(en) Hiraga K, Kure S, Yamamoto M,, «Cloning of cDNA encoding human H-protein, a constituent of the glycine cleavage system», Biochem. Biophys. Res. Commun., vol.151, no2, , p.758–62 (PMID3348809, DOI10.1016/S0006-291X(88)80345-0)
(en) Gründig E, Birnbaumer E, Hawrylewicz A, «Influence of phenothiazines or reserpine on the formation of 14C-glycine from U-14C-serine», Enzyme, vol.26, no1, , p.43–8 (PMID6111451)
(en) Hiraga K, Kochi H, Hayasaka K,, «Defective glycine cleavage system in nonketotic hyperglycinemia. Occurrence of a less active glycine decarboxylase and an abnormal aminomethyl carrier protein», J. Clin. Invest., vol.68, no2, , p.525–34 (PMID6790577, PMCID370827, DOI10.1172/JCI110284)
(en) Kure S, Kojima K, Kudo T,, «Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemia», J. Hum. Genet., vol.46, no7, , p.378–84 (PMID11450847, DOI10.1007/s100380170057)
(en) Kure S, Kojima K, Ichinohe A,, «Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemia», Ann. Neurol., vol.52, no5, , p.643–6 (PMID12402263, DOI10.1002/ana.10367)
(en) Strausberg RL, Feingold EA, Grouse LH,, «Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences», Proc. Natl. Acad. Sci. U.S.A., vol.99, no26, , p.16899–903 (PMID12477932, PMCID139241, DOI10.1073/pnas.242603899)
(en) Gerhard DS, Wagner L, Feingold EA,, «The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)», Genome Res., vol.14, no10B, , p.2121–7 (PMID15489334, PMCID528928, DOI10.1101/gr.2596504)
(en) Rual JF, Venkatesan K, Hao T,, «Towards a proteome-scale map of the human protein-protein interaction network», Nature, vol.437, no7062, , p.1173–8 (PMID16189514, DOI10.1038/nature04209)
