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Corrective gene transfer in the human skin disorder lamellar ichthyosis

Author

Jeffrey R. Morgan

Published in: Nature Medicine

Date of publication: November 1, 1996

Language: English

Main subject: skin disease

Bibliographic databases:

Cites articles 23

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Title

Authors

November 1975

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Localization of the defect in skin diseases analyzed in the human skin graft-nude mouse model
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Permanent coverage of large burn wounds with autologous cultured human epithelium
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New monoclonal antibodies recognizing epidermal differentiation-associated keratins in formalin-fixed, paraffin-embedded tissue. Keratin 10 expression in carcinoma of the vulva
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BRG1 contains a conserved domain of the SWI2/SNF2 family necessary for normal mitotic growth and transcription
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Towards gene therapy for haemophilia B using primary human keratinocytes
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Barrier function parameters in various keratinization disorders: transepidermal water loss and vascular response to hexyl nicotinate
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The genetics of ichthyosis: a primer for epidemiologists
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Semipermeable dressings improve epidermal barrier function in premature infants.
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Mutations of keratinocyte transglutaminase in lamellar ichthyosis
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Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis
January 1, 1995

Defects in the barrier
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Cutaneous permeability barrier disruption increases fatty acid synthetic enzyme activity in the epidermis of hairless mice
January 1, 1996

Evidence for separate control mechanisms at the message, protein, and enzyme activation levels for transglutaminase during calcium-induced differentiation of normal and transformed human keratinocytes
July 1, 1996

Evaluation of human skin reconstituted from composite grafts of cultured keratinocytes and human acellular dermis transplanted to athymic mice
March 1, 1996

Loss of expression of a retrovirus-transduced gene in human keratinocytes
August 1, 1996

Episomal vectors rapidly and stably produce high-titer recombinant retrovirus
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Cutaneous gene therapy

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