42 related articles for article (PubMed ID: 18362318)
1. A novel DLX3 mutation causes tricho-dento-osseous syndrome with abnormal enamel structure and formation.
Quan J; Liu Y; Ji L; Zhao Y; Zheng S
Arch Oral Biol; 2024 Jan; 157():105849. PubMed ID: 38006713
[TBL] [Abstract][Full Text] [Related]
2. DLX3-Dependent Regulation of Ion Transporters and Carbonic Anhydrases is Crucial for Enamel Mineralization.
Duverger O; Ohara T; Bible PW; Zah A; Morasso MI
J Bone Miner Res; 2017 Mar; 32(3):641-653. PubMed ID: 27760456
[TBL] [Abstract][Full Text] [Related]
3. Inherited defects in tooth structure.
Witkop CJ; Rao S
Birth Defects Orig Artic Ser; 1971 Jun; 7(7):153-84. PubMed ID: 4375507
[No Abstract] [Full Text] [Related]
4. Woolly hair in tricho-dento-osseous syndrome.
Perandones-González H; Rusiñol-Batlle L; Bosquez D; Brunet-Llobet L; Ivars M; Yubero D; Sarig O; Malki L; Peled A; Sprecher E; Baselga E
Pediatr Dermatol; 2023; 40(6):1094-1096. PubMed ID: 36973173
[TBL] [Abstract][Full Text] [Related]
5. Ophthalmic Manifestations of Heimler Syndrome in Two Siblings With
Miranda V; Cortez L; Rosmaninho-Salgado J; Ramos F; Paiva C
J Pediatr Ophthalmol Strabismus; 2024; 61(1):59-66. PubMed ID: 37092661
[TBL] [Abstract][Full Text] [Related]
6. Non-syndromic generalised hypotaurodontism in a case of Stage III Grade C periodontitis.
Sethuraman P; Baliah J; Reddy JRC; Umar M
BMJ Case Rep; 2023 Apr; 16(4):. PubMed ID: 37116957
[TBL] [Abstract][Full Text] [Related]
7. [Analysis of phenotype and pathogenic variant in a case of Heimler syndrome].
Zuo B; Wang LL; Mao L; Xu GE; Sun SP; Lu W
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2024 Mar; 59(3):249-252. PubMed ID: 38561264
[TBL] [Abstract][Full Text] [Related]
8. Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho-dento-osseous syndrome.
Whitehouse LLE; Smith CEL; Poulter JA; Brown CJ; Patel A; Lamb T; Brown LR; O'Sullivan EA; Mitchell RE; Berry IR; Charlton R; Inglehearn CF; Mighell AJ
Oral Dis; 2019 Jan; 25(1):182-191. PubMed ID: 30095208
[TBL] [Abstract][Full Text] [Related]
9. Craniofacial syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis.
Faria-Teixeira MC; Tordera C; Salvado E Silva F; Vaz-Carneiro A; Iglesias-Linares A
Pediatr Res; 2024 May; 95(6):1455-1475. PubMed ID: 38347173
[TBL] [Abstract][Full Text] [Related]
10. BMP Signaling Pathway in Dentin Development and Diseases.
Liu M; Goldman G; MacDougall M; Chen S
Cells; 2022 Jul; 11(14):. PubMed ID: 35883659
[TBL] [Abstract][Full Text] [Related]
11. Novel
Lee Y; Zhang H; Seymen F; Kim YJ; Kasimoglu Y; Koruyucu M; Simmer JP; Hu JC; Kim JW
J Pers Med; 2022 Jan; 12(2):. PubMed ID: 35207639
[TBL] [Abstract][Full Text] [Related]
12. Amelogenesis Imperfecta; Genes, Proteins, and Pathways.
Smith CEL; Poulter JA; Antanaviciute A; Kirkham J; Brookes SJ; Inglehearn CF; Mighell AJ
Front Physiol; 2017; 8():435. PubMed ID: 28694781
[TBL] [Abstract][Full Text] [Related]
13. DLX3 interacts with GCM1 and inhibits its transactivation-stimulating activity in a homeodomain-dependent manner in human trophoblast-derived cells.
Li S; Roberson MS
Sci Rep; 2017 May; 7(1):2009. PubMed ID: 28515447
[TBL] [Abstract][Full Text] [Related]
14. Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.
Zhao N; Han D; Liu H; Li Y; Wong SW; Cao Z; Xu J; Zhang X; Cai T; Wang Y; Feng H
Sci Rep; 2016 Dec; 6():38680. PubMed ID: 27924851
[TBL] [Abstract][Full Text] [Related]
15. Tricho-dento-osseous syndrome: diagnosis and dental management.
Al-Batayneh OB
Int J Dent; 2012; 2012():514692. PubMed ID: 22969805
[TBL] [Abstract][Full Text] [Related]
16. Neural crest deletion of Dlx3 leads to major dentin defects through down-regulation of Dspp.
Duverger O; Zah A; Isaac J; Sun HW; Bartels AK; Lian JB; Berdal A; Hwang J; Morasso MI
J Biol Chem; 2012 Apr; 287(15):12230-40. PubMed ID: 22351765
[TBL] [Abstract][Full Text] [Related]
17. New roles and mechanism of action of BMP4 in postnatal tooth cytodifferentiation.
Gluhak-Heinrich J; Guo D; Yang W; Harris MA; Lichtler A; Kream B; Zhang J; Feng JQ; Smith LC; Dechow P; Harris SE
Bone; 2010 Jun; 46(6):1533-45. PubMed ID: 20206312
[TBL] [Abstract][Full Text] [Related]
18. DLX3 mutation in a new family and its phenotypic variations.
Lee SK; Lee ZH; Lee SJ; Ahn BD; Kim YJ; Lee SH; Kim JW
J Dent Res; 2008 Apr; 87(4):354-7. PubMed ID: 18362318
[TBL] [Abstract][Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]