Detalhe da pesquisa
1.
Tbx2a Modulates Switching of RH2 and LWS Opsin Gene Expression.
Mol Biol Evol
; 37(7): 2002-2014, 2020 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32191319
2.
Movement of transposable elements contributes to cichlid diversity.
Mol Ecol
; 29(24): 4956-4969, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33049090
3.
Multiple trans QTL and one cis-regulatory deletion are associated with the differential expression of cone opsins in African cichlids.
BMC Genomics
; 19(1): 945, 2018 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30563463
4.
Adult plasticity in African cichlids: Rapid changes in opsin expression in response to environmental light differences.
Mol Ecol
; 26(21): 6036-6052, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28926160
5.
Determination of the Genetic Architecture Underlying Short Wavelength Sensitivity in Lake Malawi Cichlids.
J Hered
; 108(4): 379-390, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28498989
6.
Proximate and ultimate causes of variable visual sensitivities: Insights from cichlid fish radiations.
Genesis
; 54(6): 299-325, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27061347
7.
The unusual eyes of Xenos peckii (Strepsiptera: Xenidae) have green- and UV--sensitive photoreceptors.
J Exp Biol
; 219(Pt 24): 3866-3874, 2016 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27974533
8.
Loss of zebrafish dzip1 results in inappropriate recruitment of periocular mesenchyme to the optic fissure and ocular coloboma.
PLoS One
; 17(3): e0265327, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35286359
9.
Chromosome-scale assemblies reveal the structural evolution of African cichlid genomes.
Gigascience
; 8(4)2019 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30942871
10.
Diurnal variation in opsin expression and common housekeeping genes necessitates comprehensive normalization methods for quantitative real-time PCR analyses.
Mol Ecol Resour
; 19(6): 1447-1460, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31325910
11.
Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.
Nat Genet
; 44(11): 1265-71, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23023331