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EGF hijacks miR-198/FSTL1 wound-healing switch and steers a two-pronged pathway toward metastasis

The Journal of experimental medicine, 2017-10, Vol.214 (10), p.2889-2900

2017

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Somatic mutations in facial skin from countries of contrasting skin cancer risk

Nature genetics, 2023-09, Vol.55 (9), p.1440-1447

2023

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Desmoplakin CSM models unravel mechanisms regulating the binding to intermediate filaments and putative therapeutics for cardiocutaneous diseases

Scientific reports, 2024-10, Vol.14 (1), p.23206-24, Article 23206

2024

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‘See-saw’ expression of microRNA-198 and FSTL1 from a single transcript in wound healing

Nature (London), 2013-03, Vol.495 (7439), p.103-106

2013

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Desmosome dualism - most of the junction is stable, but a plakophilin moiety is persistently dynamic

Journal of cell science, 2021-11, Vol.134 (21)

2021

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Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1

Nature genetics, 2011-04, Vol.43 (4), p.365-369

2011

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Optical visualisation of thermogenesis in stimulated single-cell brown adipocytes

Scientific reports, 2017-05, Vol.7 (1), p.1383-1383, Article 1383

2017

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New consensus nomenclature for mammalian keratins

The Journal of cell biology, 2006-07, Vol.174 (2), p.169-174

2006

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Improving 2D and 3D Skin In Vitro Models Using Macromolecular Crowding

Journal of visualized experiments, 2016-08 (114)

2016

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Multiple Self-Healing Squamous Epithelioma (MSSE): Rare Variants in an Adjacent Region of Chromosome 9q22.3 to Known TGFBR1 Mutations Suggest a Digenic or Multilocus Etiology

Journal of investigative dermatology, 2013-07, Vol.133 (7), p.1907-1910

2013

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Therapeutic siRNAs for dominant genetic skin disorders including pachyonychia congenita

Journal of dermatological science, 2008-09, Vol.51 (3), p.151-157

2008

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Phenotypes, genotypes and their contribution to understanding keratin function

Trends in genetics, 2003-05, Vol.19 (5), p.278-285

2003

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Fabrication of a 3D hair follicle-like hydrogel by soft lithography

Journal of biomedical materials research. Part A, 2013-11, Vol.101 (11), p.3159-3169

2013

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Characterization of Fetal Keratinocytes, Showing Enhanced Stem Cell-Like Properties: A Potential Source of Cells for Skin Reconstruction

Stem cell reports, 2014-08, Vol.3 (2), p.324-338

2014

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Self‐improving dystrophic epidermolysis bullosa: First report of clinical, molecular, and genetic characterization of five patients from Southeast Asia

American journal of medical genetics. Part A, 2021-02, Vol.185 (2), p.625-630

2021

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Keratin K6c Mutations Cause Focal Palmoplantar Keratoderma

Journal of investigative dermatology, 2010-02, Vol.130 (2), p.425-429

2010

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Generation and characterisation of keratin 7 (K7) knockout mice

PloS one, 2013-05, Vol.8 (5), p.e64404-e64404

2013

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Xeno‐free self‐assembling peptide scaffolds for building 3D organotypic skin cultures

FASEB bioAdvances, 2022-10, Vol.4 (10), p.631-637

2022

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The mechanical behavior of mutant K14-R125P keratin bundles and networks in NEB-1 keratinocytes

PloS one, 2012-02, Vol.7 (2), p.e31320

2012

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Intermediate filaments and stress

Experimental cell research, 2007-06, Vol.313 (10), p.2244-2254

2007

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Detrimental Effects of IFN-γ on an Epidermolysis Bullosa Simplex Cell Model and Protection by a Humanized Anti–IFN-γ Monoclonal Antibody

JID innovations, 2022-03, Vol.2 (2), p.100096, Article 100096

2022

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The intermediate filament network in cultured human keratinocytes is remarkably extensible and resilient

PloS one, 2008-06, Vol.3 (6), p.e2327-e2327

2008

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Keratin 14-Null Cells as a Model to Test the Efficacy of Gene Therapy Approaches in Epithelial Cells

Journal of investigative dermatology, 2011-07, Vol.131 (7), p.1412-1419

2011

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EGF hijacks miR-198/FSTL1 wound-healing switch and steers a two-pronged pathway toward metastasis

Somatic mutations in facial skin from countries of contrasting skin cancer risk

Desmoplakin CSM models unravel mechanisms regulating the binding to intermediate filaments and putative therapeutics for cardiocutaneous diseases

‘See-saw’ expression of microRNA-198 and FSTL1 from a single transcript in wound healing

Desmosome dualism - most of the junction is stable, but a plakophilin moiety is persistently dynamic

Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1

Optical visualisation of thermogenesis in stimulated single-cell brown adipocytes

New consensus nomenclature for mammalian keratins

Improving 2D and 3D Skin In Vitro Models Using Macromolecular Crowding

Multiple Self-Healing Squamous Epithelioma (MSSE): Rare Variants in an Adjacent Region of Chromosome 9q22.3 to Known TGFBR1 Mutations Suggest a Digenic or Multilocus Etiology

Therapeutic siRNAs for dominant genetic skin disorders including pachyonychia congenita

Phenotypes, genotypes and their contribution to understanding keratin function

Fabrication of a 3D hair follicle-like hydrogel by soft lithography

Characterization of Fetal Keratinocytes, Showing Enhanced Stem Cell-Like Properties: A Potential Source of Cells for Skin Reconstruction

Self‐improving dystrophic epidermolysis bullosa: First report of clinical, molecular, and genetic characterization of five patients from Southeast Asia

Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria

Keratin K6c Mutations Cause Focal Palmoplantar Keratoderma

Generation and characterisation of keratin 7 (K7) knockout mice

Xeno‐free self‐assembling peptide scaffolds for building 3D organotypic skin cultures

The mechanical behavior of mutant K14-R125P keratin bundles and networks in NEB-1 keratinocytes

Intermediate filaments and stress

Detrimental Effects of IFN-γ on an Epidermolysis Bullosa Simplex Cell Model and Protection by a Humanized Anti–IFN-γ Monoclonal Antibody

The intermediate filament network in cultured human keratinocytes is remarkably extensible and resilient

Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation

Keratin 14-Null Cells as a Model to Test the Efficacy of Gene Therapy Approaches in Epithelial Cells

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