Lista de obras -

A Novel Fully Humanized 3D Skin Equivalent to Model Early Melanoma Invasion.

artículo científico publicado en 2015

A profile of lipid dysregulation in harlequin ichthyosis.

artículo científico publicado en 2017

Acral peeling skin syndrome associated with a novel CSTA gene mutation.

artículo científico publicado en 2015

Acute sun damage and photoprotective responses in whales.

artículo científico publicado en 2010

An unusual case of vulval papulonecrotic tuberculid

artículo científico publicado en 2010

Analysis of hedgehog signaling in periocular sebaceous carcinoma.

artículo científico publicado en 2018

Axl promotes cutaneous squamous cell carcinoma survival through negative regulation of pro-apoptotic Bcl-2 family members.

artículo científico publicado en 2010

Case 1. Systematic lupus erythematosus (SLE)

artículo científico publicado en 2002

Connexins in epidermal homeostasis and skin disease.

artículo científico

Cytoskeletal protein Flightless I inhibits apoptosis, enhances tumor cell invasion and promotes cutaneous squamous cell carcinoma progression

artículo científico publicado en 2015

Desmoglein 3 promotes cancer cell migration and invasion by regulating activator protein 1 and protein kinase C-dependent-Ezrin activation.

artículo científico publicado en 2013

Development of an ELISA for rapid detection of anti-type VII collagen autoantibodies in epidermolysis bullosa acquisita

scientific article published on 01 January 1997

Disseminated herpes zoster in the elderly

scientific article published on 01 July 1997

Enhanced modulation of keratinocyte motility by transforming growth factor-alpha (TGF-alpha) relative to epidermal growth factor (EGF)

scientific article published on 01 April 1996

Epidermal grafting for wound healing: a review on the harvesting systems, the ultrastructure of the graft and the mechanism of wound healing.

artículo científico publicado en 2016

Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes

scientific article published on 30 May 2018

Exoming into rare skin disease: EGFR deficiency.

artículo científico publicado en 2014

Expanding the Phenotypic Spectrum of Olmsted Syndrome

artículo científico publicado en 2015

Expression of eotaxin, an eosinophil-selective chemokine, parallels eosinophil accumulation in the vesiculobullous stage of incontinentia pigmenti

artículo científico publicado en 2002

Extracellular matrix and keratinocyte migration.

artículo científico publicado en 2001

Filaggrin mutations are associated with ichthyosis vulgaris in the Bangladeshi population.

artículo científico publicado en 2009

Focal PPK secondary to a novel KRT6C mutation (Pachyonychia congenita-K6c)

artículo científico publicado en 2015

Generalized pustular psoriasis and cryptogenic organizing pneumonia.

artículo científico publicado en 2008

Genotype-phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis

artículo científico publicado en 2019

Granulomatous mycosis fungoides presenting as an acquired ichthyosis

scientific article published on 01 March 2003

Hypoxia increases human keratinocyte motility on connective tissue.

artículo científico publicado en 1997

Hypoxia induces epidermal keratinocyte matrix metalloproteinase-9 secretion via the protein kinase C pathway.

artículo científico publicado en 2008

Increased invasive behaviour in cutaneous squamous cell carcinoma with loss of basement-membrane type VII collagen.

artículo científico publicado en 2009

Induction of keratinocyte IL-8 expression and secretion by IgG autoantibodies as a novel mechanism of epidermal neutrophil recruitment in a pemphigus variant

artículo científico publicado en 2000

Inherited palmoplantar keratodermas: the heart of the matter.

artículo científico publicado en 2017

Integrin alpha 5 beta 1 expression is required for inhibition of keratinocyte migration by ganglioside GT1b.

artículo científico publicado en 1998

Jessner's lymphocytic infiltrate and probable discoid lupus erythematosus occurring separately in two sisters

artículo científico publicado en 1999

Keratins and skin disease.

artículo científico publicado en 2015

Laminin-5 inhibits human keratinocyte migration.

