Cargando…

Association between PTCH1 and RAD54B Single-Nucleotide Polymorphisms and Non-syndromic Orofacial Clefts in the Northeast Population of Iran

BACKGROUND: Non-Syndromic Cleft Lip with or without cleft Palate (NSCL/P) is a common developmental disorder of the head and neck with a multifactorial etiology. The current study aimed to evaluate the potential association of PTCH1 (rs10512248) and RAD54B (rs12681366) polymorphisms with NSCL/P in t...

Descripción completa

Detalles Bibliográficos
Autores principales:	Morvaridi Farimani, Reza, Azimi-Nezhad, Mohsen, KhorramKhorshid, Hamid Reza, Ebadifar, Asghar, Tohidkhah, Saba, Jafarian, Zahra, Kamali, Koorosh, Nazari, Zeinab, Ebrahimzadeh-Vesal, Reza
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Avicenna Research Institute 2022
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706251/ https://www.ncbi.nlm.nih.gov/pubmed/36504563

Ejemplares similares

Parental cigarette smoking, transforming growth factor-alpha gene variant and the risk of orofacial cleft in Iranian infants
por: Ebadifar, Asghar, et al.
Publicado: (2016)

Maternal Supplementary Folate Intake, Methylenetetrahydrofolate Reductase (MTHFR) C677T and A1298C Polymorphisms and the Risk of Orofacial Cleft in Iranian Children
por: Ebadifar, Asghar, et al.
Publicado: (2015)

Evaluating the role of maternal folic acid supplementation in modifying the effects of methylenetetrahydrofolate reductase (C677T and A1298C) gene polymorphisms in oral cleft children
por: Ebadifar, Asghar, et al.
Publicado: (2016)

Interaction Effect of RsaI and BamHI Polymorphisms of TGFα, BMP2 and BMP4 on the Occurrence of Non-Syndromic Cleft Lip and Palate in Iranian Patients
por: Samadi, Saba, et al.
Publicado: (2018)

Association of MMP2 and MMP9 gene polymorphisms with nonsyndromic cleft lip/palate in an Iranian population
por: Zahedipour, Fatemeh, et al.
Publicado: (2023)

The study of association between reduced folate carrier 1 (RFC1) polymorphism and non-syndromic cleft lip/palate in Iranian population
por: Soghani, Behnoosh, et al.
Publicado: (2017)

Association of the WNT3 Variations and the Risk of Non-Syndromic Cleft Lip and Palate in a Population of Iranian Infants
por: Farrokhi Karibozorg, Homa, et al.
Publicado: (2018)

Effect of Bioinductive Cavity Liners on Shear Bond Strength of Dental Composite to Dentin
por: Tohidkhah, Saba, et al.
Publicado: (2022)

Evaluation of One- and Two-Step Impression Techniques and Vertical Marginal Misfit in Fixed Prothesis
por: Radfar, Sina, et al.
Publicado: (2023)

Association of Transforming Growth Factor Alpha Polymorphisms with Nonsyndromic Cleft Lip and Palate in Iranian Population
por: Ebadifar, Asghar, et al.
Publicado: (2015)

Identification of a novel nonsense mutation in kyphoscoliosis peptidase gene in an Iranian patient with myofibrillar myopathy
por: Ebrahimzadeh-Vesal, Reza, et al.
Publicado: (2018)

Neuroprotective Effects of Herbal Extract (Rosa canina, Tanacetum vulgare and Urtica dioica) on Rat Model of Sporadic Alzheimer’s Disease
por: Daneshmand, Parvaneh, et al.
Publicado: (2016)

Effects of Ectoine on Behavior and Candidate Genes Expression in ICV-STZ Rat Model of Sporadic Alzheimer’s Disease
por: Bazazzadegan, Niloofar, et al.
Publicado: (2017)

Lack of Association between Tumor Necrosis Factor-alpha -308 G/A Polymorphism and Risk of Developing Late-Onset Alzheimer's Disease in an Iranian Population
por: Manoochehri, Mehdi, et al.
Publicado: (2009)

Ccr2-64i and Ccr5 Δ32 Polymorphisms in Patients with Late-Onset Alzheimer’s disease; A Study from Iran (Ccr2-64i And Ccr5 Δ32 Polymorphisms in Alzheimer’s disease)
por: Khorram Khorshid, Hamid Reza, et al.
Publicado: (2012)

Vitamin D Receptor (VDR) Polymorphisms and Late-Onset Alzheimer’s Disease: An Association Study
por: Khorram Khorshid, Hamid Reza, et al.
Publicado: (2013)

Mutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification
por: Ashtari, Fereshteh, et al.
Publicado: (2013)

Arylamine N-acetyltransferase 2 Polymorphisms and the Risk of Endometriosis
por: Fayez, Diman, et al.
Publicado: (2018)

Association study of Glutathione S-Transferase polymorphisms and risk of endometriosis in an Iranian population
por: Hassani, Mina, et al.
Publicado: (2016)

Incidence Assessment of MTHFR C677T and A1298C Polymorphisms in Iranian Non-syndromic Cleft Lip and/or Palate Patients
por: Ebadifar, Asghar, et al.
Publicado: (2015)

Association of rs2013162 and rs2235375 Polymorphisms in IRF6 Gene with Susceptibility to Non-Syndromic Cleft Lip and Palate
por: Soleymani, Masoumeh, et al.
Publicado: (2022)

Effects of Herbal Compound (IMOD) on Behavior and Expression of Alzheimer's Disease Related Genes in Streptozotocin-Rat Model of Sporadic Alzheimer’s Disease
por: Bazazzadegan, Niloofar, et al.
Publicado: (2017)

The Effects of Melilotus officinalis Extract on Expression of Daxx, Nfkb and Vegf Genes in the Streptozotocin-Induced Rat Model of Sporadic Alzheimer’s Disease
por: Bazazzadegan, Niloofar, et al.
Publicado: (2017)

An Association Study on IL16 Gene Polymorphisms with the Risk of Sporadic Alzheimer's Disease
por: Khoshbakht, Tayyebeh, et al.
Publicado: (2015)

Treatment for Severe Class II Open Bite Using a Bonded Hyrax Expander, IZC Mini-Implants, and MEAW Technique in an Adolescent Patient
por: Farahani, Mohammad, et al.
Publicado: (2023)

Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's Disease
por: Mehrjoo, Zohreh, et al.
Publicado: (2015)

Association of CALHM1 Gene Polymorphism with Late Onset Alzheimer's Disease in Iranian Population
por: Aqdam, Meysam Jafari, et al.
Publicado: (2010)

The effect of Setarud (IMOD(TM)) on angiogenesis in transplanted human ovarian tissue to nude mice
por: Hormozi, Maryam, et al.
Publicado: (2015)

Methodological errors in screening of Yq microdeletion in Iranian azoospermic men
por: Saliminejad, Kioomars, et al.
Publicado: (2012)

Discrepancy in the results of Y chromosome microdeletions in an Iranian population
por: Saliminejad, Kioomars, et al.
Publicado: (2011)

Do we need a replacement medication for influenza with good efficacy?
por: Arastoo, Mahmoud, et al.
Publicado: (2014)

Fetal Sex Determination using Non-Invasive Method of Cell-free Fetal DNA in Maternal Plasma of Pregnant Women During 6(th)– 10(th) Weeks of Gestation
por: Zargari, Maryam, et al.
Publicado: (2011)

Factors affecting average grain size changes in rivers of a catchment area (Ardak catchment area, northeast Iran)
por: Javanbakht, Mohammad, et al.
Publicado: (2022)

Identification of rare PTCH1 nonsense variant causing orofacial cleft in a Chinese family and an up-to-date genotype-phenotype analysis
por: Zhong, Wenjie, et al.
Publicado: (2020)

Molecular analysis of a consanguineous Iranian polycystic kidney disease family identifies a PKD2 mutation that aids diagnostics
por: Vazifehmand, Reza, et al.
Publicado: (2013)

Screening PAX9, MSX1 and WNT10A Mutations in 4 Iranian Families with Non-Syndromic Tooth Agenesis
por: Safari, Shiva, et al.
Publicado: (2020)

Combination of IMOD™ and Arbidol to increase their immunomodulatory effects as a novel medicine to prevent and cure influenza and some other infectious diseases
por: Arastoo, Mahmoud, et al.
Publicado: (2014)

Electrophysiology of Human Gametes: A Systematic Review
por: Darbandi, Sara, et al.
Publicado: (2022)

Prevalence of intratubular germ cell neoplasia in cryptorchid testes of infertile men
por: Pourkeramati, Fatemeh, et al.
Publicado: (2013)

Association of Vascular Endothelial Growth Factor (VEGF) +405 G>C Polymorphism with Endometriosis in an Iranian Population
por: Memariani, Toktam, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_c6ni9s4lenii6rjm50qgr7l5ku