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Keratinocyte-specific deletion of SHARPIN induces atopic dermatitis-like inflammation in mice

PloS one, 2020-07, Vol.15 (7), p.e0235295

2020

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Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia

PloS one, 2018-10, Vol.13 (10), p.e0205775-e0205775

2018

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Chronic proliferative dermatitis in Sharpin null mice: development of an autoinflammatory disease in the absence of B and T lymphocytes and IL4/IL13 signaling

PloS one, 2014-01, Vol.9 (1), p.e85666

2014

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Systematic screening for skin, hair, and nail abnormalities in a large-scale knockout mouse program

PloS one, 2017-07, Vol.12 (7), p.e0180682-e0180682

2017

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Hyaline Arteriolosclerosis in 30 Strains of Aged Inbred Mice

Veterinary pathology, 2019-09, Vol.56 (5), p.799-806

2019

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Gain of function p.E138A alteration in Card14 leads to psoriasiform skin inflammation and implicates genetic modifiers in disease severity

Experimental and molecular pathology, 2019-10, Vol.110, p.104286-104286, Article 104286

2019

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2‐deoxy D‐glucose treatment does not elicit a hair growth response in alopecia areata

Experimental dermatology, 2019-09, Vol.28 (9), p.1091-1093

2019

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Nail abnormalities identified in an ageing study of 30 inbred mouse strains

Experimental dermatology, 2019-04, Vol.28 (4), p.383-390

2019

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Lack of Response to Laser Comb in Spontaneous and Graft-Induced Alopecia Areata in C3H/HeJ Mice

Journal of investigative dermatology, 2014-01, Vol.134 (1), p.264-266

2014

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Angiogenesis in the skin of SHARPIN-deficient mice with chronic proliferative dermatitis

Experimental and molecular pathology, 2016-12, Vol.101 (3), p.303-307

2016

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Identification of Fat4 and Tsc22d1 as Novel Candidate Genes for Spontaneous Pulmonary Adenomas

Cancer research (Chicago, Ill.), 2011-09, Vol.71 (17), p.5779-5791

2011

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Loss of FAS/FASL signalling does not reduce apoptosis in Sharpin null mice

Experimental dermatology, 2017-09, Vol.26 (9), p.820-822

2017

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The pathogenesis of chronic eosinophilic esophagitis in SHARPIN-deficient mice

Experimental and molecular pathology, 2015-12, Vol.99 (3), p.460-467

2015

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Mouse genome-wide association study identifies polymorphisms on chromosomes 4, 11, and 15 for age-related cardiac fibrosis

Mammalian genome, 2016-06, Vol.27 (5-6), p.179-190

2016

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Genetic determinants of fibro-osseous lesions in aged inbred mice

Experimental and molecular pathology, 2016-02, Vol.100 (1), p.92-100

2016

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Mouse Alopecia Areata and Heart Disease: Know Your Mouse

Journal of investigative dermatology, 2014-01, Vol.134 (1), p.279-281

2014

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Dermal lymphatic dilation in a mouse model of alopecia areata

Experimental and molecular pathology, 2016-04, Vol.100 (2), p.332-336

2016

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Excavating the Genome: Large-Scale Mutagenesis Screening for the Discovery of New Mouse Models

The Journal of investigative dermatology symposium proceedings, 2015-11, Vol.17 (2), p.27-29

2015

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Alopecia Areata: Updates from the Mouse Perspective

The Journal of investigative dermatology symposium proceedings, 2013-12, Vol.16 (1), p.S23-S24

2013

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Systematic Evaluation of Skin and Adnexa in Mutant Laboratory Mice

Current protocols in mouse biology, 2014-09, Vol.4 (3), p.105-119

2014

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Sebaceous gland abnormalities in fatty acyl CoA reductase 2

PloS one, 2018-10, Vol.13 (10), p.e0205775

2018

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Chronic Proliferative Dermatitis in Sharpin Null Mice: Development of an Autoinflammatory Disease in the Absence of B and T Lymphocytes and IL4/IL13 Signaling: e85666

PloS one, 2014-01, Vol.9 (1)

2014

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Model of tumor dormancy/recurrence after short-term chemotherapy

PloS one, 2014-05, Vol.9 (5), p.e98021-e98021

2014

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Childhood Outcomes after Hypothermia for Neonatal Encephalopathy

The New England journal of medicine, 2012-05, Vol.366 (22), p.2085-2092

2012

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Dissecting ELANE neutropenia pathogenicity by human HSC gene editing

Cell stem cell, 2021-05, Vol.28 (5), p.833-845.e5

2021

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Keratinocyte-specific deletion of SHARPIN induces atopic dermatitis-like inflammation in mice

Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia

Chronic proliferative dermatitis in Sharpin null mice: development of an autoinflammatory disease in the absence of B and T lymphocytes and IL4/IL13 signaling

Systematic screening for skin, hair, and nail abnormalities in a large-scale knockout mouse program

Hyaline Arteriolosclerosis in 30 Strains of Aged Inbred Mice

Gain of function p.E138A alteration in Card14 leads to psoriasiform skin inflammation and implicates genetic modifiers in disease severity

2‐deoxy D‐glucose treatment does not elicit a hair growth response in alopecia areata

Nail abnormalities identified in an ageing study of 30 inbred mouse strains

Lack of Response to Laser Comb in Spontaneous and Graft-Induced Alopecia Areata in C3H/HeJ Mice

Angiogenesis in the skin of SHARPIN-deficient mice with chronic proliferative dermatitis

Identification of Fat4 and Tsc22d1 as Novel Candidate Genes for Spontaneous Pulmonary Adenomas

Loss of FAS/FASL signalling does not reduce apoptosis in Sharpin null mice

The pathogenesis of chronic eosinophilic esophagitis in SHARPIN-deficient mice

Mouse genome-wide association study identifies polymorphisms on chromosomes 4, 11, and 15 for age-related cardiac fibrosis

Genetic determinants of fibro-osseous lesions in aged inbred mice

Mouse Alopecia Areata and Heart Disease: Know Your Mouse

Dermal lymphatic dilation in a mouse model of alopecia areata

Excavating the Genome: Large-Scale Mutagenesis Screening for the Discovery of New Mouse Models

Alopecia Areata: Updates from the Mouse Perspective

Systematic Evaluation of Skin and Adnexa in Mutant Laboratory Mice

Sebaceous gland abnormalities in fatty acyl CoA reductase 2

Chronic Proliferative Dermatitis in Sharpin Null Mice: Development of an Autoinflammatory Disease in the Absence of B and T Lymphocytes and IL4/IL13 Signaling: e85666

Model of tumor dormancy/recurrence after short-term chemotherapy

Childhood Outcomes after Hypothermia for Neonatal Encephalopathy

Dissecting ELANE neutropenia pathogenicity by human HSC gene editing

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