(Q46175556)

20 December 2017

title

Development of an ichthyosiform phenotype in Alox12b-deficient mouse skin transplants (English)

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20 December 2017

8

Peter Krieg

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20 December 2017

author name string

Silvia de Juanes

1

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20 December 2017

Nikolas Epp

2

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20 December 2017

Susanne Latzko

3

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20 December 2017

Mareen Neumann

4

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20 December 2017

Gerhard Fürstenberger

5

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20 December 2017

Ingrid Hausser

6

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20 December 2017

Hans-Jürgen Stark

7

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20 December 2017

language of work or name

English

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publication date

1 January 2009

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20 December 2017

Journal of Investigative Dermatology

published in

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20 December 2017

volume

129

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20 December 2017

issue

6

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20 December 2017

page(s)

1429-1436

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20 December 2017

A novel ABCA12 mutation 3270delT causes harlequin ichthyosis

cites work

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

New techniques for the grafting of cultured human epidermal cells onto athymic animals

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https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Lipoxygenases: occurrence, functions, catalysis, and acquisition of substrate

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https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

The hepoxilin connection in the epidermis

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https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Wound healing and inflammation genes revealed by array analysis of 'macrophageless' PU.1 null mice

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https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.

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https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity

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https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Mutation spectrum and functional analysis of epidermis-type lipoxygenases in patients with autosomal recessive congenital ichthyosis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

12R-lipoxygenase deficiency disrupts epidermal barrier function

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Claudin-based tight junctions are crucial for the mammalian epidermal barrier: a lesson from claudin-1-deficient mice

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Self-healing collodion membrane and mild nonbullous congenital ichthyosiform erythroderma due to 2 novel mutations in the ALOX12B gene

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

cDNA cloning, genomic structure, and chromosomal localization of a novel murine epidermis-type lipoxygenase

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https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Epidermis-type lipoxygenases.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Repetin (Rptn), a new member of the "fused gene" subgroup within the S100 gene family encoding a murine epidermal differentiation protein

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Murine 12(R)-lipoxygenase: functional expression, genomic structure and chromosomal localization

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Development of ichthyosiform skin compensates for defective permeability barrier function in mice lacking transglutaminase 1

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

The epidermal barrier function is dependent on the serine protease CAP1/Prss8

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Matriptase/MT-SP1 is required for postnatal survival, epidermal barrier function, hair follicle development, and thymic homeostasis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype association

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

A mouse mutation in the 12R-lipoxygenase, Alox12b, disrupts formation of the epidermal permeability barrier.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Mouse Sprr locus: a tandem array of coordinately regulated genes

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Loss of normal profilaggrin and filaggrin in flaky tail (ft/ft) mice: an animal model for the filaggrin-deficient skin disease ichthyosis vulgaris

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Complex redundancy to build a simple epidermal permeability barrier

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Lipopenia and skin barrier abnormalities in DGAT2-deficient mice

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Mutations associated with a congenital form of ichthyosis (NCIE) inactivate the epidermal lipoxygenases 12R-LOX and eLOX3

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

The lipoxygenase gene ALOXE3 implicated in skin differentiation encodes a hydroperoxide isomerase

1 reference

https://api.crossref.org/works/10.1038%2FJID.2008.410

7 January 2021

Identifiers

DOI

10.1038/JID.2008.410

1 reference

20 December 2017

1 reference

20 December 2017