artículo científico

Loss of function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype

artículo científico publicado en 2019

Loss-of-function mutations in CAST cause peeling skin, leukonychia, acral punctate keratoses, cheilitis, and knuckle pads.

artículo científico publicado en 2015

Management of congenital ichthyoses: European guidelines of care, part one

scientific article published on 03 December 2018

Management of congenital ichthyoses: European guidelines of care, part two

scientific article published on 03 December 2018

Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa.

artículo científico publicado en 2016

Matrix metalloproteinases and epidermal wound repair.

artículo científico

Metalloproteinases and Wound Healing

artículo científico publicado en 2015

Metastatic dissemination of human ovarian epithelial carcinoma is promoted by alpha2beta1-integrin-mediated interaction with type I collagen

artículo científico publicado en 1998

MicroRNA and transcriptome analysis in periocular Sebaceous Gland Carcinoma.

artículo científico publicado en 2018

Modeling the Structure of Keratin 1 and 10 Terminal Domains and their Misassembly in Keratoderma.

artículo científico publicado en 2017

Modulation of type VII collagen (anchoring fibril) expression by retinoids in human skin cells

artículo científico publicado en 1997

Molecular cloning and characterization of a cDNA encoding canine type VII collagen non-collagenous (NC1) domain, the target antigen of autoimmune disease epidermolysis bullosa acquisita (EBA).

artículo científico publicado en 1998

Molecular cloning of canine bullous pemphigoid antigen 2 cDNA and immunomapping of NC16A domain by canine bullous pemphigoid autoantibodies.

artículo científico publicado en 2000

Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis. ⬇️

artículo científico publicado en 2005

Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratoderma.

artículo científico publicado en 2013

Necrobiosis lipoidica: only a minority of patients have diabetes mellitus.

artículo científico publicado en 1999

Noonan syndrome with multiple lentigines and associated craniosynostosis.

artículo científico publicado en 2018

Novel and recurrent connexin 30.3 and connexin 31 mutations associated with erythrokeratoderma variabilis

scientific article published on 01 January 2011

Novel mutations in desmoglein 1: focal palmoplantar keratoderma in milder phenotypes

scientific article published on 02 June 2019

Pachyonychia congenita cornered: report on the 11th Annual International Pachyonychia Congenita Consortium Meeting

artículo científico publicado en 2014

Pachyonychia congenita, a paradigm for rare skin disorders

artículo científico publicado en 2020

Patients with recessive dystrophic epidermolysis bullosa develop squamous-cell carcinoma regardless of type VII collagen expression.

artículo científico publicado en 2007

Phosphorylation of focal adhesion kinase (pp125(FAK)) is increased in human keratinocytes induced to migrate by extracellular matrices.

artículo científico publicado en 2001

Plantar pain in pachyonychia congenita

scientific article published on 01 July 2018

Platelike osteoma cutis

artículo científico publicado en 2011

RNA-seq analysis of host and viral gene expression highlights interaction between varicella zoster virus and keratinocyte differentiation.

artículo científico publicado en 2014

Recent advances in the genetics and management of harlequin ichthyosis

artículo científico publicado en 2014

Recessive mutation in FAM83G associated with palmoplantar keratoderma and exuberant scalp hair

artículo científico publicado en 2017

Specific loss of connexin 26 expression in ductal sweat gland epithelium associated with the deletion mutation del(GJB6-D13S1830).

artículo científico publicado en 2005

Stopping pachyonychia congenita plantar pain with a statin?

scientific article published on 06 August 2019

Striate palmoplantar keratoderma resulting from a missense mutation in DSG1.

artículo científico publicado en 2018

Subungual melanoma: a relation to direct injury?

artículo científico publicado en 1995

Suppression of TGFβ and Angiogenesis by Type VII Collagen in Cutaneous SCC.

artículo científico

Targeted sequence capture and high-throughput sequencing in the molecular diagnosis of ichthyosis and other skin diseases.

artículo científico publicado en 2012

Thalidomide increases human keratinocyte migration and proliferation

artículo científico publicado en 1999

The epidermolysis bullosa acquisita antigen (type VII collagen) is present in human colon and patients with crohn's disease have autoantibodies to type VII collagen.

