Detalhe da pesquisa
1.
Characterization and mitigation of artifacts derived from NGS library preparation due to structure-specific sequences in the human genome.
BMC Genomics
; 25(1): 227, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38429743
2.
OncoPubMiner: a platform for mining oncology publications.
Brief Bioinform
; 23(5)2022 09 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36058206
3.
Astragaloside IV targeting autophagy of T cells improves inflammation of asthma.
J Asian Nat Prod Res
; 26(6): 699-713, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38213072
4.
Atp6v1h Deficiency Blocks Bone Loss in Simulated Microgravity Mice through the Fos-Jun-Src-Integrin Pathway.
Int J Mol Sci
; 25(1)2024 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38203808
5.
Comprehensive fundamental somatic variant calling and quality management strategies for human cancer genomes.
Brief Bioinform
; 22(3)2021 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32510555
6.
Comprehensive review and evaluation of computational methods for identifying FLT3-internal tandem duplication in acute myeloid leukaemia.
Brief Bioinform
; 22(5)2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33851200
7.
MSIsensor-ct: microsatellite instability detection using cfDNA sequencing data.
Brief Bioinform
; 22(5)2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33461213
8.
Genotype-phenotype analysis of selective failure of tooth eruption-A systematic review.
Clin Genet
; 104(3): 287-297, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37448157
9.
Molecular-based phenotype variations in amelogenesis imperfecta.
Oral Dis
; 29(6): 2334-2365, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37154292
10.
Hereditary dentin defects with systemic diseases.
Oral Dis
; 29(6): 2376-2393, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37094075
11.
MSX1 involved selective tooth agenesis and abnormal labial frenum, pedigree, and retrospective study.
Oral Dis
; 29(8): 3168-3172, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36478500
12.
A unified DNA- and RNA-based NGS strategy for the analysis of multiple types of variants at the dual nucleic acid level in solid tumors.
J Clin Lab Anal
; 37(19-20): e24977, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37877443
13.
Molecular Mechanisms of Craniofacial and Dental Abnormalities in Osteopetrosis.
Int J Mol Sci
; 24(12)2023 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37373559
14.
Potential Theranostic Roles of SLC4 Molecules in Human Diseases.
Int J Mol Sci
; 24(20)2023 Oct 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37894847
15.
[Research progress on structure, function and disease correlation of solute carrier family 4].
Sheng Li Xue Bao
; 75(1): 137-150, 2023 Feb 25.
Artigo
em Zh
| MEDLINE | ID: mdl-36859843
16.
ATP6V1H deficiency impairs glucose tolerance by augmenting endoplasmic reticulum stress in high fat diet fed mice.
Arch Biochem Biophys
; 716: 109116, 2022 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34990584
17.
K205R specific nanobody-horseradish peroxidase fusions as reagents of competitive ELISA to detect African swine fever virus serum antibodies.
BMC Vet Res
; 18(1): 321, 2022 Aug 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35987654
18.
HotSpot3D web server: an integrated resource for mutation analysis in protein 3D structures.
Bioinformatics
; 36(12): 3944-3946, 2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32315389
19.
CircRNA pappalysin 1 facilitates prostate cancer development through miR-515-5p/FKBP1A axis.
Andrologia
; 53(11): e14227, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34469009
20.
ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13.
PLoS Genet
; 13(2): e1006481, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28158191