Associated Papers
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy.
Karali M et al.
Scientific Reports, 2022
36460718 (PubMed )
Supplement: 41598_2022_24636_MOESM2_ESM.xlsx › Supplementary_Table_S2
Ligand binding to the human MT2 melatonin receptor: the role of residues in transmembrane domains 3, 6, and 7.
Mazna P et al.
Biochemical and Biophysical Research Communications, 2005
The spectrum of human rhodopsin disease mutations through the lens of interspecific variation.
Briscoe AD et al.
Gene, 2004
Partial agonist activity of 11-cis-retinal in rhodopsin mutants.
Han M et al.
The Journal of Biological Chemistry, 1997
The effects of amino acid replacements of glycine 121 on transmembrane helix 3 of rhodopsin.
Han M et al.
The Journal of Biological Chemistry, 1996
Select a paper to view details