Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
about
Pemphigus vulgaris antibody identifies pemphaxin. A novel keratinocyte annexin-like molecule binding acetylcholineFunctional expression in yeast of the human secretory pathway Ca(2+), Mn(2+)-ATPase defective in Hailey-Hailey diseaseSubstrate specificity, membrane topology, and activity regulation of human alkaline ceramidase 2 (ACER2)Effect of Hailey-Hailey Disease mutations on the function of a new variant of human secretory pathway Ca2+/Mn2+-ATPase (hSPCA1)SLC24A5 encodes a trans-Golgi network protein with potassium-dependent sodium-calcium exchange activity that regulates human epidermal melanogenesisFunctional comparison between secretory pathway Ca2+/Mn2+-ATPase (SPCA) 1 and sarcoplasmic reticulum Ca2+-ATPase (SERCA) 1 isoforms by steady-state and transient kinetic analysesNewly characterized Golgi-localized family of proteins is involved in calcium and pH homeostasis in yeast and human cellsHow do keratinizing disorders and blistering disorders overlap?TRP Channels in Skin Biology and PathophysiologyATP2C1 gene mutations in Hailey-Hailey disease and possible roles of SPCA1 isoforms in membrane trafficking"Manganese-induced neurotoxicity: a review of its behavioral consequences and neuroprotective strategies"Manganese homeostasis in the nervous systemMutation analysis of ATP2C1 gene in Taiwanese patients with Hailey-Hailey diseaseAcidic calcium stores open for business: expanding the potential for intracellular Ca2+ signalingMarked disturbance of calcium homeostasis in mice with targeted disruption of the Trpv6 calcium channel geneCharacterization of Cos-7 cells overexpressing the rat secretory pathway Ca2+-ATPaseGene knockout studies of Ca2+-transporting ATPasesTwo patients with Hailey-Hailey disease, multiple primary melanomas, and other cancers.The Concise Guide to PHARMACOLOGY 2013/14: transporters.Unique characteristics of Ca2+ homeostasis of the trans-Golgi compartment.Intracutaneous botulinum toxin A versus ablative therapy of Hailey-Hailey disease--a case report.Upregulation of P-cadherin expression in the lesional skin of pemphigus, Hailey-Hailey disease and Darier's disease.The Golgi PMR1 P-type ATPase of Caenorhabditis elegans. Identification of the gene and demonstration of calcium and manganese transport.Immunohistological study of involucrin expression in Darier's disease skin.[Familial benign chronic pemphigus (Hailey-Hailey disease): successful treatment with carbon dioxide laser].Apoptosis-linked gene-2 (ALG-2)/Sec31 interactions regulate endoplasmic reticulum (ER)-to-Golgi transport: a potential effector pathway for luminal calciumKeratinocyte adhesion and the missing link: from Dowling-Meara to Hay-Wells. St John's Hospital Dermatological Society Annual Oration 2000.Desmosomes: structure and function in normal and diseased epidermis.The genetics of human skin disease.Desmosome assembly and dynamicsLaser therapy for Hailey-Hailey disease: review of the literature and a case reportCombined therapeutic use of oral alitretinoin and narrowband ultraviolet-B therapy in the treatment of hailey-hailey diseasePemphigus vulgaris autoantibody profiling by proteomic technique.Efficacy of the melanocortin analogue Nle4-D-Phe7-α-melanocyte-stimulating hormone in the treatment of patients with Hailey-Hailey disease.The secretory pathway calcium ATPase PMR-1/SPCA1 has essential roles in cell migration during Caenorhabditis elegans embryonic development.Calcium regulation in photoreceptors.Plasma membrane Ca-ATPases in the nervous system during development and ageingMechanisms of desmosome assembly and disassembly.PMR1/SPCA Ca2+ pumps and the role of the Golgi apparatus as a Ca2+ store.Mathematical modeling of calcium waves induced by mechanical stimulation in keratinocytes.
P2860
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P2860
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
description
2000 nî lūn-bûn
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2000 թվականի հունվարին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
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name
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@ast
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@en
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@en-gb
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@nl
type
label
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@ast
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@en
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@en-gb
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@nl
prefLabel
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@ast
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@en
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@en-gb
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@nl
P2093
P2860
P3181
P356
P1433
P1476
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
@en
P2093
E H Epstein
J M Bonifas
T Shigihara
P2860
P2888
P3181
P356
10.1038/71701
P407
P577
2000-01-01T00:00:00Z
P5875
P6179
1033782789