Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2013 | 1 |
2014 | 1 |
2016 | 1 |
2018 | 1 |
2019 | 1 |
2020 | 1 |
2021 | 1 |
2024 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
Page 1
Intrauterine growth restriction compromises cerebellar development by affecting radial migration of granule cells via the JamC/Pard3a molecular pathway.
Exp Neurol. 2021 Feb;336:113537. doi: 10.1016/j.expneurol.2020.113537. Epub 2020 Nov 28.
Exp Neurol. 2021.
PMID: 33259808
Free PMC article.
Early dorsomedial tissue interactions regulate gyrification of distal neocortex.
Chizhikov VV, Iskusnykh IY, Steshina EY, Fattakhov N, Lindgren AG, Shetty AS, Roy A, Tole S, Millen KJ.
Chizhikov VV, et al.
Nat Commun. 2019 Nov 15;10(1):5192. doi: 10.1038/s41467-019-12913-z.
Nat Commun. 2019.
PMID: 31729356
Free PMC article.
Item in Clipboard
Preterm birth disrupts cerebellar development by affecting granule cell proliferation program and Bergmann glia.
Iskusnykh IY, Buddington RK, Chizhikov VV.
Iskusnykh IY, et al.
Exp Neurol. 2018 Aug;306:209-221. doi: 10.1016/j.expneurol.2018.05.015. Epub 2018 May 14.
Exp Neurol. 2018.
PMID: 29772246
Free PMC article.
Item in Clipboard
Loss of Ptf1a Leads to a Widespread Cell-Fate Misspecification in the Brainstem, Affecting the Development of Somatosensory and Viscerosensory Nuclei.
Iskusnykh IY, Steshina EY, Chizhikov VV.
Iskusnykh IY, et al.
J Neurosci. 2016 Mar 2;36(9):2691-710. doi: 10.1523/JNEUROSCI.2526-15.2016.
J Neurosci. 2016.
PMID: 26937009
Free PMC article.
Item in Clipboard
Transformation of the cerebellum into more ventral brainstem fates causes cerebellar agenesis in the absence of Ptf1a function.
Millen KJ, Steshina EY, Iskusnykh IY, Chizhikov VV.
Millen KJ, et al.
Proc Natl Acad Sci U S A. 2014 Apr 29;111(17):E1777-86. doi: 10.1073/pnas.1315024111. Epub 2014 Apr 14.
Proc Natl Acad Sci U S A. 2014.
PMID: 24733890
Free PMC article.
Item in Clipboard
The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.
Curry CJ, Rosenfeld JA, Grant E, Gripp KW, Anderson C, Aylsworth AS, Saad TB, Chizhikov VV, Dybose G, Fagerberg C, Falco M, Fels C, Fichera M, Graakjaer J, Greco D, Hair J, Hopkins E, Huggins M, Ladda R, Li C, Moeschler J, Nowaczyk MJ, Ozmore JR, Reitano S, Romano C, Roos L, Schnur RE, Sell S, Suwannarat P, Svaneby D, Szybowska M, Tarnopolsky M, Tervo R, Tsai AC, Tucker M, Vallee S, Wheeler FC, Zand DJ, Barkovich AJ, Aradhya S, Shaffer LG, Dobyns WB.
Curry CJ, et al.
Am J Med Genet A. 2013 Aug;161A(8):1833-52. doi: 10.1002/ajmg.a.35996. Epub 2013 Jun 27.
Am J Med Genet A. 2013.
PMID: 23813913
Free PMC article.
Item in Clipboard
Cite
Cite