Detalhe da pesquisa
1.
Pulchelloid A, a sesquiterpene lactone from the Canadian prairie plant Gaillardia aristata inhibits mitosis in human cells.
Mol Biol Rep
; 48(7): 5459-5471, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34304367
2.
Pathogenic Effects of Mineralocorticoid Pathway Activation in Retinal Pigment Epithelium.
Int J Mol Sci
; 22(17)2021 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34502527
3.
JNK Inhibition Reduced Retinal Ganglion Cell Death after Ischemia/Reperfusion In Vivo and after Hypoxia In Vitro.
Adv Exp Med Biol
; 854: 677-83, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26427475
4.
Mutations in ALDH1A3 represent a frequent cause of microphthalmia/anophthalmia in consanguineous families.
Hum Mutat
; 35(8): 949-53, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24777706
5.
Mutations in the SPARC-related modular calcium-binding protein 1 gene, SMOC1, cause waardenburg anophthalmia syndrome.
Am J Hum Genet
; 88(1): 92-8, 2011 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21194680
6.
IROme, a new high-throughput molecular tool for the diagnosis of inherited retinal dystrophies-a price comparison with Sanger sequencing.
Adv Exp Med Biol
; 801: 171-6, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24664695
7.
Polymeric micelle mediated follicular delivery of spironolactone: Targeting the mineralocorticoid receptor to prevent glucocorticoid-induced activation and delayed cutaneous wound healing.
Int J Pharm
; 604: 120773, 2021 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34090990
8.
Tuning SAS-6 architecture with monobodies impairs distinct steps of centriole assembly.
Nat Commun
; 12(1): 3805, 2021 06 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34155202
9.
Gene expression analysis using single molecule detection.
Nucleic Acids Res
; 31(16): e89, 2003 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12907741
10.
Novel ADAM9 homozygous mutation in a consanguineous Egyptian family with severe cone-rod dystrophy and cataract.
Br J Ophthalmol
; 98(12): 1718-23, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25091951
11.
IROme, a new high-throughput molecular tool for the diagnosis of inherited retinal dystrophies.
Biomed Res Int
; 2013: 198089, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23484092