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Publications by Elisabeth Steichen-Gersdorf

SLC10A7 Mutations Cause a Skeletal Dysplasia With Amelogenesis Imperfecta Mediated by GAG Biosynthesis Defects

Nature Communications

Molecular Biology

English

Deletions of the RUNX2 Gene Are Present in About 10% of Individuals With Cleidocranial Dysplasia

English

Maternal ABCA1 Genotype Is Associated With Severity of Smith–Lemli–Opitz Syndrome and With Viability of Patients Homozygous for Null Mutations

European Journal of Human Genetics

English

A Newborn With Arterial Tortuosity Syndrome: The Importance of Timely Diagnostic Work-Up in Patients Presenting With Cutis Laxa

Journal of Functional Morphology and Kinesiology

Sports Medicine

Physical Therapy

English

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Multidimensional Proteomics for Cell Biology

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DNA Methylation Pathways and Their Crosstalk With Histone Methylation

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Transcriptional Integration of Metabolism by the Nuclear Sterol-Activated Receptors LXR and FXR

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Tail-Anchored Membrane Protein Insertion Into the Endoplasmic Reticulum

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Dynamin, a Membrane-Remodelling GTPase

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Regulating the Regulator: Post-Translational Modification of RAS

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Trithorax Group Proteins: Switching Genes on and Keeping Them Active

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