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Retrotransposition of Long Interspersed Element 1 Induced by Methamphetamine or Cocaine

The Journal of biological chemistry, 2014-09, Vol.289 (37), p.25476-25485

2014

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Sudden Unexpected Death of Infantile Dilated Cardiomyopathy with JPH2 and PKD1 Gene Variants

International Heart Journal, 2020/09/29, Vol.61(5), pp.1079-1083

2020

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Postmortem Identification of Genetic Variations Associated with Sudden Unexpected Death in Young People

International Heart Journal, 2024/01/31, Vol.65(1), pp.55-62

2024

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Molecular autopsy for sudden death in Japan

Journal of Toxicologic Pathology, 2024, Vol.37(1), pp.1-10

2024

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Identification of Arrhythmogenic Right Ventricular Cardiomyopathy-Causing Gene Mutations in Young Sudden Unexpected Death Autopsy Cases

Journal of forensic sciences, 2015-03, Vol.60 (2), p.457-461

2015

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PROS1 variant in sudden death case of pulmonary embolism caused by calcification in the inferior vena cava: The importance of postmortem genetic analysis

Legal medicine (Tokyo, Japan), 2022-03, Vol.55, p.102029-102029, Article 102029

2022

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Hypertrophy of lymphoid organs is a possible phenotypic characteristic of R420W mutation of the cardiac ryanodine receptor gene: A study using a knock-in mouse model

Legal medicine (Tokyo, Japan), 2014-11, Vol.16 (6), p.326-332

2014

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Postmortem Molecular Screening for Cardiac Ryanodine Receptor Type 2 Mutations in Sudden Unexplained Death: R420W Mutated Case With Characteristics of Status Thymico-Lymphaticus

Circulation Journal, 2006, Vol.70(11), pp.1402-1406

2006

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Bromide detection in blood using energy dispersive X-ray fluorescence; a chemical marker supportive of drowning in seawater

Legal medicine (Tokyo, Japan), 2010-05, Vol.12 (3), p.132-136

2010

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Detection of metallic elements from paraffin-embedded tissue blocks by energy dispersive X-ray fluorescence spectrometry

Legal medicine (Tokyo, Japan), 2010-03, Vol.12 (2), p.102-103

2010

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Sudden death during exercise in a juvenile with arrhythmogenic right ventricular cardiomyopathy and desmoglein-2 gene substitution: A case report

Legal medicine (Tokyo, Japan), 2011-11, Vol.13 (6), p.298-300

2011

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Sudden death of a child because of an intestinal obstruction caused by a large congenital mesenteric defect

Legal medicine (Tokyo, Japan), 2012-05, Vol.14 (3), p.157-159

2012

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Usefulness of serum mast cell-specific chymase levels for postmortem diagnosis of anaphylaxis

International journal of legal medicine, 2005-11, Vol.119 (6), p.331-334

2005

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Postmortem molecular analysis for fatal arrhythmogenic disease in sudden unexplained death

Legal medicine (Tokyo, Japan), 2009-04, Vol.11, p.S119-S120

2009

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Identification of malignant hyperthermia-susceptible ryanodine receptor type 1 gene (RYR1) mutations in a child who died in a car after exposure to a high environmental temperature

Legal medicine (Tokyo, Japan), 2009-05, Vol.11 (3), p.142-143

2009

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Development of Fibrosis in Nonalcoholic Steatosis through Combination of a Synthetic Diet Rich in Disaccharide and Low-Dose Lipopolysaccharides in the Livers of Zucker (fa/fa) Rats

Journal of Clinical Biochemistry and Nutrition, 2009, Vol.45(3), pp.322-328

2009

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Traumatic basal subarachnoid hemorrhage suspected to have been caused by contrecoup cerebellar contusions: A case report

Legal medicine (Tokyo, Japan), 2014-03, Vol.16 (2), p.92-94

2014

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Postmortem genetic analysis for a sudden death case complicated with Marfan syndrome

Legal medicine (Tokyo, Japan), 2010-11, Vol.12 (6), p.305-307

2010

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Determination of acephate and methamidophos in tissues: appearance of matrix effect in gas chromatography–mass spectrometry

