𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A cleaved form of the receptor for urokinase-type plasminogen activator in invasive transplanted human and murine tumors

✍ Scribed by Helene Solberg; John Rømer; Nils Brünner; Arne Holm; Nicolai Sidenius; Keld Danø; Gunilla Høyer-Hansen


Publisher
John Wiley and Sons
Year
1994
Tongue
French
Weight
638 KB
Volume
58
Category
Article
ISSN
0020-7136

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Expression and cellular localization of
✍ Dubuisson, L.; Monvoisin, A.; Nielsen, B. S.; Le Bail, B.; Bioulac-Sage, P.; Ros 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 437 KB 👁 1 views

The urokinase-type plasminogen activator (uPA) and its receptor (uPAR) play an important role in tumour invasion. Previous studies have shown by RT-PCR that uPA and uPAR mRNAs are expressed in human hepatocellular carcinoma (HCC). Here, in situ hybridization, immunohistochemistry, and double immuno¯

ChemInform Abstract: The Role and Regula
✍ Yao Wang 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 25 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Urinary levels of urokinase-type plasmin
✍ Roberto Casella; Shahrokh F. Shariat; Mara A. Monoski; Seth P. Lerner 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 75 KB 👁 1 views

## Background: The authors found previously that plasma levels of urokinase-type plasminogen activator (upa) and its receptor (upar) were elevated in patients with bladder carcinoma and were associated with features of biologically aggressive disease. in the current study, they tested the hypothesi

Free PSA isoforms and intact and cleaved
✍ Thomas Steuber; Andrew Vickers; Alexander Haese; Michael W. Kattan; James A. Eas 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 French ⚖ 108 KB

## Abstract Clinicians currently use simple cut‐points, such as serum prostate‐specific antigen (PSA) ≥≥4 ng/ml, to decide whether to recommend further work‐up for prostate cancer (PCa). As an alternative strategy, we evaluated multivariable models giving probabilities of a PCa diagnosis based on P