Publications by authors named "Masae Morishima"

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Ultrastructural changes in the choriocapillaris of N-methyl-N-nitrosourea-induced retinal degeneration in C57BL/6 mice.
Ruriko Hayakawa, Kaori Komoike, Hayato Kawakami, Masae Morishima, Kazuhiko Shimizu

Med Mol Morphol· December 2020

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Foxc2 influences alveolar epithelial cell differentiation during lung development.
Mayoko Tsuji, Masae Morishima, Kazuhiko Shimizu, Shunichi Morikawa, Mikael Heglind

Dev Growth Differ· August 2017

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Engineered chromosome-based genetic mapping establishes a 3.7 Mb critical genomic region for Down syndrome-associated heart defects in mice.
Chunhong Liu, Masae Morishima, Xiaoling Jiang, Tao Yu, Kai Meng

Hum Genet· June 2014

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Vasohibin-2 modulates tumor onset in the gastrointestinal tract by normalizing tumor angiogenesis.
Shuji Kitahara, Yasuhiro Suzuki, Masae Morishima, Asuka Yoshii, Sachiko Kikuta

Mol Cancer· May 2014

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Genetic analysis of Down syndrome-associated heart defects in mice.
Chunhong Liu, Masae Morishima, Tao Yu, Sei-Ichi Matsui, Li Zhang

Hum Genet· November 2011

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Ripply3, a Tbx1 repressor, is required for development of the pharyngeal apparatus and its derivatives in mice.
Tadashi Okubo, Akinori Kawamura, Jun Takahashi, Hisato Yagi, Masae Morishima

Development· January 2011

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Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities.
Zhongyou Li, Tao Yu, Masae Morishima, Annie Pao, Jeffrey LaDuca

Hum Mol Genet· June 2007

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A pivotal role for endogenous TGF-beta-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway.
Min Xie, Dou Zhang, Jason R B Dyck, Yi Li, Hui Zhang, Masae Morishima

Proc Natl Acad Sci U S A· November 2006

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A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice.
Y Eugene Yu, Masae Morishima, Annie Pao, Ding-Yan Wang, Xiao-Yan Wen

Genetics· May 2006

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Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development.
Zhen Zhang, Fabiana Cerrato, Huansheng Xu, Francesca Vitelli, Masae Morishima

Development· December 2005

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Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract.
Huansheng Xu, Masae Morishima, John N Wylie, Robert J Schwartz, Benoit G Bruneau

Development· July 2004

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Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis.
Masae Morishima, Hiromi Yanagisawa, Masashi Yanagisawa, Antonio Baldini

Dev Dyn· September 2003

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TBX1 is required for inner ear morphogenesis.
Francesca Vitelli, Antonella Viola, Masae Morishima, Tiziano Pramparo, Antonio Baldini

Hum Mol Genet· August 2003

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A genetic link between Tbx1 and fibroblast growth factor signaling.
Francesca Vitelli, Ilaria Taddei, Masae Morishima, Erik N Meyers, Elizabeth A Lindsay

Development· October 2002

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Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways.
Francesca Vitelli, Masae Morishima, Ilaria Taddei, Elizabeth A Lindsay, Antonio Baldini

Hum Mol Genet· April 2002

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