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CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome.
Stem Cell Res. 2020 Jun 29;47:101889. doi: 10.1016/j.scr.2020.101889. Online ahead of print.
Stem Cell Res. 2020.
PMID: 32682288
Free article.
GSK3ß-dependent dysregulation of neurodevelopment in SPG11-patient induced pluripotent stem cell model.
Mishra HK, Prots I, Havlicek S, Kohl Z, Perez-Branguli F, Boerstler T, Anneser L, Minakaki G, Wend H, Hampl M, Leone M, Brückner M, Klucken J, Reis A, Boyer L, Schuierer G, Behrens J, Lampert A, Engel FB, Gage FH, Winkler J, Winner B.
Mishra HK, et al. Among authors: boerstler t.
Ann Neurol. 2016 May;79(5):826-840. doi: 10.1002/ana.24633.
Ann Neurol. 2016.
PMID: 26971897
Free PMC article.
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A novel human stem cell model for Coffin-Siris syndrome-like syndrome reveals the importance of SOX11 dosage for neuronal differentiation and survival.
Turan S, Boerstler T, Kavyanifar A, Loskarn S, Reis A, Winner B, Lie DC.
Turan S, et al. Among authors: boerstler t.
Hum Mol Genet. 2019 Aug 1;28(15):2589-2599. doi: 10.1093/hmg/ddz089.
Hum Mol Genet. 2019.
PMID: 31035284
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Aberrant NOVA1 function disrupts alternative splicing in early stages of amyotrophic lateral sclerosis.
Krach F, Wheeler EC, Regensburger M, Boerstler T, Wend H, Vu AQ, Wang R, Reischl S, Boldt K, Batra R, Aigner S, Ravits J, Winkler J, Yeo GW, Winner B.
Krach F, et al. Among authors: boerstler t.
Acta Neuropathol. 2022 Sep;144(3):413-435. doi: 10.1007/s00401-022-02450-3. Epub 2022 Jul 1.
Acta Neuropathol. 2022.
PMID: 35778567
Free PMC article.
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An alternative splicing modulator decreases mutant HTT and improves the molecular fingerprint in Huntington's disease patient neurons.
Krach F, Stemick J, Boerstler T, Weiss A, Lingos I, Reischl S, Meixner H, Ploetz S, Farrell M, Hehr U, Kohl Z, Winner B, Winkler J.
Krach F, et al. Among authors: boerstler t.
Nat Commun. 2022 Nov 10;13(1):6797. doi: 10.1038/s41467-022-34419-x.
Nat Commun. 2022.
PMID: 36357392
Free PMC article.
Clinical Trial.
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