Dystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells

Proteomic profiling of fatty acid binding proteins in muscular dystrophy

(2020) Paul Dowling et al.   Expert Review of Proteomics

Exploring the HeLa Dark Mitochondrial Proteome

(2020) Federica Marini et al.   Frontiers in Cell and Developmental Biology

Expression of the organic cation/carnitine transporter family (Octn1,-2 and-3) in mdx muscle and heart: Implications for early carnitine therapy in Duchenne muscular dystrophy to improve cellular carnitine homeostasis

(2020) Anne-Marie Lamhonwah et al.   CLINICA CHIMICA ACTA

Mitochondrial Dysfunction Is an Early Consequence of Partial or Complete Dystrophin Loss in mdx Mice

(2020) Timothy M. Moore et al.   Frontiers in Physiology

Power of mitochondrial drug delivery systems to produce innovative nanomedicines

(2020) Yuma Yamada et al.   ADVANCED DRUG DELIVERY REVIEWS

Transport of Ca2+ and Ca2+-dependent permeability transition in heart mitochondria in the early stages of Duchenne muscular dystrophy

(2020) Mikhail V. Dubinin et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS

Dystrophin Dp71ab is monoclonally expressed in human satellite cells and enhances proliferation of myoblast cells

(2020) Manal Farea et al.   Scientific Reports

Effect of Dp71 deficiency on the oxytocin hypothalamic axis in osmoregulation function in mice

(2019) Roza Benabdesselam et al.   ACTA HISTOCHEMICA

Reduced mitochondrial respiration and increased calcium deposits in the EDL muscle, but not in soleus, from 12-week-old dystrophic mdx mice

(2019) Rhayanna B. Gaglianone et al.   Scientific Reports

Early myopathy in Duchenne muscular dystrophy is associated with elevated mitochondrial H 2 O 2 emission during impaired oxidative phosphorylation

(2019) Meghan C. Hughes et al.   Journal of Cachexia Sarcopenia and Muscle

Recurrent DMD Deletions Highlight Specific Role of Dp71 Isoform in Soft-Tissue Sarcomas

(2019) Olivier Mauduit et al.   Cancers

Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy

(2019) Michael Naidoo et al.   MOLECULAR NEUROBIOLOGY

Detection of Dystrophin Dp71 in Human Skeletal Muscle Using an Automated Capillary Western Assay System

(2018) Tatsuya Kawaguchi et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Quantifying and Localizing the Mitochondrial Proteome Across Five Tissues in A Mouse Population

(2018) Evan Graehl Williams et al.   MOLECULAR & CELLULAR PROTEOMICS

Mass spectrometric identification of dystrophin, the protein product of the Duchenne muscular dystrophy gene, in distinct muscle surface membranes

(2017) Sandra Murphy et al.   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

Dystrophin Dp71 Isoforms Are Differentially Expressed in the Mouse Brain and Retina: Report of New Alternative Splicing and a Novel Nomenclature for Dp71 Isoforms

(2017) Jorge Aragón et al.   MOLECULAR NEUROBIOLOGY

Patients with Duchenne muscular dystrophy are significantly shorter than those with Becker muscular dystrophy, with the higher incidence of short stature in Dp71 mutated subgroup

(2017) Masaaki Matsumoto et al.   NEUROMUSCULAR DISORDERS

Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophy

(2016) Maria C Vila et al.   CELL DEATH AND DIFFERENTIATION

HEK293 cells express dystrophin Dp71 with nucleus-specific localization of Dp71ab

(2016) Atsushi Nishida et al.   HISTOCHEMISTRY AND CELL BIOLOGY

Delivery of drugs and macromolecules to the mitochondria for cancer therapy

(2016) Phong Lu et al.   JOURNAL OF CONTROLLED RELEASE

Overexpression of mutant dystrophin Dp71[INCREMENT]78–79 stimulates cell proliferation

(2016) Alma Herrera-Salazar et al.   NEUROREPORT

Purity matters: A workflow for the valid high-resolution lipid profiling of mitochondria from cell culture samples

(2016) Lisa Kappler et al.   Scientific Reports

The Pathogenesis and Therapy of Muscular Dystrophies

(2015) Simon Guiraud et al.   Annual Review of Genomics and Human Genetics

Short stature and pubertal delay in Duchenne muscular dystrophy

(2015) Claire L Wood et al.   ARCHIVES OF DISEASE IN CHILDHOOD

Knocking down Dp71 expression in A549 cells reduces its malignancyin vivoandin vitro

(2015) Sichuang Tan et al.   CANCER INVESTIGATION

Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations

(2015) Valeria Ricotti et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Neuronal SH-SY5Y cells use the C-dystrophin promoter coupled with exon 78 skipping and display multiple patterns of alternative splicing including two intronic insertion events

