ab31865 を使用した論文を発表された方は、こちらまでお知らせください。データシートに掲載させていただきます。

ab31865 は 9 報の論文で使用されています。

  • Mason AG  et al. SMCHD1 regulates a limited set of gene clusters on autosomal chromosomes. Skelet Muscle 7:12 (2017). PubMed: 28593035
  • Gaillard MC  et al. Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report. BMC Med Genet 17:66 (2016). WB ; Human . PubMed: 27634379
  • Kelsey AD  et al. Impact of flanking chromosomal sequences on localization and silencing by the human non-coding RNA XIST. Genome Biol 16:208 (2015). IF . PubMed: 26429547
  • Balog J  et al. Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4. Epigenetics 10:1133-42 (2015). ChIP . PubMed: 26575099
  • Brideau NJ  et al. Independent Mechanisms Target SMCHD1 to Trimethylated Histone H3 Lysine 9-Modified Chromatin and the Inactive X Chromosome. Mol Cell Biol 35:4053-68 (2015). PubMed: 26391951
  • Massah S  et al. Epigenetic characterization of the growth hormone gene identifies SmcHD1 as a regulator of autosomal gene clusters. PLoS One 9:e97535 (2014). WB ; Mouse . PubMed: 24818964
  • Tang M  et al. Structural maintenance of chromosomes flexible hinge domain containing 1 (SMCHD1) promotes non-homologous end joining and inhibits homologous recombination repair upon DNA damage. J Biol Chem 289:34024-32 (2014). WB, ICC/IF ; Human . PubMed: 25294876
  • Lemmers RJ  et al. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2. Nat Genet 44:1370-4 (2012). WB, ChIP ; Human . PubMed: 23143600
  • Nikolov M  et al. Chromatin affinity purification and quantitative mass spectrometry defining the interactome of histone modification patterns. Mol Cell Proteomics 10:M110.005371 (2011). WB . PubMed: 21836164

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