fibrillin

fibrillin

fibrillin

fibrillin

fibrillin

fibrillin

Genetic and gene expression analyses of the polycystic ovary syndrome candidate gene fibrillin-3 and other fibrillin family members in human ovaries

Dermal tissue and cellular expression of fibrillin-1 in diffuse cutaneous systemic sclerosis

Mechanical assessment of elastin integrity in fibrillin-1-deficient carotid arteries: implications for Marfan syndrome

Localization of fibrillin-1 in human endometrium and decidua during the menstrual cycle and pregnancy.

Mutation of the gene encoding fibrillin-2 results in syndactyly in mice

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

NMR analysis of cbEGF domains gives new insights into the structural consequences of a P1148A substitution in fibrillin-1.

Increased expression of latent TGF-ß binding protein-1 and fibrillin-1 in human uterine leiomyomata

Expression of latent TGF-beta binding proteins and association with TGF-beta1 and fibrillin-1 following arterial injury

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration

Inhibition of Fibrillin 1 Expression Using U1 snRNA as a Vehicle for the Presentation of Antisense Targeting Sequence

Defective secretion of recombinant fragments of fibrillin-1: implications of protein misfolding for the pathogenesis of Marfan syndrome and related disorders

Mutant Fibrillin-1 Monomers Lacking EGF-Like Domains Disrupt Microfibril Assembly and Cause Severe Marfan Syndrome

Delivery of a Hammerhead Ribozyme Specifically Down-Regulates the Production of Fibrillin-1 by Cultured Dermal Fibroblasts