logo
科言猫学术研究的AI总结
language
手机端手机端
  • Phone Feature微信小程序
简体中文简体中文
notice消息通知
博客博客
arrow
H

Hisato Yagi

National Institute for Basic Biology
H指数:18
被引数:3,481
浏览量:0

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Mitotic block and epigenetic repression underlie neurodevelopmental defects and neurobehavioral deficits in congenital heart disease

有丝分裂阻滞和表观遗传抑制是先天性心脏病中神经发育缺陷和神经行为障碍的基础。

NATURE COMMUNICATIONS
IF15.7
2025-01-070
OA
Gabriel, George C.; Yagi, Hisato; Tan, Tuantuan; Bais, Abha; Glennon, Benjamin J.; Stapleton, Margaret C.; Huang, Lihua; Reynolds, William T.; Shaffer, Marla G.; Ganapathiraju, Madhavi; Simon, Dennis; Panigrahy, Ashok; Wu, Yijen L.; Lo, Cecilia W.
Validation of a Paralimbic-Related Subcortical Brain Dysmaturation MRI Score in Infants with Congenital Heart Disease
JOURNAL OF CLINICAL MEDICINE
IF2.9
2024-09-270
OAAI
Reynolds, William T.; Votava-Smith, Jodie K.; Gabriel, George; Lee, Vincent K.; Rajagopalan, Vidya; Wu, Yijen; Liu, Xiaoqin; Yagi, Hisato; Slabicki, Ruby; Gibbs, Brian; Tran, Nhu N.; Weisert, Molly; Cabral, Laura; Subramanian, Subramanian; Wallace, Julia; del Castillo, Sylvia; Baust, Tracy; Weinberg, Jacqueline G.; Lorenzi Quigley, Lauren; Gaesser, Jenna; O'Neil, Sharon H.; Schmithorst, Vanessa; Panigrahy, Ashok; Ceschin, Rafael; Lo, Cecilia W.
Cardiomyocyte-Targeting Peptide to Deliver Amiodarone
PHARMACEUTICS
IF5.5
2023-08-093
OAAI
Zahid, Maliha; Weber, Beth; Yurko, Ray; Islam, Kazi; Agrawal, Vaishavi; Lopuszynski, Jack; Yagi, Hisato; Salama, Guy
Uncompensated mitochondrial oxidative stress underlies heart failure in an iPSC-derived model of congenital heart disease
CELL STEM CELL
IF20.4
2022-05-0136
OAAI
Xu, Xinxiu; Jin, Kang; Bais, Abha S.; Zhu, Wenjuan; Yagi, Hisato; Feinstein, Timothi N.; Nguyen, Phong K.; Criscione, Joseph D.; Liu, Xiaoqin; Beutner, Gisela; Karunakaran, Kalyani B.; Rao, Krithika S.; He, Haoting; Adams, Philips; Kuo, Catherine K.; Kostka, Dennis; Pryhober, Gloria S.; Shiva, Sruti; Ganapathiraju, Madhavi K.; Porter, George A.; Ivy-Lin, Jiuann-Huey; Aronow, Bruce; Lo, Cecilia W.
Vertebrate myosin 1d regulates left-right organizer morphogenesis and laterality
NATURE COMMUNICATIONS
IF15.7
2018-08-2326
OAAI
Saydmohammed, Manush; Yagi, Hisato; Calderon, Michael; Clark, Madeline J.; Feinstein, Timothy; Sun, Ming; Stolz, Donna B.; Watkins, Simon C.; Amack, Jeffrey D.; Lo, Cecilia W.; Tsang, Michael
The complex genetics of hypoplastic left heart syndrome
NATURE GENETICS
IF31.8
2017-05-22161
OAAI
Liu, Xiaoqin; Yagi, Hisato; Saeed, Shazina; Bais, Abha S.; Gabriel, George C.; Chen, Zhaohan; Peterson, Kevin A.; Li, You; Schwartz, Molly C.; Reynolds, William T.; Saydmohammed, Manush; Gibbs, Brian; Wu, Yijen; Devine, William; Chatterjee, Bishwanath; Klena, Nikolai T.; Kostka, Dennis; Bentley, Karen L. de Mesy; Ganapathiraju, Madhavi K.; Dexheimer, Phillip; Leatherbury, Linda; Khalifa, Omar; Bhagat, Anchit; Zahid, Maliha; Pu, William; Watkins, Simon; Grossfeld, Paul; Murray, Stephen A.; Porter, George A., Jr.; Tsang, Michael; Martin, Lisa J.; Benson, D. Woodrow; Aronow, Bruce J.; Lo, Cecilia W.
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates
NATURE GENETICS
IF31.8
2015-10-0562
OAAI
Guimier, Anne; Gabriel, George C.; Bajolle, Fanny; Tsang, Michael; Liu, Hui; Noll, Aaron; Schwartz, Molly; El Malti, Rajae; Smith, Laurie D.; Klena, Nikolai T.; Jimenez, Gina; Miller, Neil A.; Oufadem, Myriam; de Bellaing, Anne Moreau; Yagi, Hisato; Saunders, Carol J.; Baker, Candice N.; Di Filippo, Sylvie; Peterson, Kevin A.; Thiffault, Isabelle; Bole-Feysot, Christine; Cooley, Linda D.; Farrow, Emily G.; Masson, Cecile; Schoen, Patric; Deleuze, Jean-Francois; Nitschke, Patrick; Lyonnet, Stanislas; de Pontual, Loic; Murray, Stephen A.; Bonnet, Damien; Kingsmore, Stephen F.; Amiel, Jeanne; Bouvagnet, Patrice; Lo, Cecilia W.; Gordon, Christopher T.
High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy
CIRCULATION
IF38.6
2012-05-08131
OAAI
Nakhleh, Nader; Francis, Richard; Giese, Rachel A.; Tian, Xin; Li, You; Zariwala, Maimoona A.; Yagi, Hisato; Khalifa, Omar; Kureshi, Safina; Chatterjee, Bishwanath; Sabol, Steven L.; Swisher, Matthew; Connelly, Patricia S.; Daniels, Mathew P.; Srinivasan, Ashok; Kuehl, Karen; Kravitz, Nadav; Burns, Kimberlie; Sami, Iman; Omran, Heymut; Barmada, Michael; Olivier, Kenneth; Chawla, Kunal K.; Leigh, Margaret; Jonas, Richard; Knowles, Michael; Leatherbury, Linda; Lo, Cecilia W.
Ripply3, a Tbx1 repressor, is required for development of the pharyngeal apparatus and its derivatives in mice
DEVELOPMENT
IF3.6
2011-01-1552
OAAI
Okubo, Tadashi; Kawamura, Akinori; Takahashi, Jun; Yagi, Hisato; Morishima, Masae; Matsuoka, Rumiko; Takada, Shinji
RETRACTED: Distinct function of 2 chromatin remodeling complexes that share a common subunit, Williams syndrome transcription factor (WSTF) (Retracted article. See vol. 111, pg. 2398, 2014)

