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Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|January 1, 1994
In vitro cytokine modulation of intercellular adhesion molecule-1 expression on systemic sclerosis dermal fibroblastsM M Cho, S A Jimenez, B A Johnson, et al.
Journal of Cellular Physiology|June 26, 2010
MED and PSACH COMP mutations affect chondrogenesis in chicken limb bud micromass culturesJ Roman-Blas, A S Dion, M R Seghatoleslami, et al.
The Journal of Cell Biology|April 18, 1998
The Tight skin mouse: demonstration of mutant fibrillin-1 production and assembly into abnormal microfibrilsC M Kielty, M Raghunath, L D Siracusa, et al.
Arthritis and Rheumatism|July 1, 1994
Familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis associated with an arginine 75-->cysteine mutation in the procollagen type II gene in a kindred of Chiloe Islanders. I. Clinical, radiographic, and pathologic findingsA J Reginato, G M Passano, G Neumann, et al.
Annals of Internal Medicine|July 1, 1994
Pulmonary function and gastroesophageal reflux in systemic sclerosisM B Troshinsky, G C Kane, J Varga, et al.
Genome Research|April 1, 1996
A tandem duplication within the fibrillin 1 gene is associated with the mouse tight skin mutationL D Siracusa, R McGrath, Q Ma, et al.
American Journal of Medical Genetics|February 1, 1993
Exclusion of type II and type VI procollagen gene mutations in a five-generation family with multiple epiphyseal dysplasiaE J Weaver, G P Summerville, G Yeh, et al.
Clinical and Experimental Immunology|July 11, 2000
Polymorphisms in the IL-1 receptor antagonist gene VNTR are possible risk factors for juvenile idiopathic inflammatory myopathiesL G Rider, C M Artlett, C B Foster, et al.
The Journal of Clinical Investigation|November 7, 2001
Role of protein kinase C-delta in the regulation of collagen gene expression in scleroderma fibroblastsS A Jimenez, S Gaidarova, B Saitta, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy)N N Ahmad, L Ala-Kokko, R G Knowlton, et al.
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