Detalhe da pesquisa
1.
Apolipoprotein E is an effective biomarker for orthodontic tooth movement in patients treated with transmission straight wire appliances.
Am J Orthod Dentofacial Orthop
; 161(2): 255-262.e1, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34756485
2.
Thymomatous myasthenia gravis: 10-year experience of a single center.
Acta Neurol Scand
; 143(1): 96-102, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32762063
3.
AChRAb and MuSKAb double-seropositive myasthenia gravis: a distinct subtype?
Neurol Sci
; 42(3): 863-869, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33438140
4.
A novel IRF6 mutation causing non-syndromic cleft lip with or without cleft palate in a pedigree.
Mutagenesis
; 33(3): 195-202, 2018 09 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-30053123
5.
A novel PTCH1 mutation underlies nonsyndromic cleft lip and/or palate in a Han Chinese family.
Oral Dis
; 24(7): 1318-1325, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29908092
6.
Nonsurgical correction using miniscrew-assisted vertical control of a severe high angle with mandibular retrusion and gummy smile in an adult.
Am J Orthod Dentofacial Orthop
; 151(5): 978-988, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28457276
7.
Miniscrew-assisted customized lingual appliances for predictable treatment of skeletal Class II malocclusion with severe deep overbite and overjet.
Am J Orthod Dentofacial Orthop
; 152(1): 104-115, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28651755
8.
Exosome analysis: a promising biomarker system with special attention to saliva.
J Membr Biol
; 247(11): 1129-36, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25135166
9.
Rare loss-of-function variants in FLNB cause non-syndromic orofacial clefts.
J Genet Genomics
; 51(2): 222-229, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37003352
10.
Quantitative evaluation of vertical control in orthodontic camouflage treatment for skeletal class II with hyperdivergent facial type.
Head Face Med
; 20(1): 31, 2024 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38745246
11.
Inclination of mandibular incisors and symphysis in severe skeletal class III malocclusion.
Head Face Med
; 19(1): 16, 2023 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37165461
12.
End-to-End Automatic Classification of Retinal Vessel Based on Generative Adversarial Networks with Improved U-Net.
Diagnostics (Basel)
; 13(6)2023 Mar 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36980456
13.
Magnetic bead-based salivary peptidome profiling analysis during orthodontic treatment durations.
Biochem Biophys Res Commun
; 421(4): 844-9, 2012 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22554512
14.
Magnetic bead-based salivary peptidome profiling for periodontal-orthodontic treatment.
Proteome Sci
; 10(1): 63, 2012 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23126675
15.
The role of genotype and diet in shaping gut microbiome in a genetic vitamin A deficient mouse model.
J Genet Genomics
; 49(2): 155-164, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34537414
16.
Impacts of Delivery Mode and Maternal Factors on Neonatal Oral Microbiota.
Front Microbiol
; 13: 915423, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35832807
17.
A Novel PAX3 Variant in a Chinese Pedigree with Nonsyndromic Cleft Lip With or Without Palate.
Genet Test Mol Biomarkers
; 25(12): 749-756, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34918979
18.
Functional identification of a rare vascular endothelial growth factor a (VEGFA) variant associating with the nonsyndromic cleft lip with/without cleft palate.
Bioengineered
; 12(1): 1471-1483, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33947308
19.
A novel FZD6 mutation revealed the cause of cleft lip and/or palate in a Chinese family.
Genes Dis
; 7(3): 440-447, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32884998
20.
Functional Characterization of a Novel IRF6 Frameshift Mutation From a Van Der Woude Syndrome Family.
Front Genet
; 11: 562, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32582293