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Human keratin 1/10‐1B tetramer structures reveal a knob‐pocket mechanism in intermediate filament assembly

The EMBO journal, 2019-06, Vol.38 (11), p.n/a

2019

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Mitotic Recombination in Patients with Ichthyosis Causes Reversion of Dominant Mutations in KRT10

Science (American Association for the Advancement of Science), 2010-10, Vol.330 (6000), p.94-97

2010

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Hyperglycemia Induces Skin Barrier Dysfunctions with Impairment of Epidermal Integrity in Non-Wounded Skin of Type 1 Diabetic Mice

PloS one, 2016-11, Vol.11 (11), p.e0166215-e0166215

2016

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The X-Ray Crystal Structure of the Keratin 1-Keratin 10 Helix 2B Heterodimer Reveals Molecular Surface Properties and Biochemical Insights into Human Skin Disease

Journal of investigative dermatology, 2017-01, Vol.137 (1), p.142-150

2017

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Kallikrein-Mediated Cytokeratin 10 Degradation Is Required for Varicella Zoster Virus Propagation in Skin

Journal of investigative dermatology, 2020-04, Vol.140 (4), p.774-784.e11

2020

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Nuclear IL-33 Plays an Important Role in IL-31‒Mediated Downregulation of FLG, Keratin 1, and Keratin 10 by Regulating Signal Transducer and Activator of Transcription 3 Activation in Human Keratinocytes

Journal of investigative dermatology, 2022-01, Vol.142 (1), p.136-144.e3

2022

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A proteomic approach to compare saliva from individuals with and without oral leukoplakia

Journal of proteomics, 2017-01, Vol.151, p.43-52

2017

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Ichthyosis with confetti caused by new and recurrent mutations in KRT10 associated with varying degrees of keratin 10 mis-localization

Journal of dermatological science, 2020-04, Vol.98 (1), p.35-40

2020

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Live imaging reveals chromatin compaction transitions and dynamic transcriptional bursting during stem cell differentiation in vivo

eLife, 2023-03, Vol.12

2023

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Arginine‐ but not alanine‐rich carboxy‐termini trigger nuclear translocation of mutant keratin 10 in ichthyosis with confetti

Journal of cellular and molecular medicine, 2019-12, Vol.23 (12), p.8442-8452

2019

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CLDN1 knock out keratinocytes as a model to investigate multiple skin disorders

Experimental dermatology, 2024-05, Vol.33 (5), p.e15084-n/a

2024

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In Vitro Assessment of IL-4- or IL-13-Mediated Changes in the Structural Components of Keratinocytes in Mice and Humans

Journal of investigative dermatology, 2014-05, Vol.134 (5), p.1342-1350

2014

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An Autoimmune Basis for Raynaud's Phenomenon: Murine Model and Human Disease

Arthritis & rheumatology (Hoboken, N.J.), 2018-09, Vol.70 (9), p.1489-1499

2018

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AKT1-mediated Lamin A/C degradation is required for nuclear degradation and normal epidermal terminal differentiation

Cell death and differentiation, 2015-12, Vol.22 (12), p.2123-2132

2015

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Expression of keratin 1, keratin 10, desmoglein 1 and desmocollin 1 in the epidermis: possible downregulation by interleukin-4 and interleukin-13 in atopic dermatitis

EJD. European journal of dermatology, 2017-05, Vol.27 (3), p.247-253

2017

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Mosaicism in Cutaneous Disorders

Annual review of genetics, 2017-11, Vol.51, p.123

2017

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Serum lipids, retinoic acid and phenol red differentially regulate expression of keratins K1, K10 and K2 in cultured keratinocytes

Scientific reports, 2020-03, Vol.10 (1), p.4829-14, Article 4829

2020

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Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation

Journal of investigative dermatology, 2014-10, Vol.134 (10), p.2579-2588

2014

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Cellular senescence increases expression of bacterial ligands in the lungs and is positively correlated with increased susceptibility to pneumococcal pneumonia

