DNA-Binding Specificities of Human Transcription Factors von Jolma, Arttu, Yan, Jian, Whitington, Thomas, Toivonen, Jarkko, Nitta, Kazuhiro R., Rastas, Pasi, Morgunova, Ekaterina, Enge, Martin, Taipale, Mikko, Wei, Gonghong, Palin, Kimmo, Vaquerizas, Juan M., Vincentelli, Renaud, Luscombe, Nicholas M., Hughes, Timothy R., Lemaire, Patrick, Ukkonen, Esko, Kivioja, Teemu, Taipale, Jussi

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Impact of cytosine methylation on DNA binding specificities of human transcription factors von Yin, Yimeng, Morgunova, Ekaterina, Jolma, Arttu, Kaasinen, Eevi, Sahu, Biswajyoti, Khund-Sayeed, Syed, Das, Pratyush K., Kivioja, Teemu, Dave, Kashyap, Zhong, Fan, Nitta, Kazuhiro R., Taipale, Minna, Popov, Alexander, Ginno, Paul A., Domcke, Silvia, Yan, Jian, Schübeler, Dirk, Vinson, Charles, Taipale, Jussi

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The interaction landscape between transcription factors and the nucleosome von Zhu, Fangjie, Farnung, Lucas, Kaasinen, Eevi, Sahu, Biswajyoti, Yin, Yimeng, Wei, Bei, Dodonova, Svetlana O., Nitta, Kazuhiro R., Morgunova, Ekaterina, Taipale, Minna, Cramer, Patrick, Taipale, Jussi

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DNA-dependent formation of transcription factor pairs alters their binding specificity von Jolma, Arttu, Yin, Yimeng, Nitta, Kazuhiro R., Dave, Kashyap, Popov, Alexander, Taipale, Minna, Enge, Martin, Kivioja, Teemu, Morgunova, Ekaterina, Taipale, Jussi

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ANISEED 2019: 4D exploration of genetic data for an extended range of tunicates von Dardaillon, Justine, Dauga, Delphine, Simion, Paul, Faure, Emmanuel, Onuma, Takeshi A, DeBiasse, Melissa B, Louis, Alexandra, Nitta, Kazuhiro R, Naville, Magali, Besnardeau, Lydia, Reeves, Wendy, Wang, Kai, Fagotto, Marie, Guéroult-Bellone, Marion, Fujiwara, Shigeki, Dumollard, Rémi, Veeman, Michael, Volff, Jean-Nicolas, Roest Crollius, Hugues, Douzery, Emmanuel, Ryan, Joseph F, Davidson, Bradley, Nishida, Hiroki, Dantec, Christelle, Lemaire, Patrick

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High-Throughput Protein Production Combined with High- Throughput SELEX Identifies an Extensive Atlas of Ciona robusta Transcription Factor DNA-Binding Specificities von Nitta, Kazuhiro R., Vincentelli, Renaud, Jacox, Edwin, Cimino, Agnès, Ohtsuka, Yukio, Sobral, Daniel, Satou, Yutaka, Cambillau, Christian, Lemaire, Patrick

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Conservation of transcription factor binding specificities across 600 million years of bilateria evolution von Nitta, Kazuhiro R, Jolma, Arttu, Yin, Yimeng, Morgunova, Ekaterina, Kivioja, Teemu, Akhtar, Junaid, Hens, Korneel, Toivonen, Jarkko, Deplancke, Bart, Furlong, Eileen E M, Taipale, Jussi

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ANISEED 2017: extending the integrated ascidian database to the exploration and evolutionary comparison of genome-scale datasets von Brozovic, Matija, Dantec, Christelle, Dardaillon, Justine, Dauga, Delphine, Faure, Emmanuel, Gineste, Mathieu, Louis, Alexandra, Naville, Magali, Nitta, Kazuhiro R, Piette, Jacques, Reeves, Wendy, Scornavacca, Céline, Simion, Paul, Vincentelli, Renaud, Bellec, Maelle, Aicha, Sameh Ben, Fagotto, Marie, Guéroult-Bellone, Marion, Haeussler, Maximilian, Jacox, Edwin, Lowe, Elijah K, Mendez, Mickael, Roberge, Alexis, Stolfi, Alberto, Yokomori, Rui, Brown, C Titus, Cambillau, Christian, Christiaen, Lionel, Delsuc, Frédéric, Douzery, Emmanuel, Dumollard, Rémi, Kusakabe, Takehiro, Nakai, Kenta, Nishida, Hiroki, Satou, Yutaka, Swalla, Billie, Veeman, Michael, Volff, Jean-Nicolas, Lemaire, Patrick

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Novel ITPA variants identified by whole genome sequencing and RNA sequencing von Omichi, Nanako, Kishita, Yoshihito, Nakama, Mina, Sasai, Hideo, Terazawa, Atsushi, Kobayashi, Emiko, Fushimi, Takuya, Sugiyama, Yohei, Ichimoto, Keiko, Nitta, Kazuhiro R, Yatsuka, Yukiko, Ohtake, Akira, Murayama, Kei, Okazaki, Yasushi

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Ten-Year Clinical Observation of Immunoglobulin G4-Related Coronary Periarteritis with Aneurysms von Nitta, Kazuhiro, Hamamoto, Masaki, Fujii, Takashi, Shokawa, Tomoki, Zaitsu, Junichi

