|
XB-GENEPAGE-961018
Papers associated with pde6b
???pagination.result.count???
???pagination.result.page??? 1
| Sort Newest To Oldest | Sort Oldest To Newest |
TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B, Borday C, Erkilic N, Mamaeva D, Donval A, Masson C, Parain K, Kaminska K, Quinodoz M, Perea-Romero I, Garcia-Garcia G, Jimenez-Medina C, Boukhaddaoui H, Coget A, Leboucq N, Calzetti G, Gandolfi S, Percesepe A, Barili V, Uliana V, Delsante M, Bozzetti F, Scholl HP, Corton M, Ayuso C, Millan JM, Rivolta C, Meunier I, Perron M, Kalatzis V., JCI Insight. November 8, 2023; 8 (21):  |
|
A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit., Manes G, Cheguru P, Majumder A, Bocquet B, Sénéchal A, Artemyev NO, Hamel CP, Brabet P., PLoS One. January 1, 2014; 9 (4): e95768.  |
|
Atypical retinal degeneration 3 in mice is caused by defective PDE6B pre-mRNA splicing., Muradov H, Boyd KK, Kerov V, Artemyev NO., Vision Res. March 15, 2012; 57 1-8. |
|
Rod phosphodiesterase-6 PDE6A and PDE6B subunits are enzymatically equivalent., Muradov H, Boyd KK, Artemyev NO., J Biol Chem. December 17, 2010; 285 (51): 39828-34. |
???pagination.result.page??? 1