Results 91 to 100 of about 10,438 (212)

Familial aggregation of maxillary lateral incisor agenesis [PDF]

open access: yes, 2010
In spite of recent developments, data regarding the genes responsible for the less severe forms of hypodontia are still scarce and controversial. This study addressed the hypothesis that agenesis of maxillary lateral incisors (MLIA) is a distinct type of
A. Sousa   +10 more
core   +1 more source

The effect of tooth agenesis on dentofacial structures [PDF]

open access: yesThe European Journal of Orthodontics, 1997
The purpose of this study was to investigate the effect of tooth agenesis on dentofacial structures according to the location of the absent teeth. A total of 74 subjects were classified to three main groups and four subgroups according to the location of the absent teeth. Thirteen subjects without tooth agenesis were selected as the control group.
Ucem, Tuba, Yuksel, S
openaire   +3 more sources

The Homeobox Genes: Classification, Regulation, Biological Functions, and Diseases

open access: yesMedComm, Volume 7, Issue 4, April 2026.
Overview of the homeobox gene superfamily and its pathophysiological roles. The homeobox superfamily comprises several major classes, including ANTP, PRD, TALE, LIM, POU, and others. Among these, the HOX clusters (A–D) play critical roles in embryonic development specifically in conferring cellular identity, regulating morphogenesis, and guiding axial ...
Maedeh Dadzadi   +5 more
wiley   +1 more source

Detection of the Heterozygous Recurrent MAX p.(Arg60Gln) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly–Macrocephaly Syndrome

open access: yesClinical Genetics, Volume 109, Issue 4, Page 788-795, April 2026.
We identified a recurrent heterozygous MAX c.179G>A:p.Arg60Gln variant in two unrelated females affected with the emerging phenotypes of MAX‐associated polydactyly‐macrocephaly syndrome. We propose that genitourinary abnormalities, including Mayer–Rokitanski–Kuster–Hauser syndrome in one individual, are an expansion of the known phenotypes associated ...
Iftekhar A. Showpnil   +9 more
wiley   +1 more source

Delayed Dental Development in Children With Non‐Syndromic Hypodontia: A Cross‐Sectional Study Using a Machine Learning Approach to Dental Age Estimation

open access: yesOrthodontics &Craniofacial Research, Volume 29, Issue 2, Page 347-356, April 2026.
ABSTRACT Objectives To investigate the influence of non‐syndromic hypodontia on radiographic dental development and to estimate dental age in children with bilateral mandibular agenesis using a machine learning approach. Materials and Methods This retrospective cross‐sectional study included 626 children aged 6–15 years (311 with dental agenesis, 315 ...
Marine Crosnier   +3 more
wiley   +1 more source

An implant periapical lesion associated with presence of residual root fragments: Report of case treated with apicoectomy [PDF]

open access: yes, 2018
Indexación: Scopus.Chemicals and CAS Registry Numbers: azithromycin, 83905-01-5, 117772-70-0, 121470-24-4; chlorhexidine, 3697-42-5, 55-56-1; erythromycin, 114-07-8, 70536-18-4The present study reports a case of a periapical lesion in an implant placed ...
Alves, N., Honorato, L., Trillos, V.
core   +1 more source

Application of Artificial Intelligence in Detecting Dental Anomalies: Current Models, Imaging Modalities, and Future Directions

open access: yesHealth Science Reports, Volume 9, Issue 3, March 2026.
ABSTRACT Background and Aim As dental anomalies can significantly affect esthetic and function, early detection and diagnosis are crucial for treatment and minimizing potential negative effects. Artificial intelligence (AI) has emerged as a promising tool for the segmentation and detection of dental anomalies in number, morphology, size, position, and ...
Mobina Sadat Zarabadi   +4 more
wiley   +1 more source

Agenesia dos incisivos laterais superiores: prevalência, diagnóstico e tratamento [PDF]

open access: yes, 2017
A agenesia dentária é uma das anomalias mais comuns da dentição humana, afectando 20% da população mundial, já a agenesia dos incisivos laterais superiores afecta 2% conforme a população estudada.
Moreira, Fernanda Alves
core  

Kdf1 Regulates Molar Cusp Morphogenesis via the PI3K/AKT/mTOR Signalling Axis

open access: yesCell Proliferation, Volume 59, Issue 3, March 2026.
Epithelial Kdf1 knockout disrupts molar cusp morphogenesis by promoting inner enamel epithelium proliferation and invagination via PI3K/AKT/mTOR signalling. ABSTRACT Keratinocyte differentiation factor 1 (Kdf1) reportedly plays a significant role in enamel formation.
Jiayu Wang   +9 more
wiley   +1 more source

Novel frameshift variant of WNT10A in a Japanese patient with hypodontia

open access: yesHuman Genome Variation
Congenital tooth agenesis is caused by the impairment of crucial genes related to tooth development, such as Wnt signaling pathway genes. Here, we investigated the genetic causes of sporadic congenital tooth agenesis. Exome sequencing, followed by Sanger
Michiyo Ando   +11 more
doaj   +1 more source

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