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ESDR around the Millennium Change

Journal of investigative dermatology, 2020-09, Vol.140 (9S), p.S158-S159

Bruckner-Tuderman, Leena

2020

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Jouni Uitto (1943–2022)

Journal of investigative dermatology, 2023-04, Vol.143 (4), p.527-528

2023

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Molecular Heterogeneity of Blistering Disorders: The Paradigm of Epidermolysis Bullosa

Journal of investigative dermatology, 2012-11, Vol.132 (E1), p.E2-E5

2012

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295 Donor-dependent variation and bias of transforming growth factor-β activating mechanisms in recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2019-09, Vol.139 (9), p.S265-S265

2019

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Amlexanox Enhances Premature Termination Codon Read-Through in COL7A1 and Expression of Full Length Type VII Collagen: Potential Therapy for Recessive Dystrophic Epidermolysis Bullosa

Journal of investigative dermatology, 2017-09, Vol.137 (9), p.1842-1849

2017

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EB2017—Progress in Epidermolysis Bullosa Research toward Treatment and Cure

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.1010-1016

2018

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Collagen VII Half-Life at the Dermal-Epidermal Junction Zone: Implications for Mechanisms and Therapy of Genodermatoses

Journal of investigative dermatology, 2016-06, Vol.136 (6), p.1116-1123

2016

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Demonstration of Epitope-Spreading Phenomena in Bullous Pemphigoid: Results of a Prospective Multicenter Study

Journal of investigative dermatology, 2011-11, Vol.131 (11), p.2271-2280

2011

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403 Genetically corrected fibroblasts from individuals with recessive dystrophic epidermolysis bullosa reveal collagen VII dependent proteomic perturbations in cell cycling

Journal of investigative dermatology, 2024-08, Vol.144 (8), p.S70-S70

2024

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274 Oleogel-S10 reduces dressing changes burden and associated costs in patients with epidermolysis bullosa

Journal of investigative dermatology, 2024-08, Vol.144 (8), p.S47-S47

2024

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713 The RNA-based reprogramming of renal epithelial cells derived from recessive dystrophic epidermolysis bullosa patients into induced pluripotent stem cells

Journal of investigative dermatology, 2022-08, Vol.142 (8), p.S123

2022

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LB1730 Concordance in the secretome of recessive dystrophic epidermolysis bullosa and cellular senescence reveals COL7A1 dependent perturbations

Journal of investigative dermatology, 2023-09, Vol.143 (9), p.B21

2023

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Diversity of Mechanisms Underlying Latent TGF-β Activation in Recessive Dystrophic Epidermolysis Bullosa

Journal of investigative dermatology, 2021-06, Vol.141 (6), p.1450-1460.e9

2021

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A Perspective on Clinical and Translational Research in Pediatric Dermatology

Journal of investigative dermatology, 2012-03, Vol.132 (3), p.497-498

Bruckner, Anna L.

2012

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Impact of Atopic Skin Diathesis on Occupational Skin Disease Incidence in a Working Population

Journal of investigative dermatology, 2003-07, Vol.121 (1), p.37-40

2003

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425 Functional and scalable keratinocytes and fibroblasts produced via iPSC-derived skin organoids for the treatment of RDEB

Journal of investigative dermatology, 2024-08, Vol.144 (8), p.S74-S74

2024

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615 Efficacy and safety of Oleogel-S10 (birch triterpenes) for recessive dystrophic epidermolysis bullosa (RDEB): Results of 3 months double-blind treatment of the phase 3 study ‘EASE’

Journal of investigative dermatology, 2021-05, Vol.141 (5), p.S107

2021

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486 Systemic collagen VII protein therapy for treatment of advanced RDEB

Journal of investigative dermatology, 2021-05, Vol.141 (5), p.S84

2021

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Genotype, Clinical Course, and Therapeutic Decision Making in 76 Infants with Severe Generalized Junctional Epidermolysis Bullosa

Journal of investigative dermatology, 2016-11, Vol.136 (11), p.2150-2157

2016

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903 Utilizing an organoid-based approach for the derivation of genetically corrected keratinocytes and fibroblasts in an induced pluripotent stem cell therapy for skin diseases

