Cargando…
Detection of Dystrophin Dp71 in Human Skeletal Muscle Using an Automated Capillary Western Assay System
Background: Dystrophin Dp71 is one of the isoforms produced by the DMD gene which is mutated in patients with Duchenne muscular dystrophy (DMD). Although Dp71 is expressed ubiquitously, it has not been detected in normal skeletal muscle. This study was performed to assess the expression of Dp71 in h...
Autores principales: | Kawaguchi, Tatsuya, Niba, Emma Tabe Eko, Rani, Abdul Qawee Mahyoob, Onishi, Yoshiyuki, Koizumi, Makoto, Awano, Hiroyuki, Matsumoto, Masaaki, Nagai, Masashi, Yoshida, Shinobu, Sakakibara, Sachiko, Maeda, Naoyuki, Sato, Osamu, Nishio, Hisahide, Matsuo, Masafumi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032138/ https://www.ncbi.nlm.nih.gov/pubmed/29789502 http://dx.doi.org/10.3390/ijms19061546 |
Ejemplares similares
-
Dystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells
por: Niba, Emma Tabe Eko, et al.
Publicado: (2021) -
Dystrophin Dp71ab is monoclonally expressed in human satellite cells and enhances proliferation of myoblast cells
por: Farea, Manal, et al.
Publicado: (2020) -
DMD transcripts in CRL-2061 rhabdomyosarcoma cells show high levels of intron retention by intron-specific PCR amplification
por: Niba, Emma Tabe Eko, et al.
Publicado: (2017) -
Schwann cell-specific Dp116 is expressed in glioblastoma cells, revealing two novel DMD gene splicing patterns
por: Mahyoob Rani, Abdul Qawee, et al.
Publicado: (2019) -
Intronic Alternative Polyadenylation in the Middle of the DMD Gene Produces Half-Size N-Terminal Dystrophin with a Potential Implication of ECG Abnormalities of DMD Patients
por: Rani, Abdul Qawee Mahyoob, et al.
Publicado: (2020)