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...

Cellular Hypoxia Promotes Heterotopic Ossification by Amplifying BMP Signaling

Journal of bone and mineral research, 2016-09, Vol.31 (9), p.1652-1665

2016

Volltextzugriff (PDF)

Functional modeling of the ACVR1 (R206H) mutation in FOP

Clinical orthopaedics and related research, 2007-09, Vol.462, p.87-92

2007

Volltextzugriff (PDF)

Polypeptide Substrate Accessibility Hypothesis: Gain-of-Function R206H Mutation Allosterically Affects Activin Receptor-like Protein Kinase Activity

Biomolecules (Basel, Switzerland), 2023-07, Vol.13 (7), p.1129

2023

Volltextzugriff (PDF)

Induced degradation of protein kinases by bifunctional small molecules: a next-generation strategy

Expert opinion on drug discovery, 2019-12, Vol.14 (12), p.1237-1253

Groppe, Jay C.

2019

Volltextzugriff (PDF)

Multi-system involvement in a severe variant of fibrodysplasia ossificans progressiva (ACVR1 c.772G>A; R258G): A report of two patients

American journal of medical genetics. Part A, 2015-10, Vol.167A (10), p.2265-2271

2015

Volltextzugriff (PDF)

Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN

PLoS genetics, 2009-11, Vol.5 (11), p.e1000747-e1000747

2009

Volltextzugriff (PDF)

Regarding the mechanism of action of a proposed peptide agonist of the bone morphogenetic protein receptor activin-like kinase 3

Nature medicine, 2013-07, Vol.19 (7), p.809-810

2013

Volltextzugriff (PDF)

Matrix metalloproteinase-9 deficiency confers resilience in fibrodysplasia ossificans progressiva in a man and mice

Journal of bone and mineral research, 2024-05, Vol.39 (4), p.382-398

2024

Volltextzugriff (PDF)

Functional Testing of Bone Morphogenetic Protein (BMP) Pathway Variants Identified on Whole‐Exome Sequencing in a Patient with Delayed‐Onset Fibrodysplasia Ossificans Progressiva (FOP) Using ACVR1R206H‐Specific Human Cellular and Zebrafish Models

Journal of bone and mineral research, 2022-11, Vol.37 (11), p.2058-2076

2022

Volltextzugriff (PDF)

Intricacies of BMP receptor assembly

Cytokine & growth factor reviews, 2009-10, Vol.20 (5), p.367-377

2009

Volltextzugriff (PDF)

Functional analysis of alleged NOGGIN mutation G92E disproves its pathogenic relevance

PloS one, 2012-04, Vol.7 (4), p.e35062

2012

Volltextzugriff (PDF)

Hypoxia-selective allosteric destabilization of activin receptor-like kinases: A potential therapeutic avenue for prophylaxis of heterotopic ossification

Bone (New York, N.Y.), 2018-07, Vol.112, p.71-89

2018

Volltextzugriff (PDF)

An ACVR1 R375P pathogenic variant in two families with mild fibrodysplasia ossificans progressiva

American journal of medical genetics. Part A, 2022-03, Vol.188 (3), p.806-817

2022

Volltextzugriff (PDF)

In vitro Analyses of the Dysregulated R206H ALK2 Kinase-FKBP12 Interaction Associated with Heterotopic Ossification in FOP

Cells, tissues, organs, 2011-08, Vol.194 (2-4), p.291-295

2011

Volltextzugriff (PDF)

An ACVR1R375P pathogenic variant in two families with mild fibrodysplasia ossificans progressiva

American journal of medical genetics. Part A, 2022-03, Vol.188 (3), p.806-817

2022

Volltextzugriff (PDF)

Structure and Dynamics of the Homodimeric Dynein Light Chain km23

Journal of molecular biology, 2005-09, Vol.352 (2), p.338-354

2005

Volltextzugriff (PDF)

Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9

Human molecular genetics, 2009-08, Vol.18 (15), p.2863-2874

2009

Volltextzugriff (PDF)

The TβR-I Pre-Helix Extension Is Structurally Ordered in the Unbound Form and Its Flanking Prolines Are Essential for Binding

Journal of molecular biology, 2011-09, Vol.412 (4), p.601-618

2011

Volltextzugriff (PDF)

Nucleotide Polymorphisms in the Canine Noggin Gene and Their Distribution Among Dog (Canis lupus familiaris) Breeds

Biochemical genetics, 2012-02, Vol.50 (1-2), p.12-18

2012

Volltextzugriff (PDF)

Expression, Purification, and Characterization of a Soluble Form of the First Extracellular Domain of the Human Type 1 Corticotropin Releasing Factor Receptor

The Journal of biological chemistry, 2001-08, Vol.276 (34), p.31528-31534

2001

Volltextzugriff (PDF)

Functional Testing of Bone Morphogenetic Protein (BMP) Pathway Variants Identified on Whole-Exome Sequencing in a Patient with Delayed-Onset Fibrodysplasia Ossificans Progressiva (FOP) Using ACVR1 R206H -Specific Human Cellular and Zebrafish Models

