UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 38

Sortiert nach

iRhoms 1 and 2 are essential upstream regulators of ADAM17-dependent EGFR signaling

Proceedings of the National Academy of Sciences - PNAS, 2015-05, Vol.112 (19), p.6080-6085

2015

Link zum Volltext

Verfügbarkeit prüfen

The Disintegrin/Metalloproteinase ADAM10 Is Essential for the Establishment of the Brain Cortex

The Journal of neuroscience, 2010-04, Vol.30 (14), p.4833-4844

2010

Link zum Volltext

Verfügbarkeit prüfen

Structural modeling defines transmembrane residues in ADAM17 that are crucial for Rhbdf2-ADAM17-dependent proteolysis

Journal of cell science, 2017-03, Vol.130 (5), p.868-878

2017

Link zum Volltext

Verfügbarkeit prüfen

Distinct Roles for ADAM10 and ADAM17 in Ectodomain Shedding of Six EGFR Ligands

The Journal of cell biology, 2004-03, Vol.164 (5), p.769-779

2004

Link zum Volltext

Verfügbarkeit prüfen

VEGF-A Stimulates ADAM17-Dependent Shedding of VEGFR2 and Crosstalk Between VEGFR2 and ERK Signaling

Circulation research, 2008-10, Vol.103 (9), p.916-918

2008

Link zum Volltext

Verfügbarkeit prüfen

Characterization of the catalytic properties of the membrane-anchored metalloproteinase ADAM9 in cell-based assays

Biochemical journal, 2017-05, Vol.474 (9), p.1467-1479

2017

Link zum Volltext

Verfügbarkeit prüfen

Role of iRhoms 1 and 2 in Endochondral Ossification

International journal of molecular sciences, 2020-11, Vol.21 (22), p.8732

2020

Link zum Volltext

Verfügbarkeit prüfen

ADAM10 is a principal 'sheddase' of the low-affinity immunoglobulin E receptor CD23

Nature Immunology, 2006-12, Vol.7 (12), p.1293-1298

2006

Link zum Volltext

Verfügbarkeit prüfen

ADAM8 is a negative regulator of retinal neovascularization and of the growth of heterotopically injected tumor cells in mice

Journal of molecular medicine (Berlin, Germany), 2010-05, Vol.88 (5), p.497-505

2010

Link zum Volltext

Verfügbarkeit prüfen

Mice Lacking the Metalloprotease-Disintegrin MDC9 (ADAM9) Have No Evident Major Abnormalities during Development or Adult Life

Molecular and Cellular Biology, 2002-03, Vol.22 (5), p.1537-1544

2002

Link zum Volltext

Verfügbarkeit prüfen

Potential Role for ADAM15 in Pathological Neovascularization in Mice

Molecular and Cellular Biology, 2003-08, Vol.23 (16), p.5614-5624

2003

Link zum Volltext

Verfügbarkeit prüfen

Essential Role for ADAM19 in Cardiovascular Morphogenesis

Molecular and Cellular Biology, 2004-01, Vol.24 (1), p.96-104

2004

Link zum Volltext

Verfügbarkeit prüfen

Metalloprotease-Disintegrin MDC9: Intracellular Maturation and Catalytic Activity

The Journal of biological chemistry, 1999-02, Vol.274 (6), p.3531-3540

1999

Link zum Volltext

Verfügbarkeit prüfen

Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice

Journal of cell science, 2023-07, Vol.136 (13)

2023

Link zum Volltext

Verfügbarkeit prüfen

ADAM10-Dependent Signaling Through Notch1 and Notch4 Controls Development of Organ-Specific Vascular Beds

Circulation research, 2016-08, Vol.119 (4), p.519-531

2016

Link zum Volltext

Verfügbarkeit prüfen

ADAM17 stabilizes its interacting partner inactive Rhomboid 2 (iRhom2) but not inactive Rhomboid 1 (iRhom1)

The Journal of biological chemistry, 2020-03, Vol.295 (13), p.4350-4358

2020

Link zum Volltext

Verfügbarkeit prüfen

Characterization of the Catalytic Properties of the Membrane-anchored Metalloprotease ADAM9 in Cell-based assays

Biochemical journal, 2017-04, Vol.474 (9), p.1467-1479

2017

Link zum Volltext

Verfügbarkeit prüfen

Targeted truncation of the ADAM17 cytoplasmic domain in mice results in protein destabilization and a hypomorphic phenotype

The Journal of biological chemistry, 2021-01, Vol.296, p.100733-100733, Article 100733

2021

Link zum Volltext

Verfügbarkeit prüfen

Intravitreal injection of TIMP3 or the EGFR inhibitor erlotinib offers protection from oxygen-induced retinopathy in mice

