Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Dharminder Panesar"'
Autor:
Yusuke Echigoya, Yoshitsugu Aoki, Bailey Miskew, Dharminder Panesar, Aleksander Touznik, Tetsuya Nagata, Jun Tanihata, Akinori Nakamura, Kanneboyina Nagaraju, Toshifumi Yokota
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 4, Iss C (2015)
Antisense-mediated exon skipping, which can restore the reading frame, is a most promising therapeutic approach for Duchenne muscular dystrophy. Remaining challenges include the limited applicability to patients and unclear function of truncated dyst
Externí odkaz:
https://doaj.org/article/6bc18960718c4289bda5d2ae2bc32605
Autor:
Yusuke Echigoya, Joshua Lee, Merryl Rodrigues, Tetsuya Nagata, Jun Tanihata, Ashkan Nozohourmehrabad, Dharminder Panesar, Bailey Miskew, Yoshitsugu Aoki, Toshifumi Yokota
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e69194 (2013)
Duchenne muscular dystrophy (DMD), one of the most common and lethal genetic disorders, and the mdx mouse myopathies are caused by a lack of dystrophin protein. These dystrophic muscles contain sporadic clusters of dystrophin-expressing revertant fib
Externí odkaz:
https://doaj.org/article/1ddac4de1d0e4d3182a09b6404df8041
Autor:
Ryszard Kole, Rika Maruyama, Yoshitsugu Aoki, Tetsuya Nagata, Yusuke Echigoya, T. Partridge, Nhu Trieu, Shin'ichi Takeda, Toshifumi Yokota, Peter Sazani, Kenji Rowel Q. Lim, Dharminder Panesar, Nobuyuki Urasawa, Akinori Nakamura, Hong M. Moulton, Mutsuki Kuraoka, Patrick L. Iversen, Takashi Saito
Publikováno v:
Proceedings of the National Academy of Sciences. 114:4213-4218
Duchenne muscular dystrophy (DMD) is a lethal genetic disorder caused by an absence of the dystrophin protein in bodywide muscles, including the heart. Cardiomyopathy is a leading cause of death in DMD. Exon skipping via synthetic phosphorodiamidate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20b6817f8b4a384b306e9a413a0c0724
https://doi.org/10.1073/pnas.1613203114
https://doi.org/10.1073/pnas.1613203114
Autor:
Bailey Miskew, Tetsuya Nagata, Jun Tanihata, Dharminder Panesar, Merryl Rodrigues, Ashkan Nozohourmehrabad, Joshua Lee, Yoshitsugu Aoki, Yusuke Echigoya, Toshifumi Yokota
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e69194 (2013)
PLoS ONE
PLoS ONE
Duchenne muscular dystrophy (DMD), one of the most common and lethal genetic disorders, and the mdx mouse myopathies are caused by a lack of dystrophin protein. These dystrophic muscles contain sporadic clusters of dystrophin-expressing revertant fib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ce7ab1caf2d86693b46b2c74869d2d7
http://europepmc.org/articles/PMC3722172?pdf=render
http://europepmc.org/articles/PMC3722172?pdf=render
Autor:
Tetsuya Nagata, Yusuke Echigoya, Jun Tanihata, Akinori Nakamura, Yoshitsugu Aoki, Kanneboyina Nagaraju, Toshifumi Yokota, Aleksander Touznik, Dharminder Panesar, Bailey Miskew
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 4, Iss C (2015)
Molecular Therapy. Nucleic Acids
Molecular Therapy. Nucleic Acids
Antisense-mediated exon skipping, which can restore the reading frame, is a most promising therapeutic approach for Duchenne muscular dystrophy. Remaining challenges include the limited applicability to patients and unclear function of truncated dyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94f7127177cf0655a5d8a99b5ad67ae5
https://doi.org/10.1038/mtna.2014.76
https://doi.org/10.1038/mtna.2014.76