Results 1 to 10 of about 169,527 (113)

Comparison of the solophenyl-red polarization method and the immunohistochemical analysis for collagen type III [PDF]

open access: yes, 1992
In the present study, we have compared the staining pattern of the Solophenyl-Red 3 BL-method for the visualization of collagen type III with the immunohistochemical staining in serial sections from 7 skin wounds (wound age 3 days up to 4 weeks) to ...
A Nerlich   +22 more
core   +1 more source

Changes in histoanatomical distribution of types I, III and V collagen promote adaptative remodeling in posterior tibial tendon rupture [PDF]

open access: yes, 2008
INTRODUCTION: Posterior tibial tendon dysfunction is a common cause of adult flat foot deformity, and its etiology is unknown. PURPOSE: In this study, we characterized the morphologic pattern and distribution of types I, III and V collagen in posterior ...
SATOMI, Érika   +6 more
core   +2 more sources

Accumulation of properly folded human type III procollagen molecules in specific intracellular membranous compartments in the yeast Pichia pastoris [PDF]

open access: yes, 2000
It was recently reported that co-expression of the proal(III) chain of human type III procollagen with the subunits of human prolyl 4-hydroxylase in Pichia pastoris produces fully hydroxylated and properly folded recombinant type III procollagen ...
Keizer-Gunnink, [No Value]   +7 more
core   +6 more sources

Age-related collagen turnover of the interstitial matrix and basement membrane: Implications of age- and sex-dependent remodeling of the extracellular matrix [PDF]

open access: yes, 2018
The extracellular matrix (ECM) plays a vital role in maintaining normal tissue function. Collagens are major components of the ECM and there is a tight equilibrium between degradation and formation of these proteins ensuring tissue health and homeostasis.
Armbrecht, Gabriele   +6 more
core   +2 more sources

Excessive collagen turnover products are released during colorectal cancer progression and elevated in serum from metastatic colorectal cancer patients [PDF]

open access: yes, 2016
During cancer progression, the homeostasis of the extracellular matrix becomes imbalanced with an excessive collagen remodeling by matrix metalloproteinases.
Brix, S.   +5 more
core   +1 more source

Tendinopathy—from basic science to treatment [PDF]

open access: yes, 2008
Chronic tendon pathology (tendinopathy), although common, is difficult to treat. Tendons possess a highly organized fibrillar matrix, consisting of type I collagen and various 'minor' collagens, proteoglycans and glycoproteins.
A McCormick   +69 more
core   +1 more source

Multiple antigenic determinants on type III collagen [PDF]

open access: yesBiochemical Journal, 1991
Eight monoclonal antibodies have been produced against human pepsin-soluble type III collagen. All antibodies were shown to be highly specific for type III collagen and did not cross-react with a range of other collagen types or connective-tissue proteins. Examination of type III collagen from other species showed that these antibodies had a wide range
J A, Werkmeister, J A, Ramshaw
openaire   +2 more sources

Multifactor complex containing B element binding factor, BBF, and repressors regulate the human alpha 1(III) collagen gene (COL3A1). [PDF]

open access: yes, 2006
Type III collagen is found in fetal skin and blood vessels. Previously, we characterized the proximal promoter of the human alpha1(III) collagen gene (COL3A1) using the human rhabdomyosarcoma cell line, A204, and NIH3T3 cells (Yoshino et al., Biochim ...
Matsuo, Noritaka   +4 more
core   +1 more source

The novel missense mutation Met48Lys in FKBP22 changes its structure and functions. [PDF]

open access: yes, 2020
Mutations in the FKBP14 gene encoding FKBP22 (FK506 Binding Protein 22 kDa) cause kyphoscoliotic Ehlers-Danlos Syndrome (kEDS). The first clinical report showed that a lack of FKBP22 protein due to mutations causing nonsense-mediated decay of the mRNA ...
Bächinger, Hans Peter   +7 more
core  

Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients [PDF]

open access: yes, 2019
Osteogenesis imperfecta (OI) is a rare genetic disorder of the connective tissue and 90% of cases are due to dominant mutations in COL1A1 and COL1A2 genes.
Boarini, Manila   +11 more
core   +1 more source

Home - About - Disclaimer - Privacy