Aging cell, 2011-10, Vol.10 (5), p.798-806

2011

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Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis

Acta dermato-venereologica, 2016-01, Vol.96 (4), p.473-478

2016

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Cytokeratin 10 and Cytokeratin 19: Predictive Markers for Poor Prognosis in Hepatocellular Carcinoma Patients after Curative Resection

Clinical cancer research, 2008-06, Vol.14 (12), p.3850-3859

2008

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Key role for clumping factor B in Staphylococcus aureus nasal colonization of humans

PLoS medicine, 2008-01, Vol.5 (1), p.e17-e17

2008

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Role of the keratin 1 and keratin 10 tails in the pathogenesis of ichthyosis hystrix of Curth Macklin

PloS one, 2018-04, Vol.13 (4), p.e0195792

2018

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Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis

Journal of investigative dermatology, 2015-12, Vol.135 (12), p.3041-3050

2015

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In silico predicted structural and functional insights of all missense mutations on 2B domain of K1/K10 causing genodermatoses

Oncotarget, 2016-08, Vol.7 (33), p.52766-52780

2016

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Human keratin 1/10‐1B tetramer structures reveal a knob‐pocket mechanism in intermediate filament assembly

Mitotic Recombination in Patients with Ichthyosis Causes Reversion of Dominant Mutations in KRT10

Hyperglycemia Induces Skin Barrier Dysfunctions with Impairment of Epidermal Integrity in Non-Wounded Skin of Type 1 Diabetic Mice

The X-Ray Crystal Structure of the Keratin 1-Keratin 10 Helix 2B Heterodimer Reveals Molecular Surface Properties and Biochemical Insights into Human Skin Disease

Kallikrein-Mediated Cytokeratin 10 Degradation Is Required for Varicella Zoster Virus Propagation in Skin

Nuclear IL-33 Plays an Important Role in IL-31‒Mediated Downregulation of FLG, Keratin 1, and Keratin 10 by Regulating Signal Transducer and Activator of Transcription 3 Activation in Human Keratinocytes

A proteomic approach to compare saliva from individuals with and without oral leukoplakia

Ichthyosis with confetti caused by new and recurrent mutations in KRT10 associated with varying degrees of keratin 10 mis-localization

Live imaging reveals chromatin compaction transitions and dynamic transcriptional bursting during stem cell differentiation in vivo

Arginine‐ but not alanine‐rich carboxy‐termini trigger nuclear translocation of mutant keratin 10 in ichthyosis with confetti

CLDN1 knock out keratinocytes as a model to investigate multiple skin disorders

In Vitro Assessment of IL-4- or IL-13-Mediated Changes in the Structural Components of Keratinocytes in Mice and Humans

An Autoimmune Basis for Raynaud's Phenomenon: Murine Model and Human Disease

AKT1-mediated Lamin A/C degradation is required for nuclear degradation and normal epidermal terminal differentiation

Expression of keratin 1, keratin 10, desmoglein 1 and desmocollin 1 in the epidermis: possible downregulation by interleukin-4 and interleukin-13 in atopic dermatitis

Mosaicism in Cutaneous Disorders

Serum lipids, retinoic acid and phenol red differentially regulate expression of keratins K1, K10 and K2 in cultured keratinocytes

Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation

Cellular senescence increases expression of bacterial ligands in the lungs and is positively correlated with increased susceptibility to pneumococcal pneumonia

Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis

Cytokeratin 10 and Cytokeratin 19: Predictive Markers for Poor Prognosis in Hepatocellular Carcinoma Patients after Curative Resection

Key role for clumping factor B in Staphylococcus aureus nasal colonization of humans

Role of the keratin 1 and keratin 10 tails in the pathogenesis of ichthyosis hystrix of Curth Macklin

Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis

In silico predicted structural and functional insights of all missense mutations on 2B domain of K1/K10 causing genodermatoses

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