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Items: 6


Placental transcriptomes in the common aneuploidies reveal critical regions on the trisomic chromosomes and genome-wide effects.

Bianco K, Gormley M, Farrell J, Zhou Y, Oliverio O, Tilden H, McMaster M, Fisher SJ.

Prenat Diagn. 2016 Sep;36(9):812-22. doi: 10.1002/pd.4862. Epub 2016 Jul 25.


Deficits in human trisomy 21 iPSCs and neurons.

Weick JP, Held DL, Bonadurer GF 3rd, Doers ME, Liu Y, Maguire C, Clark A, Knackert JA, Molinarolo K, Musser M, Yao L, Yin Y, Lu J, Zhang X, Zhang SC, Bhattacharyya A.

Proc Natl Acad Sci U S A. 2013 Jun 11;110(24):9962-7. doi: 10.1073/pnas.1216575110. Epub 2013 May 28.


Gene expression changes in the MAPK pathway in both Fragile X and Down syndrome human neural progenitor cells.

McMillan EL, Kamps AL, Lake SS, Svendsen CN, Bhattacharyya A.

Am J Stem Cells. 2012 Jun 30;1(2):154-162. Epub 2012 Jun 3.


A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions.

Yu T, Li Z, Jia Z, Clapcote SJ, Liu C, Li S, Asrar S, Pao A, Chen R, Fan N, Carattini-Rivera S, Bechard AR, Spring S, Henkelman RM, Stoica G, Matsui S, Nowak NJ, Roder JC, Chen C, Bradley A, Yu YE.

Hum Mol Genet. 2010 Jul 15;19(14):2780-91. doi: 10.1093/hmg/ddq179. Epub 2010 May 4.


A critical period in cortical interneuron neurogenesis in down syndrome revealed by human neural progenitor cells.

Bhattacharyya A, McMillan E, Chen SI, Wallace K, Svendsen CN.

Dev Neurosci. 2009;31(6):497-510. doi: 10.1159/000236899. Epub 2009 Sep 9.


Genes, pseudogenes, and Alu sequence organization across human chromosomes 21 and 22.

Chen C, Gentles AJ, Jurka J, Karlin S.

Proc Natl Acad Sci U S A. 2002 Mar 5;99(5):2930-5. Epub 2002 Feb 26.

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