Steenpaß L - Search Results

1

Generation of two human isogenic iPSC lines from fetal dermal fibroblasts.

Tandon R, Brändl B, Baryshnikova N, Landshammer A, Steenpaß L, Keminer O, Pless O, Müller FJ. Tandon R, et al. Among authors: steenpass l. Stem Cell Res. 2018 Dec;33:120-124. doi: 10.1016/j.scr.2018.10.004. Epub 2018 Oct 12. Stem Cell Res. 2018. PMID: 30343101 Free article.

2

Generation of two H1 hESC sublines carrying a heterozygous and homozygous knock-out of RB1.

Steenpass L. Steenpass L. Stem Cell Res. 2017 Dec;25:270-273. doi: 10.1016/j.scr.2017.07.005. Epub 2017 Jul 11. Stem Cell Res. 2017. PMID: 29246572 Free article.

3

Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect.

Neureiter A, Brändl B, Hiber M, Tandon R, Müller FJ, Steenpass L. Neureiter A, et al. Among authors: steenpass l. Stem Cell Res. 2018 Dec;33:20-24. doi: 10.1016/j.scr.2018.09.015. Epub 2018 Sep 24. Stem Cell Res. 2018. PMID: 30296670 Free article.

4

Generation of heterozygous and homozygous hESC H9 sublines carrying inactivating mutations in RB1.

Schipper L, Kanber D, Steenpass L. Schipper L, et al. Among authors: steenpass l. Stem Cell Res. 2018 Dec;33:41-45. doi: 10.1016/j.scr.2018.09.016. Epub 2018 Sep 26. Stem Cell Res. 2018. PMID: 30312872 Free article.

5

Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC lines.

Döpper H, Horstmann M, Menges J, Bozet M, Kanber D, Steenpass L. Döpper H, et al. Among authors: steenpass l. Stem Cell Res. 2020 May;45:101779. doi: 10.1016/j.scr.2020.101779. Epub 2020 Mar 29. Stem Cell Res. 2020. PMID: 32268247 Free article.

6

Differentiation Protocol for 3D Retinal Organoids, Immunostaining and Signal Quantitation.

Döpper H, Menges J, Bozet M, Brenzel A, Lohmann D, Steenpass L, Kanber D. Döpper H, et al. Among authors: steenpass l. Curr Protoc Stem Cell Biol. 2020 Dec;55(1):e120. doi: 10.1002/cpsc.120. Curr Protoc Stem Cell Biol. 2020. PMID: 32956559

7

Angelman syndrome-derived neurons display late onset of paternal UBE3A silencing.

Stanurova J, Neureiter A, Hiber M, de Oliveira Kessler H, Stolp K, Goetzke R, Klein D, Bankfalvi A, Klump H, Steenpass L. Stanurova J, et al. Among authors: steenpass l. Sci Rep. 2016 Aug 3;6:30792. doi: 10.1038/srep30792. Sci Rep. 2016. PMID: 27484051 Free PMC article.

8

Generation of two H1 hESC sublines carrying deletions of RB1 exon 1/promoter in heterozygous or compound heterozygous state.

Menges J, Cremanns M, Steenpass L. Menges J, et al. Among authors: steenpass l. Stem Cell Res. 2019 Aug;39:101517. doi: 10.1016/j.scr.2019.101517. Epub 2019 Jul 29. Stem Cell Res. 2019. PMID: 31404748 Free article.

9

Comprehensive characterization of RB1 mutant and MYCN amplified retinoblastoma cell lines.

Schwermer M, Hiber M, Dreesmann S, Rieb A, Theißen J, Herold T, Schramm A, Temming P, Steenpass L. Schwermer M, et al. Among authors: steenpass l. Exp Cell Res. 2019 Feb 15;375(2):92-99. doi: 10.1016/j.yexcr.2018.12.018. Epub 2018 Dec 22. Exp Cell Res. 2019. PMID: 30584916 Free article.

10

Corrigendum to "Comprehensive characterization of RB1 mutant and MYCN amplified retinoblastoma cell lines" [Exp. Cell Res. 375 (2019) 92-99].

Schwermer M, Hiber M, Dreesmann S, Rieb A, Theißen J, Herold T, Schramm A, Temming P, Steenpass L. Schwermer M, et al. Among authors: steenpass l. Exp Cell Res. 2023 May 1;426(1):113569. doi: 10.1016/j.yexcr.2023.113569. Epub 2023 Mar 27. Exp Cell Res. 2023. PMID: 36989729 No abstract available.

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