Detalhe da pesquisa
1.
Guidelines for investigating causality of sequence variants in human disease.
Nature
; 508(7497): 469-76, 2014 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-24759409
2.
Revisiting mutagenesis at non-B DNA motifs in the human genome.
Nat Struct Mol Biol
; 30(4): 417-424, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36914796
3.
SNP frequencies in human genes an excess of rare alleles and differing modes of selection.
Trends Genet
; 16(8): 335-7, 2000 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-10904261
4.
Are knowledge-based potentials derived from protein structure sets discriminative with respect to amino acid types?
Proteins
; 31(3): 225-46, 1998 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-9593195
5.
PSIC: profile extraction from sequence alignments with position-specific counts of independent observations.
Protein Eng
; 12(5): 387-94, 1999 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-10360979