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References from PRELP, collagen, and a theory of Hutchinson–Gilford progeria. Local targets link to admitted publications; unresolved targets remain external evidence.
Hutchinson–Gilford progeria syndrome: a pathologic study, pediatric pathology
10.1080/15227950252774110 · 2002 · External reference
Abnormal collagen fibrils in tendons of Biglycan/Fibromodulin-deficient mice lead to gait impairment, ectopic ossification, and osteoarthritis
10.1096/fj.01-0848com · 2002 · External reference
Perlecan is essential for cartilage and cephalic development
10.1038/15537 · 1999 · External reference
Dyssegmental dysplasia, Silverman–Handmaker type: unexpected role of perlecan in cartilage development
10.1002/ajmg.10229 · 2001 · External reference
The primary structure of a basic leucine-rich repeat protein, prelp, found in connective tissues
10.1074/jbc.270.43.25639 · 1995 · External reference
The amino-terminal part of PRELP binds to heparin and heparan sulfate
10.1074/jbc.m007917200 · 2000 · External reference
The Leucine-rich repeat protein prelp binds perlecan and collagens and may function as a basement membrane anchor
10.1074/jbc.m108285200 · 2002 · External reference
Hutchinson–Gilford progeria syndrome: clinical, chromosomal and metabolic abnormalities
1990 · External reference
Degraded collagen fragments promote rapid disassembly of smooth muscle focal adhesions that correlates with cleavage of Pp125 (Fak), Paxillin, and Talin
10.1083/jcb.147.3.619 · 1999 · External reference
Hutchinson–Gilford progeria types defined by differential binding of Lectin Dsa
10.1016/0925-4439(94)00081-z · 1995 · External reference
Differential expression of lumican and fibromodulin regulate collagen fibrillogenesis in developing mouse tendons
10.1083/jcb.151.4.779 · 2000 · External reference
Characterization of the human Proline/Arginine-rich end Leucine-rich repeat protein (prelp) gene promoter and identification of a repressor element
10.1042/bj3360077 · 1998 · External reference
The gene organization, chromosome location, and expression of a 55-KDa matrix protein (prelp) of human articular cartilage
10.1006/geno.1996.0605 · 1996 · External reference
Swiss-Model and the Swiss-Pdb viewer: an environment for comparative protein modeling
10.1002/elps.1150181505 · 1997 · External reference
Unresolved reference
External reference
Dyssegmental dwarfism: a new syndrome of lethal dwarfism
1977 · External reference
Progeria: autopsy report of one case, with a review of pathologic findings reported in the literature
10.1111/j.1532-5415.1976.tb06779.x · 1976 · External reference
Mitotic misregulation and human aging
10.1126/science.287.5462.2486 · 2000 · External reference
Genetic syndromes in man with potential relevance to the pathobiology of aging
1978 · External reference
A matrix protein of Mr 55,000 that accumulates in human articular cartilage with age
10.1016/0304-4165(90)90037-w · 1990 · External reference
Changes in collagen fibril diameters across artery walls including a correlation with glycosaminoglycan content
10.3109/03008208709006979 · 1987 · External reference
Gene profile of replicative senescence is different from progeria or elderly donor
10.1006/bbrc.2001.4632 · 2001 · External reference
10.1073/pnas.87.4.1342
10.1073/pnas.87.4.1342 · External reference
Histological and ultrastructural features of atherosclerosis in progeria
10.1016/s1054-8807(98)00023-4 · 1999 · External reference
Smooth muscle cell depletion and collagen types in progeric arteries
10.1016/s1054-8807(01)00069-2 · 2001 · External reference
Fibromodulin-null mice have abnormal collagen fibrils, tissue organization, and altered lumican deposition in tendon
10.1074/jbc.274.14.9636 · 1999 · External reference
Serum cholesterol and triglyceride levels in progeria as a model of aging
10.1016/0047-6374(84)90024-1 · 1984 · External reference
Searching for clues to premature aging
10.1016/s1043-2760(02)00595-7 · 2002 · External reference