The XLMR gene PHF8 encodes a histone H4K20/H3K9 demethylase and regulates zebrafish brain and craniofacial development

[1]  R. Shiekhattar,et al.  PHF8 Targets Histone Methylation and RNA Polymerase II To Activate Transcription , 2010, Molecular and Cellular Biology.

[2]  Juri Rappsilber,et al.  A Functional Link between the Histone Demethylase PHF8 and the Transcription Factor ZNF711 in X-Linked Mental Retardation , 2010, Molecular cell.

[3]  T. Jenuwein,et al.  PHF8 activates transcription of rRNA genes through H3K4me3 binding and H3K9me1/2 demethylation , 2010, Nature Structural &Molecular Biology.

[4]  Zhongzhou Chen,et al.  Structural insights into a novel histone demethylase PHF8 , 2010, Cell Research.

[5]  R. Klose,et al.  PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an N-dimethyl lysine demethylase , 2009 .

[6]  Yang Shi,et al.  Enzymatic and structural insights for substrate specificity of a family of jumonji histone lysine demethylases , 2010, Nature Structural &Molecular Biology.

[7]  Ian M. Fingerman,et al.  One-pot shotgun quantitative mass spectrometry characterization of histones. , 2009, Journal of proteome research.

[8]  D. Reinberg,et al.  The Target of the NSD Family of Histone Lysine Methyltransferases Depends on the Nature of the Substrate , 2009, The Journal of Biological Chemistry.

[9]  P. Blader,et al.  Notch activity in the nervous system: to switch or not switch? , 2009, Neural Development.

[10]  Dustin E. Schones,et al.  Genome-wide Mapping of HATs and HDACs Reveals Distinct Functions in Active and Inactive Genes , 2009, Cell.

[11]  Chen Zeng,et al.  A clustering approach for identification of enriched domains from histone modification ChIP-Seq data , 2009, Bioinform..

[12]  J. Gécz,et al.  The genetic landscape of intellectual disability arising from chromosome X. , 2009, Trends in genetics : TIG.

[13]  M. Tetel,et al.  Nuclear Receptor Coactivators: Essential Players for Steroid Hormone Action in the Brain and in Behaviour , 2009, Journal of neuroendocrinology.

[14]  W. Oyen,et al.  FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome , 2009, Neurology.

[15]  Dustin E. Schones,et al.  Chromatin signatures in multipotent human hematopoietic stem cells indicate the fate of bivalent genes during differentiation. , 2009, Cell stem cell.

[16]  P. Ongusaha,et al.  Prolyl 4-hydroxylation regulates Argonaute 2 stability , 2008, Nature.

[17]  P. Boccuni,et al.  Histone H4 lysine 20 monomethylation promotes transcriptional repression by L3MBTL1 , 2008, Oncogene.

[18]  K. McManus,et al.  Catalytic Function of the PR-Set7 Histone H4 Lysine 20 Monomethyltransferase Is Essential for Mitotic Entry and Genomic Stability* , 2008, Journal of Biological Chemistry.

[19]  Michael Q. Zhang,et al.  Combinatorial patterns of histone acetylations and methylations in the human genome , 2008, Nature Genetics.

[20]  P. Chiurazzi,et al.  XLMR genes: update 2007 , 2008, European Journal of Human Genetics.

[21]  David Haussler,et al.  The UCSC Genome Browser Database: 2008 update , 2007, Nucleic Acids Res..

[22]  N. Kelleher,et al.  Certain and Progressive Methylation of Histone H4 at Lysine 20 during the Cell Cycle , 2007, Molecular and Cellular Biology.

[23]  A. Koivisto,et al.  Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate , 2007, Clinical genetics.

[24]  R. Young,et al.  A Chromatin Landmark and Transcription Initiation at Most Promoters in Human Cells , 2007, Cell.

[25]  D. Reinberg,et al.  L3MBTL1, a Histone-Methylation-Dependent Chromatin Lock , 2007, Cell.

[26]  Dustin E. Schones,et al.  High-Resolution Profiling of Histone Methylations in the Human Genome , 2007, Cell.

[27]  Maite Huarte,et al.  The X-Linked Mental Retardation Gene SMCX/JARID1C Defines a Family of Histone H3 Lysine 4 Demethylases , 2007, Cell.

[28]  Tatiana Tatusova,et al.  NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins , 2004, Nucleic Acids Res..

[29]  Christopher R. Vakoc,et al.  Profile of Histone Lysine Methylation across Transcribed Mammalian Chromatin , 2006, Molecular and Cellular Biology.

[30]  A. Fritz,et al.  Zebrafish msxB, msxC and msxE function together to refine the neural-nonneural border and regulate cranial placodes and neural crest development. , 2006, Developmental biology.

[31]  H. Ropers X-linked mental retardation: many genes for a complex disorder. , 2006, Current opinion in genetics & development.

[32]  W. Harris,et al.  Mechanisms of ventral patterning in the vertebrate nervous system , 2006, Nature Reviews Neuroscience.

[33]  J. Postlethwait The zebrafish genome: a review and msx gene case study. , 2006, Genome dynamics.

[34]  R. Jäger,et al.  The AP-2 family of transcription factors , 2005, Genome Biology.

[35]  B. Robert,et al.  msh/Msx gene family in neural development. , 2005, Trends in genetics : TIG.

[36]  Juri Rappsilber,et al.  Detection of arginine dimethylated peptides by parallel precursor ion scanning mass spectrometry in positive ion mode. , 2003, Analytical chemistry.

[37]  Paul Tempst,et al.  PR-Set7 is a nucleosome-specific methyltransferase that modifies lysine 20 of histone H4 and is associated with silent chromatin. , 2002, Molecular cell.

[38]  C. Ball,et al.  Identification of genes periodically expressed in the human cell cycle and their expression in tumors. , 2002, Molecular biology of the cell.

[39]  Z. Darżynkiewicz,et al.  Determining Cell Cycle Stages by Flow Cytometry , 1999, Current protocols in cell biology.