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S155-S155

2023

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024 Development and validation of an investigators global assessment scale to evaluate overall disease severity in patients with epidermolysis bullosa simplex

Journal of investigative dermatology, 2017-10, Vol.137 (10), p.S196-S196

2017

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Dipeptidyl Peptidase-4–Mediated Fibronectin Processing Evokes a Profibrotic Extracellular Matrix

Journal of investigative dermatology, 2024-04

2024

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438 A phase 1/2 trial of PTR-01, a collagen 7 (C7) protein replacement therapy, in patients with recessive dystrophic epidermolysis bullosa (RDEB)

Journal of investigative dermatology, 2021-05, Vol.141 (5), p.S76

2021

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Loss of Collagen VII Is Associated with Reduced Transglutaminase 2 Abundance and Activity

Journal of investigative dermatology, 2014-09, Vol.134 (9), p.2381-2389

2014

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499 A novel preclinical model for translating an induced pluripotent stem cell therapy for the treatment of skin diseases

Journal of investigative dermatology, 2022-08, Vol.142 (8), p.S85

2022

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ESDR around the Millennium Change

Jouni Uitto (1943–2022)

Molecular Heterogeneity of Blistering Disorders: The Paradigm of Epidermolysis Bullosa

295 Donor-dependent variation and bias of transforming growth factor-β activating mechanisms in recessive dystrophic epidermolysis bullosa

Amlexanox Enhances Premature Termination Codon Read-Through in COL7A1 and Expression of Full Length Type VII Collagen: Potential Therapy for Recessive Dystrophic Epidermolysis Bullosa

EB2017—Progress in Epidermolysis Bullosa Research toward Treatment and Cure

Collagen VII Half-Life at the Dermal-Epidermal Junction Zone: Implications for Mechanisms and Therapy of Genodermatoses

Demonstration of Epitope-Spreading Phenomena in Bullous Pemphigoid: Results of a Prospective Multicenter Study

403 Genetically corrected fibroblasts from individuals with recessive dystrophic epidermolysis bullosa reveal collagen VII dependent proteomic perturbations in cell cycling

274 Oleogel-S10 reduces dressing changes burden and associated costs in patients with epidermolysis bullosa

713 The RNA-based reprogramming of renal epithelial cells derived from recessive dystrophic epidermolysis bullosa patients into induced pluripotent stem cells

LB1730 Concordance in the secretome of recessive dystrophic epidermolysis bullosa and cellular senescence reveals COL7A1 dependent perturbations

Diversity of Mechanisms Underlying Latent TGF-β Activation in Recessive Dystrophic Epidermolysis Bullosa

A Perspective on Clinical and Translational Research in Pediatric Dermatology

Impact of Atopic Skin Diathesis on Occupational Skin Disease Incidence in a Working Population

425 Functional and scalable keratinocytes and fibroblasts produced via iPSC-derived skin organoids for the treatment of RDEB

615 Efficacy and safety of Oleogel-S10 (birch triterpenes) for recessive dystrophic epidermolysis bullosa (RDEB): Results of 3 months double-blind treatment of the phase 3 study ‘EASE’

486 Systemic collagen VII protein therapy for treatment of advanced RDEB

Genotype, Clinical Course, and Therapeutic Decision Making in 76 Infants with Severe Generalized Junctional Epidermolysis Bullosa

903 Utilizing an organoid-based approach for the derivation of genetically corrected keratinocytes and fibroblasts in an induced pluripotent stem cell therapy for skin diseases

024 Development and validation of an investigators global assessment scale to evaluate overall disease severity in patients with epidermolysis bullosa simplex

Dipeptidyl Peptidase-4–Mediated Fibronectin Processing Evokes a Profibrotic Extracellular Matrix

438 A phase 1/2 trial of PTR-01, a collagen 7 (C7) protein replacement therapy, in patients with recessive dystrophic epidermolysis bullosa (RDEB)

Loss of Collagen VII Is Associated with Reduced Transglutaminase 2 Abundance and Activity

499 A novel preclinical model for translating an induced pluripotent stem cell therapy for the treatment of skin diseases

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