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Loss of Keratin 17 induces tissue-specific cytokine polarization and cellular differentiation in HPV16-driven cervical tumorigenesis in vivo

Oncogene, 2016-10, Vol.35 (43), p.5653-5662

2016

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Pathophysiology of pachyonychia congenita‐associated palmoplantar keratoderma: new insights into skin epithelial homeostasis and avenues for treatment

British journal of dermatology (1951), 2020-03, Vol.182 (3), p.564-573

2020

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Pain mechanisms in hereditary palmoplantar keratodermas

British journal of dermatology (1951), 2020-03, Vol.182 (3), p.543-551

2020

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Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype

Journal of investigative dermatology, 2000-06, Vol.114 (6), p.1101-1107

2000

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Loss of Keratin 6 (K6) Proteins Reveals a Function for Intermediate Filaments during Wound Repair

The Journal of cell biology, 2003-10, Vol.163 (2), p.327-337

2003

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Elucidating the Early Stages of Keratin Filament Assembly

The Journal of cell biology, 1990-07, Vol.111 (1), p.153-169

1990

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Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: Genetic and functional analyses

Cell, 1991-09, Vol.66 (6), p.1301-1311

1991

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Increased levels of keratin 16 alter epithelialization potential of mouse skin keratinocytes in vivo and ex vivo

Molecular biology of the cell, 2001-11, Vol.12 (11), p.3439-3450

2001

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Transgenic Mice Expressing a Mutant Keratin 10 Gene Reveal the Likely Genetic Basis for Epidermolytic Hyperkeratosis

Proceedings of the National Academy of Sciences - PNAS, 1992-08, Vol.89 (15), p.6906-6910

1992

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The Genetic Basis of Epidermolysis Bullosa Simplex with Mottled Pigmentation

Proceedings of the National Academy of Sciences - PNAS, 1996-08, Vol.93 (17), p.9079-9084

1996

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Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease

Cell, 1991-01, Vol.64 (2), p.365-380

1991

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Re-epithelialization of Porcine Skin By The Sweat Apparatus

Journal of investigative dermatology, 1998-01, Vol.110 (1), p.13-19

1998

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Expression of Keratin K14 in the Epidermis and Hair Follicle: Insights into Complex Programs of Differentiation

The Journal of cell biology, 1989-11, Vol.109 (5), p.2295-2312

1989

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The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs

Genomics (San Diego, Calif.), 1998-10, Vol.53 (2), p.170-183

1998

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Disease Severity Correlates with Position of Keratin Point Mutations in Patients with Epidermolysis Bullosa Simplex

Proceedings of the National Academy of Sciences - PNAS, 1993-04, Vol.90 (8), p.3197-3201

1993

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Onset of Keratin 17 Expression Coincides with the Definition of Major Epithelial Lineages during Skin Development

The Journal of cell biology, 1998-10, Vol.143 (2), p.469-486

1998

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Of mice and men: Genetic skin diseases of keratin

Cell, 1992-06, Vol.69 (6), p.899-902

1992

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A 'hot-spot' mutation alters the mechanical properties of keratin filament networks

Nature cell biology, 2001-05, Vol.3 (5), p.503-506

2001

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The ‘ins’ and ‘outs’ of intermediate filament organization

Trends in Cell Biology, 2000-10, Vol.10 (10), p.420-428

2000

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Deletions in Epidermal Keratins Leading to Alterations in Filament Organization in Vivo and in Intermediate Filament Assembly in Vitro

The Journal of cell biology, 1990-12, Vol.111 (6), p.3049-3064

1990

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Keratin 17 null mice exhibit age- and strain-dependent alopecia

Genes & development, 2002-06, Vol.16 (11), p.1412-1422

2002

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A study of the rare disease pachyonychia congenita (PC)

British journal of dermatology (1951), 2020-03, Vol.182 (3), p.e91-e91

2020

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罕见疾病先天性厚甲症 (PC) 研究

British journal of dermatology (1951), 2020-03, Vol.182 (3), p.e104-e104

2020

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Pathophysiology of pachyonychia congenita-associated palmoplantar keratoderma:New insight into skin epithelial homeostasis and avenues for treatment

British journal of dermatology (1951), 2019-07, Vol.182 (3), p.564-573

2019

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Towards a Molecular Definition of Keratinocyte Activation after Acute Injury to Stratified Epithelia

Biochemical and biophysical research communications, 1997-07, Vol.236 (2), p.231-238

Coulombe, Pierre A.

1997

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Loss of Keratin 17 induces tissue-specific cytokine polarization and cellular differentiation in HPV16-driven cervical tumorigenesis in vivo

Pathophysiology of pachyonychia congenita‐associated palmoplantar keratoderma: new insights into skin epithelial homeostasis and avenues for treatment

Pain mechanisms in hereditary palmoplantar keratodermas

Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype

Loss of Keratin 6 (K6) Proteins Reveals a Function for Intermediate Filaments during Wound Repair

Elucidating the Early Stages of Keratin Filament Assembly

Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: Genetic and functional analyses

Increased levels of keratin 16 alter epithelialization potential of mouse skin keratinocytes in vivo and ex vivo

Transgenic Mice Expressing a Mutant Keratin 10 Gene Reveal the Likely Genetic Basis for Epidermolytic Hyperkeratosis

The Genetic Basis of Epidermolysis Bullosa Simplex with Mottled Pigmentation

Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease

Re-epithelialization of Porcine Skin By The Sweat Apparatus

Expression of Keratin K14 in the Epidermis and Hair Follicle: Insights into Complex Programs of Differentiation

The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs

Disease Severity Correlates with Position of Keratin Point Mutations in Patients with Epidermolysis Bullosa Simplex

Onset of Keratin 17 Expression Coincides with the Definition of Major Epithelial Lineages during Skin Development

Of mice and men: Genetic skin diseases of keratin

A 'hot-spot' mutation alters the mechanical properties of keratin filament networks

The ‘ins’ and ‘outs’ of intermediate filament organization

Deletions in Epidermal Keratins Leading to Alterations in Filament Organization in Vivo and in Intermediate Filament Assembly in Vitro

Keratin 17 null mice exhibit age- and strain-dependent alopecia

A study of the rare disease pachyonychia congenita (PC)

罕见疾病先天性厚甲症 (PC) 研究

Pathophysiology of pachyonychia congenita-associated palmoplantar keratoderma:New insight into skin epithelial homeostasis and avenues for treatment

Towards a Molecular Definition of Keratinocyte Activation after Acute Injury to Stratified Epithelia

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