Query author contributions in Reactome

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Details on Person Fischer, Alain

Class:Id	Person:5228882
_displayName	Fischer, Alain
_timestamp	2014-01-14 17:53:12
created	[InstanceEdit:5228861] Shamovsky, V, 2014-01-14
firstname	Alain
initial	A
surname	Fischer
(author)	[LiteratureReference:5228855] A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency [LiteratureReference:5262860] New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein [LiteratureReference:5602641] A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedside [LiteratureReference:5602678] Severe combined immunodeficiency. A model disease for molecular immunology and therapy [LiteratureReference:5686716] Phosphorylation of Artemis following irradiation-induced DNA damage [LiteratureReference:5687239] Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly [LiteratureReference:9686596] Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability [LiteratureReference:9689682] Neutralization of IFNgamma defeats haemophagocytosis in LCMV-infected perforin- and Rab27a-deficient mice [LiteratureReference:9696151] Impaired type I interferon activity and inflammatory responses in severe COVID-19 patients [LiteratureReference:9856375] A newly identified isoform of Slp2a associates with Rab27a in cytotoxic T cells and participates to cytotoxic granule secretion List all 12 refering instances
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No pathways have been reviewed or authored by Fischer, Alain (5228882)