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Z

Zhe Yang

Jinan University

H指数:8

被引数:274

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GLP-1 regulates osteo-adipogenic fate of BMSCs via HIF-2-AKT signaling and supports trabecular bone in glucocorticoid-induced osteoporosis

GLP-1通过HIF-2-AKT信号通路调节BMSCs的成骨-成脂分化命运，并在糖皮质激素诱导的骨质疏松症中支持小梁骨

Stem Cell Reports

IF5.1

2026-08-010

PRE

Combined effect of nutritional inflammation as well as depression on mortality in middle-aged and elderly people with osteoporosis and osteopenia

IF2.6

2025-11-030

PRE

HIF-2α-Driven Lipogenesis and Inflammation in MASLD: Role of ATF4 Signaling

HIF-2α驱动的脂生成和炎症在MASLD中的作用：ATF4信号通路的作用

Cellular and Molecular Gastroenterology and Hepatology

IF7.4

2025-09-290

OAAI

Comprehensive analysis of immune signatures in primary biliary cholangitis and autoimmune hepatitis

JOURNAL OF LEUKOCYTE BIOLOGY

IF3.1

2024-04-231

PRE

Reactivation of PPARa alleviates myocardial lipid accumulation and cardiac dysfunction by improving fatty acid ?-oxidation in Dsg2-deficient arrhythmogenic cardiomyopathy

ACTA PHARMACEUTICA SINICA B

IF14.6

2023-01-0111

OAAI

Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2022-10-274

OAAI

SGLT2 inhibitor dapagliflozin attenuates cardiac fibrosis and inflammation by reverting the HIF-2α signaling pathway in arrhythmogenic cardiomyopathy

SGLT2抑制剂达格列净通过恢复致心律失常性心肌病的HIF-2α 信号通路减轻心脏纤维化和炎症

IF4.2

2022-06-1751

OA

Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2022-05-078

OAAI

Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2021-11-2416

OAAI

Performance and Clinical Evaluation of a Sensitive Multiplex Assay for the Rapid Detection of Common NPM1 Mutations

JOURNAL OF MOLECULAR DIAGNOSTICS

IF3.4

2010-09-0114

OAAI

A novel deletion in TNNI2 causes distal arthrogryposis in a large Chinese family with marked variability of expression

TNNI2的新缺失导致一个大型中国家庭的远端关节软化

IF3.6

2006-06-2729

PREAI