Localization of ABCA12 from Golgi apparatus to lamellar granules in human upper epidermal keratinocytes (Q28252754)

2

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Yoriko Sugiyama-Nakagiri

3

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James R McMillan

4

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Daisuke Sawamura

5

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Hiroshi Shimizu

Characterization of the human ABC superfamily: isolation and mapping of 21 new genes using the expressed sequence tags database

6

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language of work or name

English

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publication date

November 2007

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published in

Experimental Dermatology

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volume

16

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page(s)

920-6

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issue

11

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cites work

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The human ATP-binding cassette (ABC) transporter superfamily

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Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

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Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

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Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration

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Structure, function and regulation of the ABC1 gene product

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Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice

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Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer

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Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis.

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ABCA12 is the major harlequin ichthyosis gene

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ABCA3 is a lamellar body membrane protein in human lung alveolar type II cells

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Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

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Complete coding sequence, promoter region, and genomic structure of the human ABCA2 gene and evidence for sterol-dependent regulation in macrophages

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ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport

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Mammalian ABC transporters in health and disease

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Characterization of the ABCA transporter subfamily: identification of prokaryotic and eukaryotic members, phylogeny and topology.

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An inventory of the human ABC proteins

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Pathomechanisms of harlequin ichthyosis and ABCA transporters in human diseases

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Harlequin ichthyosis and other autosomal recessive congenital ichthyoses: the underlying genetic defects and pathomechanisms

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Molecular basis of cholesterol homeostasis: lessons from Tangier disease and ABCA1.

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Simple and complex ABCR: genetic predisposition to retinal disease

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Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiency

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Transport of lipids from golgi to plasma membrane is defective in tangier disease patients and Abc1-deficient mice.

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Adenosine triphosphate binding cassette (ABC) transporters are expressed and regulated during terminal keratinocyte differentiation: a potential role for ABCA7 in epidermal lipid reorganization

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Regulation of ABCA1 expression in human keratinocytes and murine epidermis.

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Phytocomponents of triterpenoids, oleanolic acid and ursolic acid, regulated differently the processing of epidermal keratinocytes via PPAR-alpha pathway

21 January 2018

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Demonstration of intra- and extracellular localization of bullous pemphigoid antigen using cryofixation and freeze substitution for postembedding immunoelectron microscopy

21 January 2018

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Detection of antigens by immunofluorescence on ultrathin cryosections of skin

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Localization of ceramide and glucosylceramide in human epidermis by immunogold electron microscopy.

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Epidermal lamellar granules transport different cargoes as distinct aggregates

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ABCA3 gene mutations in newborns with fatal surfactant deficiency

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Skin barrier formation: the membrane folding model

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A cryotransmission electron microscopy study of skin barrier formation

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21 January 2018

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

3941624

3941624

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference