Robin A. Pilz

Greifswald, MV 17475, Germany

Last Updated: 09/26/2026

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Found 14 publications

Tumor-like proliferation of CCM3 knockout endothelial cells: insights from semaxinib treatment and transcriptome profiling of co-cultures.

Tumor-like proliferation of CCM3 knockout endothelial cells: insights from semaxinib treatment and transcriptome profiling of co-cultures.

Journal: Acta neuropathologica communications

Published: November 14, 2025

Lifetime Risk of First Symptomatic ICH or Seizure in Familial Cerebral Cavernous Malformations: A Multicenter Patient Data Analysis.

Lifetime Risk of First Symptomatic ICH or Seizure in Familial Cerebral Cavernous Malformations: A Multicenter Patient Data Analysis.

Journal: Neurology

Published: July 10, 2025

Familial cerebral cavernous malformations caused by a novel germline structural variant in the KRIT1 gene.

Familial cerebral cavernous malformations caused by a novel germline structural variant in the KRIT1 gene.

Journal: Neurogenetics

Published: June 11, 2025

High-throughput differentiation of human blood vessel organoids reveals overlapping and distinct functions of the cerebral cavernous malformation proteins.

High-throughput differentiation of human blood vessel organoids reveals overlapping and distinct functions of the cerebral cavernous malformation proteins.

Journal: Angiogenesis

Published: December 06, 2024

Oxford Nanopore long-read sequencing with CRISPR/Cas9-mediated target selection for accurate characterization of copy number variants in the LDLR gene.

Oxford Nanopore long-read sequencing with CRISPR/Cas9-mediated target selection for accurate characterization of copy number variants in the LDLR gene.

Journal: European journal of medical genetics

Published: August 15, 2024

Novel postzygotic RASA1 mutation in a patient with Parkes Weber syndrome: A case report and literature review.

Novel postzygotic RASA1 mutation in a patient with Parkes Weber syndrome: A case report and literature review.

Journal: Clinical case reports

Published: June 06, 2024

Cas9-Mediated Nanopore Sequencing Enables Precise Characterization of Structural Variants in CCM Genes.

Cas9-Mediated Nanopore Sequencing Enables Precise Characterization of Structural Variants in CCM Genes.

Journal: International journal of molecular sciences

Published: October 28, 2022

Endothelial Differentiation of CCM1 Knockout iPSCs Triggers the Establishment of a Specific Gene Expression Signature.

Endothelial Differentiation of CCM1 Knockout iPSCs Triggers the Establishment of a Specific Gene Expression Signature.

Journal: International journal of molecular sciences

Published: October 28, 2022

Using CRISPR/Cas9 genome editing in human iPSCs for deciphering the pathogenicity of a novel CCM1 transcription start site deletion.

Using CRISPR/Cas9 genome editing in human iPSCs for deciphering the pathogenicity of a novel CCM1 transcription start site deletion.

Journal: Frontiers in molecular biosciences

Published: May 25, 2022

Contact-dependent signaling triggers tumor-like proliferation of CCM3 knockout endothelial cells in co-culture with wild-type cells.

Contact-dependent signaling triggers tumor-like proliferation of CCM3 knockout endothelial cells in co-culture with wild-type cells.

Journal: Cellular and molecular life sciences : CMLS

Published: November 17, 2021

Bringing CCM into a dish: cell culture models for cerebral cavernous malformations.

Bringing CCM into a dish: cell culture models for cerebral cavernous malformations.

Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

Published: June 23, 2021

First interchromosomal insertion in a patient with cerebral and spinal cavernous malformations.

First interchromosomal insertion in a patient with cerebral and spinal cavernous malformations.

Journal: Scientific reports

Published: January 07, 2020

Showing 1-12 of 14

Last Updated: 09/26/2026