Castrén ML - Search Results

1

Integrative Analysis Identifies Key Molecular Signatures Underlying Neurodevelopmental Deficits in Fragile X Syndrome.

Utami KH, Skotte NH, Colaço AR, Yusof NABM, Sim B, Yeo XY, Bae HG, Garcia-Miralles M, Radulescu CI, Chen Q, Chaldaiopoulou G, Liany H, Nama S, Peteri UA, Sampath P, Castrén ML, Jung S, Mann M, Pouladi MA. Utami KH, et al. Among authors: castren ml. Biol Psychiatry. 2020 Sep 15;88(6):500-511. doi: 10.1016/j.biopsych.2020.05.005. Epub 2020 May 13. Biol Psychiatry. 2020. PMID: 32653109

2

Differentiation of neuronal cells in fragile X syndrome.

Castrén M. Castrén M. Cell Cycle. 2006 Jul;5(14):1528-30. doi: 10.4161/cc.5.14.3096. Epub 2006 Jul 17. Cell Cycle. 2006. PMID: 16861896 Review.

3

Aberrant differentiation of glutamatergic cells in neocortex of mouse model for fragile X syndrome.

Tervonen TA, Louhivuori V, Sun X, Hokkanen ME, Kratochwil CF, Zebryk P, Castrén E, Castrén ML. Tervonen TA, et al. Among authors: castren ml, castren e. Neurobiol Dis. 2009 Feb;33(2):250-9. doi: 10.1016/j.nbd.2008.10.010. Epub 2008 Nov 6. Neurobiol Dis. 2009. PMID: 19056494

4

Reduction of BDNF expression in Fmr1 knockout mice worsens cognitive deficits but improves hyperactivity and sensorimotor deficits.

Uutela M, Lindholm J, Louhivuori V, Wei H, Louhivuori LM, Pertovaara A, Akerman K, Castrén E, Castrén ML. Uutela M, et al. Among authors: castren ml, castren e. Genes Brain Behav. 2012 Jul;11(5):513-23. doi: 10.1111/j.1601-183X.2012.00784.x. Epub 2012 Apr 11. Genes Brain Behav. 2012. PMID: 22435671 Free article.

5

BDNF in fragile X syndrome.

Castrén ML, Castrén E. Castrén ML, et al. Among authors: castren e. Neuropharmacology. 2014 Jan;76 Pt C:729-36. doi: 10.1016/j.neuropharm.2013.05.018. Epub 2013 May 29. Neuropharmacology. 2014. PMID: 23727436 Review.

6

Cortical neurogenesis in fragile X syndrome.

Castrén ML. Castrén ML. Front Biosci (Schol Ed). 2016 Jan 1;8(1):160-8. doi: 10.2741/s455. Front Biosci (Schol Ed). 2016. PMID: 26709905 Free article. Review.

7

Modeling FXS with Mouse Neural Progenitors.

Peteri UK, Castrén ML. Peteri UK, et al. Among authors: castren ml. Methods Mol Biol. 2019;1942:71-78. doi: 10.1007/978-1-4939-9080-1_6. Methods Mol Biol. 2019. PMID: 30900176

8

Elevated de novo protein synthesis in FMRP-deficient human neurons and its correction by metformin treatment.

Utami KH, Yusof NABM, Kwa JE, Peteri UK, Castrén ML, Pouladi MA. Utami KH, et al. Among authors: castren ml. Mol Autism. 2020 May 27;11(1):41. doi: 10.1186/s13229-020-00350-5. Mol Autism. 2020. PMID: 32460900 Free PMC article.

9

Generation of the Human Pluripotent Stem-Cell-Derived Astrocyte Model with Forebrain Identity.

Peteri UK, Pitkonen J, Utami KH, Paavola J, Roybon L, Pouladi MA, Castrén ML. Peteri UK, et al. Among authors: castren ml. Brain Sci. 2021 Feb 9;11(2):209. doi: 10.3390/brainsci11020209. Brain Sci. 2021. PMID: 33572154 Free PMC article.

10

Urokinase plasminogen activator mediates changes in human astrocytes modeling fragile X syndrome.

Peteri UK, Pitkonen J, de Toma I, Nieminen O, Utami KH, Strandin TM, Corcoran P, Roybon L, Vaheri A, Ethell I, Casarotto P, Pouladi MA, Castrén ML. Peteri UK, et al. Among authors: castren ml. Glia. 2021 Dec;69(12):2947-2962. doi: 10.1002/glia.24080. Epub 2021 Aug 24. Glia. 2021. PMID: 34427356

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