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Title:	Activating hotspot L205R mutation in PRKACA and adrenal Cushing's syndrome
Source:	Science [0036-8075] Cao, Y yr:2014

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description	4.	Wu, G. "Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas." Nature Genetics 44.3 (2012): 251-253.
description	5.	Schwartzentruber, J. "Driver mutations in histone H3. 3 and chromatin remodelling genes in paediatric glioblastoma." Nature 482.7384 (2012): 226-231.
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description	8.	Bjerke, L. "Histone H3.3 Mutations Drive Pediatric Glioblastoma through Upregulation of MYCN." Cancer discovery 3.5 (2013): 512-519.
description	9.	Hsu, H-T T. "TRANSCRIPTION. Recruitment of RNA polymerase II by the pioneer transcription factor PHA-4." Science 348.6241 (2015): 1372-6.
description	10.	Papazyan, R. "Methylation of histone H3K23 blocks DNA damage in pericentric heterochromatin during meiosis." eLife 3 (2014).
description	11.	Drmanac, R. "Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays." Science 327.5961 (2009): 78-81.
description	12.	LIN, J. "National disability registers report on causes of intellectual disability in Taiwan: 2000-2007." Research in Developmental Disabilities 30.2 (2009): 301-307.
description	13.	Walkley, Carl R. "A Microenvironment-Induced Myeloproliferative Syndrome Caused by Retinoic Acid Receptor gamma Deficiency." Cell 129.6 (2007): 1097-1110.
description	14.	Buschdorf, Jan P P. "A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome." Journal of molecular medicine 82.2 (2004): 135-43.
description	15.	Zautra, A J J. "Some everyday life consequences of disability and bereavement for older adults." Journal of personality and social psychology 59.3 (1990): 550-61.
description	16.	Sturm, D. "Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma." Cancer cell 22.4 (2012): 425-437.
description	17.	Khuong Quang, D. "K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas." Acta neuropathologica 124.3 (2012): 439-447.
description	18.	Luger, K. "Crystal structure of the nucleosome core particle at 2.8 A resolution." Nature 389.6648: 251-260.
description	19.	Muir, Tom W. "Ultrafast Protein Splicing is Common among Cyanobacterial Split Inteins: Implications for Protein Engineering." Journal of the American Chemical Society 134.28 (2012): 11338-11341.
description	20.	Porreca, G. "Genome sequencing on nanoballs." Nature Biotechnology 28.1 (2010): 43-44.