Query author contributions in Reactome

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Details on Person Kondo, N

Class:Id	Person:110782
_displayName	Kondo, N
_timestamp	2004-02-07 12:40:35
firstname	Naomi
initial	N
surname	Kondo
(author)	[LiteratureReference:83544] Functional link between BLM defective in Bloom's syndrome and the ataxia-telangiectasia-mutated protein, ATM. [LiteratureReference:200206] Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient [LiteratureReference:480294] Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders [LiteratureReference:508383] Crystallographic and kinetic studies of human mitochondrial acetoacetyl-CoA thiolase: the importance of potassium and chloride ions for its structure and function [LiteratureReference:2210386] Mutation analysis in the iduronate-2-sulphatase gene in 43 Japanese patients with mucopolysaccharidosis type II (Hunter disease) [LiteratureReference:5228775] A rapid screening method to detect autosomal-dominant ectodermal dysplasia with immune deficiency syndrome [LiteratureReference:5602580] Structural basis for the multiple interactions of the MyD88 TIR domain in TLR4 signaling [LiteratureReference:5602589] Functional assessment of the mutational effects of human IRAK4 and MyD88 genes [LiteratureReference:9012398] TRAM is involved in IL-18 signaling and functions as a sorting adaptor for MyD88 [LiteratureReference:9012820] The structure and binding mode of interleukin-18 List all 11 refering instances
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No pathways have been reviewed or authored by Kondo, N (110782)