Turan S - Search Results

1

Store-operated calcium entry is reduced in spastin-linked hereditary spastic paraplegia.

Rizo T, Gebhardt L, Riedlberger J, Eberhardt E, Fester L, Alansary D, Winkler J, Turan S, Arnold P, Niemeyer BA, Fischer MJM, Winner B. Rizo T, et al. Among authors: turan s. Brain. 2022 Sep 14;145(9):3131-3146. doi: 10.1093/brain/awac122. Brain. 2022. PMID: 36103408 Free PMC article.

2

Tideglusib Rescues Neurite Pathology of SPG11 iPSC Derived Cortical Neurons.

Pozner T, Schray A, Regensburger M, Lie DC, Schlötzer-Schrehardt U, Winkler J, Turan S, Winner B. Pozner T, et al. Among authors: turan s. Front Neurosci. 2018 Dec 6;12:914. doi: 10.3389/fnins.2018.00914. eCollection 2018. Front Neurosci. 2018. PMID: 30574063 Free PMC article.

3

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. Hum Mol Genet. 2019 Aug 1;28(15):2589-2599. doi: 10.1093/hmg/ddz089. Hum Mol Genet. 2019. PMID: 31035284

4

CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome.

Boerstler T, Wend H, Krumbiegel M, Kavyanifar A, Reis A, Lie DC, Winner B, Turan S. Boerstler T, et al. Among authors: turan s. 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.

5

Generation and characterization of an endogenously tagged SPG11-human iPSC line by CRISPR/Cas9 mediated knock-in.

Krumm L, Pozner T, Kaindl J, Regensburger M, Günther C, Turan S, Asadollahi R, Rauch A, Winner B. Krumm L, et al. Among authors: turan s. Stem Cell Res. 2021 Oct;56:102520. doi: 10.1016/j.scr.2021.102520. Epub 2021 Aug 26. Stem Cell Res. 2021. PMID: 34479069 Free article.

6

Generation of a homozygous and a heterozygous SNCA gene knockout human-induced pluripotent stem cell line by CRISPR/Cas9 mediated allele-specific tuning of SNCA expression.

Schneider Y, Turan S, Koller A, Krumbiegel M, Farrell M, Plötz S, Winkler J, Xiang W. Schneider Y, et al. Among authors: turan s. Stem Cell Res. 2022 Dec;65:102952. doi: 10.1016/j.scr.2022.102952. Epub 2022 Oct 20. Stem Cell Res. 2022. PMID: 36283273 Free article.

7

SoxC transcription factors: multifunctional regulators of neurodevelopment.

Kavyanifar A, Turan S, Lie DC. Kavyanifar A, et al. Among authors: turan s. Cell Tissue Res. 2018 Jan;371(1):91-103. doi: 10.1007/s00441-017-2708-7. Epub 2017 Oct 27. Cell Tissue Res. 2018. PMID: 29079881 Review.

8

Precise Correction of Disease Mutations in Induced Pluripotent Stem Cells Derived From Patients With Limb Girdle Muscular Dystrophy.

Turan S, Farruggio AP, Srifa W, Day JW, Calos MP. Turan S, et al. Mol Ther. 2016 Apr;24(4):685-96. doi: 10.1038/mt.2016.40. Epub 2016 Feb 26. Mol Ther. 2016. PMID: 26916285 Free PMC article.

9

Modified lentiviral LTRs allow Flp recombinase-mediated cassette exchange and in vivo tracing of "factor-free" induced pluripotent stem cells.

Kuehle J, Turan S, Cantz T, Hoffmann D, Suerth JD, Maetzig T, Zychlinski D, Klein C, Steinemann D, Baum C, Bode J, Schambach A. Kuehle J, et al. Among authors: turan s. Mol Ther. 2014 May;22(5):919-28. doi: 10.1038/mt.2014.4. Epub 2014 Jan 17. Mol Ther. 2014. PMID: 24434935 Free PMC article.

10

Expanding Flp-RMCE options: the potential of Recombinase Mediated Twin-Site Targeting (RMTT).

Turan S, Qiao J, Madden S, Benham C, Kotz M, Schambach A, Bode J. Turan S, et al. Gene. 2014 Aug 10;546(2):135-44. doi: 10.1016/j.gene.2014.06.002. Epub 2014 Jun 4. Gene. 2014. PMID: 24905650 Review.

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