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Aurora Kinase B‐Instruct Release of AZD1152‐HQPA from Hydrogel to Enhance Cervical Cancer Suppression

Advanced functional materials, 2024-02, Vol.34 (7), p.n/a

2024

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A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene

Journal of international medical research, 2020-11, Vol.48 (11), p.300060520966499-300060520966499

2020

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A case of reversible splenial lesion syndrome secondary to Fanconi syndrome with white matter swelling as the main manifestation

Journal of international medical research, 2021-01, Vol.49 (1), p.300060520985713-300060520985713

2021

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Mitochondria-targeted fluorescent probe for visualization of exogenous and endogenous methylglyoxal in living cells

Chemical communications (Cambridge, England), 2022-05, Vol.58 (44), p.6453-6456

2022

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A highly sensitive ratiometric fluorescence probe for sensing and imaging sulfite in food samples and living cells

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2024-10, Vol.319, p.124540, Article 124540

2024

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A novel compound heterozygous SPG7 variant is associated with progressive spastic ataxia and persecutory delusions found in Chinese patients: two case reports

BMC neurology, 2022-05, Vol.22 (1), p.200-200, Article 200

2022

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Novel lysosome-targeted fluorescent molecular rotors based on a cyanine-like modular system and their application in living cells

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2022-01, Vol.265, p.120404, Article 120404

2022

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MORC2 p.R252W Mutant Axonal Charcot–Marie–Tooth Disease Causes Peripheral Neuropathies and Pathological Myofiber Destruction

Balkan medical journal, 2022-05, Vol.39 (3), p.222-223

2022

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Case Report: A Novel Splice-Site Mutation in DNAJB6 Associated With Juvenile-Onset Proximal–Distal Myopathy in a Chinese Patient

Frontiers in genetics, 2022-06, Vol.13

2022

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Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency

Balkan medical journal, 2022-07, Vol.39 (4), p.290-296

2022

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Identification of Hub Genes and Biological Pathways in Inclusion Body Myositis Using Bioinformatics Analysis

International journal of general medicine, 2022-01, Vol.15, p.1281-1293

2022

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Neutral lipid storage disease with myopathy presenting asymmetrical muscle weakness: a case report

International journal of clinical and experimental pathology, 2020-01, Vol.13 (3), p.559-562

2020

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Case Report: A Novel Splice-Site Mutation in DNAJB6 Associated With Juvenile-Onset Proximal-Distal Myopathy in a Chinese Patient

Frontiers in genetics, 2022, Vol.13, p.925926-925926

2022

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Neutral lipid storage disease with myopathy presenting asymmetrical muscle weakness: a case report

International journal of clinical and experimental pathology, 2020, Vol.13 (3), p.559-562

2020

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Ti-HMS介孔分子筛的制备及其在一氧化氮催化分解反应中的活性

催化学报, 2001, Vol.22 (2), p.157-160

2001

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Aurora Kinase B‐Instruct Release of AZD1152‐HQPA from Hydrogel to Enhance Cervical Cancer Suppression

A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene

A case of reversible splenial lesion syndrome secondary to Fanconi syndrome with white matter swelling as the main manifestation

Mitochondria-targeted fluorescent probe for visualization of exogenous and endogenous methylglyoxal in living cells

A highly sensitive ratiometric fluorescence probe for sensing and imaging sulfite in food samples and living cells

A novel compound heterozygous SPG7 variant is associated with progressive spastic ataxia and persecutory delusions found in Chinese patients: two case reports

Novel lysosome-targeted fluorescent molecular rotors based on a cyanine-like modular system and their application in living cells

MORC2 p.R252W Mutant Axonal Charcot–Marie–Tooth Disease Causes Peripheral Neuropathies and Pathological Myofiber Destruction

Case Report: A Novel Splice-Site Mutation in DNAJB6 Associated With Juvenile-Onset Proximal–Distal Myopathy in a Chinese Patient

Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency

Identification of Hub Genes and Biological Pathways in Inclusion Body Myositis Using Bioinformatics Analysis

Neutral lipid storage disease with myopathy presenting asymmetrical muscle weakness: a case report

Case Report: A Novel Splice-Site Mutation in DNAJB6 Associated With Juvenile-Onset Proximal-Distal Myopathy in a Chinese Patient

Neutral lipid storage disease with myopathy presenting asymmetrical muscle weakness: a case report

Ti-HMS介孔分子筛的制备及其在一氧化氮催化分解反应中的活性

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