Citations for
1G6PC
Large-scale transcriptome profiles reveal robust 20-signatures metabolic prediction models and novel role of G6PC in clear cell renal cell carcinoma.
Xu WH, Xu Y, Tian X, Anwaier A, Liu WR, Wang J, Zhu WK, Cao DL, Wang HK, Shi GH, Qu YY, Zhang HL, Ye DW.
J Cell Mol Med. Jun 21. doi: 10.1111/jcmm.15536. Online ahead of print 2020
2G6PC, GSD1A
Glycogen storage disease type 1a is associated with disturbed vitamin A metabolism and elevated serum retinol levels.
Saeed A, Hoogerland JA, Wessel H, Heegsma J, Derks TGJ, van der Veer E, Mithieux G, Rajas F, Oosterveer MH, Faber KN.
Hum Mol Genet. Jan 15;29(2):264-273. doi: 10.1093/hmg/ddz283 2020
3G6PC, GSD1A
Glycogen storage diseases: Twenty-seven new variants in a cohort of 125 patients.
Sperb-Ludwig F, Pinheiro FC, Bettio Soares M, Nalin T, Ribeiro EM, Steiner CE, Ribeiro Valadares E, Porta G, Fishinger Moura de Souza C, Schwartz IVD.
Mol Genet Genomic Med. Nov;7(11):e877. doi: 10.1002/mgg3.877. Epub 2019 Sep 11 2019
4CREB3L3, G6PC, PCK1, PYGL
CREBH Maintains Circadian Glucose Homeostasis by Regulating Hepatic Glycogenolysis and Gluconeogenesis.
Kim H, Zheng Z, Walker PD, Kapatos G, Zhang K.
Mol Cell Biol. Jun 29;37(14):e00048-17. doi: 10.1128/MCB.00048-17. Print 2017 Jul 15 2017
5G6PC, GSD1A
Induction of autophagy improves hepatic lipid metabolism in glucose-6-phosphatase deficiency.
Farah BL, Landau DJ, Sinha RA, Brooks ED, Wu Y, Fung SYS, Tanaka T, Hirayama M, Bay BH, Koeberl DD, Yen PM.
J Hepatol. Feb;64(2):370-379. doi: 10.1016/j.jhep.2015.10.008. Epub 2015 Oct 20 2016
6G6PC
Genetic and molecular analyses reveal G6PC as a key element connecting glucose metabolism and cell cycle control in ovarian cancer.
Guo T, Chen T, Gu C, Li B, Xu C.
Tumour Biol. Sep;36(10):7649-58. doi: 10.1007/s13277-015-3463-6. Epub 2015 Apr 30 2015
7G6PC, GSD1A
Three novel mutations of the G6PC gene identified in Chinese patients with glycogen storage disease type Ia.
Zheng BX, Lin Q, Li M, Jin Y.
Eur J Pediatr. Jan;174(1):59-63. doi: 10.1007/s00431-014-2354-y. Epub 2014 Jul 1 2015
8G6PC, PCK1, THRA, THRB
FoxO1 deacetylation regulates thyroid hormone-induced transcription of key hepatic gluconeogenic genes.
Singh BK, Sinha RA, Zhou J, Xie SY, You SH, Gauthier K, Yen PM.
J Biol Chem 18;288(42):30365-72. doi: 10.1074/jbc.M113.504845. Epub 2013 Aug 30 2013
9G6PC, GSD1A
The upstream enhancer elements of the G6PC promoter are critical for optimal G6PC expression in murine glycogen storage disease type Ia.
Lee YM, Pan CJ, Koeberl DD, Mansfield BC, Chou JY.
Mol Genet Metab. Nov;110(3):275-80. doi: 10.1016/j.ymgme.2013.06.014. Epub 2013 Jun 25 2013
10ESRRG, G6PC, PCK1
Orphan nuclear receptor estrogen-related receptor γ (ERRγ) is key regulator of hepatic gluconeogenesis.
Kim DK, Ryu D, Koh M, Lee MW, Lim D, Kim MJ, Kim YH, Cho WJ, Lee CH, Park SB, Koo SH, Choi HS.
J Biol Chem. Jun 22;287(26):21628-39. doi: 10.1074/jbc.M111.315168. Epub 2012 May 1 2012
11G6PC, 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
12G6PC
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
13VIP, 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
14G6PC, 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
15G6PC, 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
16G6PC, 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
17G6PC, 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
18G6PC, 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
19G6PC, 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
20G6PC
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
21G6PC, 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
22G6PC
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