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...

c-Met-induced epithelial carcinogenesis is initiated by the serine protease matriptase

Oncogene, 2011-04, Vol.30 (17), p.2003-2016

2011

Volltextzugriff (PDF)

Membrane-Anchored Serine Proteases in Vertebrate Cell and Developmental Biology

Annual review of cell and developmental biology, 2011-01, Vol.27 (1), p.213-235

2011

Volltextzugriff (PDF)

Suppression of Tumorigenicity-14, encoding matriptase, is a critical suppressor of colitis and colitis-associated colon carcinogenesis

Oncogene, 2012-08, Vol.31 (32), p.3679-3695

2012

Volltextzugriff (PDF)

Matriptase promotes inflammatory cell accumulation and progression of established epidermal tumors

Oncogene, 2015-08, Vol.34 (35), p.4664-4672

2015

Volltextzugriff (PDF)

Type II transmembrane serine proteases in development and disease

The international journal of biochemistry & cell biology, 2008-01, Vol.40 (6), p.1297-1316

2008

Volltextzugriff (PDF)

M2-like macrophages are responsible for collagen degradation through a mannose receptor-mediated pathway

The Journal of cell biology, 2013-09, Vol.202 (6), p.951-966

2013

Volltextzugriff (PDF)

Cellular uptake of collagens and implications for immune cell regulation in disease

Cellular and molecular life sciences : CMLS, 2020-08, Vol.77 (16), p.3161-3176

2020

Volltextzugriff (PDF)

GFRAL is the receptor for GDF15 and is required for the anti-obesity effects of the ligand

Nature medicine, 2017-10, Vol.23 (10), p.1158-1166

2017

Volltextzugriff (PDF)

Glycine inhibits NINJ1 membrane clustering to suppress plasma membrane rupture in cell death

eLife, 2022-12, Vol.11

2022

Volltextzugriff (PDF)

Matriptase inhibition by hepatocyte growth factor activator inhibitor-1 is essential for placental development

Oncogene, 2007-03, Vol.26 (11), p.1546-1556

2007

Volltextzugriff (PDF)

Deregulated matriptase causes ras-independent multistage carcinogenesis and promotes ras-mediated malignant transformation

Genes & development, 2005-08, Vol.19 (16), p.1934-1950

2005

Volltextzugriff (PDF)

Relapse from MRD Negativity As Indication for Treatment in Multiple Myeloma - the Remnant Study

Blood, 2020-11, Vol.136 (Supplement 1), p.21-22

2020

Volltextzugriff (PDF)

The source of matrix-degrading enzymes in human cancer: Problems of research reproducibility and possible solutions

The Journal of cell biology, 2015-04, Vol.209 (2), p.195-198

2015

Volltextzugriff (PDF)

Tumor-Associated Macrophages Derived from Circulating Inflammatory Monocytes Degrade Collagen through Cellular Uptake

Cell reports (Cambridge), 2017-12, Vol.21 (13), p.3662-3671

2017

Volltextzugriff (PDF)

Dense fibrillar collagen is a potent inducer of invadopodia via a specific signaling network

The Journal of cell biology, 2015-02, Vol.208 (3), p.331-350

2015

Volltextzugriff (PDF)

HAI‐2 stabilizes, inhibits and regulates SEA‐cleavage‐dependent secretory transport of matriptase

Traffic (Copenhagen, Denmark), 2017-06, Vol.18 (6), p.378-391

2017

Volltextzugriff (PDF)

Matriptase: potent proteolysis on the cell surface

Molecular medicine (Cambridge, Mass.), 2006-01, Vol.12 (1-3), p.1-7

2006

Volltextzugriff (PDF)

Loss of Proteolytically Processed Filaggrin Caused by Epidermal Deletion of Matriptase/MT-SP1

The Journal of cell biology, 2003-11, Vol.163 (4), p.901-910

2003

Volltextzugriff (PDF)

Matriptase/MT-SP1 is required for postnatal survival, epidermal barrier function, hair follicle development, and thymic homeostasis

Oncogene, 2002-05, Vol.21 (23), p.3765-3779

2002

Volltextzugriff (PDF)

The Protease Inhibitor HAI-2, but Not HAI-1, Regulates Matriptase Activation and Shedding through Prostasin

