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

Stem cell research, 2017-12, Vol.25 (C), p.270-273

Steenpass, Laura

2017

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Generation of three iPSC lines with inducible systems to be used in Angelman syndrome research

Stem cell research, 2024-08, Vol.78, p.103454, Article 103454

2024

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Generation of two human isogenic iPSC lines from fetal dermal fibroblasts

Stem cell research, 2018-12, Vol.33, p.120-124

2018

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

Stem cell research, 2019-08, Vol.39, p.101517-101517, Article 101517

2019

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

Stem cell research, 2018-12, Vol.33, p.41-45

2018

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

Stem cell research, 2020-05, Vol.45, p.101779-101779, Article 101779

2020

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Molecular Characterization and Subtyping of Breast Cancer Cell Lines Provide Novel Insights into Cancer Relevant Genes

Cells (Basel, Switzerland), 2024-02, Vol.13 (4), p.301

2024

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RB1 -Negative Retinal Organoids Display Proliferation of Cone Photoreceptors and Loss of Retinal Differentiation

Cancers, 2022-04, Vol.14 (9), p.2166

2022

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Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome

American journal of human genetics, 2014-12, Vol.95 (6), p.698-707

2014

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

Stem cell research, 2018-12, Vol.33, p.20-24

2018

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A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastoma

Communications biology, 2024-07, Vol.7 (1), p.919-16, Article 919

2024

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An in vitro ES cell imprinting model shows that imprinted expression of the Igf2r gene arises from an allele-specific expression bias

Development (Cambridge), 2009-02, Vol.136 (3), p.437-448

2009

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Silencing and transcriptional properties of the imprinted Airn ncRNA are independent of the endogenous promoter

The EMBO journal, 2008-12, Vol.27 (23), p.3116-3128

2008

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Cross contamination meets misclassification: Awakening of CHP‐100 from sleeping beauty sleep—A reviewed model for Ewing's sarcoma

International journal of cancer, 2021-05, Vol.148 (10), p.2608-2613

2021

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

Clinical & experimental ophthalmology, 2017-04, Vol.45 (3), p.288-296

2017

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

Journal of pediatric hematology/oncology, 2012-05, Vol.34 (4), p.283-292

2012

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

Generation of three iPSC lines with inducible systems to be used in Angelman syndrome research

Generation of two human isogenic iPSC lines from fetal dermal fibroblasts

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

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

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

Molecular Characterization and Subtyping of Breast Cancer Cell Lines Provide Novel Insights into Cancer Relevant Genes

RB1 -Negative Retinal Organoids Display Proliferation of Cone Photoreceptors and Loss of Retinal Differentiation

Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome

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

A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastoma

An in vitro ES cell imprinting model shows that imprinted expression of the Igf2r gene arises from an allele-specific expression bias

Silencing and transcriptional properties of the imprinted Airn ncRNA are independent of the endogenous promoter

Cross contamination meets misclassification: Awakening of CHP‐100 from sleeping beauty sleep—A reviewed model for Ewing's sarcoma

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

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

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