4.7 Article

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

Related references

Note: Only part of the references are listed.
Review Neurosciences

Stem cell-based therapies for Duchenne muscular dystrophy

Congshan Sun et al.

EXPERIMENTAL NEUROLOGY (2020)

Article Biochemistry & Molecular Biology

Dp71 Expression in Human Glioblastoma

Simona Ruggieri et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2019)

Article Biochemistry & Molecular Biology

Identification of the shortest splice variant of Dp71, together with five known variants, in glioblastoma cells

Abdul Qawee Mahyoob Rani et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2019)

Article Biochemistry & Molecular Biology

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

Tatsuya Kawaguchi et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2018)

Review Clinical Neurology

Contributions of Japanese patients to development of antisense therapy for DMD

Masafumi Matsuo et al.

BRAIN & DEVELOPMENT (2016)

Article Cell Biology

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

Atsushi Nishida et al.

HISTOCHEMISTRY AND CELL BIOLOGY (2016)

Editorial Material Endocrinology & Metabolism

The case for eteplirsen: Paving the way for precision medicine

M. Carrie Miceli et al.

MOLECULAR GENETICS AND METABOLISM (2016)

Article Neurosciences

Overexpression of mutant dystrophin Dp71Δ78-79 stimulates cell proliferation

Alma Herrera-Salazar et al.

NEUROREPORT (2016)

Review Biochemistry & Molecular Biology

Satellite Cells in Muscular Dystrophy - Lot in Polarity

Natasha C. Chang et al.

TRENDS IN MOLECULAR MEDICINE (2016)

Review Developmental Biology

Intrinsic and extrinsic mechanisms regulating satellite cell function

Nicolas A. Dumon et al.

DEVELOPMENT (2015)

Article Multidisciplinary Sciences

Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy

Frederique Rau et al.

NATURE COMMUNICATIONS (2015)

Review Biochemistry & Molecular Biology

Perspectives of stem cell therapy in Duchenne muscular dystrophy

Mirella Meregalli et al.

FEBS JOURNAL (2013)

Article Cell & Tissue Engineering

The Origin and Fate of Muscle Satellite Cells

Arif Aziz et al.

STEM CELL REVIEWS AND REPORTS (2012)

Article Biochemistry & Molecular Biology

Characterization of Dp71Δ78-79, a novel dystrophin mutant that stimulates PC12 cell differentiation

Jorge Aragon et al.

JOURNAL OF NEUROCHEMISTRY (2011)

Article Multidisciplinary Sciences

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

Atsushi Nishida et al.

NATURE COMMUNICATIONS (2011)

Article Biochemistry & Molecular Biology

Short Telomeres and Stem Cell Exhaustion Model Duchenne Muscular Dystrophy in mdx/mTR Mice

Alessandra Sacco et al.

Article Biochemistry & Molecular Biology

Neuronal differentiation modulates the dystrophin Dp71d binding to the nuclear matrix

Rafael Rodriguez-Munoz et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2008)

Article Biochemistry & Molecular Biology

Dp71ab/DAPs complex composition changes during the differentiation process in PC12 cells

J. Romo-Yanez et al.

JOURNAL OF CELLULAR BIOCHEMISTRY (2007)

Review Clinical Neurology

Dystrophin and mutations: one gene, several proteins, multiple phenotypes

F Muntoni et al.

LANCET NEUROLOGY (2003)