Evaluation of efficacy and safety of AAV8-ΔC4ATP7B gene therapy in a mutant mouse model of Wilson’s disease

Authors: Chunhua Zeng, Yunting Lin, Xinshuo Lu, Shehong Chen, Yan Xia, Kangdi Zhang, Yongxian Shao, Zhihong Guan, Rong Du, Zongcai Liu, Mingqi Zhao, Xiaoling Jiang, Yanna Cai, Taolin Li, Xueying Su, Yaoyong Chen, Xiaoyan Dong, Wen Zhang, Li Liu, Wenhao Zhou

Source: Molecular Therapy: Methods & Clinical Development, Vol 33, Iss 1, Pp 101435- (2025)

Subject Terms: AAV8, ΔC4ATP7B, gene therapy, Wilson’s disease, copper, liver disease, Genetics, QH426-470, Cytology, QH573-671

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2329050125000300; https://doaj.org/toc/2329-0501

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Reproductive hormones and sex differences in relation to brachial-ankle pulse wave velocity in obese subjects: a retrospective case–control study

Authors: Yunting Lin, Endi Song, Han Jin, Yong Jin

Source: Endocrine Connections, Vol 13, Iss 9, Pp 1-12 (2024)

Subject Terms: arterial stiffness, brachial-ankle pulse wave velocity, obese, reproductive hormones, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

File Description: electronic resource

Relation: https://ec.bioscientifica.com/view/journals/ec/13/9/EC-24-0190.xml; https://doaj.org/toc/2049-3614

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Self-adaptive pyroptosis-responsive nanoliposomes block pyroptosis in autoimmune inflammatory diseases

Authors: Kaiwang Xu, Huang Yang, Jinghua Fang, Kaijie Qiu, Haotian Shen, Guanrui Huang, Qiangqiang Zheng, Canlong Wang, Tengjing Xu, Xinning Yu, Jiajie Wang, Yunting Lin, Jiacheng Dai, Yuting Zhong, Hongyun Song, Sunan Zhu, Siheng Wang, Zhuxing Zhou, Guang Yang, Zhengwei Mao, Zongyou Pan, Xuesong Dai

Source: Bioactive Materials, Vol 36, Iss , Pp 272-286 (2024)

Subject Terms: Nanoliposome, Pyroptosis, Autoimmune inflammatory diseases, Responsive drug delivery, Anti-inflammation, Materials of engineering and construction. Mechanics of materials, TA401-492, Biology (General), QH301-705.5

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Relation: http://www.sciencedirect.com/science/article/pii/S2452199X24000677; https://doaj.org/toc/2452-199X

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Clinical and genetic analysis of methylmalonic aciduria in 60 patients from Southern China: a single center retrospective study

Authors: Ling Su, Huiying Sheng, Xiuzhen Li, Yanna Cai, Huifen Mei, Jing Cheng, Duan Li, Zhikun Lu, Yunting Lin, Xiaodan Chen, Minzhi Peng, Yonglan Huang, Wen Zhang, Li Liu

Source: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-18 (2024)

Subject Terms: Methylmalonic aciduria, MMACHC gene, MMUT gene, SUCLA2 gene, Pulmonary hypertension, Medicine

File Description: electronic resource

Relation: https://doaj.org/toc/1750-1172

Access URL: https://doaj.org/article/01ddbeba70684b68b72587b7bd0f9a05

Natural history and outcome of nonketotic hyperglycinemia in China

Authors: Zhizi Zhou, Yanna Cai, Xiuzhen Li, Zongcai Liu, Minzhi Peng, Yunting Lin, Xiaojian Mao, Chunhua Zeng, Li Liu, Wen Zhang

Source: Frontiers in Neurology, Vol 15 (2024)

Subject Terms: nonketotic hyperglycinemia, GLDC, AMT, glycine encephalopathy, genotype, Neurology. Diseases of the nervous system, RC346-429

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fneur.2024.1440883/full; https://doaj.org/toc/1664-2295

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Comparison of the ability of exosomes and ectosomes derived from adipose-derived stromal cells to promote cartilage regeneration in a rat osteochondral defect model

Authors: Tengjing Xu, Xinning Yu, Kaiwang Xu, Yunting Lin, Jiajie Wang, Zongyou Pan, Jinghua Fang, Siheng Wang, Zhuxing Zhou, Hongyun Song, Sunan Zhu, Xuesong Dai

Source: Stem Cell Research & Therapy, Vol 15, Iss 1, Pp 1-20 (2024)

Subject Terms: Cartilage regeneration, Mesenchymal stromal cells, Exosomes, Ectosomes, Macrophages, Medicine (General), R5-920, Biochemistry, QD415-436

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Relation: https://doaj.org/toc/1757-6512

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Assessment of the diagnostic value of serum ceruloplasmin for Wilson’s disease in children

