Kristina Doring

Josef Schneider Str. 2
Wuerzburg, BY 97080, Germany

Last Updated: 09/26/2026

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Found 22 publications

Author Correction: Cotranslational assembly of protein complexes in eukaryotes revealed by ribosome profiling.

Author Correction: Cotranslational assembly of protein complexes in eukaryotes revealed by ribosome profiling.

Journal: Nature

Published: February 04, 2026

Mycophenolic acid treatment drives the emergence of novel SARS-CoV-2 variants.

Mycophenolic acid treatment drives the emergence of novel SARS-CoV-2 variants.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: July 09, 2025

Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related Myopathy.

Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related Myopathy.

Journal: International journal of molecular sciences

Published: July 31, 2024

Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onset.

Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onset.

Journal: Stem cell research

Published: January 30, 2024

Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin C.

Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin C.

Journal: Stem cell research

Published: November 30, 2023

Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene.

Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene.

Journal: International journal of molecular sciences

Published: September 01, 2023

Generation of two human iPSC lines (HIMRi002-A and HIMRi003-A) derived from Caveolinopathy patients with rippling muscle disease.

Generation of two human iPSC lines (HIMRi002-A and HIMRi003-A) derived from Caveolinopathy patients with rippling muscle disease.

Journal: Stem cell research

Published: August 16, 2023

Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality Systems.

Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality Systems.

Journal: Cells

Published: March 28, 2023

Microscopic and Biochemical Hallmarks of BICD2-Associated Muscle Pathology toward the Evaluation of Novel Variants.

Microscopic and Biochemical Hallmarks of BICD2-Associated Muscle Pathology toward the Evaluation of Novel Variants.

Journal: International journal of molecular sciences

Published: February 22, 2023

Generation of a human iPSC line (HIMRi001-A) from a patient with filaminopathy.

Generation of a human iPSC line (HIMRi001-A) from a patient with filaminopathy.

Journal: Stem cell research

Published: February 17, 2023

Homeostatic calcium fluxes, ER calcium release, SOCE, and calcium oscillations in cultured astrocytes are interlinked by a small calcium toolkit.

Homeostatic calcium fluxes, ER calcium release, SOCE, and calcium oscillations in cultured astrocytes are interlinked by a small calcium toolkit.

Journal: Cell calcium

Published: June 23, 2021

A validation study revealed differences in design and performance of MEDLINE search filters for qualitative research.

A validation study revealed differences in design and performance of MEDLINE search filters for qualitative research.

Journal: Journal of clinical epidemiology

Published: September 11, 2019

Showing 1-12 of 22

Last Updated: 09/26/2026