(2015) Atsushi Nishida et al.   HUMAN GENETICS

Dystrophin Dp71 gene deletion induces retinal vascular inflammation and capillary degeneration

(2015) B. El Mathari et al.   HUMAN MOLECULAR GENETICS

Tissue- and case-specific retention of intron 40 in mature dystrophin mRNA

(2015) Atsushi Nishida et al.   JOURNAL OF HUMAN GENETICS

Revisiting the dystrophin-ATP connection: How half a century of research still implicates mitochondrial dysfunction in Duchenne Muscular Dystrophy aetiology

(2015) Cara A. Timpani et al.   MEDICAL HYPOTHESES

EF-hand domains are involved in the differential cellular distribution of dystrophin Dp40

(2015) Jorge Aragón et al.   NEUROSCIENCE LETTERS

MitoMiner v3.1, an update on the mitochondrial proteomics database

(2015) Anthony C. Smith et al.   NUCLEIC ACIDS RESEARCH

MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins

(2015) Sarah E. Calvo et al.   NUCLEIC ACIDS RESEARCH

PCR-Free Enrichment of Mitochondrial DNA from Human Blood and Cell Lines for High Quality Next-Generation DNA Sequencing

(2015) Meetha P. Gould et al.   PLoS One

Dp412e: a novel human embryonic dystrophin isoform induced by BMP4 in early differentiated cells

(2015) Emmanuelle Massouridès et al.   Skeletal Muscle

Dystrophin is a tumor suppressor in human cancers with myogenic programs

(2014) Yuexiang Wang et al.   NATURE GENETICS

Mitochondrial dysfunction as a central actor in intellectual disability-related diseases: An overview of Down syndrome, autism, Fragile X and Rett syndrome

(2014) Daniela Valenti et al.   NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS

Dystropathology Increases Energy Expenditure and Protein Turnover in the Mdx Mouse Model of Duchenne Muscular Dystrophy

(2014) Hannah G. Radley-Crabb et al.   PLoS One

Defects in Mitochondrial ATP Synthesis in Dystrophin-Deficient Mdx Skeletal Muscles May Be Caused by Complex I Insufficiency

(2014) Emma Rybalka et al.   PLoS One

Preparation of a Mitochondria-targeted and NO-Releasing Nanoplatform and its Enhanced Pro-Apoptotic Effect on Cancer Cells

(2014) Jiangsheng Xu et al.   Small

Comparative proteomic profiling of soleus, extensor digitorum longus, flexor digitorum brevis and interosseus muscles from the mdx mouse model of Duchenne muscular dystrophy

(2013) STEVEN CARBERRY et al.   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

Mitochondrial Dysfunction in Autism

(2013) Agustín Legido et al.   Seminars in Pediatric Neurology

Review on recent advances in the analysis of isolated organelles

(2012) Chad P. Satori et al.   ANALYTICA CHIMICA ACTA

Mitochondria: In Sickness and in Health

(2012) Jodi Nunnari et al.   CELL

Defects in mitochondrial localization and ATP synthesis in the mdx mouse model of Duchenne muscular dystrophy are not alleviated by PDE5 inhibition

(2012) J. M. Percival et al.   HUMAN MOLECULAR GENETICS

Anaplastic medulloblastoma in a child with Duchenne muscular dystrophy

(2012) Machiel van den Akker et al.   Journal of Neurosurgery-Pediatrics

Dystrophin Dp71: The Smallest but Multifunctional Product of the Duchenne Muscular Dystrophy Gene

(2011) Ramin Tadayoni et al.   MOLECULAR NEUROBIOLOGY

Knockdown of Dystrophin Dp71 Impairs PC12 Cells Cycle: Localization in the Spindle and Cytokinesis Structures Implies a Role for Dp71 in Cell Division

(2011) Marcela Villarreal-Silva et al.   PLoS One

Chemical treatment enhances skipping of a mutated exon in the dystrophin gene

(2011) Atsushi Nishida et al.   Nature Communications

Isolation of functional pure mitochondria by superparamagnetic microbeads

(2009) Hue-Tran Hornig-Do et al.   ANALYTICAL BIOCHEMISTRY

Loss of positive allosteric interactions between neuronal nitric oxide synthase and phosphofructokinase contributes to defects in glycolysis and increased fatigability in muscular dystrophy

(2009) M. Wehling-Henricks et al.   HUMAN MOLECULAR GENETICS

Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression

(2009) F. Daoud et al.   HUMAN MOLECULAR GENETICS

Proteome profile of functional mitochondria from human skeletal muscle using one-dimensional gel electrophoresis and HPLC-ESI-MS/MS

(2009) Natalie Lefort et al.   Journal of Proteomics