Masae Morishima - Concepedia

Author

Masae Morishima

Tokyo Women's Medical University

Also Known As

Masae Morishima

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

Tokyo Women's Medical University Baylor College of Medicine Cancer Genetics (United States)Roswell Park Comprehensive Cancer Center Center for Excellence in Education

About

Masae Morishima is an author at Tokyo Women's Medical University specializing in medicine, developmental biology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	2.1K
2	Health Sciences	2	2	1K
3	Public Health	1	1	13
4	Anatomy	1	1	23
5	Biology	1	1	17

Masae Morishima

Publications

Citations

H-Index

Page 1

	Year	Citations
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice Elizabeth A. Lindsay, Francesca Vitelli, Hong Hua Su, Nature Vascular DiseaseDevelopmental BiologyAortic Arch DefectsPhysiologyHematology	2001	1K
<i>Tbx1</i>has a dual role in the morphogenesis of the cardiac outflow tract Huansheng Xu, Masae Morishima, John N. Wylie, Development Cardiac MuscleGeneticsOft MorphogenesisCongenital Heart AnomalyCellular Physiology	2004	378
A pivotal role for endogenous TGF-β-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway Min Xie, Dou Zhang, Jason R.B. Dyck, Proceedings of the National Academy of Sciences Cardiac MuscleAmpk ActivityEndogenous Tgf-β-activated Kinase-1Congenital Heart AnomalyTak1-null Embryos	2006	342
A genetic link between<i>Tbx1</i>and fibroblast growth factor signaling Francesca Vitelli, Ilaria Taddei, Masae Morishima, Development	2002	275
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, Human Molecular Genetics	2007	210
<i>Tbx1</i>expression in pharyngeal epithelia is necessary for pharyngeal arch artery development Zhen Zhang, Fabiana Cerrato, Huansheng Xu, Development	2005	131
Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/ <i>del22q11</i> syndromes Ilaria Taddei, Masae Morishima, Tuong Huynh, Proceedings of the National Academy of Sciences Human Del22q11 SyndromeGeneticsGenetic EpidemiologyDisease Gene IdentificationGenetic Factors	2001	113
Morphological Observations on the Pathogenetic Process of Transposition of the Great Arteries Induced by Retinoic Acid in Mice Hiroshi Yasui, Makoto Nakazawa, Masae Morishima, Circulation	1995	75
Ripply3, a Tbx1 repressor, is required for development of the pharyngeal apparatus and its derivatives in mice Tadashi Okubo, Akinori Kawamura, Jun Takahashi, Development Molecular RegulationCell DeathCytoskeletonDeletion SyndromeCellular Physiology	2010	68
Genetic analysis of Down syndrome-associated heart defects in mice Chunhong Liu, Masae Morishima, Tao Yu, Human Genetics Down SyndromeGenetic AnalysisHeart FailureGenetic DisorderGenetics	2011	50

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