Literature DB >> 24257026

The search for the perfect animal model discloses the importance of biological targets for the treatment of systemic sclerosis.

Francesco Del Galdo1, Marco Matucci-Cerinic.   

Abstract

Entities:  

Keywords:  Autoimmune Diseases; Fibroblasts; Systemic Sclerosis

Mesh:

Substances:

Year:  2013        PMID: 24257026     DOI: 10.1136/annrheumdis-2013-203910

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


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  3 in total

1.  The Tsk2/+ mouse fibrotic phenotype is due to a gain-of-function mutation in the PIIINP segment of the Col3a1 gene.

Authors:  Kristen B Long; Zhenghui Li; Chelsea M Burgwin; Susanna G Choe; Viktor Martyanov; Sihem Sassi-Gaha; Josh P Earl; Rory A Eutsey; Azad Ahmed; Garth D Ehrlich; Carol M Artlett; Michael L Whitfield; Elizabeth P Blankenhorn
Journal:  J Invest Dermatol       Date:  2014-10-20       Impact factor: 8.551

2.  Searching for a good model for systemic sclerosis: the molecular profile and vascular changes occurring in UCD-200 chickens strongly resemble the early phase of human systemic sclerosis.

Authors:  Paola Cipriani; Paola Di Benedetto; Hermann Dietrich; Piero Ruscitti; Vasiliki Liakouli; Francesco Carubbi; Ilenia Pantano; Onorina Berardicurti; Roswitha Sgonc; Roberto Giacomelli
Journal:  Arch Med Sci       Date:  2016-07-01       Impact factor: 3.318

3.  The Fibrosis and Immunological Features of Hypochlorous Acid Induced Mouse Model of Systemic Sclerosis.

Authors:  Meng Meng; Jieqiong Tan; Weilin Chen; Qian Du; Bin Xie; Nian Wang; Honglin Zhu; Kangkai Wang
Journal:  Front Immunol       Date:  2019-08-20       Impact factor: 7.561

  3 in total

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