Function and regulation of Dyrk1A: towards understanding Down syndrome

Author:

Park Joongkyu,Song Woo-Joo,Chung Kwang Chul

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Cellular and Molecular Neuroscience,Pharmacology,Molecular Biology,Molecular Medicine

Reference69 articles.

1. Lejeune J, Gautier M, Turpin R (1959) Study of somatic chromosomes from 9 mongoloid children. C R Hebd Seances Acad Sci 248:1721–1722

2. Korenberg JR, Chen X-N, Schipper R, Sun Z, Gonsky R, Gerwehr S, Carpenter N, Daumer C, Dignan P, Disteche C, Graham JM Jr, Hugdins L, McGillivray B, Miyazaki K, Ogasawara N, Park JP, Pagon R, Pueschel S, Sack G, Say B, Schuffenhauer S, Soukup S, Yamanaka T (1994) Down syndrome phenotypes: the consequences of chromosomal imbalance. Proc Natl Acad Sci USA 91:4997–5001

3. Gardiner K (2007) Overview of the genes of the human chromosome 21. In: Pritchard M, Reeves RH, Dierssenc M, Patterson D, Gardiner KJ (eds) Down syndrome and the genes of human chromosome 21: current knowledge and future potentials. Report on the expert workshop on the biology of chromosome 21 genes: towards gene-phenotype correlations in Down syndrome. September 28-October 1, 2007, Washington D.C.

4. Korenberg JR, Kawashima H, Pulst S-M, Ikeuchi T, Ogasawara N, Yamamoto K, Schonberg SA, West R, Allen L, Magenis E, Ikawa K, Taniguchi N, Epstein CJ (1990) Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype. Am J Hum Genet 47:236–246

5. McCormick MK, Schinzel A, Petersen MB, Stetten G, Driscoll DJ, Cantu ES, Tranebjaerg L, Mikkelsen M, Watkins PC, Antonarakis SE (1989) Molecular genetic approach to the characterization of the “Down syndrome region” of chromosome 21. Genomics 5:325–331

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