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Periodic albinism of a widely used albino mutant of Xenopus laevis caused by deletion of two exons in the Hermansky-Pudlak syndrome type 4 gene. , Fukuzawa T ., Genes Cells. January 1, 2021; 26 (1): 31-39.
A model for investigating developmental eye repair in Xenopus laevis. , Kha CX ., Exp Eye Res. April 1, 2018; 169 38-47.
no privacy, a Xenopus tropicalis mutant, is a model of human Hermansky-Pudlak Syndrome and allows visualization of internal organogenesis during tadpole development. , Nakayama T ., Dev Biol. June 15, 2017; 426 (2): 472-486.
Overexpressed Ca(v)beta3 inhibits N-type ( Cav2.2) calcium channel currents through a hyperpolarizing shift of ultra-slow and closed-state inactivation. , Yasuda T., J Gen Physiol. April 1, 2004; 123 (4): 401-16.
Deletion of the S3-S4 linker in the Shaker potassium channel reveals two quenching groups near the outside of S4. , Sørensen JB., J Gen Physiol. February 1, 2000; 115 (2): 209-22.
Correlation between charge movement and ionic current during slow inactivation in Shaker K+ channels. , Olcese R., J Gen Physiol. November 1, 1997; 110 (5): 579-89.