Markus J. Kraiger

Neuherberg, BY 85764, Germany

Last Updated: 09/26/2026

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Found 17 publications

Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita.

Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita.

Journal: Science advances

Published: April 11, 2025

A fin-loop-like structure in GPX4 underlies neuroprotection from ferroptosis.

A fin-loop-like structure in GPX4 underlies neuroprotection from ferroptosis.

Journal: Cell

Published: March 29, 2024

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

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).

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

GPR101 loss promotes insulin resistance and diet-induced obesity risk.

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.

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

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

X-ray multiscale 3D neuroimaging to quantify cellular aging and neurodegeneration postmortem in a model of Alzheimer's disease.

X-ray multiscale 3D neuroimaging to quantify cellular aging and neurodegeneration postmortem in a model of Alzheimer's disease.

Journal: European journal of nuclear medicine and molecular imaging

Published: March 12, 2022

Showing 1-12 of 17

Last Updated: 09/26/2026