AXL targeting reduces fibrosis development in experimental unilateral ureteral obstruction-Reference-Cited by-同舟云学术

AXL targeting reduces fibrosis development in experimental unilateral ureteral obstruction

Published:2019-05 Issue:10 Volume:7 Page:e14091
ISSN:2051-817X
Container-title:Physiological Reports
language:en
Short-container-title:Physiol Rep

Author:

Landolt Lea¹^ORCID,Furriol Jessica²,Babickova Janka¹,Ahmed Lavina³,Eikrem Øystein¹,Skogstrand Trude²⁴,Scherer Andreas⁵⁶,Suliman Salwa⁷,Leh Sabine¹⁸,Lorens James B.⁹,Gausdal Gro³,Marti Hans‐Peter¹²,Osman Tarig¹

Affiliation:

1. Department of Clinical Medicine University of Bergen Bergen Norway

2. Department of Medicine Haukeland University Hospital Bergen Norway

3. BerGenBio ASA Bergen Norway

4. Department of Biomedicine University of Bergen Bergen Norway

5. Spheromics Kontiolahti Finland

6. Institute for Molecular Medicine Finland FIMM HiLIFE University of Helsinki Helsinki Finland

7. Department of Clinical Dentistry Center for Clinical Dental Research University of Bergen Bergen Norway

8. Department of Pathology Haukeland University Hospital Bergen Norway

9. Department of Biomedicine Center for Cancer Biomarkers University of Bergen Bergen Norway

Funder

BerGenBio AS

Publisher

Wiley

Subject

Physiology (medical),Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.14814/phy2.14091

Reference77 articles.

1. TAM receptor tyrosine kinases as emerging targets of innate immune checkpoint blockade for cancer therapy

2. PDGF-receptor localizes to mesangial, parietal epithelial, and interstitial cells in human and primate kidneys

3. Axl as a mediator of cellular growth and survival

4. Gas6/Axl pathway is activated in chronic liver disease and its targeting reduces fibrosis via hepatic stellate cell inactivation

5. Role of Axl in Early Kidney Inflammation and Progression of Salt-Dependent Hypertension

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