Dlk1-Dio3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in Duchenne muscular dystrophy

AV Hong, N Bourg, P Sanatine, J Poupiot… - Life Science …, 2023 - life-science-alliance.org
Duchenne muscular dystrophy (DMD) is a severe muscle disease caused by impaired
expression of dystrophin. Whereas mitochondrial dysfunction is thought to play an important …

Verification of Protein Changes Determined by 2D-DIGE Based Proteomics Using Immunofluorescence Microscopy

M Zweyer, K Ohlendieck, D Swandulla - Difference Gel Electrophoresis …, 2022 - Springer
Fluorescence two-dimensional difference gel electrophoresis (2D-DIGE) is a key
biochemical method for the comparative analysis of complex protein mixtures. The …

[HTML][HTML] Digital Pathology: A Comprehensive Review of Open-Source Histological Segmentation Software

AM Pavone, AG Giannone, D Cabibi, S D'Aprile… - …, 2024 - mdpi.com
In the era of digitalization, the biomedical sector has been affected by the spread of artificial
intelligence. In recent years, the possibility of using deep and machine learning methods for …

[HTML][HTML] Molecular and Biochemical Therapeutic Strategies for Duchenne Muscular Dystrophy

L Krishna, A Prashant, YH Kumar, S Paneyala… - Neurology …, 2024 - mdpi.com
Significant progress has been achieved in understanding Duchenne muscular dystrophy
(DMD) mechanisms and developing treatments to slow disease progression. This review …

Bioinformatic Analysis of the Subproteomic Profile of Cardiomyopathic Tissue

S Murphy, M Zweyer, D Swandulla… - … : Methods and Protocols, 2022 - Springer
Following large-scale protein separation by two-dimensional gel electrophoresis or liquid
chromatography, mass spectrometry–based proteomics can be used for the swift …

[HTML][HTML] 组织器官通讯对骨骼肌发育的作用及调控机制研究进展

张孜怡, 贺昭昭, 庞卫军 - 生物工程学报, 2023 - cjb.ijournals.cn
骨骼肌是动物机体最重要的器官之一, 研究骨骼肌发育调控机制对于肌肉相关疾病的诊断以及
家畜肉质的改善都有着重要意义. 骨骼肌发育调控是一个复杂的过程, 受到大量肌肉分泌因子和 …

Sub-region analysis of DMD gene in cases with idiopathic generalized epilepsy

ZJ Lin, BX Huang, LF Su, SY Zhu, JW He, GZ Chen… - neurogenetics, 2023 - Springer
Gene sub-region encoded protein domain is the basic unit for protein structure and function.
The DMD gene is the largest coding gene in humans, with its phenotype relevant to …

[HTML][HTML] 2023 Padua Days of Muscle and Mobility Medicine: post meeting book of abstracts

S Zampieri, I Bersch, H Kern, N Sarabon… - European Journal of …, 2023 - ncbi.nlm.nih.gov
Abstract The 2023 Padua Days of Muscle and Mobility Medicine (Pdm3) were held from
March 29 th to April 1 st, 2023. Most of the abstracts were published electronically in the …

Кардиомиопатии, вызванные патогенными вариантами в гене DMD

СЭ Нагиева, АВ Лавров, СА Смирнихина - Кардиология, 2024 - lib.ossn.ru
Аннотация DMD–ген, расположенный на хромосоме Х и отвечающий за образование
белка дистрофина. Патогенные варианты в гене DMD вызывают такие заболевания …

Spectrinopathies in rare neurological and neuromuscular diseases: large-scale efforts towards the identification of novel molecular causes

L Van de Vondel - 2024 - repository.uantwerpen.be
Rare inherited neurological and neuromuscular diseases affect the central nervous system,
peripheral nervous system, and skeletal muscles. About 80% of rare diseases are estimated …