Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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ASPsiRNA: A Resource of ASP-siRNAs Having Therapeutic Potential for Human Genetic Disorders and Algorithm for Prediction of Their Inhibitory Efficacy.

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Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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P1476

Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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P2093

Chuan Qin

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

Dennis R Roop

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

Elizabeth R Snedecor

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

Evan C Jones

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

Jiang Chen

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

Lan Huang

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

Lianfeng Zhang

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

Richard A Clark

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Xu Zhang

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

Yanfeng Xu

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P2860

An unusual Ala12Thr polymorphism in the 1A alpha-helical segment of the companion layer-specific keratin K6hf: evidence for a risk factor in the etiology of the common hair disorder pseudofolliculitis barbae

Molecular therapeutics for heritable skin diseases

Keratin disorders: from gene to therapy

A novel human type II cytokeratin, K6hf, specifically expressed in the companion layer of the hair follicle

Development of allele-specific therapeutic siRNA for keratin 5 mutations in epidermolysis bullosa simplex

Fuz controls the morphogenesis and differentiation of hair follicles through the formation of primary cilia

Hair keratin mutations in tooth enamel increase dental decay risk.

First-in-human mutation-targeted siRNA phase Ib trial of an inherited skin disorder.

The chicken frizzle feather is due to an α-keratin (KRT75) mutation that causes a defective rachis

Keratins and skin disorders.

P2888

jid.2015.375

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45-51

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scholarly article

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10.1038/JID.2015.375

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English

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136

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2016-01-01T00:00:00Z

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1019269255

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26763422

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4764097

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Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

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