Query author contributions in Reactome

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Details on Person Puel, A

Class:Id	Person:1679063
_displayName	Puel, A
_timestamp	2011-10-19 16:45:26
created	[InstanceEdit:1679075] Shamovsky, V, 2011-10-19
firstname	Anne
initial	A
surname	Puel
(author)	[LiteratureReference:1678917] Herpes simplex virus encephalitis in human UNC-93B deficiency [LiteratureReference:2428829] Human TLR-7-, -8-, and -9-mediated induction of IFN-alpha/beta and -lambda Is IRAK-4 dependent and redundant for protective immunity to viruses [LiteratureReference:5228855] A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency [LiteratureReference:5228879] A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathy [LiteratureReference:5262860] New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein [LiteratureReference:5262863] The NEMO mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translation [LiteratureReference:5262883] IRAK4 and NEMO mutations in otherwise healthy children with recurrent invasive pneumococcal disease [LiteratureReference:5433036] X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production [LiteratureReference:5602389] Pyogenic bacterial infections in humans with MyD88 deficiency [LiteratureReference:5602396] Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency List all 26 refering instances
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No pathways have been reviewed or authored by Puel, A (1679063)