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Items: 5

1.

Transcriptomic and network component analysis of glycerol kinase in skeletal muscle using a mouse model of glycerol kinase deficiency.

Rahib L, Sriram G, Harada MK, Liao JC, Dipple KM.

Mol Genet Metab. 2009 Mar;96(3):106-12. doi: 10.1016/j.ymgme.2008.11.163.

2.

Single-gene disorders: what role could moonlighting enzymes play?

Sriram G, Martinez JA, McCabe ER, Liao JC, Dipple KM.

Am J Hum Genet. 2005 Jun;76(6):911-24. Review.

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4.

Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.

Francke U, Harper JF, Darras BT, Cowan JM, McCabe ER, Kohlschütter A, Seltzer WK, Saito F, Goto J, Harpey JP, et al.

Am J Hum Genet. 1987 Mar;40(3):212-27.

5.

Targeting of hexokinase 1 to liver and hepatoma mitochondria.

Gelb BD, Adams V, Jones SN, Griffin LD, MacGregor GR, McCabe ER.

Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):202-6.

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