M. Ono

发表

Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients

C. January, C. Elayi, C. Anderson, 2020, Biomolecules.

Enhanced binding of calmodulin to RyR2 corrects arrhythmogenic channel disorder in CPVT-associated myocytes.

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2014, Biochemical and biophysical research communications.

Lower body weight and BMI at birth were associated with early adiposity rebound in 21-hydroxylase deficiency patients.

T. Morio, M. Ono, Y. Hasegawa, 2016, Endocrine journal.

Clinical, biochemical, and genetic features of non-classical 21-hydroxylase deficiency in Japanese children.

M. Ono, I. Yokota, Y. Hasegawa, 2015, Endocrine journal.

Initial high dose hydrocortisone (HDC) treatment for 21-hydroxylase deficiency (21-OHD) does not affect linear growth during the first three years of life.

S. Mizutani, M. Ono, Yohei Matsubara, 2012, Endocrine journal.

Clinical course of patients with nonclassical 21-hydroxylase deficiency (21-OHD) diagnosed in infancy and childhood.

S. Mizutani, M. Ono, K. Kashimada, 2008, Endocrine journal.

In Vitro Enzyme Assay of CYP21A2 Mutation (R483Q) by A Novel Method Using Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS)

M. Takagi, S. Mizutani, M. Ono, 2008, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Insufficiency of urinary acid excretion of overweight or obese patients with chronic kidney disease and its involvement with renal tubular injury

M. Ono, H. Nonoguchi, M. Mukoyama, 2019, Nephrology.

Longitudinal analysis of growth and body composition of Japanese 21-OHD patients in childhood.

S. Mizutani, M. Ono, Yohei Matsubara, 2013, Endocrine journal.

Liquid chromatography-tandem mass spectrometric method for determination of salivary 17alpha-hydroxyprogesterone: a noninvasive tool for evaluating efficacy of hormone replacement therapy in congenital adrenal hyperplasia.

S. Mizutani, M. Ono, T. Higashi, 2008, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Defective calmodulin binding to the cardiac ryanodine receptor plays a key role in CPVT-associated channel dysfunction.

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2010, Biochemical and biophysical research communications.

Mitochondrial deformity confined to a single cardiomyocyte in human endomyocardial biopsy specimens: Report of 4 cases.

M. Yano, Shigeki Kobayashi, M. Ono, 2017, Journal of cardiology cases.

Impact of Atrial Tachyarrhythmia Recurrence on the Development of Long‐Term Adverse Clinical Events Following Catheter Ablation in Patients With Atrial Fibrillation With Systolic Impairment: A Single‐Center Observational Study

M. Yano, Shigeki Kobayashi, M. Ono, 2022, Journal of the American Heart Association.

Catheter Ablation for Electrical Storm as Polymorphic Ventricular Tachycardia in a Case with Ischemic Cardiomyopathy after Coronary Artery Bypass Graft

M. Matsuzaki, M. Ono, A. Shimizu, 2010 .

Macroreentrant form of an adenosine 5′-triphosphate–sensitive atrial tachycardia arising from the vicinity of the atrioventricular node involving the tricuspid and mitral annuli as its reentrant circuit

M. Yano, M. Ono, A. Shimizu, 2017, HeartRhythm case reports.

Transient Hyper-17-OHPnemia Unrelated to Cross-Reactions with Residual Fetal Adrenal Cortex Products

H. Togari, M. Ono, T. Hasegawa, 2004, Hormone Research in Paediatrics.

G790del mutation in DSC2 alone is insufficient to develop the pathogenesis of ARVC in a mouse model

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2019, Biochemistry and biophysics reports.

Inferior J waves in patients with vasospastic angina might be a risk factor for ventricular fibrillation.

M. Yano, M. Ono, T. Okamura, 2017, Journal of cardiology.

Abstract 14124: A Marked Increase in Myocardial Oxidative Stress Associated With Sympathetic Hyperactivity is Related to Transient Myocardial Dysfunction in Patients With Takotsubo Cardiomyopathy

M. Yano, Shigeki Kobayashi, S. Okuda, 2015 .

Dantrolene, a therapeutic agent for malignant hyperthermia, inhibits catecholaminergic polymorphic ventricular tachycardia in a RyR2(R2474S/+) knock-in mouse model.

