Valerie Gailus-Durner

26PUBLICATIONS
213CO-AUTHORS
BiomaterialsMedical biochemistry - amino acids and metabolitesCardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (26)

|Oct 24, 2025
Loss of histone macroH2A1.1 causes kidney abnormalities secondary to a change in nutrient metabolization.

René Winkler, Gemma Comas-Armangué, David Corujo

|Apr 23, 2025
Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy.

Nadine Spielmann, Gregor Miller, Tudor I Oprea

|Dec 05, 2024
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes.

Tim P Hasenbein, Sarah Hoelzl, Zachary D Smith

|Aug 28, 2024
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy.

Nadine Spielmann, Gregor Miller, Tudor I Oprea

|Jun 18, 2024
Comparative Phenotyping of Mice Reveals Canonical and Noncanonical Physiological Functions of TRα and TRβ.

Georg Sebastian Hönes, Daniela Geist, Christina Wenzek

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