Detalhe da pesquisa
1.
Tooth agenesis related to a novel KDF1 variant: A case report and literature review.
Oral Dis
; 2024 Mar 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38501196
2.
Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG.
Oral Dis
; 30(2): 537-550, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36650945
3.
In-depth investigation of FAM20A insufficiency effects on deciduous dental pulp cells: Altered behaviours, osteogenic differentiation, and inflammatory gene expression.
Int Endod J
; 57(6): 745-758, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38477421
4.
Novel CNNM4 variant and clinical features of Jalili syndrome.
Clin Genet
; 103(2): 256-257, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36354001
5.
PTEN regulates proliferation and osteogenesis of dental pulp cells and adipogenesis of human adipose-derived stem cells.
Oral Dis
; 29(2): 735-746, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34558757
6.
Dental characteristics of patients with four different types of skeletal dysplasias.
Clin Oral Investig
; 27(10): 5827-5839, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37548766
7.
Orodental health status of patients with inborn errors of immunity.
Int J Paediatr Dent
; 2023 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38062862
8.
Patterns of nonsyndromic tooth agenesis and sexual dimorphism.
BMC Oral Health
; 23(1): 37, 2023 01 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36691053
9.
Patterns of molar agenesis associated with p.P20L and p.R77Q variants in PAX9.
Eur J Oral Sci
; 130(2): e12855, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35182440
10.
Age-related dental phenotypes and tooth characteristics of FAM83H-associated hypocalcified amelogenesis imperfecta.
Oral Dis
; 28(3): 734-744, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33486840
11.
Tooth ultrastructure of a novel COL1A2 mutation expanding its genotypic and phenotypic spectra.
Oral Dis
; 27(5): 1257-1267, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32989910
12.
Human dental pulp stem cell responses to different dental pulp capping materials.
BMC Oral Health
; 21(1): 209, 2021 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33902558
13.
Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra.
Mol Genet Genomics
; 295(4): 923-931, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32246227
14.
Genotype-phenotype correlation and expansion of orodental anomalies in LTBP3-related disorders.
Mol Genet Genomics
; 294(3): 773-787, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-30887145
15.
Female-restricted syndromic intellectual disability in a patient from Thailand.
Am J Med Genet A
; 179(5): 758-761, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30828969
16.
Compromised alveolar bone cells in a patient with dentinogenesis imperfecta caused by DSPP mutation.
Clin Oral Investig
; 23(1): 303-313, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-29679229
17.
Cole-Carpenter syndrome in a patient from Thailand.
Am J Med Genet A
; 176(8): 1706-1710, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30063094
18.
Amelogenesis imperfecta: A novel FAM83H mutation and characteristics of periodontal ligament cells.
Oral Dis
; 24(8): 1522-1531, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29949226
19.
Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG.
Oral Dis
; 2023 Oct 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37794759
20.
R-spondins/Lgrs expression in tooth development.
Dev Dyn
; 243(6): 844-51, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24616052