sameAs
Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytesA novel marker of tissue junctions, collagen XXIIProgress toward Treatment and Cure of Epidermolysis Bullosa: Summary of the DEBRA International Research Symposium EB2015Laminin 332 in junctional epidermolysis bullosaOne goal, different strategies--molecular and cellular approaches for the treatment of inherited skin fragility disordersDiscrete integration of collagen XVI into tissue-specific collagen fibrils or beaded microfibrilsProteinases of the bone morphogenetic protein-1 family convert procollagen VII to mature anchoring fibril collagenA simplified laminin nomenclatureShedding of collagen XVII ectodomain depends on plasma membrane microenvironmentThe classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EBExtracellular phosphorylation of collagen XVII by ecto-casein kinase 2 inhibits ectodomain sheddingLack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entityCleavage and oligomerization of gliomedin, a transmembrane collagen required for node of ranvier formationExpanding the COL7A1 mutation database: novel and recurrent mutations and unusual genotype-phenotype constellations in 41 patients with dystrophic epidermolysis bullosa.Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.Kindlin-1 Is required for RhoGTPase-mediated lamellipodia formation in keratinocytesEpidermal ADAM17 maintains the skin barrier by regulating EGFR ligand-dependent terminal keratinocyte differentiation.Abstracts of the 52nd Workshop for Pediatric Research : Frankfurt, Germany. 27-28 October 2016.Mechanisms of fibroblast cell therapy for dystrophic epidermolysis bullosa: high stability of collagen VII favors long-term skin integrityMutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.Altered MCM protein levels and autophagic flux in aged and systemic sclerosis dermal fibroblastsExpression of innate defense antimicrobial peptides in hidradenitis suppurativa.Collagen XVII and BPAG1 expression in the retina: evidence for an anchoring complex in the central nervous system.The flavonoid luteolin inhibits Fcγ-dependent respiratory burst in granulocytes, but not skin blistering in a new model of pemphigoid in adult mice.Prevalence of collagen VII-specific autoantibodies in patients with autoimmune and inflammatory diseasesCollagenous transmembrane proteins: recent insights into biology and pathology.Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.Compound heterozygous desmoplakin mutations result in a phenotype with a combination of myocardial, skin, hair, and enamel abnormalitiesNo evidence that human papillomavirus is responsible for the aggressive nature of recessive dystrophic epidermolysis bullosa-associated squamous cell carcinoma.Shedding of collagen XXIII is mediated by furin and depends on the plasma membrane microenvironment.Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification.Rat model for dominant dystrophic epidermolysis bullosa: glycine substitution reduces collagen VII stability and shows gene-dosage effectMolecular diagnostics facilitate distinction between lethal and non-lethal subtypes of junctional epidermolysis bullosa: a case report and review of the literature.Transmembrane collagen XVII modulates integrin dependent keratinocyte migration via PI3K/Rac1 signaling.Keratinocytes from patients lacking collagen XVII display a migratory phenotypeDynamic interactions of epidermal collagen XVII with the extracellular matrix: laminin 332 as a major binding partnerCollagenous transmembrane proteins: collagen XVII as a prototype.Definitions and outcome measures for mucous membrane pemphigoid: recommendations of an international panel of experts.Revertant mosaicism in a human skin fragility disorder results from slipped mispairing and mitotic recombination.Integrin α3 mutations with kidney, lung, and skin disease.
P50
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P50
description
Duits dermatologe
@nl
Finnish-German dermatologist, professor of dermatology (University of Freiburg, Germany)
@en
finnisch-deutsche Dermatologin
@de
suomalais-saksalainen ihotautilääkäri, Freiburgin yliopiston ihotautiopin professori
@fi
tysk professor
@da
tysk professor
@sv
name
Leena Bruckner-Tuderman
@ast
Leena Bruckner-Tuderman
@ca
Leena Bruckner-Tuderman
@da
Leena Bruckner-Tuderman
@de
Leena Bruckner-Tuderman
@en
Leena Bruckner-Tuderman
@es
Leena Bruckner-Tuderman
@fi
Leena Bruckner-Tuderman
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Leena Bruckner-Tuderman
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Leena Bruckner-Tuderman
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type
label
Leena Bruckner-Tuderman
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Leena Bruckner-Tuderman
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Leena Bruckner-Tuderman
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Leena Bruckner-Tuderman
@de
Leena Bruckner-Tuderman
@en
Leena Bruckner-Tuderman
@es
Leena Bruckner-Tuderman
@fi
Leena Bruckner-Tuderman
@fr
Leena Bruckner-Tuderman
@nb
Leena Bruckner-Tuderman
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altLabel
Leena Kaarina Bruckner-Tuderman
@de
Leena Kaarina Bruckner-Tuderman
@en
Leena Kaarina Bruckner-Tuderman
@nl
prefLabel
Leena Bruckner-Tuderman
@ast
Leena Bruckner-Tuderman
@ca
Leena Bruckner-Tuderman
@da
Leena Bruckner-Tuderman
@de
Leena Bruckner-Tuderman
@en
Leena Bruckner-Tuderman
@es
Leena Bruckner-Tuderman
@fi
Leena Bruckner-Tuderman
@fr
Leena Bruckner-Tuderman
@nb
Leena Bruckner-Tuderman
@nds
P1412
P214
P227
P269
P1559
Leena Bruckner-Tuderman
@de
P19
P2080
P21
P214
P227
1088453562
P269
P31
P4872
P569
1952-09-01T00:00:00Z