Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Miwako Kitazume"'
Autor:
Shingo Suzuki, Swati Ranade, Ken Osaki, Sayaka Ito, Atsuko Shigenari, Yuko Ohnuki, Akira Oka, Anri Masuya, John Harting, Primo Baybayan, Miwako Kitazume, Junichi Sunaga, Satoko Morishima, Yasuo Morishima, Hidetoshi Inoko, Jerzy K. Kulski, Takashi Shiina
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Although NGS technologies fuel advances in high-throughput HLA genotyping methods for identification and classification of HLA genes to assist with precision medicine efforts in disease and transplantation, the efficiency of these methods are impeded
Externí odkaz:
https://doaj.org/article/8032d101fa594b51968f6f8a8870a9d0
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0151963 (2016)
A majority of facioscapulohumeral muscular dystrophy (FSHD) is caused by contraction of macrosatellite repeats called D4Z4 that are located in the subtelomeric region of human chromosome 4q35. Sequencing the FSHD locus has been technically challengin
Externí odkaz:
https://doaj.org/article/527490a1f3d047bb9411580094cbbfe8
Autor:
Ken Osaki, Yuko Ohnuki, Akira Oka, Yasuo Morishima, Anri Masuya, John Harting, Jerzy K. Kulski, Shingo Suzuki, Takashi Shiina, Satoko Morishima, Atsuko Shigenari, Sayaka Ito, Miwako Kitazume, Primo Baybayan, Hidetoshi Inoko, Swati Ranade, Junichi Sunaga
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Frontiers in Immunology
Frontiers in Immunology
Although NGS technologies fuel advances in high-throughput HLA genotyping methods for identification and classification of HLA genes to assist with precision medicine efforts in disease and transplantation, the efficiency of these methods are impeded
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c7a54d0c10731516e61bacaf0513bb4
https://www.frontiersin.org/article/10.3389/fimmu.2018.02294/full
https://www.frontiersin.org/article/10.3389/fimmu.2018.02294/full
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0151963 (2016)
PLoS ONE
PLoS ONE
A majority of facioscapulohumeral muscular dystrophy (FSHD) is caused by contraction of macrosatellite repeats called D4Z4 that are located in the subtelomeric region of human chromosome 4q35. Sequencing the FSHD locus has been technically challengin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d196e65e9f72c3a9f1f5052321db94a4
http://europepmc.org/articles/PMC4803325?pdf=render
http://europepmc.org/articles/PMC4803325?pdf=render
Autor:
Satowa Suzuki, Makoto Kuroda, Mari Matsui, Kengo Kato, Tamaki Ito, Tsuyoshi Sekizuka, Kumiko Kai, Masanori Hashino, Miwako Kitazume
Publikováno v:
Journal of Biological Methods
This study demonstrated that bead-beating method facilitates a simple and rapid protocol for genomic DNA isolation for Pacific BioSciences (PacBio) sequencing with library construction of sufficient length. The protocol may also be beneficial for ina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff5f3447fb7d26b1b49646690c0faa5f
https://doi.org/10.14440/jbm.2017.169
https://doi.org/10.14440/jbm.2017.169
Autor:
John Harting, Takashi Shiina, Miwako Kitazume, Ken Osaki, Swati Ranade, Shingo Suzuki, Junichi Sunaga, Primo Baybayan
Publikováno v:
Human Immunology. 77:55
Aim We previously reported on the use of the Ion PGM next generation sequencing (NGS) platform to genotype HLA class I and class II genes by a super-high resolution, single-molecule, sequence-based typing (SS-SBT) method. However, HLA alleles could n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f7653da1cdc1509398c7b7aa8c316f2
https://doi.org/10.1016/j.humimm.2016.07.084
https://doi.org/10.1016/j.humimm.2016.07.084