Sabine Jyrch

Berlin, BE 13353, Germany

Last Updated: 09/26/2026

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Found 8 publications

Generation of an isogenic iPSC line via CRISPR correction of the POMC:W84X mutation for monogenic obesity modeling.

Generation of an isogenic iPSC line via CRISPR correction of the POMC:W84X mutation for monogenic obesity modeling.

Journal: Stem cell research
Published: June 17, 2025

Generation of human induced pluripotent stem cell line from an obesity patient with POMC deficiency due to POMC:W84X mutation.

Generation of human induced pluripotent stem cell line from an obesity patient with POMC deficiency due to POMC:W84X mutation.

Journal: Stem cell research
Published: June 16, 2025

Correction of the Allan-Herndon-Dudley syndrome-causing SLC16A2 mutation G401R in a patient derived hiPSC line.

Correction of the Allan-Herndon-Dudley syndrome-causing SLC16A2 mutation G401R in a patient derived hiPSC line.

Journal: Stem cell research
Published: February 24, 2025

Generation of iPSC lines with SLC16A2:G401R or SLC16A2 knock out.

Generation of iPSC lines with SLC16A2:G401R or SLC16A2 knock out.

Journal: Stem cell research
Published: September 20, 2023

A Setmelanotide-like Effect at MC4R Is Achieved by MC4R Dimer Separation.

A Setmelanotide-like Effect at MC4R Is Achieved by MC4R Dimer Separation.

Journal: Biomolecules
Published: June 21, 2022

3-Iodothyronamine Activates a Set of Membrane Proteins in Murine Hypothalamic Cell Lines.

3-Iodothyronamine Activates a Set of Membrane Proteins in Murine Hypothalamic Cell Lines.

Journal: Frontiers in endocrinology
Published: June 18, 2018

Investigation of Naturally Occurring Single-Nucleotide Variants in Human TAAR1.

Investigation of Naturally Occurring Single-Nucleotide Variants in Human TAAR1.

Journal: Frontiers in pharmacology
Published: August 18, 2017

Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.

Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.

Journal: Journal of medical genetics
Published: April 10, 2014
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Last Updated: 09/26/2026