PLAID: a Syndrome of Complex Patterns of Disease and Unique Phenotypes (Q26800003)

familial cold autoinflammatory syndrome 3

Europe PubMed Central

title

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

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main subject

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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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exact match

https://scigraph.springernature.com/pub.10.1007/s10875-015-0177-x

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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

7 April 2017

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

28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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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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