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Heterogeneous addiction to transforming growth factor‐beta signalling in recessive dystrophic epidermolysis bullosa‐associated cutaneous squamous cell carcinoma

British journal of dermatology (1951), 2021-04, Vol.184 (4), p.697-708

2021

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1128 Trametinib treatment causes an increase in disease severity and reduced dermal immune cell infiltration in a mouse model of junctional epidermolysis bullosa

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S193-S193

2023

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113 The endogenous deaminase APOBEC3A readily localizes to the nucleus of cultured keratinocytes

Journal of investigative dermatology, 2022-08, Vol.142 (8), p.S19

2022

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257 Fibroblasts can mediate partial-epithelial to mesenchymal transition in squamous cell carcinoma keratinocytes in the absence of canonical TGF-beta response

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S44-S44

2023

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811 Fibroblasts isolated from chronic wound dressings differentiate chronicity in recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S139-S139

2023

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Acantholytic ectodermal dysplasia: clinicopathological study of a new desmosomal disorder

British journal of dermatology (1951), 2009-04, Vol.160 (4), p.868-874

2009

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155 Notch intracellular domain is partitioned into extracellular vesicles: Implications for squamous cell carcinoma progression

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S26-S26

2018

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224 Mechanisms of squamous cell carcinoma development in patients with recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S38-S38

2018

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141 Potential consequences of the interaction of squamous cell carcinoma cells with EDA fibronectin in recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S24-S24

2018

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114 Blood-borne exosomes as biomarkers in head and neck squamous cell carcinoma (HNSCC)

Journal of investigative dermatology, 2022-08, Vol.142 (8), p.S19

2022

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089 Desmoglein 2 promotes tumor development through miR-146a/IRAK1/IL-8 signaling axis

Journal of investigative dermatology, 2022-08, Vol.142 (8), p.S15

2022

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Echocardiographic detection of pulmonary hypertension in extremely low birth weight infants with bronchopulmonary dysplasia requiring prolonged positive pressure ventilation

Journal of perinatology, 2011-10, Vol.31 (10), p.635-640

2011

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741 Reduced microbial diversity is a feature of recessive dystrophic epidermolysis bullosa wounds

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S126-S126

2018

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862 Absence of collagen VII binding to thrombospondin 1 promotes activation of TGF-beta in recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S147-S147

2018

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759 Successful in vivo COL7A1 gene delivery and correction of recessive dystrophic epidermolysis bullosa (RDEB) skin using an off the shelf HSV-1 vector (KB103)

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S129-S129

2018

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639 Metabolic reprogramming maintains skin integrity in the absence of glucose transport and identifies a therapeutic vulnerability in psoriasiform hyperplasia

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S109-S109

2018

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Cardiomyopathy diagnosed in the eldest child harbouring p.S24X mutation in JUP

British journal of dermatology (1951), 2016-09, Vol.175 (3), p.644-646

2016

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High levels of type VII collagen expression in recessive dystrophic epidermolysis bullosa cutaneous squamous cell carcinoma keratinocytes increases PI3K and MAPK signalling, cell migration and invasion

British journal of dermatology (1951), 2014-06, Vol.170 (6), p.1256-1265

2014

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Integrative mRNA profiling comparing cultured primary cells with clinical samples reveals PLK1 and C20orf20 as therapeutic targets in cutaneous squamous cell carcinoma

Oncogene, 2011-11, Vol.30 (46), p.4666-4677

2011

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Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology

British journal of dermatology (1951), 2012-07, Vol.167 (1), p.134-144

2012

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Growth and neurodevelopment at 16 to 24 months of age for infants born with gastroschisis

Journal of Perinatology, 2008-10, Vol.28 (10), p.702-706

2008

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Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology: Transcriptomic profiling of AEC syndrome skin

British journal of dermatology (1951), 2012-07, Vol.167 (1), p.134-144

2012

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Hospital readmission among infants with gastroschisis

Journal of perinatology, 2011-08, Vol.31 (8), p.546-550

2011

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Unusual molecular findings in Kindler syndrome

British journal of dermatology (1951), 2007-12, Vol.157 (6), p.1252-1256

2007

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Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network

British journal of dermatology (1951), 2004-05, Vol.150 (5), p.878-891

2004

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Heterogeneous addiction to transforming growth factor‐beta signalling in recessive dystrophic epidermolysis bullosa‐associated cutaneous squamous cell carcinoma

1128 Trametinib treatment causes an increase in disease severity and reduced dermal immune cell infiltration in a mouse model of junctional epidermolysis bullosa

113 The endogenous deaminase APOBEC3A readily localizes to the nucleus of cultured keratinocytes

257 Fibroblasts can mediate partial-epithelial to mesenchymal transition in squamous cell carcinoma keratinocytes in the absence of canonical TGF-beta response

811 Fibroblasts isolated from chronic wound dressings differentiate chronicity in recessive dystrophic epidermolysis bullosa

Acantholytic ectodermal dysplasia: clinicopathological study of a new desmosomal disorder

155 Notch intracellular domain is partitioned into extracellular vesicles: Implications for squamous cell carcinoma progression

224 Mechanisms of squamous cell carcinoma development in patients with recessive dystrophic epidermolysis bullosa

141 Potential consequences of the interaction of squamous cell carcinoma cells with EDA fibronectin in recessive dystrophic epidermolysis bullosa

114 Blood-borne exosomes as biomarkers in head and neck squamous cell carcinoma (HNSCC)

089 Desmoglein 2 promotes tumor development through miR-146a/IRAK1/IL-8 signaling axis

Echocardiographic detection of pulmonary hypertension in extremely low birth weight infants with bronchopulmonary dysplasia requiring prolonged positive pressure ventilation

741 Reduced microbial diversity is a feature of recessive dystrophic epidermolysis bullosa wounds

862 Absence of collagen VII binding to thrombospondin 1 promotes activation of TGF-beta in recessive dystrophic epidermolysis bullosa

759 Successful in vivo COL7A1 gene delivery and correction of recessive dystrophic epidermolysis bullosa (RDEB) skin using an off the shelf HSV-1 vector (KB103)

639 Metabolic reprogramming maintains skin integrity in the absence of glucose transport and identifies a therapeutic vulnerability in psoriasiform hyperplasia

Cardiomyopathy diagnosed in the eldest child harbouring p.S24X mutation in JUP

High levels of type VII collagen expression in recessive dystrophic epidermolysis bullosa cutaneous squamous cell carcinoma keratinocytes increases PI3K and MAPK signalling, cell migration and invasion

Integrative mRNA profiling comparing cultured primary cells with clinical samples reveals PLK1 and C20orf20 as therapeutic targets in cutaneous squamous cell carcinoma

Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology

Growth and neurodevelopment at 16 to 24 months of age for infants born with gastroschisis

Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology: Transcriptomic profiling of AEC syndrome skin

Hospital readmission among infants with gastroschisis

Unusual molecular findings in Kindler syndrome

Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network

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