Williams-Beureni sündroomi kromosoomi regiooni 22 valgu ...

histone methyltransferase with transcriptional repression activity. Mol Cell Biol 28,
2023–2034.
13. Lange A, Mills RE., Lange CJ., Stewart M, Devine SE. ja Corbett AH. (2007).
Classical Nuclear Localization Signals: Definition, Function, and Interactions with
Importin α. THE JOURNAL OF BIOLOGICAL CHEMISTRY, VOL. 282, NO. 8,
pp. 5101–5105.
14. Li X ja Zhao X (2008). Epigenetic regulation of mammalian stem cells. Stem Cells
Dev 17, 1043–1052 .
15. Meyer-Lindenberg A, Mervis CB. ja Berma KF (2006). Neural mechanisms in
Williams syndrome: a unique window to genetic influences on cognition and
behaviour. NATURE REVIEWS | NEUROSCIENCE 381, volume 7.
16. Nakazawa Y, Arai ja Fujita N (2011).The Novel Metastasis Promoter
Merm1/Wbscr22 Enhances Tumor Cell Survival in the Vasculature by Suppressing
Zac1/p53-Dependent Apoptosis. Cancer Res 71 1146-1155
17. Nelson DL. ja Cox MM. (2004). Lehninger Principles of Biochemistry, Fourth
Edition, 1071-1072
18. Osborn LR. (2010). Animal Models of Williams Syndrome. Am J Med Genet C
Semin Med Genet. 154C, 209-219.
19. Osborne LR. ja Mervis CB. (2010). Rearrangements of the Williams–Beuren
syndrome locus: molecular basis and implications for speech and language
development. Expert Rev Mol Med. ; 9(15): 1–16.
20. Schubert C. (2009). The genomic basis of the Williams – Beuren syndrome. Cell.
Mol. Life Sci. 66, 1178 – 1197.
21. Varrault A, Ciani E, Apiou F, Bilanges B, Hoffmann A, Pantaloni C, Bockaert J,
Spengler D ja Journot L (1998). hZAC encodes a zinc finger protein with
antiproliferative properties and maps to a chromosomal region frequently lost in
cancer. Proc Natl Acad Sci U S A 95, 8835–8840.
22. van Hagen JM, van der Geest JN, van der Giessen RS, Lagers-van Haselen GC,
Eussen HJ, Gille JJ, Govaerts LC, Wouters CH, de Coo IF, Hoogenraad CC,
Koekkoek SK, Frens MA, van Camp N, van der Linden A, Jansweijer MC,
Thorgeirsson SS, De Zeeuw CI (2007). Contribution of CYLN2 and GTF2IRD1 to
neurological and cognitive symptoms in Williams Syndrome. Neurobiology of
Disease 26, 112-124.
23. Wang YK, Samos CH, Peoples R, Pérez-Jurado LA, Nusse R ja Francke U
(1997). A novel human homologue of the Drosophila frizzled wnt receptor gene binds
28