Publications by authors named "Sayoko Nishimura"

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Global trends in mortality related to pulmonary embolism: an epidemiological analysis of data from the World Health Organization mortality database from 2001 to 2023.
Hideharu Hagiya, Ko Harada, Yoshito Nishimura, Maki Yamamoto, Sayoko Nishimura

EClinicalMedicine· August 2025

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Dysregulation of mTOR signalling is a converging mechanism in lissencephaly.
Ce Zhang, Dan Liang, A Gulhan Ercan-Sencicek, Aybike S Bulut, Joelly Cortes, Sayoko Nishimura

Nature· February 2025

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International Trends in Adverse Drug Event-Related Mortality from 2001 to 2019: An Analysis of the World Health Organization Mortality Database from 54 Countries.
Toshihiro Koyama, Shunya Iinuma, Michio Yamamoto, Takahiro Niimura, Yuka Osaki, Sayoko Nishimura

Drug Saf· March 2024

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Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease.
Ketu Mishra-Gorur, Tanyeri Barak, Leon D Kaulen, Octavian Henegariu, Sheng Chih Jin, Sayoko Nishimura

Proc Natl Acad Sci U S A· March 2024

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Super-enhancer hijacking drives ectopic expression of hedgehog pathway ligands in meningiomas.
Mark W Youngblood, Zeynep Erson-Omay, Chang Li, Hinda Najem, Süleyman Coșkun, Sayoko Nishimura

Nat Commun· October 2023

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Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease.
Ketu Mishra-Gorur, Tanyeri Barak, Leon D Kaulen, Octavian Henegariu, Sheng Chih Jin, Sayoko Nishimura

Proc Natl Acad Sci U S A· April 2023

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Altered Expression of Several Molecular Mediators of Cerebrospinal Fluid Production in Mice.
Jared Kaplan, Steven Tommasini, Gang-Qing Yao, Meiling Zhu, Sayoko Nishimura

J Endocr Soc· February 2023

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Cerebrovascular disorders associated with genetic lesions.
Philipp Karschnia, Sayoko Nishimura, Angeliki Louvi

Cell Mol Life Sci· January 2019

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Combined HMG-COA reductase and prenylation inhibition in treatment of CCM.
Sayoko Nishimura, Ketu Mishra-Gorur, JinSeok Park, Yulia V Surovtseva, Said M Sebti

Proc Natl Acad Sci U S A· May 2017

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Functional synergy between cholecystokinin receptors CCKAR and CCKBR in mammalian brain development.
Sayoko Nishimura, Kaya Bilgüvar, Keiko Ishigame, Nenad Sestan, Murat Günel

PLoS One· January 2016

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Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.
A Gulhan Ercan-Sencicek, Samira Jambi, Daniel Franjic, Sayoko Nishimura, Mingfeng Li

Eur J Hum Genet· February 2015

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Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors.
Ketu Mishra-Gorur, Ahmet Okay Çağlayan, Ashleigh E Schaffer, Chiswili Chabu, Octavian Henegariu, Sayoko Nishimura

Neuron· January 2015

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Mutations in KATNB1 cause complex cerebral malformations by disrupting asymmetrically dividing neural progenitors.
Ketu Mishra-Gorur, Ahmet Okay Çağlayan, Ashleigh E Schaffer, Chiswili Chabu, Octavian Henegariu, Sayoko Nishimura

Neuron· December 2014

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Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migration.
Angeliki Louvi, Sayoko Nishimura, Murat Günel

Development· March 2014

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ATF3 protects against renal ischemia-reperfusion injury.
Takumi Yoshida, Hidekazu Sugiura, Michihiro Mitobe, Ken Tsuchiya, Satsuki Shirota, Sayoko Nishimura

J Am Soc Nephrol· February 2008

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Klotho reduces apoptosis in experimental ischaemic acute renal failure.
Hidekazu Sugiura, Takumi Yoshida, Ken Tsuchiya, Michihiro Mitobe, Sayoko Nishimura

Nephrol Dial Transplant· December 2005

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CD2AP expression in a renal ischemia/reperfusion injury model and analysis of its related genes using overexpression and RNA interference technique.
Sayoko Nishimura, Takumi Yoshida, Hidekazu Sugiura, Satsuki Shirota, Ken Tsuchiya

Am J Nephrol· November 2005

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Trans-heterozygous Pkd1 and Pkd2 mutations modify expression of polycystic kidney disease.
Guanqing Wu, Xin Tian, Sayoko Nishimura, Glen S Markowitz, Vivette D'Agati

Hum Mol Genet· August 2002

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Polycystin-2 is an intracellular calcium release channel.
Peter Koulen, Yiqiang Cai, Lin Geng, Yoshiko Maeda, Sayoko Nishimura

Nat Cell Biol· March 2002

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