Mutation of Membrane Type-1 Metalloproteinase, MT1-MMP, Causes the Multicentric Osteolysis and Arthritis Disease Winchester Syndrome
- 7 September 2012
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 91 (3), 572-576
- https://doi.org/10.1016/j.ajhg.2012.07.022
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- SignalP 4.0: discriminating signal peptides from transmembrane regionsNature Methods, 2011
- Recognition of a signal peptide by the signal recognition particleNature, 2010
- Biological implications of SNPs in signal peptide domains of human proteinsProteins: Structure, Function, and Bioinformatics, 2007
- Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growthHuman Molecular Genetics, 2007
- Don't mess with the matrixNature Genetics, 2001
- Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndromeNature Genetics, 2001
- Impaired endochondral ossification and angiogenesis in mice deficient in membrane-type matrix metalloproteinase IProceedings of the National Academy of Sciences of the United States of America, 2000
- MT1-MMP-Deficient Mice Develop Dwarfism, Osteopenia, Arthritis, and Connective Tissue Disease due to Inadequate Collagen TurnoverCell, 1999
- Unaltered Secretion of β-Amyloid Precursor Protein in Gelatinase A (Matrix Metalloproteinase 2)-deficient MiceOnline Journal of Public Health Informatics, 1997
- A NEW ACID MUCOPOLYSACCHARIDOSIS WITH SKELETAL DEFORMITIES SIMULATING RHEUMATOID ARTHRITISAmerican Journal of Roentgenology, 1969