Papers associated with proximal (and pou2f1)

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	Genetic variants of organic cation transporter 2 (OCT2) significantly reduce metformin uptake in oocytes., Song IS., Xenobiotica. September 1, 2008; 38 (9): 1252-62.
	An Oct-1 binding site mediates activation of the gata2 promoter by BMP signaling., Oren T., Nucleic Acids Res. August 1, 2005; 33 (13): 4357-67.
	Comparative genomics on Dkk1 orthologs., Katoh Y., Int J Oncol. July 1, 2005; 27 (1): 275-9.
	A consensus Oct1 binding site is required for the activity of the Xenopus Cdx4 promoter., Reece-Hoyes JS., Dev Biol. June 15, 2005; 282 (2): 509-23.
	Transport of the dopamine D2 agonist pramipexole by rat organic cation transporters OCT1 and OCT2 in kidney., Ishiguro N., Drug Metab Dispos. April 1, 2005; 33 (4): 495-9.
	The organic cation transporters rOCT1 and hOCT2 are inhibited by cGMP., Schlatter E., J Membr Biol. October 1, 2002; 189 (3): 237-44.
	Developmentally regulated expression of organic ion transporters NKT (OAT1), OCT1, NLT (OAT2), and Roct., Pavlova A., Am J Physiol Renal Physiol. April 1, 2000; 278 (4): F635-43.
	Molecular cloning and characterization of NKT, a gene product related to the organic cation transporter family that is almost exclusively expressed in the kidney., Lopez-Nieto CE., J Biol Chem. March 7, 1997; 272 (10): 6471-8.
	Functional redundancy of promoter elements ensures efficient transcription of the human 7SK gene in vivo., Boyd DC., J Mol Biol. November 10, 1995; 253 (5): 677-90.
	Drug excretion mediated by a new prototype of polyspecific transporter., Gründemann D., Nature. December 8, 1994; 372 (6506): 549-52.

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