artículo científico publicado en 2002

The future of U.K. dermatology translational research through the Oracle of Delphi.

artículo científico publicado en 2015

The receptor tyrosine kinase Axl regulates cell-cell adhesion and stemness in cutaneous squamous cell carcinoma

artículo científico publicado en 2013

Type VII collagen and squamous cell carcinoma.

artículo científico publicado en 2014

Ultra-deformable liposomes containing bleomycin: in vitro stability and toxicity on human cutaneous keratinocyte cell lines.

artículo científico publicado en 2005

Ultraviolet A irradiation upregulates type VII collagen expression in human dermal fibroblasts

scientific article published on 01 February 1997

Unilateral Beau's lines in childhood reflex sympathetic dystrophy

scientific article published on 01 September 1995

Unusual distribution of punctate dysplastic keratoses and skin cancers in sunbed users: a report of three cases

artículo científico publicado en 2005

Update on pachyonychia congenita research

artículo científico publicado en 2019

Zosteriform Kaposi's sarcoma

artículo científico publicado en 2001

iRHOM2-dependent regulation of ADAM17 in cutaneous disease and epidermal barrier function

artículo científico publicado en 2014

Lista de obras de

A Novel Fully Humanized 3D Skin Equivalent to Model Early Melanoma Invasion.

A profile of lipid dysregulation in harlequin ichthyosis.

Acral peeling skin syndrome associated with a novel CSTA gene mutation.

Acute sun damage and photoprotective responses in whales.

An unusual case of vulval papulonecrotic tuberculid

Analysis of hedgehog signaling in periocular sebaceous carcinoma.

Axl promotes cutaneous squamous cell carcinoma survival through negative regulation of pro-apoptotic Bcl-2 family members.

Case 1. Systematic lupus erythematosus (SLE)

Connexins in epidermal homeostasis and skin disease.

Cytoskeletal protein Flightless I inhibits apoptosis, enhances tumor cell invasion and promotes cutaneous squamous cell carcinoma progression

Desmoglein 3 promotes cancer cell migration and invasion by regulating activator protein 1 and protein kinase C-dependent-Ezrin activation.

Development of an ELISA for rapid detection of anti-type VII collagen autoantibodies in epidermolysis bullosa acquisita

Disseminated herpes zoster in the elderly

Enhanced modulation of keratinocyte motility by transforming growth factor-alpha (TGF-alpha) relative to epidermal growth factor (EGF)

Epidermal grafting for wound healing: a review on the harvesting systems, the ultrastructure of the graft and the mechanism of wound healing.

Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes

Exoming into rare skin disease: EGFR deficiency.

Expanding the Phenotypic Spectrum of Olmsted Syndrome

Expression of eotaxin, an eosinophil-selective chemokine, parallels eosinophil accumulation in the vesiculobullous stage of incontinentia pigmenti

Extracellular matrix and keratinocyte migration.

Filaggrin mutations are associated with ichthyosis vulgaris in the Bangladeshi population.

Focal PPK secondary to a novel KRT6C mutation (Pachyonychia congenita-K6c)

Generalized pustular psoriasis and cryptogenic organizing pneumonia.

Genotype-phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis

Granulomatous mycosis fungoides presenting as an acquired ichthyosis

Hypoxia increases human keratinocyte motility on connective tissue.

Hypoxia induces epidermal keratinocyte matrix metalloproteinase-9 secretion via the protein kinase C pathway.

Increased invasive behaviour in cutaneous squamous cell carcinoma with loss of basement-membrane type VII collagen.

Induction of keratinocyte IL-8 expression and secretion by IgG autoantibodies as a novel mechanism of epidermal neutrophil recruitment in a pemphigus variant

Inherited palmoplantar keratodermas: the heart of the matter.

Integrin alpha 5 beta 1 expression is required for inhibition of keratinocyte migration by ganglioside GT1b.

Jessner's lymphocytic infiltrate and probable discoid lupus erythematosus occurring separately in two sisters

Keratins and skin disease.

