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MiR-206, a key modulator of skeletal muscle development and disease

International journal of biological sciences, 2015-01, Vol.11 (3), p.345-352

2015

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Emerging roles of SIRT1 activator, SRT2104, in disease treatment

Scientific reports, 2024-03, Vol.14 (1), p.5521-5521, Article 5521

2024

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Protection of Fecal Microbiota Transplantation in a Mouse Model of Multiple Sclerosis

Mediators of inflammation, 2020, Vol.2020 (2020), p.1-13

2020

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Pan-cancer integrated analysis of ANKRD1 expression, prognostic value, and potential implications in cancer

Scientific reports, 2024-03, Vol.14 (1), p.5268-5268, Article 5268

2024

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Cardiovascular disease contributes to Alzheimer's disease: evidence from large-scale genome-wide association studies

Neurobiology of aging, 2014-04, Vol.35 (4), p.786-792

2014

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Isolated steroid-resistant nephrotic syndrome in a Chinese child carrying a de novo mutation in WT1 gene:a case report and literature review

BMC pediatrics, 2022-06, Vol.22 (1), p.349-349, Article 349

2022

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Research progress of ankyrin repeat domain 1 protein: an updated review

Cellular & molecular biology letters, 2024-10, Vol.29 (1), p.131-28, Article 131

2024

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Mesenchymal Stem/Stromal Cells in Asthma Therapy: Mechanisms and Strategies for Enhancement

Cell Transplantation, 2023-01, Vol.32, p.9636897231180128-9636897231180128

2023

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miR-137: a new player in schizophrenia

International Journal of Molecular Sciences, 2014-02, Vol.15 (2), p.3262-3271

2014

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miR-137: A Novel Therapeutic Target for Human Glioma

Molecular therapy. Nucleic acids, 2020-09, Vol.21, p.614-622

2020

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The roles of sirtuins in ferroptosis

Frontiers in physiology, 2023-04, Vol.14, p.1131201-1131201

2023

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Case report: Familial glycogen storage disease type IV caused by novel compound heterozygous mutations in a glycogen branching enzyme 1 gene

Frontiers in genetics, 2022-11, Vol.13

2022

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Genetic Association of MiR-146a with Multiple Sclerosis Susceptibility in the Chinese Population

Cellular physiology and biochemistry, 2015-01, Vol.35 (1), p.281-291

2015

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Genetic contribution of synapse-associated protein 97 to cerebellar functional connectivity changes in first-episode schizophrenia

BMC psychiatry, 2023-08, Vol.23 (1), p.1-630, Article 630

2023

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The contribution of a novel PHEX gene mutation to X-linked hypophosphatemic rickets: a case report and an analysis of the gene mutation dosage effect in a rat model

Frontiers in endocrinology (Lausanne), 2023-12, Vol.14, p.1251718-1251718

2023

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Direct targeting of DOCK4 by miRNA-181d in oxygen-glucose deprivation/reoxygenation-mediated neuronal injury

Lipids in health and disease, 2023-03, Vol.22 (1), p.34-34, Article 34

2023

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A functional polymorphism in the promoter region of microRNA-146a is associated with the risk of Alzheimer disease and the rate of cognitive decline in patients

PloS one, 2014-02, Vol.9 (2), p.e89019-e89019

2014

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The 10-Repeat 3'-UTR VNTR Polymorphism in the SLC6A3 Gene May Confer Protection Against Parkinson's Disease: A Meta-analysis

Frontiers in genetics, 2021-09, Vol.12, p.757601-757601

2021

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A syndrome featuring developmental disorder of the nervous system induced by a novel mutation in the TCF20 gene, rarely concurrent immune disorders: a case report

Frontiers in genetics, 2023-05, Vol.14, p.1192668

2023

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Cloning and expression profiling of muscle regulator ANKRD2 in domestic chicken Gallus gallus

Histochemistry and cell biology, 2020-10, Vol.154 (4), p.383-396

2020

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Corrigendum: The 10-Repeat 3′-UTR VNTR Polymorphism in the SLC6A3 Gene May Confer Protection Against Parkinson’s Disease: A Meta-Analysis

Frontiers in genetics, 2021-10, Vol.12, p.789112-789112

2021

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Association study of a genetic variant in the long intergenic noncoding RNA (linc01080) with schizophrenia in Han Chinese

BMC psychiatry, 2021-12, Vol.21 (1), p.613-613, Article 613

2021

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Association between the RETN -420C/G polymorphism and type 2 diabetes mellitus susceptibility: A meta-analysis of 23 studies

Frontiers in endocrinology (Lausanne), 2022-12, Vol.13, p.1039919-1039919

2022

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Different Associations Between the IREB2 Variants and Chronic Obstructive Pulmonary Disease Susceptibility

Frontiers in genetics, 2020-11, Vol.11, p.598053-598053

2020

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Increases in peripheral SIRT1: A new biological characteristic of asthma

Respirology (Carlton, Vic.), 2015-10, Vol.20 (7), p.1066-1072

2015

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MiR-206, a key modulator of skeletal muscle development and disease

Emerging roles of SIRT1 activator, SRT2104, in disease treatment

Protection of Fecal Microbiota Transplantation in a Mouse Model of Multiple Sclerosis

Pan-cancer integrated analysis of ANKRD1 expression, prognostic value, and potential implications in cancer

Cardiovascular disease contributes to Alzheimer's disease: evidence from large-scale genome-wide association studies

Isolated steroid-resistant nephrotic syndrome in a Chinese child carrying a de novo mutation in WT1 gene:a case report and literature review

Research progress of ankyrin repeat domain 1 protein: an updated review

Mesenchymal Stem/Stromal Cells in Asthma Therapy: Mechanisms and Strategies for Enhancement

miR-137: a new player in schizophrenia

miR-137: A Novel Therapeutic Target for Human Glioma

The roles of sirtuins in ferroptosis

Case report: Familial glycogen storage disease type IV caused by novel compound heterozygous mutations in a glycogen branching enzyme 1 gene

Genetic Association of MiR-146a with Multiple Sclerosis Susceptibility in the Chinese Population

Genetic contribution of synapse-associated protein 97 to cerebellar functional connectivity changes in first-episode schizophrenia

The contribution of a novel PHEX gene mutation to X-linked hypophosphatemic rickets: a case report and an analysis of the gene mutation dosage effect in a rat model

Direct targeting of DOCK4 by miRNA-181d in oxygen-glucose deprivation/reoxygenation-mediated neuronal injury

A functional polymorphism in the promoter region of microRNA-146a is associated with the risk of Alzheimer disease and the rate of cognitive decline in patients

The 10-Repeat 3'-UTR VNTR Polymorphism in the SLC6A3 Gene May Confer Protection Against Parkinson's Disease: A Meta-analysis

A syndrome featuring developmental disorder of the nervous system induced by a novel mutation in the TCF20 gene, rarely concurrent immune disorders: a case report

Cloning and expression profiling of muscle regulator ANKRD2 in domestic chicken Gallus gallus

Corrigendum: The 10-Repeat 3′-UTR VNTR Polymorphism in the SLC6A3 Gene May Confer Protection Against Parkinson’s Disease: A Meta-Analysis

Association study of a genetic variant in the long intergenic noncoding RNA (linc01080) with schizophrenia in Han Chinese

Association between the RETN -420C/G polymorphism and type 2 diabetes mellitus susceptibility: A meta-analysis of 23 studies

Different Associations Between the IREB2 Variants and Chronic Obstructive Pulmonary Disease Susceptibility

Increases in peripheral SIRT1: A new biological characteristic of asthma

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