Publications by authors named "Laura Steenpass"

18Publications

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

Curr Protoc Stem Cell Biol 2020 Dec;55(1):e120

Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

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http://dx.doi.org/10.1002/cpsc.120DOI Listing
December 2020

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

Stem Cell Res 2020 05 29;45:101779. Epub 2020 Mar 29.

Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Hufelandstr. 55, 45147 Essen, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2020.101779DOI Listing
May 2020

A human somatic cell culture system for modelling gene silencing by transcriptional interference.

Heliyon 2020 Jan 29;6(1):e03261. Epub 2020 Jan 29.

Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Hufelandstr 55, 45147 Essen, Germany.

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http://dx.doi.org/10.1016/j.heliyon.2020.e03261DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994850PMC
January 2020

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

Stem Cell Res 2019 08 29;39:101517. Epub 2019 Jul 29.

Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Hufelandstr. 55, 45147 Essen, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2019.101517DOI Listing
August 2019

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

Stem Cell Res 2018 12 12;33:120-124. Epub 2018 Oct 12.

Zentrum für Integrative Psychiatrie, University Hospital Schleswig-Holstein, Kiel, Germany; Max-Planck-Institute for Molecular Genetics, Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2018.10.004DOI Listing
December 2018

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

Stem Cell Res 2018 12 26;33:41-45. Epub 2018 Sep 26.

Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Hufelandstr 55, 45147 Essen, Germany. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S18735061183023
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http://dx.doi.org/10.1016/j.scr.2018.09.016DOI Listing
December 2018

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

Stem Cell Res 2018 12 24;33:20-24. Epub 2018 Sep 24.

Institute of Human Genetics, University Hospital Essen, Essen, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2018.09.015DOI Listing
December 2018

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

Authors:
Laura Steenpass

Stem Cell Res 2017 12 11;25:270-273. Epub 2017 Jul 11.

Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Hufelandstr. 55, 45147 Essen, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2017.07.005DOI Listing
December 2017

Pharmaceutically inhibiting polo-like kinase 1 exerts a broad anti-tumour activity in retinoblastoma cell lines.

Clin Exp Ophthalmol 2017 Apr 10;45(3):288-296. Epub 2016 Nov 10.

Department of Pediatric Oncology and Hematology, University Hospital Essen, Essen, Germany.

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http://dx.doi.org/10.1111/ceo.12838DOI Listing
April 2017

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

Sci Rep 2016 08 3;6:30792. Epub 2016 Aug 3.

Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Hufelandstr. 55, 45147 Essen, Germany.

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http://dx.doi.org/10.1038/srep30792DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971516PMC
August 2016

A Mouse Model for Imprinting of the Human Retinoblastoma Gene.

PLoS One 2015 14;10(8):e0134672. Epub 2015 Aug 14.

Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0134672PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537222PMC
May 2016

Human PPP1R26P1 functions as cis-repressive element in mouse Rb1.

PLoS One 2013 3;8(9):e74159. Epub 2013 Sep 3.

Institut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, Essen, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0074159PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760807PMC
May 2014

A novel mtDNA large-scale mutation clinically exclusively presenting with refractory anemia: is there a chance to predict disease progression?

J Pediatr Hematol Oncol 2012 May;34(4):283-92

Department of Pediatric Oncology, Hematology and Clinical Immunology, Center for Child and Adolescent Health, Medical Faculty, Heinrich Heine University, Duesseldorf, Germany.

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http://Insights.ovid.com/crossref?an=00043426-201205000-0000
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http://dx.doi.org/10.1097/MPH.0b013e3182288249DOI Listing
May 2012