7 results on '"Kadota, Masayo"'
Search Results
2. A resource of targeted mutant mouse lines for 5,061 genes
- Author
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Birling, Marie-Christine, Yoshiki, Atsushi, Chiani, Francesco, Kaloff, Cornelia, Hörlein, Andreas, Teichmann, Sandy, Tasdemir, Adriane, Krause, Heidi, German, Dorota, Könitzer, Anne, Weber, Sarah, Beig, Joachim, McKay, Matthew, Chin, Hsian-Jean Genie, Bedigian, Richard, Dion, Stephanie, Kutny, Peter, Kelmenson, Jennifer, Perry, Emily, Nguyen-Bresinsky, Dong, Seluke, Audrie, Leach, Timothy, Perkins, Sara, Slater, Amanda, Christou, Skevoulla, Petit, Michaela, Urban, Rachel, Kales, Susan, DaCosta, Michael, McFarland, Michael, Palazola, Rick, Peterson, Kevin A, Svenson, Karen, Braun, Robert E, Taft, Robert, Codner, Gemma F, Rhue, Mark, Garay, Jose, Clary, Dave, Araiza, Renee, Grimsrud, Kristin, Bower, Lynette, Anchell, Nicole L, Jager, Kayla M, Young, Diana L, Dao, Phuong T, DeMayo, Francesco J, Gardiner, Wendy, Bell, Toni, Kenyon, Janet, Stewart, Michelle E, Lynch, Denise, Loeffler, Jorik, Caulder, Adam, Hillier, Rosie, Quwailid, Mohamed M, Zaman, Rumana, Dickinson, Mary E, Santos, Luis, Obata, Yuichi, Iwama, Mizuho, Nakata, Hatsumi, Hashimoto, Tomomi, Kadota, Masayo, Masuya, Hiroshi, Tanaka, Nobuhiko, Miura, Ikuo, Yamada, Ikuko, Doe, Brendan, Furuse, Tamio, Selloum, Mohammed, Jacquot, Sylvie, Ayadi, Abdel, Ali-Hadji, Dalila, Charles, Philippe, Le Marchand, Elise, El Amri, Amal, Kujath, Christelle, Fougerolle, Jean-Victor, Donahue, Leah Rae, Mellul, Peggy, Legeay, Sandrine, Vasseur, Laurent, Moro, Anne-Isabelle, Lorentz, Romain, Schaeffer, Laurence, Dreyer, Dominique, Erbs, Valérie, Eisenmann, Benjamin, Rossi, Giovanni, Fray, Martin D, Luppi, Laurence, Mertz, Annelyse, Jeanblanc, Amélie, Grau, Evelyn, Sinclair, Caroline, Brown, Ellen, Kundi, Helen, Madich, Alla, Woods, Mike, Pearson, Laila, Gambadoro, Alessia, Mayhew, Danielle, Griggs, Nicola, Houghton, Richard, Bussell, James, Ingle, Catherine, Valentini, Sara, Gleeson, Diane, Sethi, Debarati, Bayzetinova, Tanya, Burvill, Jonathan, Adams, David J, Gao, Xiang, Habib, Bishoy, Weavers, Lauren, Maswood, Ryea, Miklejewska, Evelina, Cook, Ross, Platte, Radka, Price, Stacey, Vyas, Sapna, Collinson, Adam, Hardy, Matt, Gertsenstein, Marina, Dalvi, Priya, Iyer, Vivek, West, Tony, Thomas, Mark, Mujica, Alejandro, Sins, Elodie, Barrett, Daniel, Dobbie, Michael, Grobler, Anne, Loots, Glaudina, Gomez-Segura, Alba, Hayeshi, Rose, Scholtz, Liezl-Marie, Bester, Cor, Pheiffer, Wihan, Venter, Kobus, Bosch, Fatima, Goodwin, Leslie O, Heaney, Jason D, Hérault, Yann, de Angelis, Martin Hrabě, Jiang, Si-Tse, Justice, Monica J, Kasparek, Petr, Ayabe, Shinya, King, Ruairidh E, Kühn, Ralf, Lee, Ho, Lee, Youngik, Liu, Zhiwei, Lloyd, K C Kent, Lorenzo, Isabel, Mallon, Ann-Marie, McKerlie, Colin, Meehan, Terrence F, Beaudet, Arthur L, Fuentes, Violeta Munoz, Newman, Stuart, Nutter, Lauryl M J, Oh, Goo Taeg, Pavlovic, Guillaume, Ramirez-Solis, Ramiro, Rosen, Barry, Ryder, Edward J, Santos, Luis A, Schick, Joel, Bottomley, Joanna, Seavitt, John R, Sedlacek, Radislav, Seisenberger, Claudia, Seong, Je Kyung, Skarnes, William C, Sorg, Tania, Steel, Karen P, Tamura, Masaru, Tocchini-Valentini, Glauco P, Wang, Chi-Kuang Leo, Bradley, Allan, Wardle-Jones, Hannah, Wattenhofer-Donzé, Marie, Wells, Sara, Wiles, Michael V, Willis, Brandon J, Wood, Joshua A, Wurst, Wolfgang, Xu, Ying, Consortium, International Mouse Phenotyping, Teboul, Lydia, Brown, Steve D M, Murray, Stephen A, Gallegos, Juan J, Green, Jennie R, Bohat, Ritu, Zimmel, Katie, Pereira, Monica, MacMaster, Suzanne, Tondat, Sandra, Wei, Linda, Carroll, Tracy, Bürger, Antje, Cabezas, Jorge, Fan-Lan, Qing, Jacob, Elsa, Creighton, Amie, Castellanos-Penton, Patricia, Danisment, Ozge, Clarke, Shannon, Joeng, Joanna, Kelly, Deborah, To, Christine, Bushell, Wendy, van Bruggen, Rebekah, Gailus-Durner, Valerie, Fuchs, Helmut, Marschall, Susan, Dunst, Stefanie, Romberger, Markus, Rey, Bernhard, Fessele, Sabine, Gormanns, Philipp, Friedel, Roland, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), and Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
- Subjects
