The association of gene polymorphisms in catechol-O'methyltransferase (COMT) and β2-adrenergic receptor (ADRB2) with temporomandibular joint disorders

Author:

Ekici Ömer,Arıkan Söylemez Evrim Suna

Publisher

Elsevier BV

Subject

Cell Biology,General Dentistry,General Medicine,Otorhinolaryngology

Reference34 articles.

1. Altered central sensitization and pain modulation in the CNS in chronic joint pain;Arendt-Nielsen;Current Osteoporosis Reports,2015

2. Pain modality- and sex-specific effects of COMT genetic functional variants;Belfer;Pain,2013

3. Polymorphisms in COMT, ADRB2 and HTR1A genes are associated with temporomandibular disorders in individuals with other arthralgias;Bonato;Cranio The Journal of Craniomandibular Practice,2021

4. Is catechol-O-methyltransferase gene associated with temporomandibular disorders? A systematic review and meta-analysis.;Brancher;International Journal of Paediatric Dentistry,2021

5. The association of genetic polymorphisms in serotonin transporter and catechol-O-methyltransferase on temporomandibular disorders and anxiety in adolescents;Brancher;Journal of Oral Rehabilitation,2019

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