Tanja Rodewald-Klein

Neuherberg, BY, Germany

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 23 publications

Loss of histone macroH2A1.1 causes kidney abnormalities secondary to a change in nutrient metabolization.

Loss of histone macroH2A1.1 causes kidney abnormalities secondary to a change in nutrient metabolization.

Journal: Science advances
Published: October 24, 2025

Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).

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).

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.

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

Knockout mouse models as a resource for the study of rare diseases.

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.

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

Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolism.

Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolism.

Journal: iScience
Published: April 21, 2022

Monitoring longitudinal disease progression in a novel murine Kit tumor model using high-field MRI.

Monitoring longitudinal disease progression in a novel murine Kit tumor model using high-field MRI.

Journal: Scientific reports
Published: April 08, 2022

New C3H KitN824K/WT cancer mouse model develops late-onset malignant mammary tumors with high penetrance.

New C3H KitN824K/WT cancer mouse model develops late-onset malignant mammary tumors with high penetrance.

Journal: Scientific reports
Published: April 08, 2022

Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice.

Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice.

Journal: Nature communications
Published: March 25, 2022

Dietary intervention improves health metrics and life expectancy of the genetically obese Titan mouse.

Dietary intervention improves health metrics and life expectancy of the genetically obese Titan mouse.

Journal: Communications biology
Published: June 18, 2021

Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes.

Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes.

Journal: EMBO molecular medicine
Published: April 08, 2021
Showing 1-12 of 23

Last Updated: 09/26/2026