Brigitte Pokora-Royer

Duesseldorf, NW, Germany

Last Updated: 09/26/2026

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Found 27 publications

Gene expression studies of WT1 mutant Wilms tumor cell lines in the frame work of published kidney development data reveals their early kidney stem cell origin.

Gene expression studies of WT1 mutant Wilms tumor cell lines in the frame work of published kidney development data reveals their early kidney stem cell origin.

Journal: PloS one
Published: June 07, 2022

Bromodomain 4 inhibition leads to MYCN downregulation in Wilms tumor.

Bromodomain 4 inhibition leads to MYCN downregulation in Wilms tumor.

Journal: Pediatric blood & cancer
Published: January 21, 2021

Comprehensive Biology and Genetics Compendium of Wilms Tumor Cell Lines with Different WT1 Mutations.

Comprehensive Biology and Genetics Compendium of Wilms Tumor Cell Lines with Different WT1 Mutations.

Journal: Cancers
Published: November 05, 2020

WT1-Mutant Wilms Tumor Progression Is Associated With Diverting Clonal Mutations of CTNNB1.

WT1-Mutant Wilms Tumor Progression Is Associated With Diverting Clonal Mutations of CTNNB1.

Journal: Journal of pediatric hematology/oncology
Published: August 10, 2019

Efficacy of azacitidine is independent of molecular and clinical characteristics - an analysis of 128 patients with myelodysplastic syndromes or acute myeloid leukemia and a review of the literature.

Efficacy of azacitidine is independent of molecular and clinical characteristics - an analysis of 128 patients with myelodysplastic syndromes or acute myeloid leukemia and a review of the literature.

Journal: Oncotarget
Published: January 10, 2018

Chemotherapy and terminal skeletal muscle differentiation in WT1-mutant Wilms tumors.

Chemotherapy and terminal skeletal muscle differentiation in WT1-mutant Wilms tumors.

Journal: Cancer medicine
Published: November 17, 2017

Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome.

Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome.

Journal: The Journal of pathology
Published: January 30, 2017

Comparative performance analysis of human iPSC-derived and primary neural progenitor cells (NPC) grown as neurospheres in vitro.

Comparative performance analysis of human iPSC-derived and primary neural progenitor cells (NPC) grown as neurospheres in vitro.

Journal: Stem cell research
Published: October 28, 2016

Reduction of the tumorigenic potential of human retinoblastoma cell lines by TFF1 overexpression involves p53/caspase signaling and miR-18a regulation.

Reduction of the tumorigenic potential of human retinoblastoma cell lines by TFF1 overexpression involves p53/caspase signaling and miR-18a regulation.

Journal: International journal of cancer
Published: October 14, 2016

A novel C8orf37 splice mutation and genotype-phenotype correlation for cone-rod dystrophy.

A novel C8orf37 splice mutation and genotype-phenotype correlation for cone-rod dystrophy.

Journal: Ophthalmic genetics
Published: February 12, 2016

Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15.

Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15.

Journal: PloS one
Published: October 09, 2015

Structural chromosome abnormalities, increased DNA strand breaks and DNA strand break repair deficiency in dermal fibroblasts from old female human donors.

Structural chromosome abnormalities, increased DNA strand breaks and DNA strand break repair deficiency in dermal fibroblasts from old female human donors.

Journal: Aging
Published: February 14, 2015
Showing 1-12 of 27

Last Updated: 09/26/2026