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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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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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Pain mechanisms in hereditary palmoplantar keratodermas

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

2020

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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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DNA replication origin activation in space and time

Nature reviews. Molecular cell biology, 2015-06, Vol.16 (6), p.360

2015

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Intermediate filaments and tissue repair

Experimental cell research, 2004-11, Vol.301 (1), p.68-76

2004

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132 Spatiotemporal interplay between epidermal keratinocytes and neutrophils in inflamed skin

Journal of investigative dermatology, 2022-08, Vol.142 (8), p.S23

2022

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388 The balance between K14 and K15 regulates progenitor keratinocyte identity and commitment to differentiation in epidermis

Journal of investigative dermatology, 2024-08, Vol.144 (8), p.S67-S67

2024

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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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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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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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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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Impact of operations at low anode-cathode distance on energy consumption and greenhouse gas emissions at Aluminerie Alouette

JOM (1989), 2011-08, Vol.63 (8), p.109-115

2011

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Genetic and epigenetic determinants of DNA replication origins, position and activation

Current opinion in genetics & development, 2013-04, Vol.23 (2), p.124-131

2013

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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

Volltextzugriff (PDF)

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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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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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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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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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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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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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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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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A Dysfunctional Desmin Mutation in a Patient with Severe Generalized Myopathy

Proceedings of the National Academy of Sciences - PNAS, 1998-09, Vol.95 (19), p.11312-11317

1998

Volltextzugriff (PDF)

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

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

Pain mechanisms in hereditary palmoplantar keratodermas

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

DNA replication origin activation in space and time

Intermediate filaments and tissue repair

132 Spatiotemporal interplay between epidermal keratinocytes and neutrophils in inflamed skin

388 The balance between K14 and K15 regulates progenitor keratinocyte identity and commitment to differentiation in epidermis

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

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

A study of the rare disease pachyonychia congenita (PC)

罕见疾病先天性厚甲症 (PC) 研究

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

Impact of operations at low anode-cathode distance on energy consumption and greenhouse gas emissions at Aluminerie Alouette

Genetic and epigenetic determinants of DNA replication origins, position and activation

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

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

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

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

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

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

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

Elucidating the Early Stages of Keratin Filament Assembly

The Genetic Basis of Epidermolysis Bullosa Simplex with Mottled Pigmentation

A Dysfunctional Desmin Mutation in a Patient with Severe Generalized Myopathy

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