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Banks versus Venture Capital: Project Evaluation, Screening, and Expropriation

The Journal of finance (New York), 2004-04, Vol.59 (2), p.601-621

Ueda, Masako

2004

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Apolipoprotein C-II: New findings related to genetics, biochemistry, and role in triglyceride metabolism

Atherosclerosis, 2017-12, Vol.267, p.49-60

2017

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The SUN1 splicing variants SUN1_888 and SUN1_916 differentially regulate nucleolar structure

Genes to cells : devoted to molecular & cellular mechanisms, 2020-11, Vol.25 (11), p.730-740

2020

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VENTURE CAPITAL AND INNOVATION: WHICH IS FIRST?

Pacific economic review (Oxford, England), 2011-10, Vol.16 (4), p.421-465

2011

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A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation

The journal of clinical endocrinology and metabolism, 2018-03, Vol.103 (3), p.1005-1014

2018

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The Interaction between Clause-Level Parameters and Context in Russian Morphosyntax: Genitive of Negation and Predicate Adjectives

Ueda, Masako

1992

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Familial chylomicronemia syndrome: importance of diagnostic vigilance

Translational pediatrics, 2022-10, Vol.11 (10), p.1588-1594

Ueda, Masako

2022

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Rare Diagnosis of Familial Partial Lipodystrophy in a Patient With Life-Threatening Pancreatitis due to Hypertriglyceridemia

AACE clinical case reports, 2022-01, Vol.8 (1), p.11-14

2022

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Pretreatment Gastric Lavage Reduces Postoperative Bleeding after Endoscopic Submucosal Dissection for Gastric Neoplasms

PloS one, 2016-02, Vol.11 (2), p.e0149235-e0149235

2016

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Long-term follow-up of well-treated nephropathic cystinosis patients

The Journal of pediatrics, 2004-10, Vol.145 (4), p.555-560

2004

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Experimental Therapeutics for Challenging Clinical Care of a Patient with an Extremely Rare Homozygous APOC2 Mutation

Case reports in endocrinology, 2020, Vol.2020, p.1865489-6

2020

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Challenges in Interpreting Genetic Reports in Familial Hypercholesterolemia: Variants of Uncertain Significance

Journal of clinical lipidology, 2017-05, Vol.11 (3), p.790-791

2017

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The Majority of Outpatients With Severe Hypercholesterolemia at an Academic Tertiary Centre Have Not Been Screened for FH

Journal of clinical lipidology, 2017-05, Vol.11 (3), p.800-801

2017

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An Electronic Health Records Query for Severe Hypercholesterolemia Identifies Individuals With Undiagnosed Clinical and Molecular FH at a Tertiary Academic Centre

Journal of clinical lipidology, 2017-05, Vol.11 (3), p.801-801

2017

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Familial Chylomicron Syndrome: Importance of Discerning the Rare Among the Common

Journal of clinical lipidology, 2017-05, Vol.11 (3), p.818-819

2017

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Familial Hypercholesterolemia Prevalence of 1.5% in a Clinical Database of 542,214 Patients: Refined Risk Stratification Using ApoB:LDL-C Ratio

Journal of clinical lipidology, 2015-05, Vol.9 (3), p.414-414

2015

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Lack of Hirsutism in an XX Woman With History of Hyperandrogenism and Oligomenorrhea: Two Coexisting Disorders or Novel Syndrome of Androgen Insensitivity?

Journal of the Endocrine Society, 2021-05, Vol.5 (Supplement_1), p.A781-A782

2021

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Estimated Atherosclerotic Cardiovascular Disease Risk Score: An Automated Decision Aid for Statin Therapy

Clinical chemistry (Baltimore, Md.), 2022-10, Vol.68 (10), p.1302-1310

2022

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Coronary Artery and Other Vascular Calcifications in Patients with Cystinosis after Kidney Transplantation

Clinical journal of the American Society of Nephrology, 2006-05, Vol.1 (3), p.555-562

2006

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Optimal Project Rejection and New Firm Start-ups

