Babenko AP - Search Results

1

Insulin secretagogues, sulfonylurea receptors and K(ATP) channels.

Bryan J, Crane A, Vila-Carriles WH, Babenko AP, Aguilar-Bryan L. Bryan J, et al. Among authors: babenko ap. Curr Pharm Des. 2005;11(21):2699-716. doi: 10.2174/1381612054546879. Curr Pharm Des. 2005. PMID: 16101450 Review.

2

Toward linking structure with function in ATP-sensitive K+ channels.

Bryan J, Vila-Carriles WH, Zhao G, Babenko AP, Aguilar-Bryan L. Bryan J, et al. Among authors: babenko ap. Diabetes. 2004 Dec;53 Suppl 3:S104-12. doi: 10.2337/diabetes.53.suppl_3.s104. Diabetes. 2004. PMID: 15561897 Review.

3

Toward understanding the assembly and structure of KATP channels.

Aguilar-Bryan L, Clement JP 4th, Gonzalez G, Kunjilwar K, Babenko A, Bryan J. Aguilar-Bryan L, et al. Physiol Rev. 1998 Jan;78(1):227-45. doi: 10.1152/physrev.1998.78.1.227. Physiol Rev. 1998. PMID: 9457174 Free article. Review.

4

Sulfonylurea receptors set the maximal open probability, ATP sensitivity and plasma membrane density of KATP channels.

Babenko AP, Gonzalez G, Aguilar-Bryan L, Bryan J. Babenko AP, et al. FEBS Lett. 1999 Feb 19;445(1):131-6. doi: 10.1016/s0014-5793(99)00102-7. FEBS Lett. 1999. PMID: 10069387 Free article.

5

Two regions of sulfonylurea receptor specify the spontaneous bursting and ATP inhibition of KATP channel isoforms.

Babenko AP, Gonzalez G, Bryan J. Babenko AP, et al. J Biol Chem. 1999 Apr 23;274(17):11587-92. doi: 10.1074/jbc.274.17.11587. J Biol Chem. 1999. PMID: 10206966 Free article.

6

The C terminus of SUR1 is required for trafficking of KATP channels.

Sharma N, Crane A, Clement JP 4th, Gonzalez G, Babenko AP, Bryan J, Aguilar-Bryan L. Sharma N, et al. Among authors: babenko ap. J Biol Chem. 1999 Jul 16;274(29):20628-32. doi: 10.1074/jbc.274.29.20628. J Biol Chem. 1999. PMID: 10400694 Free article.

7

The tolbutamide site of SUR1 and a mechanism for its functional coupling to K(ATP) channel closure.

Babenko AP, Gonzalez G, Bryan J. Babenko AP, et al. FEBS Lett. 1999 Oct 15;459(3):367-76. doi: 10.1016/s0014-5793(99)01215-6. FEBS Lett. 1999. PMID: 10526167 Free article.

8

Pharmaco-topology of sulfonylurea receptors. Separate domains of the regulatory subunits of K(ATP) channel isoforms are required for selective interaction with K(+) channel openers.

Babenko AP, Gonzalez G, Bryan J. Babenko AP, et al. J Biol Chem. 2000 Jan 14;275(2):717-20. doi: 10.1074/jbc.275.2.717. J Biol Chem. 2000. PMID: 10625598 Free article.

9

Hetero-concatemeric KIR6.X4/SUR14 channels display distinct conductivities but uniform ATP inhibition.

Babenko AP, Gonzalez GC, Bryan J. Babenko AP, et al. J Biol Chem. 2000 Oct 13;275(41):31563-6. doi: 10.1074/jbc.C000553200. J Biol Chem. 2000. PMID: 10956638 Free article.

10

A conserved inhibitory and differential stimulatory action of nucleotides on K(IR)6.0/SUR complexes is essential for excitation-metabolism coupling by K(ATP) channels.

Babenko AP, Bryan J. Babenko AP, et al. J Biol Chem. 2001 Dec 28;276(52):49083-92. doi: 10.1074/jbc.M108763200. Epub 2001 Oct 22. J Biol Chem. 2001. PMID: 11673467 Free article.

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