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2010, Circulation journal : official journal of the Japanese Circulation Society.

Correction of impaired calmodulin binding to RyR2 as a novel therapy for lethal arrhythmia in the pressure-overloaded heart failure.

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2017, Heart rhythm.

The Differential Prognostic Impact of Long-Duration Atrial High-Rate Episodes Detected by Cardiac Implantable Electronic Devices between Patients with and without a History of Atrial Fibrillation

M. Yano, Shigeki Kobayashi, M. Ono, 2022, Journal of clinical medicine.

Investigation of electrocardiographic changes after intracoronary injection of acetylcholine in symptomatic patients with Brugada syndrome

M. Matsuzaki, M. Ono, A. Shimizu, 2008 .

Clinical characteristics in patients with Brugada type ECG associated with only supuraventricular arrhythmias

A. Sawa, M. Matsuzaki, M. Ono, 2007 .

Two preterm infants with late onset circulatory collapse induced by levothyroxine sodium

S. Mizutani, M. Ono, K. Kashimada, 2009, Pediatrics international : official journal of the Japan Pediatric Society.

Mutation-linked, excessively tight interaction between the calmodulin binding domain and the C-terminal domain of the cardiac ryanodine receptor as a novel cause of catecholaminergic polymorphic ventricular tachycardia.

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2018, Heart rhythm.

Nationwide surveillance of circulatory collapse associated with levothyroxine administration in very‐low‐birthweight infants in Japan

M. Ono, M. Kawai, Kazutoshi Cho, 2012, Pediatrics international : official journal of the Japan Pediatric Society.

Strict sequential catheter ablation strategy targeting the pulmonary veins and superior vena cava for persistent atrial fibrillation.

M. Yano, Shigeki Kobayashi, M. Ono, 2018, Journal of cardiology.

Identification of a new case of hepatocyte nuclear factor-1β mutation with highly varied phenotypes

M. Ono, Y. Horikawa, J. Takeda, 2004, Diabetologia.

Circadian clocks regulate cardiac arrhythmia susceptibility, repolarization, and ion channels.

B. Delisle, M. Ono, D. Burgess, 2020, Current opinion in pharmacology.

Disorders of sex development: new genes, new concepts

Makoto Ono, M. Ono, V. Harley, 2013, Nature Reviews Endocrinology.

An impact of superior vena cava isolation in non‐paroxysmal atrial fibrillation patients with low voltage areas

M. Yano, Shigeki Kobayashi, M. Ono, 2021, Journal of Arrhythmia.

A 45,X/46,XY DSD (Disorder of Sexual Development) case with an extremely uneven distribution of 46,XY cells between lymphocytes and gonads

T. Ogata, M. Sekine, T. Akashi, 2015, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Social cognition in individuals with agenesis of the corpus callosum

W. Brown, L. Paul, M. Ono, 2010, Social neuroscience.

FGFR2 mutation in 46,XY sex reversal with craniosynostosis.

M. Ono, P. Koopman, R. Lai, 2015, Human molecular genetics.

Two novel HSD3B2 missense mutations with diverse residual enzymatic activities for Δ5‐steroids

O. Ohara, T. Morio, M. Takagi, 2014, Clinical endocrinology.

Elevated C‐Reactive Protein Is Related to Cognitive Decline in Older Adults with Cardiovascular Disease

Robert H. Paul, D. Tate, A. Haley, 2008, Journal of the American Geriatrics Society.

Vascular Health and Cognitive Function in Older Adults with Cardiovascular Disease.

D. Tate, R. Paul, R. Cohen, 2008, Artery research.

Newborn screening for congenital adrenal hyperplasia in Tokyo, Japan from 1989 to 2013: a retrospective population-based study

T. Morio, M. Ono, T. Kitagawa, 2015, BMC Pediatrics.

Mutation and gene copy number analyses of six pituitary transcription factor genes in 71 patients with combined pituitary hormone deficiency: identification of a single patient with LHX4 deletion.

T. Ogata, M. Ono, M. Kaji, 2010, The Journal of clinical endocrinology and metabolism.

A boy with "transient" growth hormone deficiency in prepubertal stage despite normal growth hormone secretion in childhood and after puberty.

