The Bartonella autotransporter BafA activates the host VEGF pathway to drive angiogenesis von Tsukamoto, Kentaro, Shinzawa, Naoaki, Kawai, Akito, Suzuki, Masahiro, Kidoya, Hiroyasu, Takakura, Nobuyuki, Yamaguchi, Hisateru, Kameyama, Toshiki, Inagaki, Hidehito, Kurahashi, Hiroki, Horiguchi, Yasuhiko, Doi, Yohei

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Inherited Chromosomally Integrated Human Herpesvirus 6 Is a Risk Factor for Spontaneous Abortion von Miura, Hiroki, Kawamura, Yoshiki, Ohye, Tamae, Hattori, Fumihiko, Kozawa, Kei, Ihira, Masaru, Yatsuya, Hiroshi, Nishizawa, Haruki, Kurahashi, Hiroki, Yoshikawa, Tetsushi

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Clinical Consequences of Chromothripsis and Other Catastrophic Cellular Events von Fukami, Maki, Kurahashi, Hiroki

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Experimental method for haplotype phasing across the entire length of chromosome 21 in trisomy 21 cells using a chromosome elimination technique von Wakita, Sachiko, Hara, Mari, Kitabatake, Yasuji, Kawatani, Keiji, Kurahashi, Hiroki, Hashizume, Ryotaro

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Age-related decrease of meiotic cohesins in human oocytes von Tsutsumi, Makiko, Fujiwara, Reiko, Nishizawa, Haruki, Ito, Mayuko, Kogo, Hiroshi, Inagaki, Hidehito, Ohye, Tamae, Kato, Takema, Fujii, Takuma, Kurahashi, Hiroki

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CDH1 Is a Specific Marker for Undifferentiated Spermatogonia in Mouse Testes von TOKUDA, Masutaka, KADOKAWA, Yuzo, KURAHASHI, Hiroki, MARUNOUCHI, Tohru

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Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes von Mariya, Tasuku, Kato, Takema, Sugimoto, Takeshi, Miyai, Syunsuke, Inagaki, Hidehito, Ohye, Tamae, Sugihara, Eiji, Muramatsu, Yukako, Mizuno, Seiji, Kurahashi, Hiroki

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A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia von Kawamura, Rie, Kato, Takema, Miyai, Shunsuke, Suzuki, Fumihiko, Naru, Yuki, Kato, Maki, Tanaka, Keiko, Nagasaka, Miwako, Tsutsumi, Makiko, Inagaki, Hidehito, Ioroi, Tomoaki, Yoshida, Makiko, Nao, Tomoya, Conlin, Laura K, Iijima, Kazumoto, Kurahashi, Hiroki, Taniguchi-Ikeda, Mariko

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Antisense oligonucleotide induced pseudoexon skipping and restoration of functional protein for Fukuyama muscular dystrophy caused by a deep-intronic variant von Enkhjargal, Sarantuya, Sugahara, Kana, Khaledian, Behnoush, Nagasaka, Miwako, Inagaki, Hidehito, Kurahashi, Hiroki, Koshimizu, Hisatsugu, Toda, Tatsushi, Taniguchi-Ikeda, Mariko

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Incontinentia pigmenti inherited from a father with a low level atypical IKBKG deletion mosaicism: a case report von Kawai, Miki, Sugimoto, Atsuya, Ishihara, Yasunori, Kato, Takema, Kurahashi, Hiroki

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

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Identification of a Novel Mutation in Carboxyl Ester Lipase Gene in a Patient with MODY-like Diabetes von Kondoh, Tomomi, Nakajima, Yoko, Yokoi, Katsuyuki, Matsumoto, Yuji, Inagaki, Hidehito, Kato, Takema, Nakajima, Yoichi, Ito, Tetsuya, Yoshikawa, Tetsushi, Kurahashi, Hiroki

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Chromosomal translocations and palindromic AT-rich repeats von Kato, Takema, Kurahashi, Hiroki, Emanuel, Beverly S

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Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structures von Inagaki, Hidehito, Ota, Sayuri, Nishizawa, Haruki, Miyamura, Hironori, Nakahira, Kumiko, Suzuki, Machiko, Nishiyama, Sachie, Kato, Takema, Yanagihara, Itaru, Kurahashi, Hiroki

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Chromosomally integrated human herpesvirus 6 in the Japanese population von Miura, Hiroki, Kawamura, Yoshiki, Hattori, Fumihiko, Kozawa, Kei, Ihira, Masaru, Ohye, Tamae, Kurahashi, Hiroki, Yoshikawa, Tetsushi

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Familial cardiac septal defect due to a novel nine‐base deletion in TBX20 von Yamamoto, Hidenori, Inagaki, Hidehito, Hayano, Satoshi, Kurahashi, Hiroki, Kato, Taichi

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Increased levels of nectin-4 as a serological marker for pre-eclampsia von Yoshizawa, Hikari, Nishizawa, Haruki, Ito, Mayuko, Ohwaki, Akiko, Sakabe, Yoshiko, Sekiya, Takao, Fujii, Takuma, Kurahashi, Hiroki

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Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy von Taniguchi-Ikeda, Mariko, Kobayashi, Kazuhiro, Kanagawa, Motoi, Yu, Chih-chieh, Mori, Kouhei, Oda, Tetsuya, Kuga, Atsushi, Kurahashi, Hiroki, Akman, Hasan O., DiMauro, Salvatore, Kaji, Ryuji, Yokota, Toshifumi, Takeda, Shin’ichi, Toda, Tatsushi

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Myoinositol to Total Choline Ratio in Glioblastomas as a Potential Prognostic Factor in Preoperative Magnetic Resonance Spectroscopy von KUMON, Masanobu, NAKAE, Shunsuke, MURAYAMA, Kazuhiro, KATO, Takema, OHBA, Shigeo, INAMASU, Joji, YAMADA, Seiji, ABE, Masato, SASAKI, Hikaru, OHNO, Yoshiharu, HASEGAWA, Mitsuhiro, KURAHASHI, Hiroki, HIROSE, Yuichi

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Comparative gene expression profiling of placentas from patients with severe pre-eclampsia and unexplained fetal growth restriction von Nishizawa, Haruki, Ota, Sayuri, Suzuki, Machiko, Kato, Takema, Sekiya, Takao, Kurahashi, Hiroki, Udagawa, Yasuhiro

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