Localization of ABCA12 from Golgi apparatus to lamellar granules in human upper epidermal keratinocytes - Wikidata - awgldk - TriplyDB

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

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

http://www.wikidata.org/entity/Q28252754

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Pathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolism Mammalian P4-ATPases and ABC transporters and their role in phospholipid transport Lipid somersaults: Uncovering the mechanisms of protein-mediated lipid flipping Defects in Stratum Corneum Desquamation Are the Predominant Effect of Impaired ABCA12 Function in a Novel Mouse Model of Harlequin Ichthyosis A mouse model of harlequin ichthyosis delineates a key role for Abca12 in lipid homeostasis Abca12-mediated lipid transport and Snap29-dependent trafficking of lamellar granules are crucial for epidermal morphogenesis in a zebrafish model of ichthyosis Loss of SNAP29 impairs endocytic recycling and cell motility Regulation of ABCG1 expression in human keratinocytes and murine epidermis.The effect of two endogenous retinoids on the mRNA expression profile in human primary keratinocytes, focusing on genes causing autosomal recessive congenital ichthyosis Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle.Cellular basis of secondary infections and impaired desquamation in certain inherited ichthyoses A-Subclass ATP-Binding Cassette Proteins in Brain Lipid Homeostasis and Neurodegeneration.Role of the calcium-sensing receptor in calcium regulation of epidermal differentiation and function A case report of fatal harlequin ichthyosis: Insights into infectious and respiratory complications.Glycosphingolipid storage in Fabry mice extends beyond globotriaosylceramide and is affected by ABCB1 depletion.Endogenous β-glucocerebrosidase activity in Abca12⁻/⁻epidermis elevates ceramide levels after topical lipid application but does not restore barrier function.Perinatal management of harlequin ichthyosis: a case report and literature review.Malignant skin tumours in patients with inherited ichthyosis.Updated molecular genetics and pathogenesis of ichthiyoses.Harlequin ichthyosis: ABCA12 mutations underlie defective lipid transport, reduced protease regulation and skin-barrier dysfunction.Role of ABC transporters in lipid transport and human disease.Discovery in genetic skin disease: the impact of high throughput genetic technologies Harlequin Infant Born to a Varicella Infected Mother: A Case Report.The role of membrane transporters in ovarian cancer chemoresistance and prognosis.Techniques for toddlers: linear band incision for harlequin ichthyosis with associated compartment syndrome.A palindromic motif in the -2084 to -2078 upstream region is essential for ABCA12 promoter function in cultured human keratinocytes.The roles of ABCA12 in keratinocyte differentiation and lipid barrier formation in the epidermis.Epidemiology, medical genetics, diagnosis and treatment of harlequin ichthyosis in Japan.Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma.

P2860

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P2860

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

http://www.wikidata.org/entity/Q28252754

description

2007 nî lūn-bûn

@nan

2007 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Localization of ABCA12 from Go ...... upper epidermal keratinocytes

@ast

Localization of ABCA12 from Go ...... upper epidermal keratinocytes

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Localization of ABCA12 from Go ...... upper epidermal keratinocytes

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type

label

Localization of ABCA12 from Go ...... upper epidermal keratinocytes

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Localization of ABCA12 from Go ...... upper epidermal keratinocytes

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Localization of ABCA12 from Go ...... upper epidermal keratinocytes

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prefLabel

Localization of ABCA12 from Go ...... upper epidermal keratinocytes

@ast

Localization of ABCA12 from Go ...... upper epidermal keratinocytes

@en

Localization of ABCA12 from Go ...... upper epidermal keratinocytes

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J.1600-0625.2007.00614.X

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Experimental Dermatology

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Localization of ABCA12 from Go ...... upper epidermal keratinocytes

@en

P2093

Daisuke Sawamura

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

Hiroshi Shimizu

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

James R McMillan

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

Kaori Sakai

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

Masashi Akiyama

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

Yoriko Sugiyama-Nakagiri

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

P2860

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

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

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

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

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

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

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

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

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

The human ATP-binding cassette (ABC) transporter superfamily

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10.1111/J.1600-0625.2007.00614.X

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11

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17927575

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P921

Golgi apparatus