Julia Wack-Calzada
Neuherberg, BY, Germany
Last Updated: 09/26/2026
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Found 49 publications
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita.
Journal: Science advances
Published: April 11, 2025
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes.
Journal: Nature communications
Published: January 26, 2024
Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Journal: medRxiv : the preprint server for health sciences
Published: March 30, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Journal: Kidney international
Published: March 16, 2023
AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) disease.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: March 09, 2023
Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria.
Journal: Human molecular genetics
Published: February 16, 2023
GPR101 loss promotes insulin resistance and diet-induced obesity risk.
Journal: Neuroscience applied
Published: December 20, 2022
Knockout mouse models as a resource for the study of rare diseases.
Journal: Mammalian genome : official journal of the International Mammalian Genome Society
Published: August 12, 2022
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 06, 2022
Monitoring longitudinal disease progression in a novel murine Kit tumor model using high-field MRI.
Journal: Scientific reports
Published: April 08, 2022
Last Updated: 09/26/2026