Investigative ophthalmology & visual science, 2013-01, Vol.54 (1), p.864-870

2013

Link zum Volltext

Verfügbarkeit prüfen

Evidence for a Critical Role of the Tumor Necrosis Factor α Convertase (TACE) in Ectodomain Shedding of the p75 Neurotrophin Receptor (p75NTR)

The Journal of biological chemistry, 2004-02, Vol.279 (6), p.4241-4249

2004

Link zum Volltext

Verfügbarkeit prüfen

Nerve Growth Factor Gene Expression in the Developing Rat Brain

Science (American Association for the Advancement of Science), 1986-10, Vol.234 (4774), p.352-355

1986

Link zum Volltext

Verfügbarkeit prüfen

Lack of ADAM10 in endothelial cells affects osteoclasts at the chondro-osseus junction

Journal of orthopaedic research, 2014-02, Vol.32 (2), p.224-230

2014

Link zum Volltext

Verfügbarkeit prüfen

A sensitive method to monitor ectodomain shedding of ligands of the epidermal growth factor receptor

Methods in molecular biology (Clifton, N.J.), 2006, Vol.327, p.99

2006

Link zum Volltext

Verfügbarkeit prüfen

ADAM17 stabilizes its interacting partner inactive Rhomboid 2 (iRhom2) but not inactive Rhomboid 1 (iRhom1)

The Journal of biological chemistry, 2020-03, Vol.295 (13), p.4350

2020

Link zum Volltext

Verfügbarkeit prüfen

Nerve Growth Factor and Its Low-Affinity Receptor Promote Schwann Cell Migration

Proceedings of the National Academy of Sciences - PNAS, 1994-03, Vol.91 (7), p.2795-2799

1994

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 38

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(37)
Mit Volltextzugriff
(37)

Publikationsform

Artikel
(38)

Sprache

Englisch
(38)
Japanisch
(15)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

iRhoms 1 and 2 are essential upstream regulators of ADAM17-dependent EGFR signaling

The Disintegrin/Metalloproteinase ADAM10 Is Essential for the Establishment of the Brain Cortex

Structural modeling defines transmembrane residues in ADAM17 that are crucial for Rhbdf2-ADAM17-dependent proteolysis

Distinct Roles for ADAM10 and ADAM17 in Ectodomain Shedding of Six EGFR Ligands

VEGF-A Stimulates ADAM17-Dependent Shedding of VEGFR2 and Crosstalk Between VEGFR2 and ERK Signaling

Characterization of the catalytic properties of the membrane-anchored metalloproteinase ADAM9 in cell-based assays

Role of iRhoms 1 and 2 in Endochondral Ossification

ADAM10 is a principal 'sheddase' of the low-affinity immunoglobulin E receptor CD23

ADAM8 is a negative regulator of retinal neovascularization and of the growth of heterotopically injected tumor cells in mice

Mice Lacking the Metalloprotease-Disintegrin MDC9 (ADAM9) Have No Evident Major Abnormalities during Development or Adult Life

Potential Role for ADAM15 in Pathological Neovascularization in Mice

Essential Role for ADAM19 in Cardiovascular Morphogenesis

Metalloprotease-Disintegrin MDC9: Intracellular Maturation and Catalytic Activity

Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice

ADAM10-Dependent Signaling Through Notch1 and Notch4 Controls Development of Organ-Specific Vascular Beds

ADAM17 stabilizes its interacting partner inactive Rhomboid 2 (iRhom2) but not inactive Rhomboid 1 (iRhom1)

Characterization of the Catalytic Properties of the Membrane-anchored Metalloprotease ADAM9 in Cell-based assays

Targeted truncation of the ADAM17 cytoplasmic domain in mice results in protein destabilization and a hypomorphic phenotype

Intravitreal injection of TIMP3 or the EGFR inhibitor erlotinib offers protection from oxygen-induced retinopathy in mice

Evidence for a Critical Role of the Tumor Necrosis Factor α Convertase (TACE) in Ectodomain Shedding of the p75 Neurotrophin Receptor (p75NTR)

Nerve Growth Factor Gene Expression in the Developing Rat Brain

Lack of ADAM10 in endothelial cells affects osteoclasts at the chondro-osseus junction

A sensitive method to monitor ectodomain shedding of ligands of the epidermal growth factor receptor

ADAM17 stabilizes its interacting partner inactive Rhomboid 2 (iRhom2) but not inactive Rhomboid 1 (iRhom1)

Nerve Growth Factor and Its Low-Affinity Receptor Promote Schwann Cell Migration

Suchergebnisse filtern