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Involvement of GLCCI1 in mouse spermatogenesis von Takada, Masaru, Fukuhara, Daisuke, Takiura, Toshihiko, Nishibori, Yukino, Kotani, Masashi, Kiuchi, Zentaro, Kudo, Akihiko, Beltcheva, Olga, Ito‐Nitta, Noriko, Nitta, Kazuhiro R., Kimura, Toru, Suehiro, Jun‐Ichi, Katada, Tomohisa, Takematsu, Hiromu, Yan, Kunimasa

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Genome sequencing and RNA‐seq analyses of mitochondrial complex I deficiency revealed Alu insertion‐mediated deletion in NDUFV2 von Kishita, Yoshihito, Shimura, Masaru, Kohda, Masakazu, Fushimi, Takuya, Nitta, Kazuhiro R., Yatsuka, Yukiko, Hirose, Shinichi, Ideguchi, Hiroshi, Ohtake, Akira, Murayama, Kei, Okazaki, Yasushi

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Long-term prognosis and genetic background of cardiomyopathy in 223 pediatric mitochondrial disease patients von Imai-Okazaki, Atsuko, Matsunaga, Ayako, Yatsuka, Yukiko, Nitta, Kazuhiro R., Kishita, Yoshihito, Sugiura, Ayumu, Sugiyama, Yohei, Fushimi, Takuya, Shimura, Masaru, Ichimoto, Keiko, Tajika, Makiko, Ogawa-Tominaga, Minako, Ebihara, Tomohiro, Matsuhashi, Tetsuro, Tsuruoka, Tomoko, Kohda, Masakazu, Hirata, Tomoko, Harashima, Hiroko, Nojiri, Shuko, Takeda, Atsuhito, Nakaya, Akihiro, Kogaki, Shigetoyo, Sakata, Yasushi, Ohtake, Akira, Murayama, Kei, Okazaki, Yasushi

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A homozygous variant in NDUFA8 is associated with developmental delay, microcephaly, and epilepsy due to mitochondrial complex I deficiency von Yatsuka, Yukiko, Kishita, Yoshihito, Formosa, Luke E., Shimura, Masaru, Nozaki, Fumihito, Fujii, Tatsuya, Nitta, Kazuhiro R., Ohtake, Akira, Murayama, Kei, Ryan, Michael T., Okazaki, Yasushi

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Associations of frontal QRS-T angle with left ventricular volume and function derived from ECG-gated SPECT in patients with advanced chronic kidney disease von Kurisu, Satoshi, Nitta, Kazuhiro, Watanabe, Noriaki, Ikenaga, Hiroki, Ishibashi, Ken, Fukuda, Yukihiro, Nakano, Yukiko

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Non-Invasive Central Venous Pressure Measurement Using Enclosed-Zone Central Venous Pressure (ezCVPTM) von Hidaka, Takayuki, Sumimoto, Yoji, Dohi, Yoshihiro, Morimoto, Haruka, Susawa, Hitoshi, Nitta, Kazuhiro, Ishibashi, Ken, Kurisu, Satoru, Fukuda, Yukihiro, Hashimoto, Haruki, Matsui, Shogo, Kishimoto, Shinji, Kajikawa, Masato, Maruhashi, Tatsuya, Ukawa, Teiji, Goto, Chikara, Nakashima, Ayumu, Noma, Kensuke, Tsuji, Toshio, Kihara, Yasuki, Higashi, Yukihito

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Author Correction: Myt1l safeguards neuronal identity by actively repressing many non-neuronal fates von Mall, Moritz, Kareta, Michael S., Chanda, Soham, Ahlenius, Henrik, Perotti, Nicholas, Zhou, Bo, Grieder, Sarah D., Ge, Xuecai, Drake, Sienna, Ang, Cheen Euong, Walker, Brandon M., Vierbuchen, Thomas, Fuentes, Daniel R., Brennecke, Philip, Nitta, Kazuhiro R., Jolma, Arttu, Steinmetz, Lars M., Taipale, Jussi, Südhof, Thomas C., Wernig, Marius

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Clinical heterogeneity in patients with m.4412G > A MT-TM mutation and different heteroplasmy levels von Imai-Okazaki, Atsuko, Yagi, Nobuyasu, Nitta, Kazuhiro R., Murayama, Kei, Ohtake, Akira, Okazaki, Yasushi

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Effects of upright T-wave in lead aVR on left ventricular volume and function derived from ECG-gated SPECT in patients with advanced chronic kidney disease von Kurisu, Satoshi, Nitta, Kazuhiro, Watanabe, Noriaki, Ikenaga, Hiroki, Ishibashi, Ken, Fukuda, Yukihiro, Nakano, Yukiko

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Impact of measuring heteroplasmy of a pathogenic mitochondrial DNA variant at the single‐cell level in individuals with mitochondrial disease von Imai‐Okazaki, Atsuko, Nitta, Kazuhiro R., Yatsuka, Yukiko, Sugiura, Ayumu, Arao, Masato, Shimura, Masaru, Ebihara, Tomohiro, Onuki, Takanori, Ichimoto, Keiko, Ohtake, Akira, Murayama, Kei, Okazaki, Yasushi

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