ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia. - sprookjes - yvandenbroek - TriplyDB

ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia.

ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia.

http://www.wikidata.org/entity/Q33693080

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STIM1 and SLC24A4 Are Critical for Enamel Maturation Human muscle economy myoblast differentiation and excitation-contraction coupling use the same molecular partners, STIM1 and STIM2 STIM proteins: dynamic calcium signal transducers Store-operated Ca2+ channels in airway epithelial cell function and implications for asthma Signature Channels of Excitability no More: L-Type Channels in Immune Cells Ion channels and transporters in lymphocyte function and immunity Orai3--the 'exceptional' Orai?Molecular regulation of CRAC channels and their role in lymphocyte function A post-classical theory of enamel biomineralization… and why we need one Store-operated Ca2+ entry in muscle physiology and diseases Store-operated Ca2+ entry (SOCE) regulates melanoma proliferation and cell migration Mechanism-Based Strategies for the Management of Autoimmunity and Immune Dysregulation in Primary Immunodeficiencies Calcium Dyshomeostasis in Tubular Aggregate Myopathy Diseases caused by mutations in ORAI1 and STIM1 Store-operated calcium entry and diabetic complications Constitutive activation of the calcium sensor STIM1 causes tubular-aggregate myopathy Autoimmunity in primary T-cell immunodeficiencies.Orai1 deficiency leads to heart failure and skeletal myopathy in zebrafish The calcium release-activated calcium channel Orai1 represents a crucial component in hypertrophic compensation and the development of dilated cardiomyopathy.Advances in basic and clinical immunology in 2009 Pore architecture of the ORAI1 store-operated calcium channel.Quality control autophagy degrades soluble ERAD-resistant conformers of the misfolded membrane protein GnRHR Molecular basis of calcium signaling in lymphocytes: STIM and ORAI Role of transient receptor potential channel 6 in the odontogenic differentiation of human dental pulp cells.Store-operated calcium entry remains fully functional in aged mouse skeletal muscle despite a decline in STIM1 protein expression.Protein kinase C-induced phosphorylation of Orai1 regulates the intracellular Ca2+ level via the store-operated Ca2+ channel.CRAC channelopathies.Pharmacology of store-operated calcium channels CD4⁺ and CD8⁺ T cell-dependent antiviral immunity requires STIM1 and STIM2.Stromal interaction molecule 1 (STIM1) and Orai1 mediate histamine-evoked calcium entry and nuclear factor of activated T-cells (NFAT) signaling in human umbilical vein endothelial cells.Polarized but differential localization and recruitment of STIM1, Orai1 and TRPC channels in secretory cells.Expression of ORAII, a plasma membrane resident subunit of the CRAC channel, in rodent and non-rodent species Ameloblast transcriptome changes from secretory to maturation stages.Epstein-Barr virus latent membrane protein 1 increases calcium influx through store-operated channels in B lymphoid cells.X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia disease: a combined immune deficiency with magnesium defect.Antibody-mediated targeting of the Orai1 calcium channel inhibits T cell function.STIM1L is a new actin-binding splice variant involved in fast repetitive Ca2+ release.Orai1-mediated I (CRAC) is essential for neointima formation after vascular injury.ORAI1 deficiency impairs activated T cell death and enhances T cell survival Store-operated calcium channels: new perspectives on mechanism and function.

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P2860

ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia.

http://www.wikidata.org/entity/Q33693080

description

2009 nî lūn-bûn

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2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

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2009年論文

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2009年論文

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2009年論文

@zh-hk

2009年論文

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2009年論文

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2009年论文

@wuu

name

ORAI1 deficiency and lack of s ...... thy, and ectodermal dysplasia.

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ORAI1 deficiency and lack of s ...... thy, and ectodermal dysplasia.

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type

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ORAI1 deficiency and lack of s ...... thy, and ectodermal dysplasia.

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ORAI1 deficiency and lack of s ...... thy, and ectodermal dysplasia.

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ORAI1 deficiency and lack of s ...... thy, and ectodermal dysplasia.

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ORAI1 deficiency and lack of s ...... thy, and ectodermal dysplasia.

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The Journal of Allergy and Clinical Immunology

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ORAI1 deficiency and lack of s ...... thy, and ectodermal dysplasia.

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Alexander Papolos

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Katrin Plogmann

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Michael H Albert

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P2860

Orai1 and STIM reconstitute store-operated calcium channel function

Orai1 is an essential pore subunit of the CRAC channel

Amplification of CRAC current by STIM1 and CRACM1 (Orai1)

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

Dual functions for the endoplasmic reticulum calcium sensors STIM1 and STIM2 in T cell activation and tolerance

Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee

Molecular identification of the CRAC channel by altered ion selectivity in a mutant of Orai

Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function

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Janbernd Kirschner

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