(Q26800003)

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PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes

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Europe PubMed Central

title

PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes (English)

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main subject

familial cold autoinflammatory syndrome 3

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Joshua D Milner

1

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language of work or name

English

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publication date

August 2015

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published in

Journal of Clinical Immunology

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volume

35

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issue

6

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page(s)

527-30

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cites work

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The autoinhibitory C-terminal SH2 domain of phospholipase C-γ2 stabilizes B cell receptor signalosome assembly

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Urticaria mimickers in children

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28 September 2017

A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency

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Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions

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Familial atypical cold urticaria: description of a new hereditary disease

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Distinct Cutaneous Manifestations and Cold-Induced Leukocyte Activation Associated With PLCG2 Mutations.

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31 May 2018

Phospholipase Cgamma2 contributes to light-chain gene activation and receptor editing

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Phospholipase C-gamma 2 is a critical signaling mediator for murine NK cell activating receptors

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21 January 2018

Autoimmunity and inflammation due to a gain-of-function mutation in phospholipase C gamma 2 that specifically increases external Ca2+ entry

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A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine model

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Phospholipase Cgamma2 is essential in the functions of B cell and several Fc receptors

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Identifiers

DOI

10.1007/S10875-015-0177-X

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Dimensions Publication ID

1014409777

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PMC publication ID

4575258

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PubMed publication ID

26206677

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(Q26800003)

PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes

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