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Auteur Li S

Documents disponibles écrits par cet auteur (48)

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The Journal of molecular diagnostics : JMD Comprehensive Analysis of Spinal Muscular Atrophy: SMN1 Copy Number, Intragenic Mutation, and 2 + 0 Carrier Analysis by Third-Generation Sequencing

Li S ; Han X ; Xu Y ; Chang C ; Gao L ; Li J ; Lu Y ; Mao A ; Wang Y | United States | 31/05/2022

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Article

Frontiers in pediatrics, 10. Circulating FGF21 and GDF15 as Biomarkers for Screening, Diagnosis, and Severity Assessment of Primary Mitochondrial Disorders in Children

Li Y ; Li S ; Qiu Y ; Zhou M ; Chen M ; Hu Y ; Hong S ; Jiang L ; Guo Y | 14/04/2022

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Article

Prenatal diagnosis Noninvasive prenatal testing of Duchenne muscular dystrophy in a twin gestation

Kong L ; Li S ; Zhao Z ; Feng J ; Liu L ; Tang W ; Zhang H ; Wu D ; Sun L ; Kong X | England | 26/02/2022

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Article

Human gene therapy Minimum Effective Dose to Achieve Biochemical Correction With AAV Vector-Mediated Gene Therapy in Mice With Pompe Disease

Han S ; Gheorghiu DB ; Li S ; Kang HR ; Koeberl D | United States | 01/02/2022

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Article

Human gene therapy Efficacious Androgen Hormone Administration in Combination With AAV Vector-Mediated Gene Therapy in Female Mice With Pompe Disease

Han S ; Gheorghiu DB ; Chang A ; Mapatano SH ; Li S ; Brooks ED ; Koeberl D | United States | 26/01/2022

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Article

Journal of translational medicine, 19, 1. Identification of the regulatory role of lncRNA HCG18 in myasthenia gravis by integrated bioinformatics and experimental analyses

Li S ; Wang X ; Wang T ; Zhang H ; Lu X ; Liu L ; Li L ; Bo C ; Kong X ; Xu S ; Ning S ; Wang J ; Wang L | 18/11/2021

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Article

British journal of pharmacology A new therapeutic effect of fenofibrate in Duchenne muscular dystrophy: The promotion of myostatin degradation

Sun Z ; Xu D ; Zhao L ; Li X ; Li S ; Huang X ; Li C ; Sun L ; Liu B ; Jiang Z ; Zhang L | England | 22/09/2021

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$The Efficacy of Tocilizumab in the Treatment of Patients with Refractory Immune-Mediated Necrotizing Myopathies: An Open-Label Pilot Study$

Article

Frontiers in pharmacology, 12. The Efficacy of Tocilizumab in the Treatment of Patients with Refractory Immune-Mediated Necrotizing Myopathies: An Open-Label Pilot Study

Li S ; Li W ; Jiang W ; He L ; Peng Q ; Wang G ; Lu X | 16/03/2021

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Article

Molecular therapy. Nucleic acids, 24. Efficient correction of Duchenne muscular dystrophy mutations by SpCas9 and dual gRNAs

Xiang X ; Zhao X ; Pan X ; Dong Z ; Yu J ; Li S ; Liang X ; Qu K ; Jensen JB ; Farup J ; Wang F ; Petersen TS ; Bolund L ; Teng H ; Lin L ; Luo Y | 13/03/2021

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Scientific Reports, 11, 1. Construction of a TF-miRNA-gene feed-forward loop network predicts biomarkers and potential drugs for myasthenia gravis

Bo C ; Zhang H ; Cao Y ; Lu X ; Zhang C ; Li S ; Kong X ; Zhang X ; Bai M ; Tian K ; Saitgareeva A ; Lyaysan G ; Wang J ; Ning S ; Wang L | 28/01/2021

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Noro psikiyatri arsivi, 58, 1. Central Role of T Follicular Helper Cells in Myasthenia Gravis

Wu N ; Wu N ; Tüzün E ; Cheng Y ; Yan L ; Wu Y ; Rao J ; Huang H ; Li S ; Shi L ; Wu X | 16/01/2021

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Article

Arthritis research & therapy, 23, 1. Expansion of circulating peripheral TIGIT+CD226+ CD4 T cells with enhanced effector functions in dermatomyositis

Li W ; Deng C ; Yang H ; Lu X ; Li S ; Liu X ; Chen F ; Chen L ; Shu X ; Zhang L ; Liu Q ; Wang G ; Peng Q | 07/01/2021

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Article

Theranostics, 11, 6. Lipin 1 deficiency causes adult-onset myasthenia with motor neuron dysfunction in humans and neuromuscular junction defects in zebrafish

Lu S ; Lyu Z ; Wang Z ; Kou Y ; Liu C ; Li S ; Hu M ; Zhu H ; Wang W ; Zhang C ; Kuan YS ; Liu YW ; Chen J ; Tian J | 01/01/2021

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Article

Rheumatology (Oxford, England) Clinical features, treatments and outcomes of calcinosis in adult patients with dermatomyositis: a single cohort study

Jiang W ; Yang H ; Li S ; Tian X ; Wang G | England | 29/11/2020

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Article

Journal of cachexia, sarcopenia and muscle TAK1 inhibition improves myoblast differentiation and alleviates fibrosis in a mouse model of Duchenne muscular dystrophy