Forensic toxicology, 2011-07, Vol.29 (2), p.159-162

2011

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Fatality due to acute fluoride poisoning in the workplace

Legal medicine (Tokyo, Japan), 2004-07, Vol.6 (3), p.197-200

2004

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Identification of an ethnic-specific variant (V207M) of the KCNQ1 cardiac potassium channel gene in sudden unexplained death and implications from a knock-in mouse model

International journal of legal medicine, 2009-05, Vol.123 (3), p.253-257

2009

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I536T variant of RBM20 affects splicing of cardiac structural proteins that are causative for developing dilated cardiomyopathy

Journal of molecular medicine (Berlin, Germany), 2022-12, Vol.100 (12), p.1741-1754

2022

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Identification of a novel mutation V2321M of the cardiac ryanodine receptor gene of sudden unexplained death and a phenotypic study of the gene mutations

Legal medicine (Tokyo, Japan), 2008-07, Vol.10 (4), p.196-200

2008

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Arrhythmia severity in mouse models harboring RyR2 mutations with varied extent of channel activity

Biophysical journal, 2023-02, Vol.122 (3), p.238a-238a

2023

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RNA sequencing reveals abnormal LDB3 splicing in sudden cardiac death

Forensic science international, 2019-09, Vol.302, p.109906-109906, Article 109906

2019

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Retrotransposition of Long Interspersed Element 1 Induced by Methamphetamine or Cocaine

Sudden Unexpected Death of Infantile Dilated Cardiomyopathy with JPH2 and PKD1 Gene Variants

Postmortem Identification of Genetic Variations Associated with Sudden Unexpected Death in Young People

Molecular autopsy for sudden death in Japan

Identification of Arrhythmogenic Right Ventricular Cardiomyopathy-Causing Gene Mutations in Young Sudden Unexpected Death Autopsy Cases

PROS1 variant in sudden death case of pulmonary embolism caused by calcification in the inferior vena cava: The importance of postmortem genetic analysis

Hypertrophy of lymphoid organs is a possible phenotypic characteristic of R420W mutation of the cardiac ryanodine receptor gene: A study using a knock-in mouse model

Postmortem Molecular Screening for Cardiac Ryanodine Receptor Type 2 Mutations in Sudden Unexplained Death: R420W Mutated Case With Characteristics of Status Thymico-Lymphaticus

Bromide detection in blood using energy dispersive X-ray fluorescence; a chemical marker supportive of drowning in seawater

Detection of metallic elements from paraffin-embedded tissue blocks by energy dispersive X-ray fluorescence spectrometry

Sudden death during exercise in a juvenile with arrhythmogenic right ventricular cardiomyopathy and desmoglein-2 gene substitution: A case report

Sudden death of a child because of an intestinal obstruction caused by a large congenital mesenteric defect

Usefulness of serum mast cell-specific chymase levels for postmortem diagnosis of anaphylaxis

Postmortem molecular analysis for fatal arrhythmogenic disease in sudden unexplained death

Identification of malignant hyperthermia-susceptible ryanodine receptor type 1 gene (RYR1) mutations in a child who died in a car after exposure to a high environmental temperature

Development of Fibrosis in Nonalcoholic Steatosis through Combination of a Synthetic Diet Rich in Disaccharide and Low-Dose Lipopolysaccharides in the Livers of Zucker (fa/fa) Rats

Traumatic basal subarachnoid hemorrhage suspected to have been caused by contrecoup cerebellar contusions: A case report

Postmortem genetic analysis for a sudden death case complicated with Marfan syndrome

Determination of acephate and methamidophos in tissues: appearance of matrix effect in gas chromatography–mass spectrometry

Fatality due to acute fluoride poisoning in the workplace

Identification of an ethnic-specific variant (V207M) of the KCNQ1 cardiac potassium channel gene in sudden unexplained death and implications from a knock-in mouse model

I536T variant of RBM20 affects splicing of cardiac structural proteins that are causative for developing dilated cardiomyopathy

Identification of a novel mutation V2321M of the cardiac ryanodine receptor gene of sudden unexplained death and a phenotypic study of the gene mutations

Arrhythmia severity in mouse models harboring RyR2 mutations with varied extent of channel activity

RNA sequencing reveals abnormal LDB3 splicing in sudden cardiac death

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