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The genomic landscape of cutaneous SCC reveals drivers and a novel azathioprine associated mutational signature

Nature communications, 2018-09, Vol.9 (1), p.3667-14, Article 3667

2018

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In vivo topical gene therapy for recessive dystrophic epidermolysis bullosa: a phase 1 and 2 trial

Nature medicine, 2022-04, Vol.28 (4), p.780-788

2022

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Impaired Wound Healing, Fibrosis, and Cancer: The Paradigm of Recessive Dystrophic Epidermolysis Bullosa

International journal of molecular sciences, 2021-05, Vol.22 (10), p.5104

2021

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Differential glucose requirement in skin homeostasis and injury identifies a therapeutic target for psoriasis

Nature medicine, 2018-05, Vol.24 (5), p.617-627

2018

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NOTCH1 Mutations Occur Early during Cutaneous Squamous Cell Carcinogenesis

Journal of investigative dermatology, 2014-10, Vol.134 (10), p.2630-2638

2014

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Innate sensing of microbial products promotes wound-induced skin cancer

Nature communications, 2015-01, Vol.6 (1), p.5932, Article 5932

2015

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Stopping a runaway train: targeting fibrosis in recessive dystrophic epidermolysis bullosa

British journal of dermatology (1951), 2024-09, Vol.191 (4), p.482

South, Andrew P

2024

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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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Loss-of-function mutations in Notch receptors in cutaneous and lung squamous cell carcinoma

Proceedings of the National Academy of Sciences - PNAS, 2011-10, Vol.108 (43), p.17761-17766

2011

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Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

American journal of human genetics, 2014-09, Vol.95 (3), p.308-314

2014

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Type VII Collagen Replacement Therapy in Recessive Dystrophic Epidermolysis Bullosa—How Much, How Often?

Journal of investigative dermatology, 2016-06, Vol.136 (6), p.1079-1081

2016

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Mutations in AQP5, Encoding a Water-Channel Protein, Cause Autosomal-Dominant Diffuse Nonepidermolytic Palmoplantar Keratoderma

American journal of human genetics, 2013-08, Vol.93 (2), p.330-335

2013

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Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma

Nature communications, 2016-08, Vol.7 (1), p.12493-14, Article 12493

2016

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Metaanalysis of the prevalence of intrauterine fetal death in gastroschisis

American journal of obstetrics and gynecology, 2013-08, Vol.209 (2), p.114.e1-114.e13

2013

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Mathematical modeling of cancer cell invasion of tissue: biological insight from mathematical analysis and computational simulation

Journal of mathematical biology, 2011-07, Vol.63 (1), p.141-171

2011

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Maintenance of chronicity signatures in fibroblasts isolated from recessive dystrophic epidermolysis bullosa chronic wound dressings under culture conditions

Biological research, 2023-05, Vol.56 (1), p.23-16, Article 23

2023

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RHBDF2 Mutations Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome

American journal of human genetics, 2012-02, Vol.90 (2), p.340-346

2012

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Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility

American journal of human genetics, 2012-12, Vol.91 (6), p.1115-1121

2012

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Wnt5a is strongly expressed at the leading edge in non-melanoma skin cancer, forming active gradients, while canonical Wnt signalling is repressed

PloS one, 2012-02, Vol.7 (2), p.e31827-e31827

2012

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Next-Generation Sequencing for Mutation Detection in Heritable Skin Diseases: The Paradigm of Pseudoxanthoma Elasticum

Journal of investigative dermatology, 2015-04, Vol.135 (4), p.937-940

2015

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Precision Medicine for Heritable Skin Diseases—The Paradigm of Epidermolysis Bullosa

The Journal of investigative dermatology symposium proceedings, 2018-12, Vol.19 (2), p.S74-S76

2018

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BPAG1-e Restricts Keratinocyte Migration through Control of Adhesion Stability

Journal of investigative dermatology, 2014-03, Vol.134 (3), p.773-782

2014

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Evaluating a Targeted Cancer Therapy Approach Mediated by RNA trans -Splicing In Vitro and in a Xenograft Model for Epidermolysis Bullosa-Associated Skin Cancer

International journal of molecular sciences, 2022-01, Vol.23 (1), p.575

2022

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The genomic landscape of cutaneous SCC reveals drivers and a novel azathioprine associated mutational signature

In vivo topical gene therapy for recessive dystrophic epidermolysis bullosa: a phase 1 and 2 trial

Impaired Wound Healing, Fibrosis, and Cancer: The Paradigm of Recessive Dystrophic Epidermolysis Bullosa

Differential glucose requirement in skin homeostasis and injury identifies a therapeutic target for psoriasis

NOTCH1 Mutations Occur Early during Cutaneous Squamous Cell Carcinogenesis

Innate sensing of microbial products promotes wound-induced skin cancer

Stopping a runaway train: targeting fibrosis 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

Loss-of-function mutations in Notch receptors in cutaneous and lung squamous cell carcinoma

Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

Type VII Collagen Replacement Therapy in Recessive Dystrophic Epidermolysis Bullosa—How Much, How Often?

Mutations in AQP5, Encoding a Water-Channel Protein, Cause Autosomal-Dominant Diffuse Nonepidermolytic Palmoplantar Keratoderma

Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma

Metaanalysis of the prevalence of intrauterine fetal death in gastroschisis

Mathematical modeling of cancer cell invasion of tissue: biological insight from mathematical analysis and computational simulation

Maintenance of chronicity signatures in fibroblasts isolated from recessive dystrophic epidermolysis bullosa chronic wound dressings under culture conditions

RHBDF2 Mutations Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome

Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility

Wnt5a is strongly expressed at the leading edge in non-melanoma skin cancer, forming active gradients, while canonical Wnt signalling is repressed

Next-Generation Sequencing for Mutation Detection in Heritable Skin Diseases: The Paradigm of Pseudoxanthoma Elasticum

Gauging NOTCH1 Activation in Cancer Using Immunohistochemistry

Precision Medicine for Heritable Skin Diseases—The Paradigm of Epidermolysis Bullosa

BPAG1-e Restricts Keratinocyte Migration through Control of Adhesion Stability

Evaluating a Targeted Cancer Therapy Approach Mediated by RNA trans -Splicing In Vitro and in a Xenograft Model for Epidermolysis Bullosa-Associated Skin Cancer

IL‐8 correlates with nonresponse to neoadjuvant nivolumab in HPV positive HNSCC via a potential extracellular vesicle miR‐146a mediated mechanism

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