[HTML][HTML] Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis
L Slavec, N Karas Kuželički, I Locatelli, K Geršak - Scientific Reports, 2022 - nature.com
To date, the involvement of various genetic markers in the aetiopathogenesis of non-
syndromic orofacial cleft (nsOFC) has been extensively studied. In the present study, we …
syndromic orofacial cleft (nsOFC) has been extensively studied. In the present study, we …
The genetic factors contributing to the risk of cleft lip-cleft palate and their clinical utility
S Askarian, M Gholami, G Khalili-Tanha… - Oral and Maxillofacial …, 2023 - Springer
Cleft lip and cleft palate (CL/P) are among the most common congenital malformations in
neonates and have syndromic or nonsyndromic forms. Nonsyndromic forms of malformation …
neonates and have syndromic or nonsyndromic forms. Nonsyndromic forms of malformation …
Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non‐syndromic tooth agenesis
A Mostowska, B Biedziak, M Zadurska… - Clinical …, 2013 - Wiley Online Library
Tooth agenesis is one of the most common dental anomalies, with a complex and not yet
fully elucidated aetiology. Given the crucial role of the Wnt signalling pathway during tooth …
fully elucidated aetiology. Given the crucial role of the Wnt signalling pathway during tooth …
Association studies and direct DNA sequencing implicate genetic susceptibility loci in the etiology of nonsyndromic orofacial clefts in sub-Saharan African populations
LJJ Gowans, WL Adeyemo, M Eshete… - Journal of dental …, 2016 - journals.sagepub.com
Orofacial clefts (OFCs) are congenital dysmorphologies of the human face and oral cavity,
with a global incidence of 1 per 700 live births. These anomalies exhibit a multifactorial …
with a global incidence of 1 per 700 live births. These anomalies exhibit a multifactorial …
A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population
Purpose The aim of this study was to use the TaqMan OpenArray system to evaluate
associations between 39 genes and the etiology of nonsyndromic cleft lip and palate …
associations between 39 genes and the etiology of nonsyndromic cleft lip and palate …
Analysis of PRICKLE 1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations
Palate development is shaped by multiple molecular signaling pathways, including the Wnt
pathway. In mice and humans, mutations in both the canonical and noncanonical arms of …
pathway. In mice and humans, mutations in both the canonical and noncanonical arms of …
Association of WNT pathway genes with nonsyndromic cleft lip with or without cleft palate
V Vijayan, R Ummer, R Weber… - The Cleft Palate …, 2018 - journals.sagepub.com
Objective: Nonsyndromic cleft lip with or without cleft palate (NSCL±P) is a common
craniofacial anomaly with multifactorial etiology. Evidence suggests that variations in WNT …
craniofacial anomaly with multifactorial etiology. Evidence suggests that variations in WNT …
[HTML][HTML] Clinical relevance of breast and gastric cancer-associated polymorphisms as potential susceptibility markers for oral clefts in the Brazilian population
RA Machado, EM de Freitas, SN de Aquino… - BMC Medical …, 2017 - Springer
Background Epidemiological studies have indicated a higher incidence of breast and gastric
cancer in patients with nonsyndromic cleft lip with or without cleft palate (NSCL±P) and their …
cancer in patients with nonsyndromic cleft lip with or without cleft palate (NSCL±P) and their …
[HTML][HTML] Association of single nucleotide polymorphisms in AXIN2, BMP4, and IRF6 with Non-Syndromic Cleft Lip with or without Cleft Palate in a sample of the …
Non-syndromic cleft lip with or without palate (NSCL/P) is a common congenital
malformation worldwide, with complex etiology. It has been proposed that interaction of …
malformation worldwide, with complex etiology. It has been proposed that interaction of …
Genetic polymorphisms in APC, DVL2, and AXIN1 are associated with susceptibility, advanced TNM stage or tumor location in colorectal cancer
MA Rosales-Reynoso… - The Tohoku journal of …, 2019 - jstage.jst.go.jp
Colorectal cancer (CRC) is the third most common cancer and the second leading cause of
death worldwide. The named “destruction complex” has a critical function in the Wnt/β …
death worldwide. The named “destruction complex” has a critical function in the Wnt/β …