Andreas Hentschel

Otto Hahn Str. 6b
Dortmund, NW 44227, Germany

Last Updated: 09/26/2026

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Found 72 publications

Hexosamine Pathway Disruption by GFPT1 Loss Drives Coordinated Defects in Glycosylation, Autophagy, and Trafficking.

Hexosamine Pathway Disruption by GFPT1 Loss Drives Coordinated Defects in Glycosylation, Autophagy, and Trafficking.

Journal: Biomolecules

Published: May 01, 2026

Drug-induced autophagic myopathies: Exploring pathophysiology with immunolabelling and proteomics.

Drug-induced autophagic myopathies: Exploring pathophysiology with immunolabelling and proteomics.

Journal: Journal of neuropathology and experimental neurology

Published: January 29, 2026

When muscles matter in SORD neuropathy.

When muscles matter in SORD neuropathy.

Journal: Journal of neuropathology and experimental neurology

Published: January 20, 2026

A dose-escalation and safety gene therapy study in a model of CMT4C neuropathy.

A dose-escalation and safety gene therapy study in a model of CMT4C neuropathy.

Journal: Gene therapy

Published: December 11, 2025

The Omics Molecule Extractor: A Web Application for the Selection of Potential Biomarker Panels.

The Omics Molecule Extractor: A Web Application for the Selection of Potential Biomarker Panels.

Journal: Journal of proteome research

Published: December 01, 2025

Clinical, morphological, and molecular characterization of patients with X-linked myopathy with excessive autophagy (XMEA).

Clinical, morphological, and molecular characterization of patients with X-linked myopathy with excessive autophagy (XMEA).

Journal: Journal of neuropathology and experimental neurology

Published: November 27, 2025

Brachio-cervical inflammatory myopathy: multilevel clinical, histopathological and multi-omic analyses of a syndrome variably associated with systemic sclerosis.

Brachio-cervical inflammatory myopathy: multilevel clinical, histopathological and multi-omic analyses of a syndrome variably associated with systemic sclerosis.

Journal: Acta neuropathologica

Published: November 18, 2025

Combined Histological and Proteomic Analysis Reveals Muscle Denervation in KMT5B-Related Neurodevelopmental Disorder: A Case Report.

Combined Histological and Proteomic Analysis Reveals Muscle Denervation in KMT5B-Related Neurodevelopmental Disorder: A Case Report.

Journal: Journal of clinical medicine

Published: October 21, 2025

A Homozygous CPSF1 Variant Causes Congenital Cataract, Intellectual Disability and Hyperphagia.

A Homozygous CPSF1 Variant Causes Congenital Cataract, Intellectual Disability and Hyperphagia.

Journal: Clinical genetics

Published: October 08, 2025

Exploring molecular signatures in PURA syndrome using muscle proteomics and serum biomarkers.

Exploring molecular signatures in PURA syndrome using muscle proteomics and serum biomarkers.

Journal: Journal of neurology

Published: September 17, 2025

A muscular dystrophy associated with bi-allelic LEMD2 variants: Expanding the genotype of nuclear envelopathies.

A muscular dystrophy associated with bi-allelic LEMD2 variants: Expanding the genotype of nuclear envelopathies.

Journal: Brain pathology (Zurich, Switzerland)

Published: August 20, 2025

Myopathy With Exercise-Induced Intolerance due to Novel Biallelic Variants in OBSCN-A Clinical, Morphological and Molecular Analysis.

Myopathy With Exercise-Induced Intolerance due to Novel Biallelic Variants in OBSCN-A Clinical, Morphological and Molecular Analysis.

Journal: Neuropathology and applied neurobiology

Published: August 05, 2025

Showing 1-12 of 72

Last Updated: 09/26/2026