Detalhe da pesquisa
1.
Molecular signaling and mechanisms of low-level laser-induced gene expression in cells involved in orthodontic tooth movement.
J Formos Med Assoc
; 123(4): 442-451, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-37805307
2.
Phenotypic variability in LAMA3-associated amelogenesis imperfecta.
Oral Dis
; 29(8): 3514-3524, 2023 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-36326426
3.
FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome.
Int Endod J
; 56(8): 943-954, 2023 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-37159186
4.
A genetic model for the secretory stage of dental enamel formation.
J Struct Biol
; 213(4): 107805, 2021 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34715329
5.
Transcriptome analysis of gingival tissues of enamel-renal syndrome.
J Periodontal Res
; 54(6): 653-661, 2019 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-31131889
6.
ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta.
Hum Mol Genet
; 23(8): 2157-63, 2014 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-24305999
7.
FAM20A mutations can cause enamel-renal syndrome (ERS).
PLoS Genet
; 9(2): e1003302, 2013.
Artigo
Inglês
| MEDLINE | ID: mdl-23468644
8.
Ameloblast transcriptome changes from secretory to maturation stages.
Connect Tissue Res
; 55 Suppl 1: 29-32, 2014 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-25158176
9.
Orthodontically induced changes to the genetic profile in periodontal ligament tissue and cytokine release in gingival crevicular fluid - A pilot investigation.
J Dent Sci
; 19(1): 387-396, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-38303827
10.
A novel ODAPH mutation causing amelogenesis imperfecta and its expression in human dental tissues.
J Dent Sci
; 19(1): 524-531, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-38303846
11.
Orodental malformations associated with human MSX1 sequence variants.
J Am Dent Assoc
; 155(6): 484-495.e21, 2024 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-38713117
12.
Craniofacial and olfactory sensory changes after long-term unilateral nasal obstruction-an animal study using MMP-3-LUC transgenic rats.
Sci Rep
; 14(1): 2616, 2024 01 31.
Artigo
Inglês
| MEDLINE | ID: mdl-38297007
13.
Secreted protein kinases?
Trends Biochem Sci
; 38(9): 424-5, 2013 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-23992947
14.
The implication of integrating pediatric education into a pediatric dentistry course for undergraduate dental students.
J Dent Sci
; 18(4): 1794-1803, 2023 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-37799870
15.
PAX9 mutations and genetic synergism in familial tooth agenesis.
Ann N Y Acad Sci
; 1524(1): 87-96, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37005710
16.
Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations.
Sci Rep
; 12(1): 16477, 2022 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36183038
17.
The Modified Shields Classification and 12 Families with Defined DSPP Mutations.
Genes (Basel)
; 13(5)2022 05 12.
Artigo
Inglês
| MEDLINE | ID: mdl-35627243
18.
Potential contribution of neural crest cells to dental enamel formation.
Biochem Biophys Res Commun
; 415(1): 114-9, 2011 Nov 11.
Artigo
Inglês
| MEDLINE | ID: mdl-22020075
19.
Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families.
Eur J Oral Sci
; 119 Suppl 1: 158-67, 2011 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-22243242
20.
Mouse Dspp frameshift model of human dentinogenesis imperfecta.
Sci Rep
; 11(1): 20653, 2021 10 19.
Artigo
Inglês
| MEDLINE | ID: mdl-34667213