Valentin Fischer

Autoimmune disease of exocrine organs in immunodeficient alymphoplasia mice: a spontaneous model for Sjören's syndrome

Cellular and molecular mechanisms of fibrosis

A tandem duplication within the fibrillin 1 gene is associated with the mouse tight skin mutation.

Genetic Defects in Tight Skin Mice Developing a Scleroderma-Like Syndrome

B-cell Deficiency does not Abrogate Development of Cutaneous Hyperplasia in Mice Inheriting the Defective Fibrillin-1 Gene

Fibrotic disease and the TH1/TH2 paradigm

Halofuginone to treat fibrosis in chronic graft-versus-host disease and scleroderma

Systemic sclerosis: a prototypic multisystem fibrotic disorder

Mechanisms of fibrosis: therapeutic translation for fibrotic disease

Anti-IL-4 treatment prevents dermal collagen deposition in the tight-skin mouse model of scleroderma

Structure of the Mutant Fibrillin-1 Gene in the Tight Skin (TSK) Mouse

Characterization of mutated protein encoded by partially duplicated fibrillin-1 gene in tight skin (TSK) mice

Quinoline, quinazoline and acridone alkaloids

The Tight Skin Mouse: Demonstration of Mutant Fibrillin-1 Production and Assembly into Abnormal Microfibrils

Tight-Skin Mouse an Experimental Model for Scleroderma

Elastic fibres

Spontaneous Occurrence of Anti-Fibrillin-1 Autoantibodies in Tight-Skin Mice

Induction of Skin Fibrosis in Mice Expressing a Mutated Fibrillin-1 Gene

Collagenous abnormalities in the heart of the tight-skin mouse