Management science, 2006-02, Vol.52 (2), p.262-275

2006

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Analysis of 'Spirituality' in the Japanese-Speaking Mediation Context : Its Contributions and Controversies

Ueda, Masako

2020

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Jiadifenolide induces the expression of cellular communication network factor (CCN) genes, and CCN2 exhibits neurotrophic activity in neuronal precursor cells derived from human induced pluripotent stem cells

Biochemical and biophysical research communications, 2019-11, Vol.519 (2), p.309-315

2019

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Effects of fatty acid and emulsifier on the complex formation and in vitro digestibility of gelatinized potato starch

International journal of food properties, 2017-07, Vol.20 (7), p.1500-1510

2017

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Effects of Novel Biologics to Treat Hypertriglyceridemia in Familial Chylomicronemia Syndrome with Two Different Genotypes

Journal of clinical lipidology, 2020-07, Vol.14 (4), p.590-591

2020

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A Novel APOC2 Missense Mutation Causing Apolipoprotein C-II Deficiency With Severe Triglyceridemia and Pancreatitis

The journal of clinical endocrinology and metabolism, 2017-05, Vol.102 (5), p.1454-1457

2017

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Banks versus Venture Capital: Project Evaluation, Screening, and Expropriation

Apolipoprotein C-II: New findings related to genetics, biochemistry, and role in triglyceride metabolism

The SUN1 splicing variants SUN1_888 and SUN1_916 differentially regulate nucleolar structure

VENTURE CAPITAL AND INNOVATION: WHICH IS FIRST?

A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation

The Interaction between Clause-Level Parameters and Context in Russian Morphosyntax: Genitive of Negation and Predicate Adjectives

Familial chylomicronemia syndrome: importance of diagnostic vigilance

Rare Diagnosis of Familial Partial Lipodystrophy in a Patient With Life-Threatening Pancreatitis due to Hypertriglyceridemia

Pretreatment Gastric Lavage Reduces Postoperative Bleeding after Endoscopic Submucosal Dissection for Gastric Neoplasms

Long-term follow-up of well-treated nephropathic cystinosis patients

Experimental Therapeutics for Challenging Clinical Care of a Patient with an Extremely Rare Homozygous APOC2 Mutation

Challenges in Interpreting Genetic Reports in Familial Hypercholesterolemia: Variants of Uncertain Significance

The Majority of Outpatients With Severe Hypercholesterolemia at an Academic Tertiary Centre Have Not Been Screened for FH

An Electronic Health Records Query for Severe Hypercholesterolemia Identifies Individuals With Undiagnosed Clinical and Molecular FH at a Tertiary Academic Centre

Familial Chylomicron Syndrome: Importance of Discerning the Rare Among the Common

Familial Hypercholesterolemia Prevalence of 1.5% in a Clinical Database of 542,214 Patients: Refined Risk Stratification Using ApoB:LDL-C Ratio

Lack of Hirsutism in an XX Woman With History of Hyperandrogenism and Oligomenorrhea: Two Coexisting Disorders or Novel Syndrome of Androgen Insensitivity?

Estimated Atherosclerotic Cardiovascular Disease Risk Score: An Automated Decision Aid for Statin Therapy

Coronary Artery and Other Vascular Calcifications in Patients with Cystinosis after Kidney Transplantation

Optimal Project Rejection and New Firm Start-ups

Analysis of 'Spirituality' in the Japanese-Speaking Mediation Context : Its Contributions and Controversies

Jiadifenolide induces the expression of cellular communication network factor (CCN) genes, and CCN2 exhibits neurotrophic activity in neuronal precursor cells derived from human induced pluripotent stem cells

Effects of fatty acid and emulsifier on the complex formation and in vitro digestibility of gelatinized potato starch

Effects of Novel Biologics to Treat Hypertriglyceridemia in Familial Chylomicronemia Syndrome with Two Different Genotypes

A Novel APOC2 Missense Mutation Causing Apolipoprotein C-II Deficiency With Severe Triglyceridemia and Pancreatitis

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