| P2093 | author name string | Muna I Naash | |
| | Zack A Nash | |
| P2860 | cites work | A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness | Q44128836 |
| | Slow binding of retinal to rhodopsin mutants G90D and T94D. | Q44318492 |
| | Light-Dependent Translocation of Arrestin in the Absence of Rhodopsin Phosphorylation and Transducin Signaling | Q44380847 |
| | The R172W mutation in peripherin/rds causes a cone-rod dystrophy in transgenic mice | Q44978539 |
| | Retinal abnormalities associated with the G90D mutation in opsin | Q45045560 |
| | Light-dependent subcellular movement of photoreceptor proteins | Q46224757 |
| | Light-dependent translocation of visual arrestin regulated by the NINAC myosin III. | Q47070026 |
| | Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness | Q72896189 |
| | Light-dependent redistribution of visual arrestins and transducin subunits in mice with defective phototransduction | Q73514847 |
| | On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention | Q24536217 |
| | Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness | Q28116173 |
| | The relationship between opsin overexpression and photoreceptor degeneration | Q32061867 |
| | Modulating expression of peripherin/rds in transgenic mice: critical levels and the effect of overexpression | Q34119855 |
| | Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation | Q34745200 |
| | Morphological, physiological, and biochemical changes in rhodopsin knockout mice | Q34853562 |
| | Phototransduction: shedding light on translocation. | Q35548399 |
| | Mouse models of human retinal disease caused by expression of mutant rhodopsin. A valuable tool for the assessment of novel gene therapies. | Q35793650 |
| | Temporal kinetics of the light/dark translocation and compartmentation of arrestin and alpha-transducin in mouse photoreceptor cells. | Q38575568 |
| | Characterization of rhodopsin congenital night blindness mutant T94I. | Q42694901 |
| | Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell loss. | Q43683686 |
| | Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutations | Q44119130 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | photoreceptor protein | Q7187894 |
| P304 | page(s) | 125-131 | |
| P577 | publication date | 2006-01-01 | |
| P1433 | published in | Advances in Experimental Medicine and Biology | Q4686385 |
| P1476 | title | Light/dark translocation of alphatransducin in mouse photoreceptor cells expressing G90D mutant opsin | |
| P478 | volume | 572 | |