Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

COL17A1 gene

Known as: BULLOUS PEMPHIGOID ANTIGEN 2, collagen type XVII alpha 1, COLLAGEN, TYPE XVII, ALPHA-1 
 
National Institutes of Health

Related topics

Related topics

1 relation
COL15A1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Bullous Pemphigoid: A Review of its Diagnosis, Associations and Treatment
Bullous pemphigoid (BP) is the most common autoimmune subepidermal blistering disease in Western countries, and typically affects… Expand
  • table 1
  • table 2
  • figure 1
  • table 3
Is this relevant?
Review
2012
Review
2012
Bullous pemphigoid: from the clinic to the bench.
Bullous pemphigoid (BP) constitutes the most frequent autoimmune subepidermal blistering disease. It is associated with… Expand
Is this relevant?
2011
2011
Enzyme-linked immunosorbent assay for the combination of bullous pemphigoid antigens 1 and 2 in the diagnosis of bullous pemphigoid.
OBJECTIVE To assess the usefulness of enzyme-linked immunosorbent assay (ELISA) assessment of the combination of bullous… Expand
  • table 2
  • table 1
Is this relevant?
Highly Cited
2000
Highly Cited
2000
The Serpin α1-Proteinase Inhibitor Is a Critical Substrate for Gelatinase B/MMP-9 In Vivo
We have identified the key protein substrate of gelatinase B/MMP-9 (GB) that is cleaved in vivo during dermal-epidermal… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
1998
Highly Cited
1998
Gelatinase B–deficient Mice Are Resistant to Experimental Bullous Pemphigoid
Bullous pemphigoid (BP) is an autoimmune subepidermal blistering disease characterized by deposition of autoantibodies at the… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
1998
Highly Cited
1998
Identification and characterization of autoreactive T cell responses to bullous pemphigoid antigen 2 in patients and healthy controls.
Antibodies against the extracellular domain of bullous pemphigoid antigen 2 (BPAG2) are thought to play a key role in the… Expand
  • figure 1
  • table I
  • table II
  • table III
  • figure 2
Is this relevant?
Highly Cited
1998
Highly Cited
1998
The 97 kDa linear IgA bullous disease antigen is identical to a portion of the extracellular domain of the 180 kDa bullous pemphigoid antigen, BPAg2.
IgA autoantibodies from the sera of some patients with linear IgA bullous dermatosis (LABD) recognize a 97 kDa antigen (LABD97… Expand
Is this relevant?
Highly Cited
1996
Highly Cited
1996
Beta4 integrin is required for hemidesmosome formation, cell adhesion and cell survival
The integrin heterodimer alpha 6 beta 4 is expressed in many epithelia and in Schwann cells. In stratified epithelia, alpha 6… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 6
Is this relevant?
Highly Cited
1996
Highly Cited
1996
Cicatricial pemphigoid autoantibodies react with multiple sites on the BP180 extracellular domain.
Cicatricial pemphigoid (CP) is an autoimmune blistering disease that primarily affects mucosal tissues. Autoantibodies to laminin… Expand
Is this relevant?
Highly Cited
1995
Highly Cited
1995
Mutations in the 180–kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa
Junctional epidermolysis bullosa (JEB) is a heterogeneous autosomal recessively inherited blistering skin disorder associated… Expand
Is this relevant?
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE