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A novel ODAPH mutation causing amelogenesis imperfecta and its expression in human dental tissues.
J Dent Sci. 2024 Jan;19(1):524-531. doi: 10.1016/j.jds.2023.09.020. Epub 2023 Sep 28.
J Dent Sci. 2024.
PMID: 38303846
Free PMC article.
Effect of hydroalcoholic extract of whole pomegranate fruit on cariogenic bacteria and its clinical effect on dental plaque formation in 8-10-year-old children.
Mahd MA, Aref P, Emadi F, Javadi F, Kharazi Fard MJ, Tavassoli-Hojjati S.
Mahd MA, et al. Among authors: aref p.
Dent Res J (Isfahan). 2023 Nov 27;20:114. eCollection 2023.
Dent Res J (Isfahan). 2023.
PMID: 38169678
Free PMC article.
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Strategy of targeting the tumor microenvironment via inhibition of fibroblast/fibrosis remodeling new era to cancer chemo-immunotherapy resistance.
Tajaldini M, Poorkhani A, Amiriani T, Amiriani A, Javid H, Aref P, Ahmadi F, Sadani S, Khori V.
Tajaldini M, et al. Among authors: aref p.
Eur J Pharmacol. 2023 Oct 15;957:175991. doi: 10.1016/j.ejphar.2023.175991. Epub 2023 Aug 22.
Eur J Pharmacol. 2023.
PMID: 37619785
Review.
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Hereditary Autonomic Neuropathy of the Oral Cavity and its Management.
Esmaeilzadeh N, Ashrafi MR, Shojaaldini Ardakani H, Seraj B, Aref P.
Esmaeilzadeh N, et al. Among authors: aref p.
Iran J Child Neurol. 2022 Winter;16(1):135-142. doi: 10.22037/ijcn.v15i4.32016. Epub 2022 Jan 1.
Iran J Child Neurol. 2022.
PMID: 35222664
Free PMC article.
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FAM20A mutations associated with enamel renal syndrome.
Wang SK, Reid BM, Dugan SL, Roggenbuck JA, Read L, Aref P, Taheri AP, Yeganeh MZ, Simmer JP, Hu JC.
Wang SK, et al. Among authors: aref p.
J Dent Res. 2014 Jan;93(1):42-8. doi: 10.1177/0022034513512653. Epub 2013 Nov 6.
J Dent Res. 2014.
PMID: 24196488
Free PMC article.
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FAM20A mutations can cause enamel-renal syndrome (ERS).
Wang SK, Aref P, Hu Y, Milkovich RN, Simmer JP, El-Khateeb M, Daggag H, Baqain ZH, Hu JC.
Wang SK, et al. Among authors: aref p.
PLoS Genet. 2013;9(2):e1003302. doi: 10.1371/journal.pgen.1003302. Epub 2013 Feb 28.
PLoS Genet. 2013.
PMID: 23468644
Free PMC article.
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Abnormal dentition in a boy with incontinentia pigmenti: case report.
Afshar H, Daneshpazhooh M, Kiani A, Aref P, Baniameri Z.
Afshar H, et al. Among authors: aref p.
J Dent (Tehran). 2012 Summer;9(3):267-70. Epub 2012 Sep 30.
J Dent (Tehran). 2012.
PMID: 23119137
Free PMC article.
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Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta.
Parry DA, Mighell AJ, El-Sayed W, Shore RC, Jalili IK, Dollfus H, Bloch-Zupan A, Carlos R, Carr IM, Downey LM, Blain KM, Mansfield DC, Shahrabi M, Heidari M, Aref P, Abbasi M, Michaelides M, Moore AT, Kirkham J, Inglehearn CF.
Parry DA, et al. Among authors: aref p.
Am J Hum Genet. 2009 Feb;84(2):266-73. doi: 10.1016/j.ajhg.2009.01.009. Epub 2009 Feb 5.
Am J Hum Genet. 2009.
PMID: 19200525
Free PMC article.
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