Search Results - Machida, Shinichi
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Chromatin architecture may dictate the target site for DMC1, but not for RAD51, during homologous pairing by Kobayashi, Wataru, Takaku, Motoki, Machida, Shinichi, Tachiwana, Hiroaki, Maehara, Kazumitsu, Ohkawa, Yasuyuki, Kurumizaka, Hitoshi
Published 2016Text -
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Recombination Activator Function of the Novel RAD51- and RAD51B-binding Protein, Human EVL by Takaku, Motoki, Machida, Shinichi, Hosoya, Noriko, Nakayama, Shugo, Takizawa, Yoshimasa, Sakane, Isao, Shibata, Takehiko, Miyagawa, Kiyoshi, Kurumizaka, Hitoshi
Published 2009Text -
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Single-stranded DNA catenation mediated by human EVL and a type I topoisomerase by Takaku, Motoki, Takahashi, Daisuke, Machida, Shinichi, Ueno, Hiroyuki, Hosoya, Noriko, Ikawa, Shukuko, Miyagawa, Kiyoshi, Shibata, Takehiko, Kurumizaka, Hitoshi
Published 2010Text -
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Cryo-EM structure of the nucleosome containing the ALB1 enhancer DNA sequence by Takizawa, Yoshimasa, Tanaka, Hiroki, Machida, Shinichi, Koyama, Masako, Maehara, Kazumitsu, Ohkawa, Yasuyuki, Wade, Paul A., Wolf, Matthias, Kurumizaka, Hitoshi
Published 2018Text -
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Exploring histone loading on HIV DNA reveals a dynamic nucleosome positioning between unintegrated and integrated viral genome by Machida, Shinichi, Depierre, David, Chen, Heng-Chang, Thenin-Houssier, Suzie, Petitjean, Gaël, Doyen, Cecile M., Takaku, Motoki, Cuvier, Olivier, Benkirane, Monsef
Published 2020Text -
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H3K14 ubiquitylation promotes H3K9 methylation for heterochromatin assembly by Oya, Eriko, Nakagawa, Reiko, Yoshimura, Yuriko, Tanaka, Mayo, Nishibuchi, Gohei, Machida, Shinichi, Shirai, Atsuko, Ekwall, Karl, Kurumizaka, Hitoshi, Tagami, Hideaki, Nakayama, Jun‐ichi
Published 2019Text -
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N-terminal phosphorylation of HP1α increases its nucleosome-binding specificity by Nishibuchi, Gohei, Machida, Shinichi, Osakabe, Akihisa, Murakoshi, Hiromu, Hiragami-Hamada, Kyoko, Nakagawa, Reiko, Fischle, Wolfgang, Nishimura, Yoshifumi, Kurumizaka, Hitoshi, Tagami, Hideaki, Nakayama, Jun-ichi
Published 2014Text -
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GATA3-dependent cellular reprogramming requires activation-domain dependent recruitment of a chromatin remodeler by Takaku, Motoki, Grimm, Sara A., Shimbo, Takashi, Perera, Lalith, Menafra, Roberta, Stunnenberg, Hendrik G., Archer, Trevor K., Machida, Shinichi, Kurumizaka, Hitoshi, Wade, Paul A.
Published 2016Text -
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Nap1 stimulates homologous recombination by RAD51 and RAD54 in higher-ordered chromatin containing histone H1 by Machida, Shinichi, Takaku, Motoki, Ikura, Masae, Sun, Jiying, Suzuki, Hidekazu, Kobayashi, Wataru, Kinomura, Aiko, Osakabe, Akihisa, Tachiwana, Hiroaki, Horikoshi, Yasunori, Fukuto, Atsuhiko, Matsuda, Ryo, Ura, Kiyoe, Tashiro, Satoshi, Ikura, Tsuyoshi, Kurumizaka, Hitoshi
Published 2014Text -
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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language by Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.
Published 2018Text -
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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language by Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.
Published 2019Text