Citations for
1AMT, GLDC
Genetic association of the glycine cleavage system genes and myelomeningocele.
Shah RH, Northrup H, Hixson JE, Morrison AC, Au KS.
Birth Defects Res A Clin Mol Teratol 106(10):847-853. doi: 10.1002/bdra.23552. 2016
2AMT, GCE2, GCE3, GLDC
Mutation analysis of glycine decarboxylase, aminomethyltransferase and glycine cleavage system protein-H genes in 13 unrelated families with glycine encephalopathy.
Azize NA, Ngah WZ, Othman Z, Md Desa N, Chin CB, Md Yunus Z, Mohan A, Hean TS, Syed Zakaria SZ, Lock-Hock N.
J Hum Genet 59(11):593-7. doi: 10.1038/jhg.2014.69. 2014
3GLDC, NKH1
A Novel Glycine Decarboxylase Gene Mutation in an Indian Family With Nonketotic Hyperglycinemia.
Love JM, Prosser D, Love DR, Chintakindi KP, Dalal AB, Aggarwal S.
J Child Neurol Child Neurol. 2013 Jan 24. [Epub ahead of print] 2013
4GLDC
Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans.
Narisawa A, Komatsuzaki S, Kikuchi A, Niihori T, Aoki Y, Fujiwara K, Tanemura M, Hata A, Suzuki Y, Relton CL, Grinham J, Leung KY, Partridge D, Robinson A, Stone V, Gustavsson P, Stanier P, Copp AJ, Greene ND, Tominaga T, Matsubara Y, Kure S.
Hum Mol Genet 21(7):1496-503. doi: 10.1093/hmg/ddr585. Epub 2011 Dec 13. 2012
5GLDC
Glycine decarboxylase activity drives non-small cell lung cancer tumor-initiating cells and tumorigenesis.
Zhang WC, Shyh-Chang N, Yang H, Rai A, Umashankar S, Ma S, Soh BS, Sun LL, Tai BC, Nga ME, Bhakoo KK, Jayapal SR, Nichane M, Yu Q, Ahmed DA, Tan C, Sing WP, Tam J, Thirugananam A, Noghabi MS, Pang YH, Ang HS, Mitchell W, Robson P, Kaldis P, Soo RA, Swarup S, Lim EH, Lim B.
Cell 148(1-2):259-72. doi: 10.1016/j.cell.2011.11.050. Epub 2012 Jan 5. Erratum in: Cell. 2012 Mar 2;148(5):1066. Mitchell, Wayne [ad 2012
6GLDC, NKH1
Late-onset nonketotic hyperglycinemia caused by a novel homozygous missense mutation in the GLDC gene.
Brunel-Guitton C, Casey B, Coulter-Mackie M, Vallance H, Hewes D, Stockler-Ipsiroglu S, Mercimek-Mahmutoglu S.
Mol Genet Metab 103(2):193-6. doi: 10.1016/j.ymgme.2011.02.009. Epub 2011 Feb 22. 2011
7AMT, GCE1, GCE2, GCE3, GCSH, GLDC
Two novel laboratory tests facilitating diagnosis of glycine encephalopathy (nonketotic hyperglycinemia).
Kure S.
Brain Dev 33(9):753-7. doi: 10.1016/j.braindev.2011.03.001. Review. 2011
8AMT, GCSH, GLDC
Glycine cleavage enzyme complex: molecular cloning and expression of the H-protein cDNA from cultured human skin fibroblasts.
Zay A, Choy FY, Patrick C, Sinclair G.
Biochem Cell Biol 89(3):299-307. doi: 10.1139/O10-156. 2011
9GLDC, NKH1
A novel missense mutation in a neonate with nonketotic hyperglycinemia.
Meyer S, Acquaviva C, Shamdeen MG, Haas D, Vianey-Saban C.
Pediatr Neurol 43(5):363-7. doi: 10.1016/j.pediatrneurol.2010.05.025. 2010
10GLDC, NKH1
Genomic deletion within GLDC is a major cause of non-ketotic hyperglycinaemia.
Kanno J, Hutchin T, Kamada F, Narisawa A, Aoki Y, Matsubara Y, Kure S.
J Med Genet 44(3):e69. 2007
11GLDC, NKH1
Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia.
Kure S, Kato K, Dinopoulos A, Gail C, DeGrauw TJ, Christodoulou J, Bzduch V, Kalmanchey R, Fekete G, Trojovsky A, Plecko B, Breningstall G, Tohyama J, Aoki Y, Matsubara Y.
Hum Mutat 27(4):343-52. 2006
12AMT, GCE1, GCE2, GCE3, GCSH, GLDC
Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotic hyperglycinemia.
Kure S, Kato K, Dinopoulos A, Gail C, DeGrauw TJ, Christodoulou J, Bzduch V, Kalmanchey R, Fekete G, Trojovsky A, Plecko B, Breningstall G, Tohyama J, Aoki Y, Matsubara Y.
Hum Mutat 27(4):343-52. 2006
13GLDC, NKH1
Detection of mutations in the glycine decarboxylase gene in patients with nonketotic hyperglycinaemia.
Sellner L, Edkins E, Greed L, Lewis B.
Mol Genet Metab 84(2):167-71. Epub 2004 Nov 23. 2005
14GLDC, NKH1
Glycine decarboxylase mutations: a distinctive phenotype of nonketotic hyperglycinemia in adults.
Dinopoulos A, Kure S, Chuck G, Sato K, Gilbert DL, Matsubara Y, Degrauw T.
Neurology 64(7):1255-7. 2005
15GCE2, GLDC
A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem.
Boneh A, Korman SH, Sato K, Kanno J, Matsubara Y, Lerer I, Ben-Neriah Z, Kure S.
J Hum Genet 50(5):230-4. 2005
16GCE1, GCE2, GCSH, GLDC
Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemia.
Kure S, Kojima K, Ichinohe A, Maeda T, Kalmanchey R, Fekete G, Berg SZ, Filiano J, Aoki Y, Suzuki Y, Izumi T, Matsubara Y.
Ann Neurol 52(5):643-6. 2002
17AMT, GLDC, NKH1, NKH2
Recurrent mutations in p- and t-proteins of the glycine cleavage complex and a novel t-protein mutation (n145i): a strategy for the molecular investigation of patients with nonketotic hyperglycinemia (nkh).
Toone JR, Applegarth DA, Coulter-Mackie MB, James ER.
Mol Genet Metab 72(4):322-5. 2001
18GLDC, GLDCP
Human glycine decarboxylase gene (GLDC) and its highly conserved processed pseudogene (psiGLDC): their structure and expression, and the identification of a large deletion in a family with nonketotic hyperglycinemia.
Takayanagi M, Kure S, Sakata Y, Kurihara Y, Ohya Y, Kajita M, Tada K, Matsubara Y, Narisawa K.
Hum Genet 106(3):298-305. 2000
19GLDC, GLDCP, NKH1
Assignment of the true and processed genes for human glycine decarboxylase to 9p23-24 and 4q12.
Isobe M, et al.
Biochem Biophys Res Commun 203 : 1483-1487. 1994
20GLDC, NKH1
Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia.
Kure S, et al.
J Clin Invest 90 : 160-164. 1992