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Items: 1 to 20 of 160

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Transmembrane topology of glucose-6-phosphatase.

Pan CJ, Lei KJ, Annabi B, Hemrika W, Chou JY.

J Biol Chem. 1998 Mar 13;273(11):6144-8.

4.

Structure-function analysis of human glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a.

Lei KJ, Pan CJ, Liu JL, Shelly LL, Chou JY.

J Biol Chem. 1995 May 19;270(20):11882-6.

5.

Identification and characterization of a cDNA and the gene encoding the mouse ubiquitously expressed glucose-6-phosphatase catalytic subunit-related protein.

Boustead JN, Martin CC, Oeser JK, Svitek CA, Hunter SI, Hutton JC, O'Brien RM.

J Mol Endocrinol. 2004 Feb;32(1):33-53.

6.

The molecular basis of type 1 glycogen storage diseases.

Chou JY.

Curr Mol Med. 2001 Mar;1(1):25-44. Review.

PMID:
11899241
7.

Squash glycerol-3-phosphate (1)-acyltransferase. Alteration of substrate selectivity and identification of arginine and lysine residues important in catalytic activity.

Slabas AR, Kroon JT, Scheirer TP, Gilroy JS, Hayman M, Rice DW, Turnbull AP, Rafferty JB, Fawcett T, Simon WJ.

J Biol Chem. 2002 Nov 15;277(46):43918-23.

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The glucose-6-phosphatase system.

van Schaftingen E, Gerin I.

Biochem J. 2002 Mar 15;362(Pt 3):513-32. Review.

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Metabolic impact of adenovirus-mediated overexpression of the glucose-6-phosphatase catalytic subunit in hepatocytes.

Seoane J, Trinh K, O'Doherty RM, Gómez-Foix AM, Lange AJ, Newgard CB, Guinovart JJ.

J Biol Chem. 1997 Oct 24;272(43):26972-7.

13.

Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex.

Chou JY, Matern D, Mansfield BC, Chen YT.

Curr Mol Med. 2002 Mar;2(2):121-43. Review.

PMID:
11949931
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The biochemistry and molecular biology of the glucose-6-phosphatase system.

Foster JD, Nordlie RC.

Exp Biol Med (Maywood). 2002 Sep;227(8):601-8. Review.

PMID:
12192101
19.

Roles of active site residues in Pseudomonas aeruginosa phosphomannomutase/phosphoglucomutase.

Naught LE, Regni C, Beamer LJ, Tipton PA.

Biochemistry. 2003 Aug 26;42(33):9946-51.

PMID:
12924943
20.

The molecular basis of glycogen storage disease type 1a: structure and function analysis of mutations in glucose-6-phosphatase.

Shieh JJ, Terzioglu M, Hiraiwa H, Marsh J, Pan CJ, Chen LY, Chou JY.

J Biol Chem. 2002 Feb 15;277(7):5047-53.

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