Cancer Research ,Genotype ,Knockout ,International Cooperation ,[SDV]Life Sciences [q-bio] ,Mutant ,Mutagenesis (molecular biology technique) ,cytology [Mouse Embryonic Stem Cells] ,Mouse Mutant Strains ,Biology ,Genome ,Medical and Health Sciences ,Article ,03 medical and health sciences ,Mice ,0302 clinical medicine ,Research community ,ddc:570 ,Genetics ,Animals ,Allele ,Gene ,Genetic Association Studies ,030304 developmental biology ,Mice, Knockout ,0303 health sciences ,Internet ,metabolism [Mouse Embryonic Stem Cells] ,Information Dissemination ,mutant mouse IMPC ,Mouse Embryonic Stem Cells ,Biological Sciences ,Null allele ,Embryonic stem cell ,Phenotype ,Mutagenesis ,Montertondo Mouse Production ,Technology Platforms ,International Mouse Phenotyping Consortium ,Function (biology) ,030217 neurology & neurosurgery ,Gene Deletion ,Developmental Biology - Abstract
The International Mouse Phenotyping Consortium reports the generation of new mouse mutant strains for over 5,000 genes from targeted embryonic stem cells on the C57BL/6N genetic background. This includes 2,850 null alleles for which no equivalent mutant mouse line exists, 2,987 novel conditional-ready alleles, and 4,433 novel reporter alleles. This nearly triples the number of genes with reporter alleles and almost doubles the number of conditional alleles available to the scientific community. When combined with more than 30 years of community effort, the total mutant allele mouse resource covers more than half of the genome. The extensively validated collection is archived and distributed through public repositories, facilitating availability to the worldwide biomedical research community, and expanding our understanding of gene function and human disease.
- Published
- 2021
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3. Development of assisted reproductive technologies for Mus spretus†
- Author
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Hasegawa, Ayumi, primary, Mochida, Keiji, additional, Matoba, Shogo, additional, Inoue, Kimiko, additional, Hama, Daiki, additional, Kadota, Masayo, additional, Hiraiwa, Noriko, additional, Yoshiki, Atsushi, additional, and Ogura, Atsuo, additional
- Published
- 2020
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4. Development of assisted reproductive technologies for Mus spretus†
- Author
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Hasegawa, Ayumi, Mochida, Keiji, Matoba, Shogo, Inoue, Kimiko, Hama, Daiki, Kadota, Masayo, Hiraiwa, Noriko, Yoshiki, Atsushi, and Ogura, Atsuo
- Abstract
The genus Musconsists of many species with high genetic diversity. However, only one species, Mus musculus(the laboratory mouse), is common in biomedical research. The unavailability of assisted reproductive technologies (ARTs) for other Musspecies might be a major reason for their limited use in laboratories. Here, we devised ARTs for Mus spretus(the Algerian mouse), a commonly used wild-derived Musspecies. We found that in vitro production of M. spretusembryos was difficult because of low efficacies of superovulation with equine chorionic gonadotropin or anti-inhibin serum (AIS) (5–8 oocytes per female) and a low fertilization rate following in vitro fertilization (IVF; 15.2%). The primary cause of this was the hardening of the zona pellucida but not the sperm’s fertilizing ability, as revealed by reciprocal IVF with laboratory mice. The largest number of embryos (16 per female) were obtained when females were injected with AIS followed by human chorionic gonadotropin and estradiol injections 24 h later, and then by natural mating. These in vivo-derived 2-cell embryos could be vitrified/warmed with a high survival rate (94%) using an ethylene glycol-based solution. Importantly, more than 60% of such embryos developed into healthy offspring following interspecific embryo transfer into (C57BL/6 × C3H) F1 female mice. Thus, we have devised practical ARTs for Mus spretusmice, enabling efficient production of embryos and animals, with safe laboratory preservation of their strains. In addition, we have demonstrated that interspecific embryo transfer is possible in murine rodents.Embryos from wild-derived Mus spretusmice can be efficiently produced, cryopreserved, and transferred into laboratory mouse females using newly developed assisted reproductive technology protocols.
