- ORCID iD
- 0000-0002-7604-3117
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- Journal Article
- A1
- open access
Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta
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Type III collagen affects dermal and vascular collagen fibrillogenesis and tissue integrity in a mutant Col3a1 transgenic mouse model
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- Journal Article
- A1
- open access
Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome : a systematic review
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- PhD Thesis
- open access
Type III collagen : a major fibrillar collagen with major issues
(2017) -
Type III collagen is important for type I collagen fibrillogenesis and for dermal and cardiovascular development
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Differential expression of type III collagen in male and female mice
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Type III collagen is important for dermal and cardiovascular development, and type I collagen fibrillogenesis
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Type III collagen is important for type I collagen fibrillogenesis and for dermal and cardiovascular development
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Type III collagen is important for type I collagen fibrillogenesis and for dermal and cardiovascular development
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Type III collagen is important for collagen fibrillogenesis and for dermal and cardiovascular development
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Genetic defects in TAPT1 disrupt ciliogenesis and cause a complex lethal osteochondrodysplasia
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Type III collagen is important for type I collagen fibrillogenesis and for dermal and cardiovascular development
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C-propeptide mutations in procollagen type I and V are associated with endoplasmic reticulum stress-specific unfolded protein responses
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- Journal Article
- A1
- open access
Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans