Julia Calzada-Wack

5PUBLICATIONS
54CO-AUTHORS
Medical biochemistry - amino acids and metabolitesEpigenetics (incl. genome methylation and epigenomics)Molecular targetsNeurology and neuromuscular diseasesGene mapping
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Publications (5)

|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 11, 2025
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita.

Adrián Sanz-Moreno, Lore Becker, Kan Xie

|May 09, 2023
Knockout mouse models as a resource for the study of rare diseases.

Patricia da Silva-Buttkus, Nadine Spielmann, Tanja Klein-Rodewald

|Dec 29, 2021
Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk.

Lillian Garrett, Patricia Da Silva-Buttkus, Birgit Rathkolb

|May 27, 2021
A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouse.

Caroline A Biagosch, Silvia Vidali, Michael Faerberboeck

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Frequent Collaborators

5 joint publications

Martin Hrabě de Angelis

5 joint publications

Lore Becker

4 joint publications

Valerie Gailus-Durner

4 joint publications

Birgit Rathkolb