EKSPRESSIYa FAKTOROV TRANSKRIPTsII SEMEYSTVA Vsx V KhODE RETINOGENEZA U KUR

I N Andreychenko , R D Zinov'eva

Medical academic journal ›› 2016, Vol. 16 ›› Issue (4) : 44 -45.

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Medical academic journal ›› 2016, Vol. 16 ›› Issue (4) : 44 -45. DOI: 10.17816/MAJ16444-45
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EKSPRESSIYa FAKTOROV TRANSKRIPTsII SEMEYSTVA Vsx V KhODE RETINOGENEZA U KUR

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I N Andreychenko, R D Zinov'eva. EKSPRESSIYa FAKTOROV TRANSKRIPTsII SEMEYSTVA Vsx V KhODE RETINOGENEZA U KUR. Medical academic journal, 2016, 16(4): 44-45 DOI:10.17816/MAJ16444-45

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VSX2 mutations in autosomal recessive microphthalmia / Reis L. M., Khan A., Kariminejad A., Ebadi F., Tyler R. C., Semina E. V. // Mol Vis. 2011. Vol. 17. P. 2527-2532.

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H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD family / Valleix S., Nedelec B., Rigaudiere F., Dighiero P., Pouliquen Y., Renard G., Gargasson J. F., Delpech M. // Invest Ophthalmol Vis Sci. 2006. Vol. 47. P. 48-54.

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Thehomeobox gene CHX10/VSX2 regulates RdCVF promoter activity in the inner retina / Reichman S., Kalathur R. K., Lambard S., Aït-Ali N., Yang Y., Lardenois A., Ripp R., Poch O., Zack D. J., Sahel J. A., Léveillard T. // Hum Mol Genet. 2010. Vol. 19. P. 250-261.

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Andreychenko I.N., Zinov'eva R.D.

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