Detalhe da pesquisa
1.
FCGR3A-V158F polymorphism is a disease-specific pharmacogenetic marker for the treatment of psoriasis with Fc-containing TNFα inhibitors.
Pharmacogenomics J
; 17(3): 237-241, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27044681
2.
Replication of PTPRC as genetic biomarker of response to TNF inhibitors in patients with rheumatoid arthritis.
Pharmacogenomics J
; 16(2): 137-40, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25896535
3.
A pharmacogenetic study of ABCB1 polymorphisms and cyclosporine treatment response in patients with psoriasis in the Greek population.
Pharmacogenomics J
; 14(6): 523-5, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24889923
4.
Association of anti-CCP positivity and carriage of TNFRII susceptibility variant with anti-TNF-α response in rheumatoid arthritis.
Clin Exp Rheumatol
; 29(4): 701-4, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21813066
5.
Major histocompatibility complex variation at class II DQA locus in the brown hare (Lepus europaeus).
Mol Ecol
; 18(22): 4631-49, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19845856
6.
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy.
Epilepsy Res
; 70(2-3): 118-26, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16707245
7.
ZNF232: structure and expression analysis of a novel human C(2)H(2) zinc finger gene, member of the SCAN/LeR domain subfamily.
Biochim Biophys Acta
; 1518(3): 300-5, 2001 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-11311944
8.
Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia.
Gene
; 282(1-2): 87-94, 2002 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-11814680
9.
Map integration at human chromosome 10: molecular and cytogenetic analysis of a chromosome-specific somatic cell hybrid panel and genomic clones, based on a well-supported genetic map.
Cytogenet Cell Genet
; 79(3-4): 257-65, 1997.
Artigo
em Inglês
| MEDLINE | ID: mdl-9605867