Publications by authors named "Mitsuru Emi"

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Germline variants predispose to mesothelioma by impairing DNA repair and calcium signaling.
Flavia Novelli, Yoshie Yoshikawa, Veronica Angela Maria Vitto, Lorenzo Modesti, Michael Minaai, Mitsuru Emi

Proc Natl Acad Sci U S A· July 2024

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HMGB1 released by mesothelial cells drives the development of asbestos-induced mesothelioma.
Joelle S Suarez, Flavia Novelli, Keisuke Goto, Michiko Ehara, Mika Steele, Mitsuru Emi

Proc Natl Acad Sci U S A· September 2023

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Medical and Surgical Care of Patients With Mesothelioma and Their Relatives Carrying Germline BAP1 Mutations.
Michele Carbone, Harvey I Pass, Guntulu Ak, H Richard Alexander, Paul Baas, Mitsuru Emi

J Thorac Oncol· July 2022

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Risk prediction for metastasis of clear cell renal cell carcinoma using digital multiplex ligation-dependent probe amplification.
Yoshie Yoshikawa, Yusuke Yamada, Mitsuru Emi, Lilit Atanesyan, Jan Smout

Cancer Sci· January 2022

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Short somatic alterations at the site of copy number variation in breast cancer.
Fumi Murakami, Yumi Tsuboi, Yuka Takahashi, Yoshiya Horimoto, Kaoru Mogushi, Mitsuru Emi

Cancer Sci· January 2021

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Heterozygous germline mutations increase susceptibility to asbestos and mesothelioma.
Angela Bononi, Keisuke Goto, Guntulu Ak, Yoshie Yoshikawa, Mitsuru Emi

Proc Natl Acad Sci U S A· December 2020

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Mesothelioma developing in carriers of inherited genetic mutations.
Yoshie Yoshikawa, Mitsuru Emi, Takashi Nakano, Giovanni Gaudino

Transl Lung Cancer Res· February 2020

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A Subset of Mesotheliomas With Improved Survival Occurring in Carriers of BAP1 and Other Germline Mutations.
Sandra Pastorino, Yoshie Yoshikawa, Harvey I Pass, Mitsuru Emi, Masaki Nasu

J Clin Oncol· October 2018

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Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disorders.
Shingo Koyama, Hidenori Sato, Manabu Wada, Toru Kawanami, Mitsuru Emi

BMC Med Genet· March 2017

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High-density array-CGH with targeted NGS unmask multiple noncontiguous minute deletions on chromosome 3p21 in mesothelioma.
Yoshie Yoshikawa, Mitsuru Emi, Tomoko Hashimoto-Tamaoki, Masaki Ohmuraya, Ayuko Sato

Proc Natl Acad Sci U S A· November 2016

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Combined Genetic and Genealogic Studies Uncover a Large BAP1 Cancer Syndrome Kindred Tracing Back Nine Generations to a Common Ancestor from the 1700s.
Michele Carbone, Erin G Flores, Mitsuru Emi, Todd A Johnson, Tatsuhiko Tsunoda

PLoS Genet· December 2015

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Frequent genomic rearrangements of BRCA1 associated protein-1 (BAP1) gene in Japanese malignant mesothelioma-characterization of deletions at exon level.
Mitsuru Emi, Yoshie Yoshikawa, Chika Sato, Ayuko Sato, Hidenori Sato

J Hum Genet· October 2015

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Somatic alteration and depleted nuclear expression of BAP1 in human esophageal squamous cell carcinoma.
Takahiro Mori, Makiko Sumii, Fumiyoshi Fujishima, Kazuko Ueno, Mitsuru Emi

Cancer Sci· September 2015

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High Incidence of Somatic BAP1 alterations in sporadic malignant mesothelioma.
Masaki Nasu, Mitsuru Emi, Sandra Pastorino, Mika Tanji, Amy Powers

J Thorac Oncol· April 2015

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Segmental copy number loss in the region of Semaphorin 4D gene in patients with acetabular dysplasia.
Tomohisa Sekimoto, Miho Ishii, Mitsuru Emi, Syuji Kurogi, Taro Funamoto

J Orthop Res· June 2013

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Frequent inactivation of the BAP1 gene in epithelioid-type malignant mesothelioma.
Yoshie Yoshikawa, Ayuko Sato, Tohru Tsujimura, Mitsuru Emi, Tomonori Morinaga

Cancer Sci· May 2012

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Genome-wide copy number analysis in primary breast cancer.
Takayuki Ueno, Mitsuru Emi, Hidenori Sato, Noriko Ito, Mariko Muta

Expert Opin Ther Targets· March 2012

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Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation.
Satoru Sakazume, Hirofumi Ohashi, Yuki Sasaki, Naoki Harada, Katsumi Nakanishi, Mitsuru Emi

Hum Genet· January 2012

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Frequent loss of genome gap region in 4p16.3 subtelomere in early-onset type 2 diabetes mellitus.
Hirohito Kudo, Mitsuru Emi, Yasushi Ishigaki, Uiko Tsunoda, Yoshinori Hinokio

Exp Diabetes Res· November 2011

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Segmental copy number loss of SFMBT1 gene in elderly individuals with ventriculomegaly: a community-based study.
Takeo Kato, Hidenori Sato, Mitsuru Emi, Tomomi Seino, Shigeki Arawaka

Intern Med· June 2011

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Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy.
Hidenao Sasaki, Mitsuru Emi, Hiroshi Iijima, Noriko Ito, Hidenori Sato

Mol Brain· June 2011

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Molecular analysis of TSC2/PKD1 contiguous gene deletion syndrome.
Yoshinobu Oyazato, Kazumoto Iijima, Mitsuru Emi, Takashi Sekine, Koichi Kamei

Kobe J Med Sci· June 2011

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Segmental copy-number gain within the region of isopentenyl diphosphate isomerase genes in sporadic amyotrophic lateral sclerosis.
Takeo Kato, Mitsuru Emi, Hidenori Sato, Shigeki Arawaka, Manabu Wada

Biochem Biophys Res Commun· November 2010

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[iNPH (Idiopathic normal pressure hydrocephalus) and AVIM (asymptomatic ventriculomegaly with features of iNPH on MRI)].
Takeo Kato, Chifumi Iseki, Yoshimi Takahashi, Manabu Wada, Toru Kawanami, Mitsuru Emi

Rinsho Shinkeigaku· November 2010

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[Copy number variation: experimental procedures and statistical analysis].
Hidenori Sato, Mitsuru Emi

Nihon Rinsho· August 2010

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