Pages that link to "Q42794061"

The following pages link to Assessment of procollagen processing defects by fibroblasts cultured in the presence of dextran sulphate (Q42794061):

Displaying 18 items.

• Procollagen II amino propeptide processing by ADAMTS-3. Insights on dermatosparaxis (Q24291329) (← links)
• Cloning and characterization of ADAMTS-14, a novel ADAMTS displaying high homology with ADAMTS-2 and ADAMTS-3 (Q28210583) (← links)
• An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome (Q33678012) (← links)
• Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen (Q35195722) (← links)
• A mutation in the pro alpha 2(I) gene (COL1A2) for type I procollagen in Ehlers-Danlos syndrome type VII: evidence suggesting that skipping of exon 6 in RNA splicing may be a common cause of the phenotype. (Q35196578) (← links)
• Immunohistochemical and mutation analyses demonstrate that procollagen VII is processed to collagen VII through removal of the NC-2 domain (Q36382726) (← links)
• Ehlers-Danlos syndrome: classifications, oral manifestations, and dental considerations (Q36628892) (← links)
• Macromolecular crowding meets oxygen tension in human mesenchymal stem cell culture - A step closer to physiologically relevant in vitro organogenesis. (Q37141160) (← links)
• Low oxygen tension and macromolecular crowding accelerate extracellular matrix deposition in human corneal fibroblast culture (Q39425106) (← links)
• EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta. (Q39701074) (← links)
• Incomplete Processing of Type II Procollagen by a Rat Chondrosarcoma Cell Line (Q41099331) (← links)
• Effect of dextran on synthesis, secretion and deposition of type III procollagen in cultured human fibroblasts (Q41775679) (← links)
• Gly85 to Val substitution in pro alpha 1(I) chain causes mild osteogenesis imperfecta and introduces a susceptibility to protease digestion (Q48099657) (← links)
• Clinical, morphological, and biochemical phenotype of a new case of Ehlers-Danlos syndrome type VIIC. (Q50531293) (← links)
• A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta (Q50772150) (← links)
• Collagen metabolism is a novel target of the neuropeptide alpha-melanocyte-stimulating hormone. (Q52767211) (← links)
• Effects of collagen-derived bioactive peptides and natural antioxidant compounds on proliferation and matrix protein synthesis by cultured normal human dermal fibroblasts. (Q55561527) (← links)
• An alpha2(I) glycine to aspartate substitution is responsible for the presence of a kink in type I collagen in a lethal case of osteogenesis imperfecta (Q77922267) (← links)