The Journal of biological chemistry, 2014-08, Vol.289 (32), p.22319-22332

2014

Volltextzugriff (PDF)

Surface Toll-like receptor 3 expression in metastatic intestinal epithelial cells induces inflammatory cytokine production and promotes invasiveness

The Journal of biological chemistry, 2017-09, Vol.292 (37), p.15408-15425

2017

Volltextzugriff (PDF)

The Membrane-anchored Serine Protease Prostasin (CAP1/PRSS8) Supports Epidermal Development and Postnatal Homeostasis Independent of Its Enzymatic Activity

The Journal of biological chemistry, 2014-05, Vol.289 (21), p.14740-14749

2014

Volltextzugriff (PDF)

A matriptase-prostasin reciprocal zymogen activation complex with unique features: prostasin as a non-enzymatic co-factor for matriptase activation

The Journal of biological chemistry, 2013-06, Vol.288 (26), p.19028-19039

2013

Volltextzugriff (PDF)

Measuring Respiratory Activity of Adipocytes and Adipose Tissues in Real Time

Methods in Enzymology, 2014, Vol.538, p.233-247

2014

Volltextzugriff (PDF)

Sodium retention in nephrotic syndrome is independent of the activation of the membrane-anchored serine protease prostasin (CAP1/PRSS8) and its enzymatic activity

Pflügers Archiv, 2022-06, Vol.474 (6), p.613-624

2022

Volltextzugriff (PDF)

1 – 25 von 83

Suche als RSS-Feed

Aktive Filter

ThemaCell Biology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(72)
Mit Volltextzugriff
(78)

Publikationsform

Artikel
(75)
Buchkapitel
(8)

Sprache

Englisch
(83)
Japanisch
(30)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

c-Met-induced epithelial carcinogenesis is initiated by the serine protease matriptase

Membrane-Anchored Serine Proteases in Vertebrate Cell and Developmental Biology

Suppression of Tumorigenicity-14, encoding matriptase, is a critical suppressor of colitis and colitis-associated colon carcinogenesis

Matriptase promotes inflammatory cell accumulation and progression of established epidermal tumors

Type II transmembrane serine proteases in development and disease

M2-like macrophages are responsible for collagen degradation through a mannose receptor-mediated pathway

Cellular uptake of collagens and implications for immune cell regulation in disease

GFRAL is the receptor for GDF15 and is required for the anti-obesity effects of the ligand

Glycine inhibits NINJ1 membrane clustering to suppress plasma membrane rupture in cell death

Matriptase inhibition by hepatocyte growth factor activator inhibitor-1 is essential for placental development

Deregulated matriptase causes ras-independent multistage carcinogenesis and promotes ras-mediated malignant transformation

Relapse from MRD Negativity As Indication for Treatment in Multiple Myeloma - the Remnant Study

The source of matrix-degrading enzymes in human cancer: Problems of research reproducibility and possible solutions

Tumor-Associated Macrophages Derived from Circulating Inflammatory Monocytes Degrade Collagen through Cellular Uptake

Dense fibrillar collagen is a potent inducer of invadopodia via a specific signaling network

HAI‐2 stabilizes, inhibits and regulates SEA‐cleavage‐dependent secretory transport of matriptase

Matriptase: potent proteolysis on the cell surface

Loss of Proteolytically Processed Filaggrin Caused by Epidermal Deletion of Matriptase/MT-SP1

Matriptase/MT-SP1 is required for postnatal survival, epidermal barrier function, hair follicle development, and thymic homeostasis

The Protease Inhibitor HAI-2, but Not HAI-1, Regulates Matriptase Activation and Shedding through Prostasin

Surface Toll-like receptor 3 expression in metastatic intestinal epithelial cells induces inflammatory cytokine production and promotes invasiveness

The Membrane-anchored Serine Protease Prostasin (CAP1/PRSS8) Supports Epidermal Development and Postnatal Homeostasis Independent of Its Enzymatic Activity

A matriptase-prostasin reciprocal zymogen activation complex with unique features: prostasin as a non-enzymatic co-factor for matriptase activation

Measuring Respiratory Activity of Adipocytes and Adipose Tissues in Real Time

Sodium retention in nephrotic syndrome is independent of the activation of the membrane-anchored serine protease prostasin (CAP1/PRSS8) and its enzymatic activity

Aktive Filter

Suchergebnisse filtern