Bhattacharyya A - Search Results

1

Identification of FMR1-regulated molecular networks in human neurodevelopment.

Li M, Shin J, Risgaard RD, Parries MJ, Wang J, Chasman D, Liu S, Roy S, Bhattacharyya A, Zhao X. Li M, et al. Among authors: bhattacharyya a. Genome Res. 2020 Mar;30(3):361-374. doi: 10.1101/gr.251405.119. Epub 2020 Mar 16. Genome Res. 2020. PMID: 32179589 Free PMC article.

2

Normal Neurogenesis but Abnormal Gene Expression in Human Fragile X Cortical Progenitor Cells.

Bhattacharyya A, McMillan E, Wallace K, Tubon TC Jr, Capowski EE, Svendsen CN. Bhattacharyya A, et al. Stem Cells Dev. 2008 Feb;17(1):107-17. doi: 10.1089/scd.2007.0073. Stem Cells Dev. 2008. PMID: 18225979

3

iPSC-derived forebrain neurons from FXS individuals show defects in initial neurite outgrowth.

Doers ME, Musser MT, Nichol R, Berndt ER, Baker M, Gomez TM, Zhang SC, Abbeduto L, Bhattacharyya A. Doers ME, et al. Among authors: bhattacharyya a. Stem Cells Dev. 2014 Aug 1;23(15):1777-87. doi: 10.1089/scd.2014.0030. Epub 2014 Apr 30. Stem Cells Dev. 2014. PMID: 24654675 Free PMC article.

4

Human pluripotent stem cell models of Fragile X syndrome.

Bhattacharyya A, Zhao X. Bhattacharyya A, et al. Mol Cell Neurosci. 2016 Jun;73:43-51. doi: 10.1016/j.mcn.2015.11.011. Epub 2015 Nov 27. Mol Cell Neurosci. 2016. PMID: 26640241 Free PMC article. Review.

5

Efficient generation of region-specific forebrain neurons from human pluripotent stem cells under highly defined condition.

Yuan F, Fang KH, Cao SY, Qu ZY, Li Q, Krencik R, Xu M, Bhattacharyya A, Su YW, Zhu DY, Liu Y. Yuan F, et al. Among authors: bhattacharyya a. Sci Rep. 2015 Dec 16;5:18550. doi: 10.1038/srep18550. Sci Rep. 2015. PMID: 26670131 Free PMC article.

6

MDM2 inhibition rescues neurogenic and cognitive deficits in a mouse model of fragile X syndrome.

Li Y, Stockton ME, Bhuiyan I, Eisinger BE, Gao Y, Miller JL, Bhattacharyya A, Zhao X. Li Y, et al. Among authors: bhattacharyya a. Sci Transl Med. 2016 Apr 27;8(336):336ra61. doi: 10.1126/scitranslmed.aad9370. Sci Transl Med. 2016. PMID: 27122614 Free PMC article.

7

Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells.

Li M, Zhao H, Ananiev GE, Musser MT, Ness KH, Maglaque DL, Saha K, Bhattacharyya A, Zhao X. Li M, et al. Among authors: bhattacharyya a. Stem Cells. 2017 Jan;35(1):158-169. doi: 10.1002/stem.2463. Epub 2016 Jul 27. Stem Cells. 2017. PMID: 27422057 Free PMC article.

8

CGG Repeats in the 5'UTR of FMR1 RNA Regulate Translation of Other RNAs Localized in the Same RNA Granules.

Rovozzo R, Korza G, Baker MW, Li M, Bhattacharyya A, Barbarese E, Carson JH. Rovozzo R, et al. Among authors: bhattacharyya a. PLoS One. 2016 Dec 22;11(12):e0168204. doi: 10.1371/journal.pone.0168204. eCollection 2016. PLoS One. 2016. PMID: 28005950 Free PMC article.

9

Human Models Are Needed for Studying Human Neurodevelopmental Disorders.

Zhao X, Bhattacharyya A. Zhao X, et al. Among authors: bhattacharyya a. Am J Hum Genet. 2018 Dec 6;103(6):829-857. doi: 10.1016/j.ajhg.2018.10.009. Am J Hum Genet. 2018. PMID: 30526865 Free PMC article. Review.

10

CRISPR/Cas9 editing of APP C-terminus attenuates β-cleavage and promotes α-cleavage.

Sun J, Carlson-Stevermer J, Das U, Shen M, Delenclos M, Snead AM, Koo SY, Wang L, Qiao D, Loi J, Petersen AJ, Stockton M, Bhattacharyya A, Jones MV, Zhao X, McLean PJ, Sproul AA, Saha K, Roy S. Sun J, et al. Among authors: bhattacharyya a. Nat Commun. 2019 Jan 3;10(1):53. doi: 10.1038/s41467-018-07971-8. Nat Commun. 2019. PMID: 30604771 Free PMC article.

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