Differential requirements for retinal degeneration slow intermolecular disulfide-linked oligomerization in rods versus cones

By Chakraborty Dibyendu   Ding Xi-Qin   Conley Shannon M.   Fliesler Steven J.   Naash Muna I.  

Human Molecular Genetics, Vol. 18, Iss. 5, 2009-03 ,pp. : 797-808

Oxford University Press

Access to resources Recommend Favorite

Loss-of-function point mutations associated with renal tubular dysgenesis provide insights about renin function and cellular trafficking

By Michaud Annie   Bur Daniel   Gribouval Olivier   Muller Laurent   Iturrioz Xavier   Clemessy Maud   Gasc Jean-Marie   Gubler Marie-Claire   Corvol Pierre  

Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 301-311

Oxford University Press

Access to resources Recommend Favorite

The R172W mutation in peripherin/ rds causes a cone–rod dystrophy in transgenic mice

By Ding Xi-Qin  

Human Molecular Genetics, Vol. 13, Iss. 18, 2004-09 ,pp. : 2075-2087

Oxford University Press

Access to resources Recommend Favorite

Gene replacement therapy in the retinal degeneration slow ( rds ) mouse: the effect on retinal degeneration following partial transduction of the retina

By Sarra G-M.  

Human Molecular Genetics, Vol. 10, Iss. 21, 2001-10 ,pp. : 2353-2361

Oxford University Press

Access to resources Recommend Favorite

Murine model of autosomal dominant retinitis pigmentosa generated by targeted deletion at codon 307 of the rds –peripherin gene

By Humphries M.M.  

Human Molecular Genetics, Vol. 11, Iss. 9, 2002-05 ,pp. : 1005-1016

Oxford University Press

Access to resources Recommend Favorite