Laminin-5 inhibits human keratinocyte migration.

Loss of function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype

Loss-of-function mutations in CAST cause peeling skin, leukonychia, acral punctate keratoses, cheilitis, and knuckle pads.

Management of congenital ichthyoses: European guidelines of care, part one

Management of congenital ichthyoses: European guidelines of care, part two

Management of cutaneous squamous cell carcinoma in patients with epidermolysis bullosa.

Matrix metalloproteinases and epidermal wound repair.

Metalloproteinases and Wound Healing

Metastatic dissemination of human ovarian epithelial carcinoma is promoted by alpha2beta1-integrin-mediated interaction with type I collagen

MicroRNA and transcriptome analysis in periocular Sebaceous Gland Carcinoma.

Modeling the Structure of Keratin 1 and 10 Terminal Domains and their Misassembly in Keratoderma.

Modulation of type VII collagen (anchoring fibril) expression by retinoids in human skin cells

Molecular cloning and characterization of a cDNA encoding canine type VII collagen non-collagenous (NC1) domain, the target antigen of autoimmune disease epidermolysis bullosa acquisita (EBA).

Molecular cloning of canine bullous pemphigoid antigen 2 cDNA and immunomapping of NC16A domain by canine bullous pemphigoid autoantibodies.

Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis. ⬇️

Mutations in AQP5, encoding a water-channel protein, cause autosomal-dominant diffuse nonepidermolytic palmoplantar keratoderma.

Necrobiosis lipoidica: only a minority of patients have diabetes mellitus.

Noonan syndrome with multiple lentigines and associated craniosynostosis.

Novel and recurrent connexin 30.3 and connexin 31 mutations associated with erythrokeratoderma variabilis

Novel mutations in desmoglein 1: focal palmoplantar keratoderma in milder phenotypes

Pachyonychia congenita cornered: report on the 11th Annual International Pachyonychia Congenita Consortium Meeting

Pachyonychia congenita, a paradigm for rare skin disorders

Patients with recessive dystrophic epidermolysis bullosa develop squamous-cell carcinoma regardless of type VII collagen expression.

Phosphorylation of focal adhesion kinase (pp125(FAK)) is increased in human keratinocytes induced to migrate by extracellular matrices.

Plantar pain in pachyonychia congenita

Platelike osteoma cutis

RNA-seq analysis of host and viral gene expression highlights interaction between varicella zoster virus and keratinocyte differentiation.

Recent advances in the genetics and management of harlequin ichthyosis

Recessive mutation in FAM83G associated with palmoplantar keratoderma and exuberant scalp hair

Specific loss of connexin 26 expression in ductal sweat gland epithelium associated with the deletion mutation del(GJB6-D13S1830).

Stopping pachyonychia congenita plantar pain with a statin?

Striate palmoplantar keratoderma resulting from a missense mutation in DSG1.

Subungual melanoma: a relation to direct injury?

Suppression of TGFβ and Angiogenesis by Type VII Collagen in Cutaneous SCC.

Targeted sequence capture and high-throughput sequencing in the molecular diagnosis of ichthyosis and other skin diseases.

Thalidomide increases human keratinocyte migration and proliferation

The epidermolysis bullosa acquisita antigen (type VII collagen) is present in human colon and patients with crohn's disease have autoantibodies to type VII collagen.

The future of U.K. dermatology translational research through the Oracle of Delphi.

The receptor tyrosine kinase Axl regulates cell-cell adhesion and stemness in cutaneous squamous cell carcinoma

Type VII collagen and squamous cell carcinoma.

Ultra-deformable liposomes containing bleomycin: in vitro stability and toxicity on human cutaneous keratinocyte cell lines.

Ultraviolet A irradiation upregulates type VII collagen expression in human dermal fibroblasts

Unilateral Beau's lines in childhood reflex sympathetic dystrophy

Unusual distribution of punctate dysplastic keratoses and skin cancers in sunbed users: a report of three cases

Update on pachyonychia congenita research

Zosteriform Kaposi's sarcoma