Artificial Intelligence in Orthodontics: Critical Review
NF Nordblom, M Büttner… - Journal of Dental …, 2024 - journals.sagepub.com
With increasing digitalization in orthodontics, certain orthodontic manufacturing processes
such as the fabrication of indirect bonding trays, aligner production, or wire bending can be …
such as the fabrication of indirect bonding trays, aligner production, or wire bending can be …
The association of gene polymorphisms in catechol-O'methyltransferase (COMT) and β2-adrenergic receptor (ADRB2) with temporomandibular joint disorders
Ö Ekici, ESA Söylemez - Archives of Oral Biology, 2024 - Elsevier
Objective Temporomandibular disorder (TMD) has a multifactorial etiology that includes
environmental, psychological, and genetic factors. This study aimed to evaluate the possible …
environmental, psychological, and genetic factors. This study aimed to evaluate the possible …
[HTML][HTML] Temporomandibular disorder in construction workers associated with ANKK1 and DRD2 genes
SSP Baratto, MN Meger, V Camargo… - Brazilian Dental …, 2022 - SciELO Brasil
The study aimed to explore the influence of genetic polymorphisms in ANKK1 and DRD2 on
the signs and symptoms of temporomandibular disorder (TMD) in construction workers. This …
the signs and symptoms of temporomandibular disorder (TMD) in construction workers. This …
Is there an association of genetic polymorphisms of the catechol-O-methyltransferase gene (rs165656 and rs174675) and the 5-hydroxytryptamine receptor 2A gene …
J Duarte, P Pauletto, H Polmann, JC Réus… - Archives of Oral …, 2022 - Elsevier
Objective To evaluate the association of single-nucleotide polymorphisms within the
catechol-O-methyltransferase and 5-hydroxytryptamine receptor 2A genes with sleep …
catechol-O-methyltransferase and 5-hydroxytryptamine receptor 2A genes with sleep …
Associations between anxiety, depression, chronic pain and oral health-related quality of life, happiness, and polymorphisms in adolescents' genes
ALP Baldiotti, G Amaral-Freitas, MCF Barbosa… - International journal of …, 2023 - mdpi.com
Adolescence is marked by changes and vulnerability to the emergence of psychological
problems. This study aimed to investigate associations between anxiety/depression/chronic …
problems. This study aimed to investigate associations between anxiety/depression/chronic …
Genetic variation in catechol‐O‐methyltransferase is associated with individual differences in conditioned pain modulation in healthy subjects
OA Korczeniewska, F Kuo, CY Huang… - The journal of gene …, 2021 - Wiley Online Library
Background Genetic variation in the catechol‐O‐methyltransferase (COMT) gene is
associated with sensitivity to both acute experimental pain and chronic pain conditions. Four …
associated with sensitivity to both acute experimental pain and chronic pain conditions. Four …
Polymorphisms in the HTR2A and HTR3A Genes Contribute to Pain in TMD Myalgia
S Louca Jounger, N Christidis… - Frontiers in Oral …, 2021 - frontiersin.org
Background: The aim of this study was to investigate if single nucleotide polymorphisms
(SNPs) related to monoaminergic neurotransmission, in particular the serotonergic pathway …
(SNPs) related to monoaminergic neurotransmission, in particular the serotonergic pathway …
[HTML][HTML] Associations Between Temporomandibular Disorders and Brain Imaging-Derived Phenotypes
J Lin, DY Cao - International Dental Journal, 2024 - Elsevier
Objective Temporomandibular disorders (TMD) affect the temporomandibular joint and
associated structures. Despite its prevalence and impact on quality of life, the underlying …
associated structures. Despite its prevalence and impact on quality of life, the underlying …
A computational data mining strategy to identify the common genetic markers of temporomandibular joint disorders and osteoarthritis
VP Jayaseelan, P Arumugam - Global Medical Genetics, 2022 - thieme-connect.com
Statement of Problem Prosthodontic planning in patients with temporomandibular joint
disorders (TMDs) is a challenge for the clinicians. Purpose A differential biomarker …
disorders (TMDs) is a challenge for the clinicians. Purpose A differential biomarker …
The polymorphism Val158Met in the COMT gene: disrupted dopamine system in fibromyalgia patients?
MC Gerra, C Dallabona, M Manfredini, R Giordano… - Pain, 2022 - journals.lww.com
The single-nucleotide polymorphism (SNP) rs4680 in the catechol-O-methyltransferase
gene (COMT) is a missense variant (Val158Met) associated with altered activity of the COMT …
gene (COMT) is a missense variant (Val158Met) associated with altered activity of the COMT …