撤回: 共有一个共同亚基的2种染色质重塑复合物的独特功能，威廉姆斯综合征转录因子 (WSTF) (撤回的文章。见111卷，2398页，2014页)

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
IF9.1
2009-06-0961
OAAI
Yoshimura, Kimihiro; Kitagawa, Hirochika; Fujiki, Ryoji; Tanabe, Masahiko; Takezawa, Shinichiro; Takada, Ichiro; Yamaoka, Ikuko; Yonezawa, Masayoshi; Kondo, Takeshi; Furutani, Yoshiyuki; Yagi, Hisato; Yoshinaga, Shin; Masuda, Takeyoshi; Fukuda, Toru; Yamamoto, Yoko; Ebihara, Kanae; Li, Dean Y.; Matsuoka, Rumiko; Takeuchi, Jun K.; Matsumoto, Takahiro; Kato, Shigeaki
A new nonsense mutation of SMAD8 associated with pulmonary arterial hypertension
JOURNAL OF MEDICAL GENETICS
IF3.7
2009-02-11192
PREAI
Shintani, M.; Yagi, H.; Nakayama, T.; Saji, T.; Matsuoka, R.
Implications of mutations of activin receptor-like kinase 1 gene (ALK1) in addition to bone morphogenetic protein receptor II gene (BMPR2) in children with pulmonary arterial hypertension
CIRCULATION JOURNAL
IF3.7
2008-01-0187
OAAI
Fujiwara, Maya; Yagi, Hisato; Matsuoka, Rumiko; Akimoto, Kaoru; Furutani, Michiko; Imamura, Shin-Ichiro; Uehara, Ritei; Nakayama, Tomotaka; Takao, Atsuyoshi; Nakazawa, Makoto; Saji, Tsutomu
Germline gain-of-function mutations in RAF1 cause Noonan syndrome
NATURE GENETICS
IF31.8
2007-07-01414
PREAI
Razzaque, M. Abdur; Nishizawa, Tsutomu; Komoike, Yuta; Yagi, Hisato; Furutani, Michiko; Amo, Ryunosuke; Kamisago, Mitsuhiro; Momma, Kazuo; Katayama, Hiroshi; Nakagawa, Masao; Fujiwara, Yuko; Matsushima, Masaki; Mizuno, Katsumi; Tokuyama, Mika; Hirota, Hamao; Muneuchi, Jun; Higashinakagawa, Toru; Matsuoka, Rumiko
Role of TBX1 in human del22q11.2 syndrome
LANCET
IF88.5
2003-10-01703
PREAI
Yagi, H; Furutani, Y; Hamada, H; Sasaki, T; Asakawa, S; Minoshima, S; Ichida, F; Joo, K; Kimura, M; Imamura, S; Kamatani, N; Momma, K; Takao, A; Nakazawa, M; Shimizu, N; Matsuoka, R

研究方向

暂未获取到该数据
C
Cecilia Lo
H 指数:44论文数:353被引数:7,318
R
Rumiko Matsuoka
H 指数:46论文数:213被引数:9,654
G
George C. Gabriel
H 指数:20论文数:64被引数:2,203
W
William Reynolds
H 指数:13论文数:64被引数:678
M
Michael Tsang
H 指数:41论文数:123被引数:5,995
Y
Yijen Wu
H 指数:29论文数:144被引数:3,724
M
Madhavi K. Ganapathiraju
H 指数:25论文数:103被引数:2,769
A
Abha Bais
H 指数:15论文数:39被引数:1,236
A
Ashok Panigrahy
H 指数:48论文数:403被引数:8,845
B
Bruce J. Aronow
H 指数:101论文数:633被引数:3.9万