Zinc finger protein 536
Zinc finger protein 536 is a protein that in humans is encoded by the ZNF536 gene.[1]
References
Further reading
- Qin Z, Ren F, Xu X, Ren Y, Li H, Wang Y, Zhai Y, Chang Z (July 2009). “ZNF536, a novel zinc finger protein specifically expressed in the brain, negatively regulates neuron differentiation by repressing retinoic acid-induced gene transcription”. Molecular and Cellular Biology. 29 (13): 3633–43. doi:10.1128/MCB.00362-09. PMC 2698762. PMID 19398580.
- Dugas JC, Tai YC, Speed TP, Ngai J, Barres BA (October 2006). “Functional genomic analysis of oligodendrocyte differentiation”. The Journal of Neuroscience. 26 (43): 10967–83. doi:10.1523/JNEUROSCI.2572-06.2006. PMID 17065439.
- Benjamin EJ, Dupuis J, Larson MG, Lunetta KL, Booth SL, Govindaraju DR, Kathiresan S, Keaney JF, Keyes MJ, Lin JP, Meigs JB, Robins SJ, Rong J, Schnabel R, Vita JA, Wang TJ, Wilson PW, Wolf PA, Vasan RS (September 2007). “Genome-wide association with select biomarker traits in the Framingham Heart Study”. BMC Medical Genetics. 8 Suppl 1: S11. doi:10.1186/1471-2350-8-S1-S11. PMC 1995615. PMID 17903293.
- Low SK, Chung S, Takahashi A, Zembutsu H, Mushiroda T, Kubo M, Nakamura Y (August 2013). “Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan”. Cancer Science. 104 (8): 1074–82. doi:10.1111/cas.12186. PMID 23648065.
- Meng W, Butterworth J, Bradley DT, Hughes AE, Soler V, Calvas P, Malecaze F (December 2012). “A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population”. Investigative Ophthalmology & Visual Science. 53 (13): 7983–8. doi:10.1167/iovs.12-10409. PMID 23049088.
- Sakai T, Hino K, Wada S, Maeda H (August 2003). “Identification of the DNA binding specificity of the human ZNF219 protein and its function as a transcriptional repressor”. DNA Research. 10 (4): 155–65. doi:10.1093/dnares/10.4.155. PMID 14621294.
- Seppälä I, Kleber ME, Lyytikäinen LP, Hernesniemi JA, Mäkelä KM, Oksala N, Laaksonen R, Pilz S, Tomaschitz A, Silbernagel G, Boehm BO, Grammer TB, Koskinen T, Juonala M, Hutri-Kähönen N, Alfthan G, Viikari JS, Kähonen M, Raitakari OT, März W, Meinitzer A, Lehtimäki T (February 2014). “Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality”. European Heart Journal. 35 (8): 524–31. doi:10.1093/eurheartj/eht447. PMID 24159190.
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