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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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Supporting conditional mouse mutagenesis with a comprehensive cre characterization resource

Nature communications, 2012, Vol.3 (1), p.1218, Article 1218

2012

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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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Witch Nails (Krt90whnl): A spontaneous mouse mutation affecting nail growth and development

PloS one, 2022-11, Vol.17 (11), p.e0277284

2022

Volltextzugriff (PDF)

Spontaneous asj-2J mutant mouse as a model for generalized arterial calcification of infancy: a large deletion/insertion mutation in the Enpp1 gene

PloS one, 2014-12, Vol.9 (12), p.e113542

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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Interrogating congenital heart defects with noninvasive fetal echocardiography in a mouse forward genetic screen

Circulation. Cardiovascular imaging, 2014-01, Vol.7 (1), p.31-42

2014

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Alopecia areata

Nature reviews. Disease primers, 2017-03, Vol.3 (1), p.17011-17011, Article 17011

2017

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Skin Diseases in Laboratory Mice: Approaches to Drug Target Identification and Efficacy Screening

Methods in molecular biology (Clifton, N.J.), 2016-01, Vol.1438, p.199

2016

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Skin fragility in the wild-derived, inbred mouse strain Mus pahari/EiJ

Experimental and molecular pathology, 2017-02, Vol.102 (1), p.128-132

2017

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Mitotic defects lead to pervasive aneuploidy and accompany loss of RB1 activity in mouse LmnaDhe dermal fibroblasts

PloS one, 2011-03, Vol.6 (3), p.e18065-e18065

2011

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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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R164C mutation in FOXQ1 H3 domain affects formation of the hair medulla

Experimental dermatology, 2013-03, Vol.22 (3), p.234-236

2013

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The Mafb cleft‐associated variant H131Q is not required for palatogenesis in the mouse

Developmental dynamics, 2021-10, Vol.250 (10), p.1463-1476

2021

Volltextzugriff (PDF)

Dsprul: A spontaneous mouse mutation in desmoplakin as a model of Carvajal-Huerta syndrome

Experimental and molecular pathology, 2015-04, Vol.98 (2), p.164-172

2015

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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

Volltextzugriff (PDF)

A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia

Investigative ophthalmology & visual science, 2015-06, Vol.56 (6), p.3776-3787

2015

Volltextzugriff (PDF)

Gnaq(M1J): An ENU-Induced Mutant Allele Affecting Pigmentation in the Mouse

Journal of investigative dermatology, 2016-01, Vol.136 (1), p.334-336

2016

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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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Witch Nails

PloS one, 2022-11, Vol.17 (11), p.e0277284

2022

Volltextzugriff (PDF)

Cleft Palate Case‐Derived ARHGAP29 Mutation Causes Lethality and Oral Adhesions in Mice

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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Patient‐derived MAFB Missense Mutation Is Associated with Cleft Palate in Mice

The FASEB journal, 2018-04, Vol.32 (S1), p.776.6-776.6

2018

Volltextzugriff (PDF)

Sebaceous gland abnormalities in fatty acyl CoA reductase 2

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

2018

Volltextzugriff (PDF)

GnaqM1J: An ENU-Induced Mutant Allele Affecting Pigmentation in the Mouse

Journal of investigative dermatology, 2016-01, Vol.136 (1), p.334-336

2016

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

Supporting conditional mouse mutagenesis with a comprehensive cre characterization resource

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

Witch Nails (Krt90whnl): A spontaneous mouse mutation affecting nail growth and development

Spontaneous asj-2J mutant mouse as a model for generalized arterial calcification of infancy: a large deletion/insertion mutation in the Enpp1 gene

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

Interrogating congenital heart defects with noninvasive fetal echocardiography in a mouse forward genetic screen

Alopecia areata

Skin Diseases in Laboratory Mice: Approaches to Drug Target Identification and Efficacy Screening

Skin fragility in the wild-derived, inbred mouse strain Mus pahari/EiJ

Mitotic defects lead to pervasive aneuploidy and accompany loss of RB1 activity in mouse LmnaDhe dermal fibroblasts

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

R164C mutation in FOXQ1 H3 domain affects formation of the hair medulla

The Mafb cleft‐associated variant H131Q is not required for palatogenesis in the mouse

Dsprul: A spontaneous mouse mutation in desmoplakin as a model of Carvajal-Huerta syndrome

Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders

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

A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia

Gnaq(M1J): An ENU-Induced Mutant Allele Affecting Pigmentation in the Mouse

Dermal lymphatic dilation in a mouse model of alopecia areata

Witch Nails

Cleft Palate Case‐Derived ARHGAP29 Mutation Causes Lethality and Oral Adhesions in Mice

Patient‐derived MAFB Missense Mutation Is Associated with Cleft Palate in Mice

Sebaceous gland abnormalities in fatty acyl CoA reductase 2

GnaqM1J: An ENU-Induced Mutant Allele Affecting Pigmentation in the Mouse

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