Citations for
1G6PC, PCK2
DNA damage induces down-regulation of PEPCK and G6P gene expression through degradation of PGC-1alpha.
Kim HJ, Jee HJ, Yun J.
Acta Biochim Biophys Sin (Shanghai) 43(8):589-94. Epub 2011 Jul 5. 2011
2G6PC
Insulin and epidermal growth factor suppress basal glucose-6-phosphatase catalytic subunit gene transcription through overlapping but distinct mechanisms.
Onuma H, Oeser JK, Nelson BA, Wang Y, Flemming BP, Scheving LA, Russell WE, O'Brien RM.
Biochem J 417(2):611-20. 2009
3VIP, CREM, G6PC, HNF1A, HNF4A
Transcriptional regulation of the glucose-6-phosphatase gene by cAMP/vasoactive intestinal peptide in the intestine. Role of HNF4alpha, CREM, HNF1alpha, and C/EBPalpha.
Gautier-Stein A, Zitoun C, Lalli E, Mithieux G, Rajas F.
J Biol Chem 281(42):31268-78. Epub 2006 Aug 7. 2006
4G6PC, GCK
Identification of novel polymorphisms in the glucokinase and glucose-6-phosphatase genes in infants who died suddenly and unexpectedly.
Forsyth L, Hume R, Howatson A, Busuttil A, Burchell A.
J Mol Med 83(8):610-8. Epub 2005 May 26. 2005
5G6PC, G6PC3
Identification and characterisation of a new human glucose-6-phosphatase isoform.
Guionie O, Clottes E, Stafford K, Burchell A.
FEBS Lett 551(1-3):159-64. 2003
6G6PC, SLC37A4, GSD1B, GSD1C
Structure-function analysis of the glucose-6-phosphate transporter deficient in glycogen storage disease type Ib.
Chen LY, Pan CJ, Shieh JJ, Chou JY.
Hum Mol Genet 11(25):3199-207. 2002
7G6PC, GSD1B
Glycogen storage disease type I: diagnosis and phenotype/genotype correlation.
Matern D, Seydewitz HH, Bali D, Lang C, Chen YT.
Eur J Pediatr 161 Suppl 1:S10-9. Epub 2002 Jul 27. 2002
8G6PC, GSD1B, GSD1C
Molecular genetics of type 1 glycogen storage disease.
Janecke AR, Mayatepek E, Utermann G.
Mol Genet Metab 73(2):117-25. Review. 2001
9G6PC, GSD1A
Glycogen storage disease type ia: molecular diagnosis of 51 japanese patients and characterization of splicing mutations by analysis of ectopically transcribed mRNA from lymphoblastoid cells.
Akanuma J, Nishigaki T, Fujii K, Matsubara Y, Inui K, Takahashi K, Kure S, Suzuki Y, Ohura T, Miyabayashi S, Ogawa E, Iinuma K, Okada S, Narisawa K.
Am J Med Genet 91(2):107-12. 2000
10G6PC
Enzymatic characterization of four new mutations in the glucose-6 phosphatase (G6PC) gene which cause glycogen storage disease type 1a.
Bruni N, Rajas F, Montano S, Chevalier-Porst F, Maire I, Mithieux G.
Ann Hum Genet 63:141-146 1999
11G6PC, GSD1A
Two new mutations in the glucose-6-phosphatase gene cause glycogen storage disease in Hungarian patients.
Parvari R, Lei KJ, Szonyi L, Narkis G, Moses S, Chou JY.
Eur J Hum Genet 5(4):191-5. 1997
12G6PC
Exon redefinition by a point mutation within exon 5 of the glucose-6-phosphatase gene is the major cause of glycogen storage disease type Ia in Japan.
Kajihara S, et al.
Am J Hum Genet 57 : 549-555. 1995