Journal of bone and mineral research, 2022-11, Vol.37 (11), p.2058

2022

Volltextzugriff (PDF)

Assembly of TβRI:TβRII:TGFβ Ternary Complex in vitro with Receptor Extracellular Domains is Cooperative and Isoform-dependent

Journal of molecular biology, 2005-12, Vol.354 (5), p.1052-1068

2005

Volltextzugriff (PDF)

Functional modeling of the ACVR1 (R206H) mutation in FOP : Genetics in Orthopaedics

Clinical orthopaedics and related research, 2007 (462), p.87-92

2007

Volltextzugriff (PDF)

Chymotrypsin mRNA expression in digestive gland amoebocytes: cell specification occurs prior to metamorphosis and gut morphogenesis in the gastropod, Haliotis rufescens

Roux's Archives of Developmental Biology, 1995-09, Vol.205 (1-2), p.97-101

1995

Volltextzugriff (PDF)

Mutations in GDF5 Reveal a Key Residue Mediating BMP Inhibition by NOGGIN: e1000747

PLoS genetics, 2009-11, Vol.5 (11)

2009

Volltextzugriff (PDF)

1 – 25 von 35

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(35)
Mit Volltextzugriff
(31)

Publikationsform

Artikel
(35)

Sprache

Englisch
(35)

Erscheinungsjahr

n.n

Thema

Science & Technology
(25)
Life Sciences & Biomedicine
(22)
Animals
(18)
Humans
(18)
Biochemistry & Molecular Biology
(12)
Amino Acid Sequence
(10)
Molecular Sequence Data
(10)
Ligands
(9)
Mutation
(9)
Models, Molecular
(8)
Activin Receptors, Type I - Metabolism
(7)
Bone Morphogenetic Proteins
(7)
Fibrodysplasia Ossificans Progressiva
(7)
Myositis Ossificans
(6)
Proteins
(6)
Activin Receptors, Type I - Genetics
(5)
Acvr1
(5)
Genetics & Heredity
(5)
Kinases
(5)
Mice
(5)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Cellular Hypoxia Promotes Heterotopic Ossification by Amplifying BMP Signaling

Functional modeling of the ACVR1 (R206H) mutation in FOP

Polypeptide Substrate Accessibility Hypothesis: Gain-of-Function R206H Mutation Allosterically Affects Activin Receptor-like Protein Kinase Activity

Induced degradation of protein kinases by bifunctional small molecules: a next-generation strategy

Multi-system involvement in a severe variant of fibrodysplasia ossificans progressiva (ACVR1 c.772G>A; R258G): A report of two patients

Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN

Regarding the mechanism of action of a proposed peptide agonist of the bone morphogenetic protein receptor activin-like kinase 3

Matrix metalloproteinase-9 deficiency confers resilience in fibrodysplasia ossificans progressiva in a man and mice

Functional Testing of Bone Morphogenetic Protein (BMP) Pathway Variants Identified on Whole‐Exome Sequencing in a Patient with Delayed‐Onset Fibrodysplasia Ossificans Progressiva (FOP) Using ACVR1R206H‐Specific Human Cellular and Zebrafish Models

Intricacies of BMP receptor assembly

Functional analysis of alleged NOGGIN mutation G92E disproves its pathogenic relevance

Hypoxia-selective allosteric destabilization of activin receptor-like kinases: A potential therapeutic avenue for prophylaxis of heterotopic ossification

An ACVR1 R375P pathogenic variant in two families with mild fibrodysplasia ossificans progressiva

In vitro Analyses of the Dysregulated R206H ALK2 Kinase-FKBP12 Interaction Associated with Heterotopic Ossification in FOP

An ACVR1R375P pathogenic variant in two families with mild fibrodysplasia ossificans progressiva

Structure and Dynamics of the Homodimeric Dynein Light Chain km23

Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9

The TβR-I Pre-Helix Extension Is Structurally Ordered in the Unbound Form and Its Flanking Prolines Are Essential for Binding

Nucleotide Polymorphisms in the Canine Noggin Gene and Their Distribution Among Dog (Canis lupus familiaris) Breeds

Expression, Purification, and Characterization of a Soluble Form of the First Extracellular Domain of the Human Type 1 Corticotropin Releasing Factor Receptor

Functional Testing of Bone Morphogenetic Protein (BMP) Pathway Variants Identified on Whole-Exome Sequencing in a Patient with Delayed-Onset Fibrodysplasia Ossificans Progressiva (FOP) Using ACVR1 R206H -Specific Human Cellular and Zebrafish Models

Assembly of TβRI:TβRII:TGFβ Ternary Complex in vitro with Receptor Extracellular Domains is Cooperative and Isoform-dependent

Functional modeling of the ACVR1 (R206H) mutation in FOP : Genetics in Orthopaedics

Chymotrypsin mRNA expression in digestive gland amoebocytes: cell specification occurs prior to metamorphosis and gut morphogenesis in the gastropod, Haliotis rufescens

Mutations in GDF5 Reveal a Key Residue Mediating BMP Inhibition by NOGGIN: e1000747

Suchergebnisse filtern