Detalhe da pesquisa
1.
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
; 52(D1): D33-D43, 2024 Jan 05.
Artigo
Inglês
| MEDLINE | ID: mdl-37994677
2.
Database resources of the National Center for Biotechnology Information in 2023.
Nucleic Acids Res
; 51(D1): D29-D38, 2023 01 06.
Artigo
Inglês
| MEDLINE | ID: mdl-36370100
3.
Database resources of the national center for biotechnology information.
Nucleic Acids Res
; 50(D1): D20-D26, 2022 01 07.
Artigo
Inglês
| MEDLINE | ID: mdl-34850941
4.
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
; 49(D1): D10-D17, 2021 01 08.
Artigo
Inglês
| MEDLINE | ID: mdl-33095870
5.
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
; 48(D1): D9-D16, 2020 01 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31602479
6.
SPDI: data model for variants and applications at NCBI.
Bioinformatics
; 36(6): 1902-1907, 2020 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31738401
7.
iCn3D, a web-based 3D viewer for sharing 1D/2D/3D representations of biomolecular structures.
Bioinformatics
; 36(1): 131-135, 2020 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31218344
8.
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
; 47(D1): D23-D28, 2019 01 08.
Artigo
Inglês
| MEDLINE | ID: mdl-30395293
9.
LitVar: a semantic search engine for linking genomic variant data in PubMed and PMC.
Nucleic Acids Res
; 46(W1): W530-W536, 2018 07 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29762787
10.
tmVar 2.0: integrating genomic variant information from literature with dbSNP and ClinVar for precision medicine.
Bioinformatics
; 34(1): 80-87, 2018 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28968638
11.
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool.
BMC Bioinformatics
; 19(1): 57, 2018 02 20.
Artigo
Inglês
| MEDLINE | ID: mdl-29463208
12.
Supporting precision medicine by data mining across multi-disciplines: an integrative approach for generating comprehensive linkages between single nucleotide variants (SNVs) and drug-binding sites.
Bioinformatics
; 33(11): 1621-1629, 2017 Jun 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28158543
13.
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
; 40(Database issue): D13-25, 2012 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-22140104
14.
Database resources of the National Center for Biotechnology Information.
Nucleic Acids Res
; 39(Database issue): D38-51, 2011 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-21097890
15.
The completion of the Mammalian Gene Collection (MGC).
Genome Res
; 19(12): 2324-33, 2009 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-19767417
16.
Tracking genetic variants in the biomedical literature using LitVar 2.0.
Nat Genet
; 55(6): 901-903, 2023 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-37268776
17.
dbVar structural variant cluster set for data analysis and variant comparison.
F1000Res
; 5: 673, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-28357035
18.
Study of translational control of eukaryotic gene expression using yeast.
Ann N Y Acad Sci
; 1038: 60-74, 2004 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-15838098
19.
Phenotype-Genotype Integrator (PheGenI): synthesizing genome-wide association study (GWAS) data with existing genomic resources.
Eur J Hum Genet
; 22(1): 144-7, 2014 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-23695286
20.
Analysis and reconstitution of translation initiation in vitro.
Methods Enzymol
; 351: 221-47, 2002.
Artigo
Inglês
| MEDLINE | ID: mdl-12073347