A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis (Q42804721)

7 November 2017

title

A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis (English)

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7 November 2017

Felix B Müller

1

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7 November 2017

Marcel Huber

2

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7 November 2017

Tamar Kinaciyan

3

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7 November 2017

Ingrid Hausser

4

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7 November 2017

Christina Schaffrath

5

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7 November 2017

Thomas Krieg

6

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7 November 2017

Daniel Hohl

7

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7 November 2017

Bernhard P Korge

8

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7 November 2017

Meral J Arin

9

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7 November 2017

publication date

27 February 2006

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7 November 2017

published in

Human Molecular Genetics

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7 November 2017

volume

15

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7 November 2017

issue

7

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7 November 2017

page(s)

1133-1141

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The Molecular Genetics of Keratin Disorders

7 November 2017

cites work

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https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Different keratin polypeptides in epidermis and other epithelia of human skin: a specific cytokeratin of molecular weight 46,000 in epithelia of the pilosebaceous tract and basal cell epitheliomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: Genetic and functional analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

A leucine----proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Deletions in epidermal keratins leading to alterations in filament organization in vivo and in intermediate filament assembly in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Expression of a truncated keratin 5 may contribute to severe palmar--plantar hyperkeratosis in epidermolysis bullosa simplex patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Epidermolysis bullosa simplex in Israel: clinical and genetic features.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Mechanistic links between nonsense-mediated mRNA decay and pre-mRNA splicing in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Intron function in the nonsense-mediated decay of beta-globin mRNA: indications that pre-mRNA splicing in the nucleus can influence mRNA translation in the cytoplasm

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Effects of keratin 14 ablation on the clinical and cellular phenotype in a kindred with recessive epidermolysis bullosa simplex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

The basal keratin network of stratified squamous epithelia: defining K15 function in the absence of K14.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Keratins of the human hair follicle: "hyperproliferative" keratins consistently expressed in outer root sheath cells in vivo and in vitro.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Onset of re-epithelialization after skin injury correlates with a reorganization of keratin filaments in wound edge keratinocytes: defining a potential role for keratin 16

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Formation of a normal epidermis supported by increased stability of keratins 5 and 14 in keratin 10 null mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Focal activation of a mutant allele defines the role of stem cells in mosaic skin disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

Diversity of cytokeratins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL028

21 January 2018

Identifiers

DOI

10.1093/HMG/DDL028

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7 November 2017

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