Darren Chambers

UCL Queen Square Institute Of Neurology, Queen Square
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 14 publications

Multi-omics approach identifies a novel recessive pathogenic variant in the TNNT3 gene in two siblings with congenital myopathy.

Multi-omics approach identifies a novel recessive pathogenic variant in the TNNT3 gene in two siblings with congenital myopathy.

Journal: Neuromuscular disorders : NMD
Published: March 11, 2025

A comprehensive spatiotemporal map of dystrophin isoform expression in the developing and adult human brain.

A comprehensive spatiotemporal map of dystrophin isoform expression in the developing and adult human brain.

Journal: Acta neuropathologica communications
Published: December 27, 2024

Somatic SNCA Copy Number Variants in Multiple System Atrophy are Related to Pathology and Inclusions.

Somatic SNCA Copy Number Variants in Multiple System Atrophy are Related to Pathology and Inclusions.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 03, 2022

High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients.

High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients.

Journal: Journal of neuropathology and experimental neurology
Published: September 09, 2021

TRAPPC11-related muscular dystrophy with hypoglycosylation of alpha-dystroglycan in skeletal muscle and brain.

TRAPPC11-related muscular dystrophy with hypoglycosylation of alpha-dystroglycan in skeletal muscle and brain.

Journal: Neuropathology and applied neurobiology
Published: December 29, 2020

The administration of antisense oligonucleotide golodirsen reduces pathological regeneration in patients with Duchenne muscular dystrophy.

The administration of antisense oligonucleotide golodirsen reduces pathological regeneration in patients with Duchenne muscular dystrophy.

Journal: Acta neuropathologica communications
Published: December 11, 2020

Importance of immunohistochemical evaluation of developmentally regulated myosin heavy chains in human muscle biopsies.

Importance of immunohistochemical evaluation of developmentally regulated myosin heavy chains in human muscle biopsies.

Journal: Neuromuscular disorders : NMD
Published: November 19, 2020

Lentiviral Hematopoietic Stem Cell Gene Therapy Rescues Clinical Phenotypes in a Murine Model of Pompe Disease.

Lentiviral Hematopoietic Stem Cell Gene Therapy Rescues Clinical Phenotypes in a Murine Model of Pompe Disease.

Journal: Molecular therapy. Methods & clinical development
Published: March 07, 2020

A high-throughput digital script for multiplexed immunofluorescent analysis and quantification of sarcolemmal and sarcomeric proteins in muscular dystrophies.

A high-throughput digital script for multiplexed immunofluorescent analysis and quantification of sarcolemmal and sarcomeric proteins in muscular dystrophies.

Journal: Acta neuropathologica communications
Published: January 31, 2020

Comparison of veterinary drugs and veterinary homeopathy: part 2.

Comparison of veterinary drugs and veterinary homeopathy: part 2.

Journal: The Veterinary record
Published: August 20, 2017

Comparison of veterinary drugs and veterinary homeopathy: part 1.

Comparison of veterinary drugs and veterinary homeopathy: part 1.

Journal: The Veterinary record
Published: August 13, 2017

A novel high-throughput immunofluorescence analysis method for quantifying dystrophin intensity in entire transverse sections of Duchenne muscular dystrophy muscle biopsy samples.

A novel high-throughput immunofluorescence analysis method for quantifying dystrophin intensity in entire transverse sections of Duchenne muscular dystrophy muscle biopsy samples.

Journal: PloS one
Published: August 03, 2017
Showing 1-12 of 14

Last Updated: 09/26/2026