Detalhe da pesquisa
1.
Dedicated transcriptomics combined with power analysis lead to functional understanding of genes with weak phenotypic changes in knockout lines.
PLoS Comput Biol
; 16(11): e1008354, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33180766
2.
Dealing with the adaptive immune system during de novo evolution of genes from intergenic sequences.
BMC Evol Biol
; 18(1): 121, 2018 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30075701
3.
Segmental duplications and evolutionary acquisition of UV damage response in the SPATA31 gene family of primates and humans.
BMC Genomics
; 18(1): 222, 2017 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28264649
4.
Primate segmental duplication creates novel promoters for the LRRC37 gene family within the 17q21.31 inversion polymorphism region.
Genome Res
; 22(6): 1050-8, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22419166
5.
Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and Africa.
BMC Genomics
; 15: 963, 2014 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25376095
6.
Death and resurrection of the human IRGM gene.
PLoS Genet
; 5(3): e1000403, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19266026
7.
Human core duplicon gene families: game changers or game players?
Brief Funct Genomics
; 18(6): 402-411, 2019 11 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31529038
8.
A de novo evolved gene in the house mouse regulates female pregnancy cycles.
Elife
; 82019 08 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-31436535
9.
Involvement of SPATA31 copy number variable genes in human lifespan.
Aging (Albany NY)
; 10(4): 674-688, 2018 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29676996
10.
Critical role for the tapasin-docking site of TAP2 in the functional integrity of the MHC class I-peptide-loading complex.
J Immunol
; 175(8): 5104-14, 2005 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16210614
11.
The interferon-inducible p47 (IRG) GTPases in vertebrates: loss of the cell autonomous resistance mechanism in the human lineage.
Genome Biol
; 6(11): R92, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16277747