Authors: Xinshuo Lu, Simin Li, Wen Zhang, Yunting Lin, Zhikun Lu, Yanna Cai, Xueying Su, Yongxian Shao, Zongcai Liu, Huiying Sheng, Yonglan Huang, Li Liu, Chunhua Zeng

Source: BMC Gastroenterology, Vol 22, Iss 1, Pp 1-9 (2022)

Subject Terms: Ceruloplasmin, Wilson’s disease, Children, Diagnosis, Diseases of the digestive system. Gastroenterology, RC799-869

File Description: electronic resource

Relation: https://doaj.org/toc/1471-230X

Access URL: https://doaj.org/article/7d33b8e632c34ab0afd4d762e8918add

Glucose-6-Phosphate dehydrogenase deficiency associated hemolysis in a cohort of new onset type 1 diabetes children in Guangdong province, China

Authors: Aijing Xu, Minyan Jiang, Wen Zhang, Yunting Lin, Yongxian Shao, Huifen Mei, Jing Cheng, Cuili Liang, Cuiling Li, Xiuzhen Li, Li Liu

Source: Diabetology & Metabolic Syndrome, Vol 14, Iss 1, Pp 1-8 (2022)

Subject Terms: Glucose-6-phosphate dehydrogenase deficiency, Hemolysis, Type 1 diabetes, Nutritional diseases. Deficiency diseases, RC620-627

File Description: electronic resource

Relation: https://doaj.org/toc/1758-5996

Access URL: https://doaj.org/article/ceebfd3306d9408e8e19430bbe9a225d

Features of chinese patients with sitosterolemia

Authors: Zhizi Zhou, Xueying Su, Yanna Cai, Tzer Hwu Ting, Wen Zhang, Yunting Lin, Aijing Xu, Xiaojian Mao, Chunhua Zeng, Li Liu, Xiuzhen Li

Source: Lipids in Health and Disease, Vol 21, Iss 1, Pp 1-10 (2022)

Subject Terms: Sitosterolemia, Xanthoma, Hypercholesterolemia, ABCG5, ABCG8, Nutritional diseases. Deficiency diseases, RC620-627

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Relation: https://doaj.org/toc/1476-511X

Access URL: https://doaj.org/article/46094b49716b49fdbca4b77e5c9c1f38

Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome

Authors: Yunting Lin, Xiaohong Chen, Bobo Xie, Zhihong Guan, Xiaodan Chen, Xiuzhen Li, Peng Yi, Rong Du, Huifen Mei, Li Liu, Wen Zhang, Chunhua Zeng

Source: Frontiers in Genetics, Vol 14 (2023)

Subject Terms: Wiedemann-Steiner syndrome, KMT2A gene, clinical characteristics, genetic spectrum, therapeutic effect, Chinese, Genetics, QH426-470

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2023.1085210/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/95dfcda6cdf842699d3002ebcc11ca75

Clinical characteristics and long-term outcomes of 12 children with vitamin D-dependent rickets type 1A: A retrospective study

Authors: Yunting Lin, Zhihong Guan, Huifen Mei, Wen Zhang, Zhizi Zhou, Ling Su, Jing Cheng, Ruidan Zheng, Cuili Liang, Yanna Cai, Xi Yin, Dongyan Wu, Li Liu, Chunhua Zeng

Source: Frontiers in Pediatrics, Vol 10 (2022)

Subject Terms: vitamin D-dependent rickets type 1A, CYP27B1 gene, clinical characteristics, genetic spectrum, therapeutic effect, Pediatrics, RJ1-570

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Relation: https://www.frontiersin.org/articles/10.3389/fped.2022.1007219/full; https://doaj.org/toc/2296-2360

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A Metaheuristic Hybrid of Double-Target Multi-Layer Perceptron for Energy Performance Analysis in Residential Buildings

Authors: Cheng Lin, Yunting Lin

Source: Buildings, Vol 13, Iss 4, p 1086 (2023)

Subject Terms: energy sustainability, building energy performance, thermal load, artificial neural networks, metaheuristic algorithms, Building construction, TH1-9745

File Description: electronic resource

Relation: https://www.mdpi.com/2075-5309/13/4/1086; https://doaj.org/toc/2075-5309

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Distinct severity of phenotype in Hajdu-Cheney syndrome: a case report and literature review

Authors: Chunhua Zeng, Yunting Lin, Zhikun Lu, Zhen Chen, Xiaoling Jiang, Xiaojian Mao, Zongcai Liu, Xinshuo Lu, Kangdi Zhang, Qiaoli Yu, Xiaoya Wang, Yonglan Huang, Li Liu

Source: BMC Musculoskeletal Disorders, Vol 21, Iss 1, Pp 1-6 (2020)

Subject Terms: NOTCH2, Hajdu-Cheney syndrome, Osteoporosis, Acro-osteolysis, Diseases of the musculoskeletal system, RC925-935

