Associated Papers
Genetic associations and parent-of-origin effects of PVRL1 in non-syndromic cleft lip with or without cleft palate across multiple ethnic populations.
Park JW et al.
Epidemiology and Health, 2024
MicroRNA-655-3p and microRNA-497-5p inhibit cell proliferation in cultured human lip cells through the regulation of genes related to human cleft lip.
Gajera M et al.
Bmc Medical Genomics, 2019
31122291 (PubMed )
Supplement: 12920_2019_535_MOESM1_ESM.zip › 3_Human_Cleft_Lip__Table_S3__Significant_R2.xlsx › Single_Gene_Significant
Identification of Novel Variants in the PVRL1 Gene in Patients With Nonsyndromic Cleft Lip With or Without Cleft Palate.
Oner DA et al.
Genetic Testing and Molecular Biomarkers, 2016
Mutation analysis of PVRL1 in patients with non-syndromic cleft of the lip and/or palate in Guangdong.
Shu SY et al.
Genetics and Molecular Research : Gmr, 2015
Novel insertion mutation in the PVRL1 gene in Turkish patients with non-syndromic cleft lip with/without cleft palate.
Aşlar D et al.
Archives of Oral Biology, 2014
PVRL1 as a candidate gene for nonsyndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in southern Han Chinese patients.
Cheng HQ et al.
Dna and Cell Biology, 2012
Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate.
Tongkobpetch S et al.
International Journal of Oral and Maxillofacial Surgery, 2008
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