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Protective effect of microRNA‐224 on acute lower extremity ischemia through activation of the mTOR signaling pathway via CHOP in mice

Journal of cellular physiology, 2019-06, Vol.234 (6), p.8888-8898

Chen, Yang‐Xi

2019

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Oxidative Stress and Antioxidative Therapy in Pulmonary Arterial Hypertension

Molecules (Basel, Switzerland), 2022-06, Vol.27 (12), p.3724

2022

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Light‐induced FeCl3‐catalyzed selective benzyl C−H chlorination with trifluoromethanesulfonyl chloride

Advanced synthesis & catalysis, 2023-12, Vol.365 (23), p.4144-4149

2023

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Altered Polarization and Impaired Phagocytic Activity of Lung Macrophages in People With Human Immunodeficiency Virus and Chronic Obstructive Pulmonary Disease

The Journal of infectious diseases, 2022-03, Vol.225 (5), p.862-867

2022

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Gene expression network analysis provides potential targets against SARS-CoV-2

Scientific reports, 2020-12, Vol.10 (1), p.21863-9, Article 21863

2020

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SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial Hypertension

International Heart Journal, 2021/05/29, Vol.62(3), pp.566-574

2021

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Association Between METS-IR and Prehypertension or Hypertension Among Normoglycemia Subjects in Japan: A Retrospective Study

Frontiers in endocrinology (Lausanne), 2022-03, Vol.13, p.851338-851338

2022

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Visible light-induced Ni-catalyzed C–heteroatom cross-coupling of aryl halides via LMCT with DBU to access a Ni(i)/Ni(iii) cycle

Organic chemistry frontiers an international journal of organic chemistry, 2022-07, Vol.9 (14), p.3847-3853

2022

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MiR‐10a‐5p restrains the aggressive phenotypes of ovarian cancer cells by inhibiting HOXA1

The Kaohsiung journal of medical sciences, 2021-04, Vol.37 (4), p.276-285

2021

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A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block

International Heart Journal, 2020/07/30, Vol.61(4), pp.761-768

2020

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KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy

Journal of the American Heart Association, 2022-11, Vol.11 (22), p.e027578-e027578

2022

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PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation

Journal of the American Heart Association, 2021-12, Vol.10 (23), p.e023517-e023517

2021

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Acute spontaneous intracerebral hemorrhage and traumatic brain injury are the most common causes of critical illness in the ICU and have high early mortality

BMC neurology, 2018-08, Vol.18 (1), p.127-127, Article 127

2018

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Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy

Clinical chemistry and laboratory medicine, 2021-04, Vol.59 (5), p.955

2021

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Multi-Enzymatic Biosynthesis of Chiral β-Hydroxy Nitriles through Co-Expression of Oxidoreductase and Halohydrin Dehalogenase

Advanced synthesis & catalysis, 2013-11, Vol.355 (16), p.3179-3190

2013

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Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy

European journal of medical genetics, 2020-04, Vol.63 (4), p.103827-103827, Article 103827

2020

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COVID-19 and nicotine as a mediator of ACE-2

The European respiratory journal, 2020-06, Vol.55 (6), p.2001261

2020

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Radiofrequency therapy improves exercise capacity of mice with emphysema

Scientific reports, 2021-10, Vol.11 (1), p.20056-20056, Article 20056

2021

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Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

Diagnostics (Basel), 2022-08, Vol.12 (8), p.1917

2022

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Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy

Diagnostics (Basel), 2023-01, Vol.13 (2), p.242

2023

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Atrial Arrhythmias in Patients with Severe COVID-19

Cardiology research and practice, 2021, Vol.2021, p.8874450-7

2021

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ISL1 loss-of-function variation causes familial atrial fibrillation

European journal of medical genetics, 2020-11, Vol.63 (11), p.104029-104029, Article 104029

2020

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Single-Center Experience of Treating Chronic Limb-Threatening Ischemia of Lower Limbs Combined with Diabetes

Sichuan da xue xue bao. Journal of Sichuan University. Yi xue ban, 2022-11, Vol.53 (6), p.988-992

2022

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Hydraulic bulging process with axial feedings and strain field of U-shaped metal bellows

Journal of Central South University, 2018-12, Vol.25 (11), p.2712-2721

2018

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Autophagy appears during the development of the mouse lower first molar

Histochemistry and cell biology, 2013-01, Vol.139 (1), p.109-118

2013

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Protective effect of microRNA‐224 on acute lower extremity ischemia through activation of the mTOR signaling pathway via CHOP in mice

Oxidative Stress and Antioxidative Therapy in Pulmonary Arterial Hypertension

Light‐induced FeCl3‐catalyzed selective benzyl C−H chlorination with trifluoromethanesulfonyl chloride

Altered Polarization and Impaired Phagocytic Activity of Lung Macrophages in People With Human Immunodeficiency Virus and Chronic Obstructive Pulmonary Disease

Gene expression network analysis provides potential targets against SARS-CoV-2

SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial Hypertension

Association Between METS-IR and Prehypertension or Hypertension Among Normoglycemia Subjects in Japan: A Retrospective Study

Visible light-induced Ni-catalyzed C–heteroatom cross-coupling of aryl halides via LMCT with DBU to access a Ni(i)/Ni(iii) cycle

MiR‐10a‐5p restrains the aggressive phenotypes of ovarian cancer cells by inhibiting HOXA1

A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block

KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy

PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation

Acute spontaneous intracerebral hemorrhage and traumatic brain injury are the most common causes of critical illness in the ICU and have high early mortality

Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy

Multi-Enzymatic Biosynthesis of Chiral β-Hydroxy Nitriles through Co-Expression of Oxidoreductase and Halohydrin Dehalogenase

Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy

COVID-19 and nicotine as a mediator of ACE-2

Radiofrequency therapy improves exercise capacity of mice with emphysema

Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy

Atrial Arrhythmias in Patients with Severe COVID-19

ISL1 loss-of-function variation causes familial atrial fibrillation

Single-Center Experience of Treating Chronic Limb-Threatening Ischemia of Lower Limbs Combined with Diabetes

Hydraulic bulging process with axial feedings and strain field of U-shaped metal bellows

Autophagy appears during the development of the mouse lower first molar

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