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- 2021
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5. Devising Assisted Reproductive Technologies for Wild-Derived Strains of Mice: 37 Strains from Five Subspecies of Mus musculus
- Author
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Mochida, Keiji, primary, Hasegawa, Ayumi, additional, Otaka, Naoki, additional, Hama, Daiki, additional, Furuya, Takashi, additional, Yamaguchi, Masaki, additional, Ichikawa, Eri, additional, Ijuin, Maiko, additional, Taguma, Kyuichi, additional, Hashimoto, Michiko, additional, Takashima, Rika, additional, Kadota, Masayo, additional, Hiraiwa, Noriko, additional, Mekada, Kazuyuki, additional, Yoshiki, Atsushi, additional, and Ogura, Atsuo, additional
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- 2014
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6. The Mouse Resources at the RIKEN BioResource Center
- Author
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YOSHIKI, Atsushi, primary, IKE, Fumio, additional, MEKADA, Kazuyuki, additional, KITAURA, Yasuyuki, additional, NAKATA, Hatsumi, additional, HIRAIWA, Noriko, additional, MOCHIDA, Keiji, additional, IJUIN, Maiko, additional, KADOTA, Masayo, additional, MURAKAMI, Ayumi, additional, OGURA, Atsuo, additional, ABE, Kuniya, additional, MORIWAKI, Kazuo, additional, and OBATA, Yuichi, additional
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- 2009
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7. Telephone Cognitive-Behavioral Therapy for Subthreshold Depression and Presenteeism in Workplace: A Randomized Controlled Trial.
- Author
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Furukawa, Toshi A., Horikoshi, Masaru, Kawakami, Norito, Kadota, Masayo, Sasaki, Megumi, Sekiya, Yuki, Hosogoshi, Hiroki, Kashimura, Masami, Asano, Kenichi, Terashima, Hitomi, Iwasa, Kazunori, Nagasaku, Minoru, and Grothaus, Louis C.
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MENTAL depression ,BEHAVIOR therapy ,COGNITIVE therapy ,PUBLIC health ,MENTAL health personnel ,PEOPLE with mental illness - Abstract
Background: Subthreshold depression is highly prevalent in the general population and causes great loss to society especially in the form of reduced productivity while at work (presenteeism). We developed a highly-structured manualized eight-session cognitive-behavioral program with a focus on subthreshold depression in the workplace and to be administered via telephone by trained psychotherapists (tCBT). Methods: We conducted a parallel-group, non-blinded randomized controlled trial of tCBT in addition to the pre-existing Employee Assistance Program (EAP) versus EAP alone among workers with subthreshold depression at a large manufacturing company in Japan. The primary outcomes were depression severity as measured with Beck Depression Inventory-II (BDI-II) and presenteeism as measured with World Health Organization Health and Work Productivity Questionnaire (HPQ). In the course of the trial the follow-up period was shortened in order to increase acceptability of the study. Results: The planned sample size was 108 per arm but the trial was stopped early due to low accrual. Altogether 118 subjects were randomized to tCBT+EAP (n = 58) and to EAP alone (n = 60). The BDI-II scores fell from the mean of 17.3 at baseline to 11.0 in the intervention group and to 15.7 in the control group after 4 months (p<0.001, Effect size = 0.69, 95%CI: 0.32 to 1.05). However, there was no statistically significant decrease in absolute and relative presenteeism (p = 0.44, ES = 0.15, -0.21 to 0.52, and p = 0.50, ES = 0.02, -0.34 to 0.39, respectively). Conclusion: Remote CBT, including tCBT, may provide easy access to quality-assured effective psychotherapy for people in the work force who present with subthreshold depression. Further studies are needed to evaluate the effectiveness of this approach in longer terms. The study was funded by Sekisui Chemicals Co. Ltd. [ABSTRACT FROM AUTHOR]
- Published
- 2012
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