共 186 条
[1]
Lower KM(2002)Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome Nature Genetics 32 661-665
[2]
Turner G(2004)A novel PHF6 mutation results in enhanced exon skipping and mild Börjeson-Forssman-Lehmann syndrome Journal of Medical Genetics 41 778-783
[3]
Kerr BA(2007)Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity Gene Expression Patterns 7 858-871
[4]
Vallée D(2012)PHF6 interacts with the nucleosome remodeling and deacetylation (NuRD) complex Journal of Proteome Research 11 4326-4337
[5]
Chevrier E(2006)The Epc-N domain: A predicted protein-protein interaction domain found in select chromatin associated proteins BMC Genomics 7 6-422
[6]
Graham GE(2021)PHF6 Mutations in Hematologic Malignancies Frontiers in Oncology 11 410-342
[7]
Voss AK(2013)The molecular profile of adult T-cell acute lymphoblastic leukemia: Mutations in RUNX1 and DNMT3A are associated with poor prognosis in T-ALL Genes, Chromosomes & Cancer 52 338-825
[8]
Gamble R(2010)PHF6 mutations in T-cell acute lymphoblastic leukemia Nature Genetics 42 819-989
[9]
Collin C(2020)PHF6 Expression Levels Impact Human Hematopoietic Stem Cell Differentiation Front Cell Dev Biol. 8 973-10083
[10]
Todd MA(2004)Clinical and behavioral features of patients with Borjeson-Forssman-Lehmann syndrome with mutations in PHF6 Journal of Pediatrics 145 10069-861