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Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Nature genetics, 1996-08, Vol.13 (4), p.450-457

1996

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Octopus arms exhibit exceptional flexibility

Scientific reports, 2020-11, Vol.10 (1), p.20872-20872, Article 20872

2020

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1552 Ruxolitinib reduces inflammation, itch and immune subsets - DETCs and macrophages in a mouse MC903 dermatitis model

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S266-S266

2023

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Keratin 16 and keratin 17 mutations cause pachyonychia congenita

Nature genetics, 1995-03, Vol.9 (3), p.273-278

1995

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105 The effect of oxygen on keratinocyte differentiation

Journal of investigative dermatology, 2016-09, Vol.136 (9), p.S178-S178

2016

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A Novel Mutation in the Keratin 13 Gene Causing Oral White Sponge Nevus

Journal of dental research, 2001-03, Vol.80 (3), p.919-923

2001

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Retrovirus-mediated transgenic keratin expression in cultured fibroblasts: Specific domain functions in keratin stabilization and filament formation

Cell, 1990-08, Vol.62 (4), p.681-696

1990

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Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations

British journal of dermatology (1951), 2011-07, Vol.165 (1), p.106-114

2011

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Ionizing radiation induces a dramatic persistence of p53 protein accumulation and DNA damage signaling in mutant p53 zebrafish

Oncogene, 2013-08, Vol.32 (34), p.4009-4016

2013

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A mutation in the mucosal keratin K4 is associated with oral white sponge nevus

Nature genetics, 1995-12, Vol.11 (4), p.450-452

1995

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Comparative biomechanics of hagfish skins: diversity in material, morphology, and movement

Zoology (Jena), 2021-04, Vol.145, p.125888-125888, Article 125888

2021

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Filaggrin mutations are associated with recurrent skin infection in Singaporean Chinese patients with atopic dermatitis

British journal of dermatology (1951), 2012-01, Vol.166 (1), p.200-203

2012

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Missing links: Weber-Cockayne keratin mutations implicate the L12 linker domain in effective cytoskeleton function

Nature genetics, 1993-11, Vol.5 (3), p.294-300

1993

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Keratinocyte differentiation in psoriatic scalp: morphology and expression of epithelial keratins

British journal of dermatology (1951), 1994-08, Vol.131 (2), p.191-200

1994

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Filaggrin mutations are associated with recurrent skin infection in Singaporean Chinese patients with atopic dermatitis: Filaggrin mutations and recurrent skin infection in AD

British journal of dermatology (1951), 2012-01, Vol.166 (1), p.200-203

2012

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Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation

British journal of dermatology (1951), 2009-12, Vol.161 (6), p.1396-1398

2009

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Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Muscle & nerve, 2007-01, Vol.35 (1), p.24-35

2007

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Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations: Wide spectrum of FLG mutations in Singaporean Chinese

British journal of dermatology (1951), 2011-07, Vol.165 (1), p.106-114

2011

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Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutations

British journal of dermatology (1951), 2003-07, Vol.149 (1), p.46-58

2003

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Disruption of the keratin filament network during epithelial cell division

The EMBO journal, 1982-01, Vol.1 (11), p.1365-1372

1982

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Psoriasis: maintenance of an intact monolayer basal cell differentiation compartment in spite of hyperproliferation

British journal of dermatology (1951), 1985-07, Vol.113 (1), p.53-64

1985

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Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation

British journal of dermatology (1951), 2001-01, Vol.144 (1), p.40-45

2001

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Functional analysis of keratin components in the mouse hair follicle inner root sheath

British journal of dermatology (1951), 2004-02, Vol.150 (2), p.195-204

2004

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A keratin 14 ‘knockout’ mutation in recessive epidermolysis bullosa simplex resulting in less severe disease

British journal of dermatology (1951), 2000-09, Vol.143 (3), p.621-627

2000

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Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans

British journal of dermatology (1951), 2001-10, Vol.145 (4), p.558-568

2001

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Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Octopus arms exhibit exceptional flexibility

1552 Ruxolitinib reduces inflammation, itch and immune subsets - DETCs and macrophages in a mouse MC903 dermatitis model

Keratin 16 and keratin 17 mutations cause pachyonychia congenita

105 The effect of oxygen on keratinocyte differentiation

A Novel Mutation in the Keratin 13 Gene Causing Oral White Sponge Nevus

Retrovirus-mediated transgenic keratin expression in cultured fibroblasts: Specific domain functions in keratin stabilization and filament formation

Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations

Ionizing radiation induces a dramatic persistence of p53 protein accumulation and DNA damage signaling in mutant p53 zebrafish

A mutation in the mucosal keratin K4 is associated with oral white sponge nevus

Comparative biomechanics of hagfish skins: diversity in material, morphology, and movement

Filaggrin mutations are associated with recurrent skin infection in Singaporean Chinese patients with atopic dermatitis

Missing links: Weber-Cockayne keratin mutations implicate the L12 linker domain in effective cytoskeleton function

Keratinocyte differentiation in psoriatic scalp: morphology and expression of epithelial keratins

Filaggrin mutations are associated with recurrent skin infection in Singaporean Chinese patients with atopic dermatitis: Filaggrin mutations and recurrent skin infection in AD

Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation

Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations: Wide spectrum of FLG mutations in Singaporean Chinese

Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutations

Disruption of the keratin filament network during epithelial cell division

Psoriasis: maintenance of an intact monolayer basal cell differentiation compartment in spite of hyperproliferation

Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation

Functional analysis of keratin components in the mouse hair follicle inner root sheath

A keratin 14 ‘knockout’ mutation in recessive epidermolysis bullosa simplex resulting in less severe disease

Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans

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