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1.
Global overview on current paediatric dentistry teaching: A survey of National Member Societies of the IAPD.
Int J Paediatr Dent
; 34(1): 58-65, 2024 Jan.
Article
in English
| MEDLINE | ID: mdl-37330970
2.
An in vitro assessment of teething gels' effects on human gingival mesenchymal stem cells.
BMC Oral Health
; 24(1): 573, 2024 May 17.
Article
in English
| MEDLINE | ID: mdl-38760715
3.
Phenotypic variability in LAMA3-associated amelogenesis imperfecta.
Oral Dis
; 29(8): 3514-3524, 2023 Nov.
Article
in English
| MEDLINE | ID: mdl-36326426
4.
FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome.
Int Endod J
; 56(8): 943-954, 2023 Aug.
Article
in English
| MEDLINE | ID: mdl-37159186
5.
Cytotoxic effects of different detergent containing children's toothpastes on human gingival epithelial cells.
BMC Oral Health
; 22(1): 66, 2022 03 09.
Article
in English
| MEDLINE | ID: mdl-35264124
6.
Assessment of Dental Arch Parameters in Turkish Twins.
J Clin Pediatr Dent
; 46(2): 160-170, 2022 Mar 01.
Article
in English
| MEDLINE | ID: mdl-35533222
7.
Assessment of Dental Arch Parameters in Turkish Twins.
J Clin Pediatr Dent
; 45(5): 359-370, 2021 Nov 01.
Article
in English
| MEDLINE | ID: mdl-34740261
8.
Recessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis Imperfecta.
Am J Hum Genet
; 99(5): 1199-1205, 2016 Nov 03.
Article
in English
| MEDLINE | ID: mdl-27843125
9.
Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta.
Am J Hum Genet
; 99(4): 984-990, 2016 Oct 06.
Article
in English
| MEDLINE | ID: mdl-27693231
10.
Mutations in RELT cause autosomal recessive amelogenesis imperfecta.
Clin Genet
; 95(3): 375-383, 2019 03.
Article
in English
| MEDLINE | ID: mdl-30506946
11.
Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfecta.
Clin Oral Investig
; 23(3): 1481-1487, 2019 Mar.
Article
in English
| MEDLINE | ID: mdl-30120606
12.
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.
Hum Mol Genet
; 25(13): 2862-2872, 2016 07 01.
Article
in English
| MEDLINE | ID: mdl-27033726
13.
Novel homozygous KREMEN1 mutation causes ectodermal dysplasia.
Oral Dis
; 28(3): 843-845, 2022 04.
Article
in English
| MEDLINE | ID: mdl-34028942
14.
Novel FGF10 mutation in autosomal dominant aplasia of lacrimal and salivary glands.
Clin Oral Investig
; 21(1): 167-172, 2017 Jan.
Article
in English
| MEDLINE | ID: mdl-26955834
15.
Genetic influences on dental enamel that impact caries differ between the primary and permanent dentitions.
Eur J Oral Sci
; 123(5): 327-334, 2015 Oct.
Article
in English
| MEDLINE | ID: mdl-26283008
16.
Effect of fibroblast growth factor and enamel matrix derivative treatment on root resorption after delayed replantation.
Dent Traumatol
; 31(1): 49-56, 2015 Feb.
Article
in English
| MEDLINE | ID: mdl-25290558
17.
Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay.
BMC Med Genet
; 15: 81, 2014 Jul 15.
Article
in English
| MEDLINE | ID: mdl-25023176
18.
The WNT10A gene in ectodermal dysplasias and selective tooth agenesis.
Am J Med Genet A
; 164A(10): 2455-60, 2014 Oct.
Article
in English
| MEDLINE | ID: mdl-24700731
19.
Novel frameshift mutations in DSPP cause dentin dysplasia type II.
Oral Dis
; 25(8): 2044-2046, 2019 11.
Article
in English
| MEDLINE | ID: mdl-31454439
20.
Traumatic dental injuries in Turkish children, Istanbul.
Dent Traumatol
; 30(4): 280-4, 2014 Aug.
Article
in English
| MEDLINE | ID: mdl-24502762