Sebastian Frohler

Berlin, BE 13125, Germany

Last Updated: 09/26/2026

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Found 21 publications

Atypical KCNQ1/Kv7 channel function in a neonatal diabetes patient: Hypersecretion preceded the failure of pancreatic β-cells.

Atypical KCNQ1/Kv7 channel function in a neonatal diabetes patient: Hypersecretion preceded the failure of pancreatic β-cells.

Journal: iScience
Published: February 29, 2024

Ethanol deprivation and central 5-HT deficiency differentially affect the mRNA editing of the 5-HT2C receptor in the mouse brain.

Ethanol deprivation and central 5-HT deficiency differentially affect the mRNA editing of the 5-HT2C receptor in the mouse brain.

Journal: Pharmacological reports : PR
Published: August 01, 2023

Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation.

Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation.

Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: March 05, 2020

Plasma-based longitudinal mutation monitoring as a potential predictor of disease progression in subjects with adenocarcinoma in advanced non-small cell lung cancer.

Plasma-based longitudinal mutation monitoring as a potential predictor of disease progression in subjects with adenocarcinoma in advanced non-small cell lung cancer.

Journal: BMC cancer
Published: December 03, 2019

A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing.

A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing.

Journal: PLoS genetics
Published: March 05, 2019

Concordance of Genomic Alterations by Next-Generation Sequencing in Tumor Tissue versus Cell-Free DNA in Stage I-IV Non-Small Cell Lung Cancer.

Concordance of Genomic Alterations by Next-Generation Sequencing in Tumor Tissue versus Cell-Free DNA in Stage I-IV Non-Small Cell Lung Cancer.

Journal: The Journal of molecular diagnostics : JMD
Published: December 20, 2018

HDAC4 mutations cause diabetes and induce β-cell FoxO1 nuclear exclusion.

HDAC4 mutations cause diabetes and induce β-cell FoxO1 nuclear exclusion.

Journal: Molecular genetics & genomic medicine
Published: October 17, 2018

Pontine Tegmental Cap Dysplasia in an Extremely Preterm Infant and Review of the Literature.

Pontine Tegmental Cap Dysplasia in an Extremely Preterm Infant and Review of the Literature.

Journal: Journal of child neurology
Published: February 15, 2017

Combining transcription factor binding affinities with open-chromatin data for accurate gene expression prediction.

Combining transcription factor binding affinities with open-chromatin data for accurate gene expression prediction.

Journal: Nucleic acids research
Published: May 27, 2016

Epigenetic dynamics of monocyte-to-macrophage differentiation.

Epigenetic dynamics of monocyte-to-macrophage differentiation.

Journal: Epigenetics & chromatin
Published: April 20, 2016

Epigenomic Profiling of Human CD4+ T Cells Supports a Linear Differentiation Model and Highlights Molecular Regulators of Memory Development.

Epigenomic Profiling of Human CD4+ T Cells Supports a Linear Differentiation Model and Highlights Molecular Regulators of Memory Development.

Journal: Immunity
Published: December 30, 2015

reChIP-seq reveals widespread bivalency of H3K4me3 and H3K27me3 in CD4(+) memory T cells.

reChIP-seq reveals widespread bivalency of H3K4me3 and H3K27me3 in CD4(+) memory T cells.

Journal: Nature communications
Published: December 18, 2015
Showing 1-12 of 21

Last Updated: 09/26/2026