File Description: electronic resource

Relation: http://link.springer.com/article/10.1186/s12891-020-3181-0; https://doaj.org/toc/1471-2474

Access URL: https://doaj.org/article/9f9a422efae44b2d84b2cec34b49442e

Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China

Authors: Aijing Xu, Jing Cheng, Huiying Sheng, Zhe Wen, Yunting Lin, Zhihong Zhou, Chunhua Zeng, Yongxian Shao, Cuiling Li, Li Liu, Xiuzhen Li

Source: JCRPE, Vol 11, Iss 4, Pp 400-409 (2019)

Subject Terms: congenital hyperinsulinism, clinical management, gene mutation, Pediatrics, RJ1-570, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

File Description: electronic resource

Relation: http://www.jcrpe.org/archives/archive-detail/article-preview/clinical-management-and-gene-mutation-analysis-of-/27785; https://doaj.org/toc/1308-5727; https://doaj.org/toc/1308-5735

Access URL: https://doaj.org/article/22bde2bf7ff0418fb682c763fb5df3d7

Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: case reports and literature review

Authors: Xiaojian Mao, Sichi Liu, Yunting Lin, Zhen Chen, Yongxian Shao, Qiaoli Yu, Haiying Liu, Zhikun Lu, Huiyin Sheng, Xinshuo Lu, Yonglan Huang, Li Liu, Chunhua Zeng

Source: BMC Pediatrics, Vol 19, Iss 1, Pp 1-8 (2019)

Subject Terms: Hypophosphatasia, Alkaline phosphatase, Mutation, Hypomineralization, Pediatrics, RJ1-570

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Relation: http://link.springer.com/article/10.1186/s12887-019-1800-4; https://doaj.org/toc/1471-2431

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Neddylation activity modulates the neurodegeneration associated with fragile X associated tremor/ataxia syndrome (FXTAS) through regulating Sima

Authors: Yunting Lin, Jin Xue, Jing Deng, Hua He, Shiyu Luo, Jia Chen, Jia Li, Li Yu, Juan Zhao, Jing Chen, Emily G. Allen, Peng Jin, Ranhui Duan

Source: Neurobiology of Disease, Vol 143, Iss , Pp 105013- (2020)

Subject Terms: FXTAS, Drosophila, Chemical screen, Neddylation, HIF1α/Sima, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

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Relation: http://www.sciencedirect.com/science/article/pii/S0969996120302886; https://doaj.org/toc/1095-953X

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Genetic and clinical characteristics of Chinese children with Glucokinase-maturity-onset diabetes of the young (GCK-MODY)

Authors: Xiuzhen Li, Tzer Hwu Ting, Huiying Sheng, Cui Li Liang, Yongxian Shao, Minyan Jiang, Aijing Xu, Yunting Lin, Li Liu

Source: BMC Pediatrics, Vol 18, Iss 1, Pp 1-8 (2018)

Subject Terms: MODY, Glucokinase, Genetics, Chinese, Children, Pediatrics, RJ1-570

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Relation: http://link.springer.com/article/10.1186/s12887-018-1060-8; https://doaj.org/toc/1471-2431

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Amyotrophic Lateral Sclerosis-associated GGGGCC repeat expansion promotes Tau phosphorylation and toxicity

Authors: Hua He, Wen Huang, Ruoxi Wang, Yunting Lin, Yichen Guo, Jing Deng, Haitao Deng, Yanping Zhu, Emily G. Allen, Peng Jin, Ranhui Duan

Source: Neurobiology of Disease, Vol 130, Iss , Pp 104493- (2019)

Subject Terms: Drosophila, C9ORF72, G4C2 repeat expansion, Tau, ALS, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

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Relation: http://www.sciencedirect.com/science/article/pii/S0969996119301482; https://doaj.org/toc/1095-953X

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UBA5 Mutations Cause a New Form of Autosomal Recessive Cerebellar Ataxia.

Authors: Ranhui Duan, Yuting Shi, Li Yu, Gehan Zhang, Jia Li, Yunting Lin, Jifeng Guo, Junling Wang, Lu Shen, Hong Jiang, Guanghui Wang, Beisha Tang

Source: PLoS ONE, Vol 11, Iss 2, p e0149039 (2016)

Subject Terms: Medicine, Science

File Description: electronic resource

Relation: http://europepmc.org/articles/PMC4752235?pdf=render; https://doaj.org/toc/1932-6203

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Activation of mTOR ameliorates fragile X premutation rCGG repeat-mediated neurodegeneration.

Authors: Yunting Lin, Chengyuan Tang, Hua He, Ranhui Duan

Source: PLoS ONE, Vol 8, Iss 4, p e62572 (2013)

Subject Terms: Medicine, Science

File Description: electronic resource

Relation: https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23626835/pdf/?tool=EBI; https://doaj.org/toc/1932-6203

Access URL: https://doaj.org/article/4dfd52dca8224e3f97f135e2a7943068