Associated Papers
PHF8/KDM7B: A Versatile Histone Demethylase and Epigenetic Modifier in Nervous System Disease and Cancers.
Fan T et al.
Epigenomes, 2024
Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology.
Sobering AK et al.
Hgg Advances, 2022
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
A functional link between the histone demethylase PHF8 and the transcription factor ZNF711 in X-linked mental retardation.
Kleine-Kohlbrecher D et al.
Molecular Cell, 2010
Structural insights into a novel histone demethylase PHF8.
Yu L et al.
Cell Research, 2010
A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate.
Abidi F et al.
Clinical Genetics, 2007
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