KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.

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On the tear proteome of the house mouse (Mus musculus musculus) in relation to chemical signalling Differential regulation of vaginal lipocalins (OBP, MUP) during the estrous cycle of the house mouse Serine protease inhibitors to treat inflammation: a patent review (2011-2016).

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P2860

KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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name

KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.

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KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.

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KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.

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KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.

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KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.

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KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.

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P1476

KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype

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P2093

Inken M Beck

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Ivan Kanchev

http://www.w3.org/2001/XMLSchema#string

Karel Chalupsky

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Maria Brattsand

http://www.w3.org/2001/XMLSchema#string

Petr Kasparek

http://www.w3.org/2001/XMLSchema#string

Zuzana Ileninova

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P2860

A conditional knockout resource for the genome-wide study of mouse gene function

Elastase 2 is expressed in human and mouse epidermis and impairs skin barrier function in Netherton syndrome through filaggrin and lipid misprocessing

LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome

Epidermal detachment, desmosomal dissociation, and destabilization of corneodesmosin in Spink5-/- mice

Matriptase initiates activation of epidermal pro-kallikrein and disease onset in a mouse model of Netherton syndrome

LEKTI fragments specifically inhibit KLK5, KLK7, and KLK14 and control desquamation through a pH-dependent interaction

KLK5 Inactivation Reverses Cutaneous Hallmarks of Netherton Syndrome

Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome

Inhibition of serine proteinases plasmin, trypsin, subtilisin A, cathepsin G, and elastase by LEKTI: a kinetic analysis

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e1006566

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10.1371/JOURNAL.PGEN.1006566

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Oldřich Benada

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2017-01-17T00:00:00Z

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KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.

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P2860

P2860

KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.

description

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P1433

P1476

P2093

P2860

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P698

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P698

P932