检索结果 - Inagaki, Hidehito

Failure of homologous synapsis and sex-specific reproduction problems 由 Kurahashi, Hiroki, Kogo, Hiroshi, Tsutsumi, Makiko, Inagaki, Hidehito, Ohye, Tamae

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Cruciform extrusion propensity of human translocation-mediating palindromic AT-rich repeats 由 Kogo, Hiroshi, Inagaki, Hidehito, Ohye, Tamae, Kato, Takema, Emanuel, Beverly S., Kurahashi, Hiroki

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Palindrome-mediated chromosomal translocations in humans 由 Kurahashi, Hiroki, Inagaki, Hidehito, Ohye, Tamae, Kogo, Hiroshi, Kato, Takema, Emanuel, Beverly S.

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Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements 由 Inagaki, Hidehito, Kato, Takema, Tsutsumi, Makiko, Ouchi, Yuya, Ohye, Tamae, Kurahashi, Hiroki

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Exonic duplication of the OTC gene by a complex rearrangement that likely occurred via a replication-based mechanism: a case report 由 Yokoi, Katsuyuki, Nakajima, Yoko, Inagaki, Hidehito, Tsutsumi, Makiko, Ito, Tetsuya, Kurahashi, Hiroki

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Deficiency of Vgll2 Gene Alters the Gene Expression Profiling of Skeletal Muscle Subjected to Mechanical Overload 由 Hitachi, Keisuke, Inagaki, Hidehito, Kurahashi, Hiroki, Okada, Hitoshi, Tsuchida, Kunihiro, Honda, Masahiko

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Molecular analysis of low‐level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti 由 Kawai, Miki, Kato, Takema, Tsutsumi, Makiko, Shinkai, Yasuko, Inagaki, Hidehito, Kurahashi, Hiroki

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An Analysis of Differentially Expressed Coding and Long Non-Coding RNAs in Multiple Models of Skeletal Muscle Atrophy 由 Hitachi, Keisuke, Nakatani, Masashi, Kiyofuji, Yuri, Inagaki, Hidehito, Kurahashi, Hiroki, Tsuchida, Kunihiro

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A Turner syndrome case associated with dic(Y;22) 由 Kawamura, Rie, Inagaki, Hidehito, Yamada, Midori, Suzuki, Fumihiko, Naru, Yuki, Kurahashi, Hiroki

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Molecular cloning of a translocation breakpoint hotspot in 22q11 由 Kurahashi, Hiroki, Inagaki, Hidehito, Hosoba, Eriko, Kato, Takema, Ohye, Tamae, Kogo, Hiroshi, Emanuel, Beverly S.

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Cruciform DNA Structure Underlies the Etiology for Palindrome-mediated Human Chromosomal Translocations 由 Kurahashi, Hiroki, Inagaki, Hidehito, Yamada, Kouji, Ohye, Tamae, Taniguchi, Mariko, Emanuel, Beverly S., Toda, Tatsushi

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Age has no effect on de novo constitutional t(11;22) translocation frequency in sperm 由 Kato, Takema, Yamada, Kouji, Inagaki, Hidehito, Kogo, Hiroshi, Ohye, Tamae, Emanuel, Beverly S., Kurahashi, Hiroki

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Palindromic AT-Rich Repeat in the NF1 Gene Is Hypervariable in Humans and Evolutionarily Conserved in Primates 由 Inagaki, Hidehito, Ohye, Tamae, Kogo, Hiroshi, Yamada, Kouji, Kowa, Hiroe, Shaikh, Tamim H., Emanuel, Beverly S., Kurahashi, Hiroki

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DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation 由 Kato, Takema, Inagaki, Hidehito, Tong, Maoqing, Kogo, Hiroshi, Ohye, Tamae, Yamada, Kouji, Tsutsumi, Makiko, Emanuel, Beverly S, Kurahashi, Hiroki

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Myogenin promoter‐associated lncRNA Myoparr is essential for myogenic differentiation 由 Hitachi, Keisuke, Nakatani, Masashi, Takasaki, Akihiko, Ouchi, Yuya, Uezumi, Akiyoshi, Ageta, Hiroshi, Inagaki, Hidehito, Kurahashi, Hiroki, Tsuchida, Kunihiro

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Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complex 由 Muto, Yoshinari, Sasaki, Hitomi, Sumitomo, Makoto, Inagaki, Hidehito, Kato, Maki, Kato, Takema, Miyai, Shunsuke, Kurahashi, Hiroki, Shiroki, Ryoichi

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Meiotic Recombination and Spatial Proximity in the Etiology of the Recurrent t(11;22) 由 Ashley, Terry, Gaeth, Ann P., Inagaki, Hidehito, Seftel, Allen, Cohen, Maimon M., Anderson, Lorinda K., Kurahashi, Hiroki, Emanuel, Beverly S.

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Chromosomal instability mediated by non-B DNA: Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans 由 Inagaki, Hidehito, Ohye, Tamae, Kogo, Hiroshi, Kato, Takema, Bolor, Hasbaira, Taniguchi, Mariko, Shaikh, Tamim H., Emanuel, Beverly S., Kurahashi, Hiroki

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Intragenic DOK7 deletion detected by whole-genome sequencing in congenital myasthenic syndromes 由 Azuma, Yoshiteru, Töpf, Ana, Evangelista, Teresinha, Lorenzoni, Paulo José, Roos, Andreas, Viana, Pedro, Inagaki, Hidehito, Kurahashi, Hiroki, Lochmüller, Hanns

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Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells 由 Kurahashi, Hiroki, Inagaki, Hidehito, Kato, Takema, Hosoba, Eriko, Kogo, Hiroshi, Ohye, Tamae, Tsutsumi, Makiko, Bolor, Hasbaira, Tong, Maoqing, Emanuel, Beverly S.

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