2021-01, Vol.22 (1), p.429

2021

Volltextzugriff (PDF)

Understanding the Role of Estrogen Receptor Status in PRODH/POX-Dependent Apoptosis/Survival in Breast Cancer Cells

Biology (Basel, Switzerland), 2021-12, Vol.10 (12), p.1314

2021

Volltextzugriff (PDF)

Compression Fractures and Partial Phenotype Rescue With a Low Phosphorus Diet in the Chihuahua Zebrafish Osteogenesis Imperfecta Model

Frontiers in endocrinology (Lausanne), 2022-02, Vol.13, p.851879-851879

2022

Volltextzugriff (PDF)

MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndrome

European journal of human genetics : EJHG, 2017-05, Vol.25 (5), p.646-650

2017

Volltextzugriff (PDF)

Calcium activated nucleotidase 1 (CANT1) is critical for glycosaminoglycan biosynthesis in cartilage and endochondral ossification

Matrix biology, 2019-08, Vol.81, p.70-90

2019

Volltextzugriff (PDF)

More Bone with Less Minerals? The Effects of Dietary Phosphorus on the Post-Cranial Skeleton in Zebrafish

International journal of molecular sciences, 2020-07, Vol.21 (15), p.5429

2020

Volltextzugriff (PDF)

Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1

Bone (New York, N.Y.), 2018-09, Vol.114, p.125-136

2018

Volltextzugriff (PDF)

Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate

Disease models & mechanisms, 2019-06, Vol.12 (6)

2019

Volltextzugriff (PDF)

Candidate Cell and Matrix Interaction Domains on the Collagen Fibril, the Predominant Protein of Vertebrates

The Journal of biological chemistry, 2008-07, Vol.283 (30), p.21187-21197

2008

Volltextzugriff (PDF)

TAPT1—at the crossroads of extracellular matrix and signaling in Osteogenesis imperfecta

EMBO molecular medicine, 2023-07, Vol.15 (7), p.e17528-n/a

2023

Volltextzugriff (PDF)

A standard set of outcome measures for the comprehensive assessment of osteogenesis imperfecta

Orphanet journal of rare diseases, 2021-03, Vol.16 (1), p.140-140, Article 140

2021

Volltextzugriff (PDF)

Shedding Light on Bone Morphogenetic Protein (BMP) Signaling Modifiers to Modulate Fibrodysplasia Ossificans Progressiva Severity

Journal of bone and mineral research, 2022-11, Vol.37 (11), p.2055-2057

Forlino, Antonella

2022

Volltextzugriff (PDF)

Testing the Cre-mediated genetic switch for the generation of conditional knock-in mice

PloS one, 2019-03, Vol.14 (3), p.e0213660-e0213660

2019

Volltextzugriff (PDF)

1 – 25 von 166

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(148)
Mit Volltextzugriff
(147)

Publikationsform

Sprache

Englisch
(166)
Japanisch
(22)

Erscheinungsjahr

n.n

Thema

Science & Technology
(96)
Life Sciences & Biomedicine
(93)
Humans
(62)
Animals
(43)
Biochemistry & Molecular Biology
(38)
Collagen
(38)
Osteogenesis Imperfecta
(37)
Mutation
(34)
Mice
(31)
Osteogenesis Imperfecta - Genetics
(27)
Cell Biology
(23)
Male
(23)
Proteins
(22)
Female
(19)
Osteogenesis Imperfecta - Metabolism
(19)
Biological And Medical Sciences
(17)
Disease Models, Animal
(17)
Endocrinology & Metabolism
(17)
Genetics & Heredity
(17)
Extracellular Matrix
(16)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(4)
... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Osteogenesis imperfecta

New perspectives on osteogenesis imperfecta

Outer Membrane Vesicles (OMVs) as Biomedical Tools and Their Relevance as Immune-Modulating Agents against H. pylori Infections: Current Status and Future Prospects

Appendage Regeneration in Vertebrates: What Makes This Possible?

Zebrafish: A Resourceful Vertebrate Model to Investigate Skeletal Disorders

4-PBA ameliorates cellular homeostasis in fibroblasts from osteogenesis imperfecta patients by enhancing autophagy and stimulating protein secretion

Dissecting the phenotypic variability of osteogenesis imperfecta

The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta

Severely Impaired Bone Material Quality in Chihuahua Zebrafish Resembles Classical Dominant Human Osteogenesis Imperfecta

Knocking out TMEM38B in human foetal osteoblasts hFOB 1.19 by CRISPR/Cas9: A model for recessive OI type XIV

Editorial: Molecular Mechanisms of Heritable Connective Tissue Disorders

Phenotypic Characterization of Immortalized Chondrocytes from a Desbuquois Dysplasia Type 1 Mouse Model: A Tool for Studying Defects in Glycosaminoglycan Biosynthesis

Intracellular and Extracellular Markers of Lethality in Osteogenesis Imperfecta: A Quantitative Proteomic Approach

Understanding the Role of Estrogen Receptor Status in PRODH/POX-Dependent Apoptosis/Survival in Breast Cancer Cells

Compression Fractures and Partial Phenotype Rescue With a Low Phosphorus Diet in the Chihuahua Zebrafish Osteogenesis Imperfecta Model

MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndrome

Calcium activated nucleotidase 1 (CANT1) is critical for glycosaminoglycan biosynthesis in cartilage and endochondral ossification

More Bone with Less Minerals? The Effects of Dietary Phosphorus on the Post-Cranial Skeleton in Zebrafish

Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1

Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate

Candidate Cell and Matrix Interaction Domains on the Collagen Fibril, the Predominant Protein of Vertebrates

TAPT1—at the crossroads of extracellular matrix and signaling in Osteogenesis imperfecta

A standard set of outcome measures for the comprehensive assessment of osteogenesis imperfecta

Shedding Light on Bone Morphogenetic Protein (BMP) Signaling Modifiers to Modulate Fibrodysplasia Ossificans Progressiva Severity

Testing the Cre-mediated genetic switch for the generation of conditional knock-in mice

Suchergebnisse filtern