Steffen Uebe

Erlangen, BY 91054, Germany

Last Updated: 09/26/2026

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Found 94 publications

Developmental and Structural Alterations at the Ductus-Aortic Isthmus Interface in Infantile Coarctation of the Aorta: A Biological Basis for Persistent Vascular Disease Beyond Anatomical Repair.

Developmental and Structural Alterations at the Ductus-Aortic Isthmus Interface in Infantile Coarctation of the Aorta: A Biological Basis for Persistent Vascular Disease Beyond Anatomical Repair.

Journal: Journal of clinical medicine
Published: June 04, 2026

LAMA5 links extracellular matrix organization to a candidate WNT-associated endothelial signaling niche during human chondrogenesis.

LAMA5 links extracellular matrix organization to a candidate WNT-associated endothelial signaling niche during human chondrogenesis.

Journal: iScience
Published: April 24, 2026

A multi-omics approach to characterize a deep intronic ARID1A deletion in Coffin-Siris syndrome.

A multi-omics approach to characterize a deep intronic ARID1A deletion in Coffin-Siris syndrome.

Journal: European journal of medical genetics
Published: February 06, 2026

A single-donor proof-of-concept single-cell analysis maps heterogeneous differentiation trajectories toward cartilage-like states in human urine-derived stem cells.

A single-donor proof-of-concept single-cell analysis maps heterogeneous differentiation trajectories toward cartilage-like states in human urine-derived stem cells.

Journal: Stem cell research & therapy
Published: November 28, 2025

Exploring Differentially Expressed Genes and Understanding the Underlying Mechanisms in Glioblastoma.

Exploring Differentially Expressed Genes and Understanding the Underlying Mechanisms in Glioblastoma.

Journal: Biochemical genetics
Published: March 03, 2025

Proteasomal activation ameliorates neuronal phenotypes linked to FBXO11-deficiency.

Proteasomal activation ameliorates neuronal phenotypes linked to FBXO11-deficiency.

Journal: HGG advances
Published: November 15, 2024

R405W Desmin Knock-In Mice Highlight Alterations of Mitochondria, Protein Quality Control and Myofibrils in Myofibrillar Myopathy.

R405W Desmin Knock-In Mice Highlight Alterations of Mitochondria, Protein Quality Control and Myofibrils in Myofibrillar Myopathy.

Journal: Journal of cachexia, sarcopenia and muscle
Published: October 21, 2024

Genetic liability to psoriasis predicts severe disease outcomes.

Genetic liability to psoriasis predicts severe disease outcomes.

Journal: Genome medicine
Published: July 07, 2024

Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia.

Acid sphingomyelinase activity suggests a new antipsychotic pharmaco-treatment strategy for schizophrenia.

Journal: Molecular psychiatry
Published: May 07, 2024

Severe manifestation of Rauch-Azzarello syndrome associated with biallelic deletion of CTNND2.

Severe manifestation of Rauch-Azzarello syndrome associated with biallelic deletion of CTNND2.

Journal: Clinical genetics
Published: February 19, 2024

P2RX7 gene variants associate with altered inflammasome assembly and reduced pyroptosis in chronic nonbacterial osteomyelitis (CNO).

P2RX7 gene variants associate with altered inflammasome assembly and reduced pyroptosis in chronic nonbacterial osteomyelitis (CNO).

Journal: Journal of autoimmunity
Published: December 01, 2023

GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets.

GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets.

Journal: medRxiv : the preprint server for health sciences
Published: October 24, 2023
Showing 1-12 of 94

Last Updated: 09/26/2026