Prevalence of collagen VII-specific autoantibodies in patients with autoimmune and inflammatory diseases - Wikidata - wikimedia - TriplyDB

Prevalence of collagen VII-specific autoantibodies in patients with autoimmune and inflammatory diseases

Prevalence of collagen VII-specific autoantibodies in patients with autoimmune and inflammatory diseases

http://www.wikidata.org/entity/Q34218525

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Molecular diagnosis in autoimmune skin blistering conditions Prevalence of specific anti-skin autoantibodies in a cohort of patients with inherited epidermolysis bullosa.Blister-inducing antibodies target multiple epitopes on collagen VII in mice.Clinical relevance of autoantibodies in patients with autoimmune bullous dermatosis Clinical presentation, pathogenesis, diagnosis, and treatment of epidermolysis bullosa acquisita Epidermolysis bullosa acquisita.Oral lichenoid tissue reactions: diagnosis and classification.Discovering potential drug-targets for personalized treatment of autoimmune disorders - what we learn from epidermolysis bullosa acquisita.Novel in silico tools for designing peptide-based subunit vaccines and immunotherapeutics.Sensitivity of different assays for the serological diagnosis of epidermolysis bullosa acquisita: analysis of a cohort of 24 Italian patients.Summary of results of serological tests and diagnoses for 4774 cases of various autoimmune bullous diseases consulted to Kurume University.Autoimmune Subepidermal Bullous Diseases of the Skin and Mucosae: Clinical Features, Diagnosis, and Management.Serological diagnostics in the detection of IgG autoantibodies against human collagen VII in epidermolysis bullosa acquisita: a multicentre analysis.Management of severe epidermolysis bullosa by haematopoietic transplant: principles, perspectives and pitfalls.Anti-Type VII Collagen Antibodies Are Identified in a Subpopulation of Bullous Pemphigoid Patients With Relapse.Humoral Epitope Spreading in Autoimmune Bullous Diseases.Molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid.Meta-analysis of the clinical and immunopathological characteristics and treatment outcomes in epidermolysis bullosa acquisita patients

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P2860

Prevalence of collagen VII-specific autoantibodies in patients with autoimmune and inflammatory diseases

http://www.wikidata.org/entity/Q34218525

description

2012 nî lūn-bûn

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2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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name

Prevalence of collagen VII-spe ...... mune and inflammatory diseases

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Prevalence of collagen VII-spe ...... mune and inflammatory diseases

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Prevalence of collagen VII-spe ...... mune and inflammatory diseases

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Prevalence of collagen VII-spe ...... mune and inflammatory diseases

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Prevalence of collagen VII-spe ...... mune and inflammatory diseases

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Prevalence of collagen VII-spe ...... mune and inflammatory diseases

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Prevalence of collagen VII-spe ...... mune and inflammatory diseases

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Prevalence of collagen VII-spe ...... mune and inflammatory diseases

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Prevalence of collagen VII-spe ...... mune and inflammatory diseases

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Prevalence of collagen VII-spe ...... mune and inflammatory diseases

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Gheorghe Hundorfean

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Giovanna Zambruno

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Jonas Mudter

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Markus F Neurath

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Martin J Recknagel

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Michael Hertl

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Susanne Ganz

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P2860

Human type VII collagen: cDNA cloning and chromosomal mapping of the gene

Identification of conformational B-cell Epitopes in an antigen from its primary sequence

Proteinases of the bone morphogenetic protein-1 family convert procollagen VII to mature anchoring fibril collagen

Epitope mapping for epidermolysis bullosa acquisita autoantibody by molecularly cloned cDNA for type VII collagen

Immunopathology and molecular diagnosis of autoimmune bullous diseases

The tissue form of type VII collagen is an antiparallel dimer

Fcgamma receptors as regulators of immune responses

Induction of dermal-epidermal separation in mice by passive transfer of antibodies specific to type VII collagen.

Epitope mapping of type VII collagen. Identification of discrete peptide sequences recognized by sera from patients with acquired epidermolysis bullosa.

Alport alloantibodies but not Goodpasture autoantibodies induce murine glomerulonephritis: protection by quinary crosslinks locking cryptic α3(IV) collagen autoepitopes in vivo.

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10.1186/1471-2172-13-16

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Leena Bruckner-Tuderman

Takashi Hashimoto

Emilia Licarete

Giovanni Di Zenzo

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2012-04-04T00:00:00Z

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