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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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Keratins and skin disorders

The Journal of pathology, 2004-11, Vol.204 (4), p.355-366

2004

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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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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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Detection of the p53 response in zebrafish embryos using new monoclonal antibodies

Oncogene, 2008-01, Vol.27 (5), p.629-640

2008

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Ex Vivo Herpes Simplex Virus Reactivation Involves a Dual Leucine Zipper Kinase-Dependent Wave of Lytic Gene Expression That Is Independent of Histone Demethylase Activity and Viral Genome Synthesis

Journal of virology, 2022-06, Vol.96 (12), p.e0047522-e0047522

2022

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Human keratin 8 mutations that disturb filament assembly observed in inflammatory bowel disease patients

Journal of cell science, 2004-04, Vol.117 (Pt 10), p.1989-1999

2004

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Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

Nature genetics, 1997-10, Vol.17 (2), p.240-244

1997

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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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Expression of individual lamins in basal cell carcinomas of the skin

British journal of cancer, 2001-02, Vol.84 (4), p.512-519

2001

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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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Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

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

2007

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Keratin mutations and intestinal pathology

The Journal of pathology, 2004-11, Vol.204 (4), p.377-385

2004

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A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering

Nature (London), 1992-03, Vol.356 (6366), p.244-246

1992

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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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Antibody markers of basal cells in complex epithelia

Journal of cell science, 1990-09, Vol.97 (1), p.39-50

1990

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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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Effects on normal fibroblasts and neuroblastoma cells of the activation of the p53 response by the nuclear export inhibitor leptomycin B

Oncogene, 1999-12, Vol.18 (51), p.7378-7386

1999

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Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress

British journal of dermatology (1951), 1998-11, Vol.139 (5), p.767-775

1998

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Functional improvement of mutant keratin cells on addition of desmin: an alternative approach to gene therapy for dominant diseases

Gene therapy, 2004-08, Vol.11 (16), p.1290-1295

2004

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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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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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Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization

Genes & development, 1996-07, Vol.10 (14), p.1724-1735

1996

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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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Octopus arms exhibit exceptional flexibility

Keratins and skin disorders

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

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

Detection of the p53 response in zebrafish embryos using new monoclonal antibodies

Ex Vivo Herpes Simplex Virus Reactivation Involves a Dual Leucine Zipper Kinase-Dependent Wave of Lytic Gene Expression That Is Independent of Histone Demethylase Activity and Viral Genome Synthesis

Human keratin 8 mutations that disturb filament assembly observed in inflammatory bowel disease patients

Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Expression of individual lamins in basal cell carcinomas of the skin

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

Plectin defects in epidermolysis bullosa simplex with muscular dystrophy

Keratin mutations and intestinal pathology

A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering

Keratin 16 and keratin 17 mutations cause pachyonychia congenita

Antibody markers of basal cells in complex epithelia

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

Effects on normal fibroblasts and neuroblastoma cells of the activation of the p53 response by the nuclear export inhibitor leptomycin B

Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress

Functional improvement of mutant keratin cells on addition of desmin: an alternative approach to gene therapy for dominant diseases

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

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

Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization

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

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