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Collagen Gene

Collagen Genes encode different forms of Collagen, the principle fibrous protein of connective tissue, all consisting of triple helix alpha… 
National Institutes of Health

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Beta Isomer of C-Terminal Telopeptide of Type I CollagenC-telopeptideC-terminal type I collagen telopeptideCell Adhesion

Papers overview

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Highly Cited
2010
Highly Cited
2010
Maternal obesity programmes offspring development of non-alcoholic fatty pancreas disease
Highly Cited
2006
Highly Cited
2006
Demineralized bone matrix gelatin as scaffold for osteochondral tissue engineering.
Highly Cited
2003
Highly Cited
2003
CC-chemokine receptor 2 required for bleomycin-induced pulmonary fibrosis.
Review
2003
Review
2003
Type XVII collagen gene mutations in junctional epidermolysis bullosa and prospects for gene therapy
Non‐Herlitz junctional epidermolysis bullosa (nH‐JEB) is caused predominantly by mutations leading to premature stop codons on… 
Highly Cited
1998
Highly Cited
1998
Expression of transforming growth factor-beta1 and type IV collagen in the renal tubulointerstitium in experimental diabetes: effects of ACE inhibition.
Transforming growth factor-beta (TGF-beta) and the renin-angiotensin system (RAS) have both been implicated in the pathogenesis… 
Highly Cited
1995
Highly Cited
1995
Pretibial epidermolysis bullosa: genetic linkage to COL7A1 and identification of a glycine-to-cysteine substitution in the triple-helical domain of type VII collagen.
Pretibial epidermolysis bullosa (PEB) is a rare variant of dominant dystrophic EB (DDEB) in which recurrent blistering with… 
Highly Cited
1994
Highly Cited
1994
Dominant dystrophic epidermolysis bullosa: identification of a Gly-->Ser substitution in the triple-helical domain of type VII collagen.
Epidermolysis bullosa (EB) represents a group of genodermatoses characterized by fragility and easy blistering of the skin. In… 
Highly Cited
1991
Highly Cited
1991
Human type VII collagen: genetic linkage of the gene (COL7A1) on chromosome 3 to dominant dystrophic epidermolysis bullosa.
Epidermolysis bullosa (EB) is a heterogeneous group of heritable blistering disorders affecting the skin and the mucous membranes… 
Highly Cited
1988
Highly Cited
1988
The type X collagen gene. Intron sequences split the 5'-untranslated region and separate the coding regions for the non-collagenous amino-terminal and triple-helical domains.
Type X collagen, expressed by hypertrophic chondrocytes, consists of homotrimeric molecules with subunits that are only about one… 
1986
1986
Use of molecular haplotypes specific for the human pro alpha 2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfecta.
Autosomal dominant osteogenesis imperfecta (OI) is a heterogeneous group of disorders. Molecular haplotypes associated with the… 
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