Enlightened therapy of the disorders of cornification (Q35565674)

8 August 2017

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title

Enlightened therapy of the disorders of cornification (English)

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8 August 2017

Mary L Williams

1

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8 August 2017

Peter M Elias

series ordinal

2

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8 August 2017

publication date

1 July 2003

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8 August 2017

published in

Clinics in Dermatology

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8 August 2017

volume

21

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8 August 2017

issue

4

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8 August 2017

page(s)

269-273

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Keratinocytes cultured from subjects with ichthyosis vulgaris are phenotypically abnormal

8 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

Does catabolism of stratum corneum proteins yield functionally active molecules?

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

Cholesterol sulfate inhibits proteases that are involved in desquamation of stratum corneum

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

The pH gradient over the stratum corneum differs in X-linked recessive and autosomal dominant ichthyosis: a clue to the molecular origin of the "acid skin mantle"?

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

Mode of action of glycolic acid on human stratum corneum: ultrastructural and functional evaluation of the epidermal barrier.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

Recessive x-linked ichthyosis: role of cholesterol-sulfate accumulation in the barrier abnormality

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

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/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

Abnormal Lamellar Granules in Harlequin Ichthyosis

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

Nature of skin fragility in patients receiving retinoids for systemic effect.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

Ichthyosis bullosa of Siemens is caused by mutations in the keratin 2e gene

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

Pathogenesis of the permeability barrier abnormality in epidermolytic hyperkeratosis

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2803%2900059-2

7 January 2021

10.1016/S0738-081X(03)00059-2

Identifiers

DOI

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8 August 2017

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