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富山大学 ホーム
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糸魚川・地域医療支援学講座
富山大学
附属病院
概要
フィンガープリント
ネットワーク
プロファイル
(4)
プロジェクト
(1)
研究成果
(136)
データセット
(8)
フィンガープリント
糸魚川・地域医療支援学講座が活動している研究トピックを掘り下げます。これらのトピックラベルは、この組織のメンバーの研究成果に基づきます。これらがまとまってユニークなフィンガープリントを構成します。
並べ替え順
重み付け
アルファベット順
Keyphrases
Left Ventricular Noncompaction
100%
Type 2 Diabetes Mellitus (T2DM)
73%
Kawasaki Disease
59%
Japanese Population
56%
3T3-L1 Adipocytes
42%
Single nucleotide Polymorphism
37%
Insulin
31%
Insulin Receptor Substrate 1 (IRS1)
28%
Insulin Resistance
25%
Replication Study
24%
Japan
24%
Insulin Receptor
22%
Advanced Gastric Cancer
22%
Insulin Signaling
22%
Hypertrophic Cardiomyopathy
21%
Meta-analysis
19%
Genome-wide Association Study
19%
Tumor Necrosis Factor-α
18%
Next-generation Sequencing
17%
Systematic Meta-analysis
17%
Interleukin-1β
17%
Dilated Cardiomyopathy
16%
Congenital Heart Disease
16%
Heart Failure
15%
Pioglitazone
14%
Nivolumab
14%
Japanese children
14%
Warfarin
14%
Phosphoinositide 3-kinase (PI3K)
14%
Pediatric Patients
13%
Cardiomyopathy
13%
Confidence Interval
13%
Clinical Significance
12%
Fibroblasts
12%
Stomach
12%
Type 2 Diabetic Patients
12%
Genetic Variants
12%
Gene Variants
12%
Glucose Uptake
11%
Suppressor of Cytokine Signaling 3 (SOCS3)
11%
Heat Shock Protein 90 (Hsp90)
11%
Gastrointestinal Stromal Tumor
11%
Neurodevelopmental Outcome
11%
Orai1
11%
Novel Variation
11%
Tadalafil
11%
Dose-response Relationship
11%
Sildenafil
11%
Single Ventricle Physiology
11%
MYH7
11%
Odds Ratio
11%
Congestive Heart Failure
11%
Fasting Plasma Glucose
10%
Tyrosine Phosphorylation
9%
Inherited Cardiomyopathy
9%
Heterozygous Variant
9%
Bilateral Adrenal Hyperplasia
9%
Pathogenic Variants
9%
Genetic Risk Score
9%
Chronic Heart Failure
9%
Fetal Onset
9%
Autopsy
9%
Diabetes
8%
Papilla of Vater
8%
Ramucirumab
8%
3-year-olds
8%
Trabeculation
8%
Genetic Background
8%
Asthma
8%
Mitogenesis
8%
Allergic Diseases
8%
MYH7 Gene
8%
Neonate
8%
Pediatric
8%
Single Ventricle
8%
School Age
8%
Interleukin-6
8%
Sarcomere Genes
8%
Sudden Death
8%
Jejunum
7%
Serum Levels
7%
Japanese Patients
7%
Genotype-phenotype Correlation
7%
Nationwide Survey
7%
Gastric Cancer
7%
Hemoglobin A1c (HbA1c)
7%
Phosphorylation
7%
Thiazolidinedione Derivatives
7%
Tyrosine
7%
Hormone-independent
7%
Adrenocorticotropic Hormone
7%
Developmental Delay
7%
Anticoagulant Effect
7%
Japanese Family
7%
Macronodule
7%
Clinical Trials
7%
School Health Screening
7%
Subclinical Cushing's Syndrome
7%
Long-term Prognosis
7%
Arrhythmia
7%
Medicine and Dentistry
Noncompaction Cardiomyopathy
89%
Maturity Onset Diabetes of the Young
35%
Congestive Heart Failure
26%
Persistent Truncus Arteriosus
22%
Myocardial Disease
21%
Abdominal Cancer
20%
Patient with Kawasaki Disease
17%
Single Nucleotide Polymorphism
15%
Next Generation Sequencing
14%
Nivolumab
14%
Heart Single Ventricle
14%
Pediatrics
12%
MYH7
12%
Coronary Artery
12%
Dilated Cardiomyopathy
12%
Corticotropin
11%
Genome Wide Association Study
11%
Pediatrics Patient
11%
Disease
10%
Sarcomere
10%
Hypertrophic Cardiomyopathy
10%
Neoplasm
9%
Electrocardiogram
9%
Coronary Artery Aneurysm
8%
Brain Natriuretic Peptide
8%
Kawasaki Disease
8%
Adrenal Hyperplasia
8%
Infancy
8%
Echocardiography
7%
Allele
7%
Jejunum
7%
Neonate
7%
Thromboembolism
7%
Amino Terminal Sequence
7%
Immunoglobulin
7%
Right Coronary Artery
7%
Cushing Syndrome
6%
Adrenalectomy
6%
Cardiac Dysrhythmia
6%
Genetic Risk
6%
Immune-Related Adverse Events
6%
Genotype Phenotype Correlation
6%
Heart Muscle Conduction Disturbance
6%
Insulin Treatment
5%
Gastrointestinal Stromal Tumor
5%
Proliferative Retinopathy
5%
Cryptorchism
5%
Pembrolizumab
5%
Hepatocyte Nuclear Factor 1beta
5%
Interstitial Lung Disease
5%
Heat Shock Protein 90
5%
Carcinoma
5%
Very Low Birth Weight
5%
Hypoplasia
5%
Sinus Arrest
5%
Multidetector Computed Tomography
5%
Cyclosporine
5%
Mitogenesis
5%
Insulin Receptor
5%
Hyperplasia
5%
Apoplexy
5%
Rectum Cancer
5%
Diverticulum
5%
Hydrocephalus
5%
Gene Mutation
5%
Peritoneum Metastasis
5%
Adenoma
5%
Macular Edema
5%
Developmental Delay
5%
Sudden Unexpected Death in Epilepsy
5%
Cardiac Resynchronization Therapy
5%
QRS Complex
5%
Reoperation
5%
Tetralogy of Fallot
5%
Interleukin 1
5%
Endothelial Cell
5%
Great Arteries
5%
Brain Development
5%
Tafazzin
5%
Ventricular Septal Defect
5%
Odds Ratio
5%
Family History
5%