12R-lipoxygenase deficiency disrupts epidermal barrier function (Q28585387)

31 January 2017

title

12R-lipoxygenase deficiency disrupts epidermal barrier function (English)

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Arachidonate 12-lipoxygenase, 12R type

31 January 2017

main subject

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GOA release 2020-03-11

Gerhard Liebisch

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Gerd Schmitz

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Peter Krieg

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31 January 2017

Nikolas Epp

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31 January 2017

Gerhard Fürstenberger

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31 January 2017

Karsten Müller

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31 January 2017

Silvia de Juanes

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31 January 2017

Michael Leitges

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31 January 2017

Ingrid Hausser

1 reference

31 January 2017

Florian Thieme

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31 January 2017

language of work or name

English

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publication date

9 April 2007

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31 January 2017

published in

Journal of Cell Biology

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31 January 2017

volume

177

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31 January 2017

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31 January 2017

page(s)

173–182

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Human and mouse eLOX3 have distinct substrate specificities: implications for their linkage with lipoxygenases in skin

31 January 2017

cites work

1 reference

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

17 March 2017

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E-cadherin is essential for in vivo epidermal barrier function by regulating tight junctions

17 March 2017

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17 March 2017

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

17 March 2017

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

17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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17 March 2017

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7 April 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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

29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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3 June 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Patterned acquisition of skin barrier function during development.

27 November 2018

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

27 November 2018

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Ceramide composition of the psoriatic scale

21 January 2018

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12 December 2020

6-Hydroxy-4-sphingenine in human epidermal ceramides

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12 December 2020

The barrier function of skin: how to keep a tight lid on water loss

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12 December 2020

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12 December 2020

Origin of the corneocyte lipid envelope (CLE): observations in harlequin ichthyosis and cultured human keratinocytes

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

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12 December 2020

Identifiers

DOI

10.1083/JCB.200612116

1 reference

1 reference

1 reference

1 reference