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Eva Lausberg

Showing results (1-10 of 12) with videos related to

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Journal of Medical Genetics|May 25, 2020
Paternal 132 bp deletion affecting <i>KCNQ1OT1</i> in 11p15.5 is associated with growth retardation but does not affect imprintingThomas Eggermann, Florian Kraft, Eva Lausberg, et al.
Journal of Medical Case Reports|February 24, 2026
Biallelic pathogenic hydroxymethylbilane synthase gene variants of a neurodegenerative disorder with progressive cystic leukoencephalopathy: a case reportGabriel Schacht, Miriam Elbracht, Anna-Elisabeth Minder, et al.
BMC Bioinformatics|December 17, 2024
CNVizard-a lightweight streamlit application for an interactive analysis of copy number variantsJeremias Krause, Carlos Classen, Daniela Dey, et al.
Journal of Medical Genetics|June 14, 2024
Complex structural variation and nonsense variant <i>in trans</i> cause <i>VPS50</i>-related disorderLaura Hecher, Esther Gorski-Alberts, Matthias Begemann, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 22, 2021
A Hypercaloric Diet Induces Early Podocyte Damage in Aged, Non-Diabetic RatsClaudia Seikrit, Eva Lausberg, Eva Miriam Buhl, et al.
Scientific Reports|May 2, 2018
Nucleolar-nucleoplasmic shuttling of TARG1 and its control by DNA damage-induced poly-ADP-ribosylation and by nucleolar transcriptionMareike Bütepage, Christian Preisinger, Alexander von Kriegsheim, et al.
Deutsches Arzteblatt International|March 19, 2026
Exome and Genome Sequencing for the Diagnosis of Rare DiseasesMiriam Elbracht, Jeremias Krause, Larissa Mattern, et al.
Brain : a Journal of Neurology|August 12, 2020
Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuolesCarola Hedberg-Oldfors, Robert Meyer, Kay Nolte, et al.
The Journal of Clinical Investigation|May 4, 2021
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammationEva Lausberg, Sebastian Gießelmann, Joseph P Dewulf, et al.
Frontiers in Cell and Developmental Biology|February 2, 2023
<i>PHIP</i>-associated Chung-Jansen syndrome: Report of 23 new individualsAntje Kampmeier, Elsa Leitão, Ilaria Parenti, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Medical Genetics|May 25, 2020
Paternal 132 bp deletion affecting <i>KCNQ1OT1</i> in 11p15.5 is associated with growth retardation but does not affect imprintingThomas Eggermann, Florian Kraft, Eva Lausberg, et al.
Journal of Medical Case Reports|February 24, 2026
Biallelic pathogenic hydroxymethylbilane synthase gene variants of a neurodegenerative disorder with progressive cystic leukoencephalopathy: a case reportGabriel Schacht, Miriam Elbracht, Anna-Elisabeth Minder, et al.
BMC Bioinformatics|December 17, 2024
CNVizard-a lightweight streamlit application for an interactive analysis of copy number variantsJeremias Krause, Carlos Classen, Daniela Dey, et al.
Journal of Medical Genetics|June 14, 2024
Complex structural variation and nonsense variant <i>in trans</i> cause <i>VPS50</i>-related disorderLaura Hecher, Esther Gorski-Alberts, Matthias Begemann, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 22, 2021
A Hypercaloric Diet Induces Early Podocyte Damage in Aged, Non-Diabetic RatsClaudia Seikrit, Eva Lausberg, Eva Miriam Buhl, et al.
Scientific Reports|May 2, 2018
Nucleolar-nucleoplasmic shuttling of TARG1 and its control by DNA damage-induced poly-ADP-ribosylation and by nucleolar transcriptionMareike Bütepage, Christian Preisinger, Alexander von Kriegsheim, et al.
Deutsches Arzteblatt International|March 19, 2026
Exome and Genome Sequencing for the Diagnosis of Rare DiseasesMiriam Elbracht, Jeremias Krause, Larissa Mattern, et al.
Brain : a Journal of Neurology|August 12, 2020
Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuolesCarola Hedberg-Oldfors, Robert Meyer, Kay Nolte, et al.
The Journal of Clinical Investigation|May 4, 2021
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammationEva Lausberg, Sebastian Gießelmann, Joseph P Dewulf, et al.
Frontiers in Cell and Developmental Biology|February 2, 2023
<i>PHIP</i>-associated Chung-Jansen syndrome: Report of 23 new individualsAntje Kampmeier, Elsa Leitão, Ilaria Parenti, et al.
Pageof 2