S. Mizutani, M. Ono, K. Kashimada, 2007, Endocrine journal.

Reduced early diastolic extension in the infarcted portion in patients with old myocardial infarction.

M. Ono, R. Katori, K. Kanamasa, 1988, Japanese circulation journal.

Early weaning induces anxiety and precocious myelination in the anterior part of the basolateral amygdala of male Balb/c mice

M. Ichikawa, T. Kikusui, Y. Mori, 2008, Neuroscience.

Neonatal Intractable Atrial Flutter Successfully Treated with Intravenous Flecainide

M. Ono, H. Suzumura, O. Arisaka, 2004, Pediatric Cardiology.

Isoform-Specific Localization of A-RAF in Mitochondria

A. Yuryev, S. Goff, L. Wennogle, 2000, Molecular and Cellular Biology.

A Low-Dose β1-Blocker in Combination with Milrinone Improves Intracellular Ca2+ Handling in Failing Cardiomyocytes by Inhibition of Milrinone-Induced Diastolic Ca2+ Leakage from the Sarcoplasmic Reticulum

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2015, PloS one.

Defective domain-domain interactions within the ryanodine receptor as a critical cause of diastolic Ca2+ leak in failing hearts.

M. Yano, T. Ohkusa, Shigeki Kobayashi, 2008, Cardiovascular research.

The role of the cardiomyocyte circadian clocks in ion channel regulation and cardiac electrophysiology

K. Esser, B. Delisle, M. Ono, 2022, The Journal of physiology.

Timing of food intake in mice unmasks a role for the cardiomyocyte circadian clock mechanism in limiting QT-interval prolongation

K. Esser, C. Elayi, B. Delisle, 2021, Chronobiology international.

Addition of a β1-Blocker to Milrinone Treatment Improves Cardiac Function in Patients with Acute Heart Failure and Rapid Atrial Fibrillation

M. Yano, Shigeki Kobayashi, S. Okuda, 2019, Cardiology.

Successful cryoballoon pulmonary vein isolation in a patient with situs inversus and dextrocardia

M. Yano, M. Ono, A. Shimizu, 2016, Journal of arrhythmia.

Correlation between asymptomatic gastroesophageal excessive transmural injury after pulmonary vein isolation and a bonus freeze protocol using the second-generation 28-mm cryoballoon for paroxysmal atrial fibrillation.

M. Yano, Shigeki Kobayashi, M. Ono, 2019, Journal of cardiology.

Mutation-Linked Defective Interdomain Interactions Within Ryanodine Receptor Cause Aberrant Ca2+ Release Leading to Catecholaminergic Polymorphic Ventricular Tachycardia

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2011, Circulation.

Dantrolene, a therapeutic agent for malignant hyperthermia, markedly improves the function of failing cardiomyocytes by stabilizing interdomain interactions within the ryanodine receptor.

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2009, Journal of the American College of Cardiology.

Subjective cognitive complaints relate to white matter hyperintensities and future cognitive decline in patients with cardiovascular disease.

D. Tate, R. Paul, R. Cohen, 2009, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Catecholaminergic Polymorphic Ventricular Tachycardia Is Caused by Mutation-Linked Defective Conformational Regulation of the Ryanodine Receptor

M. Yano, T. Ohkusa, Shigeki Kobayashi, 2010, Circulation research.

Dissociation of calmodulin from cardiac ryanodine receptor causes aberrant Ca(2+) release in heart failure.

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2010, Cardiovascular research.

FGF9 variant in 46,XY DSD patient suggests a role for dimerization in sex determination

A. Sinclair, M. Ono, T. Thomas, 2022, Clinical genetics.

Enhanced binding of calmodulin to the ryanodine receptor corrects contractile dysfunction in failing hearts.

M. Yano, Shigeki Kobayashi, Takeshi Yamamoto, 2012, Cardiovascular research.

Inactivation of a Frameshift TSH Receptor Variant Val711Phefs*18 is Due to Acquisition of a Hydrophobic Degron.

M. Ono, K. Kashimada, T. Hasegawa, 2020, The Journal of clinical endocrinology and metabolism.

Regulation of Rhcg, an ammonia transporter, by aldosterone in the kidney.

M. Ono, H. Nonoguchi, M. Mukoyama, 2021, Journal of Endocrinology.