Xu D ; Li S ; Wang L ; Jiang J ; Zhao L ; Huang X ; Sun Z ; Li C ; Sun L ; Li X ; Jiang Z ; Zhang L | Germany | 25/11/2020

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Article

Nature communications, 11, 1. CRISPR artificial splicing factors

Du M ; Jillette N ; Zhu JJ ; Li S ; Cheng AW | 06/2020

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Journal of cachexia, sarcopenia and muscle A potential therapeutic effect of catalpol in Duchenne muscular dystrophy revealed by binding with TAK1

Xu D ; Zhao L ; Jiang J ; Li S ; Sun Z ; Huang X ; Li C ; Wang T ; Sun L ; Li X ; Jiang Z ; Zhang L | Germany | 2020

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Article

Mediators of inflammation Soluble IL-2 Receptor in Dermatomyositis: Its Associations with Skin Ulcers and Disease Activity

He L ; Shu X ; Liu X ; Ge Y ; Li S ; Lu X ; Wang G | 2020

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Article

Rheumatology (Oxford, England) Prognosis of adult idiopathic inflammatory myopathy-associated interstitial lung disease: a retrospective study of 679 adult cases

Li S ; Sun Y ; Shao C ; Huang H ; Wang Q ; Xu K ; Zhang X ; Liu P ; Zeng X ; Xu Z | England | 2020

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Article

European journal of obstetrics, gynecology, and reproductive biology, 240. Haplotype-Based noninvasive prenatal diagnosis for duchenne muscular dystrophy: A pilot study in South China.

Chen M, Auteur ; Chen C ; Li Y ; Yuan Y ; Lai Z ; Guo F ; Wang Y ; Huang X ; Li S ; Wu R ; Peng Z ; Sun J ; Chen D | Ireland | 05/2019

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Article

Molecular therapy. Methods & clinical development, 13. Erratum: Low-Dose Liver-Targeted Gene Therapy for Pompe Disease Enhances Therapeutic Efficacy of ERT via Immune Tolerance Induction

Han SO, Auteur ; Ronzitti G ; Arnson B ; Leborgne C ; Li S ; Mingozzi F ; Koeberl D | 01/05/2019

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Article

Human gene therapy, 30, 7. Salmeterol with Liver Depot Gene Therapy Enhances the Skeletal Muscle Response in Murine Pompe Disease

Han SO, Auteur ; Li S ; Everitt JI ; Koeberl DD | 2019

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Article

Orphanet journal of rare diseases, 13, 1. The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients

Wang L, Auteur ; Zhang VW ; Li S ; Li H ; Sun Y ; Li J ; Zhu Y ; He R ; Lin J ; Zhang C | 14/08/2018

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Article

Seminars in arthritis and rheumatism, 47, 6. Pregnancy outcomes in adult patients with dermatomyositis and polymyositis

Kolstad KD, Auteur ; Fiorentino D ; Li S ; Chakravarty EF ; Chung L | 2018

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Article

Arthritis care & research, 69, 12. The cutaneous and systemic findings associated with nuclear matrix protein-2 antibodies in adult dermatomyositis patients

Rogers A, Auteur ; Chung L ; Li S ; Casciola-Rosen L ; Fiorentino DF | 2017

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Détail de l'auteur

Auteur Li S

Documents disponibles écrits par cet auteur (48)

The Journal of molecular diagnostics : JMD Comprehensive Analysis of Spinal Muscular Atrophy: SMN1 Copy Number, Intragenic Mutation, and 2 + 0 Carrier Analysis by Third-Generation Sequencing

Frontiers in pediatrics, 10. Circulating FGF21 and GDF15 as Biomarkers for Screening, Diagnosis, and Severity Assessment of Primary Mitochondrial Disorders in Children

Prenatal diagnosis Noninvasive prenatal testing of Duchenne muscular dystrophy in a twin gestation

Human gene therapy Minimum Effective Dose to Achieve Biochemical Correction With AAV Vector-Mediated Gene Therapy in Mice With Pompe Disease

Human gene therapy Efficacious Androgen Hormone Administration in Combination With AAV Vector-Mediated Gene Therapy in Female Mice With Pompe Disease

Journal of translational medicine, 19, 1. Identification of the regulatory role of lncRNA HCG18 in myasthenia gravis by integrated bioinformatics and experimental analyses

British journal of pharmacology A new therapeutic effect of fenofibrate in Duchenne muscular dystrophy: The promotion of myostatin degradation

Frontiers in pharmacology, 12. The Efficacy of Tocilizumab in the Treatment of Patients with Refractory Immune-Mediated Necrotizing Myopathies: An Open-Label Pilot Study

Molecular therapy. Nucleic acids, 24. Efficient correction of Duchenne muscular dystrophy mutations by SpCas9 and dual gRNAs

Scientific Reports, 11, 1. Construction of a TF-miRNA-gene feed-forward loop network predicts biomarkers and potential drugs for myasthenia gravis

Noro psikiyatri arsivi, 58, 1. Central Role of T Follicular Helper Cells in Myasthenia Gravis

Arthritis research & therapy, 23, 1. Expansion of circulating peripheral TIGIT+CD226+ CD4 T cells with enhanced effector functions in dermatomyositis

Theranostics, 11, 6. Lipin 1 deficiency causes adult-onset myasthenia with motor neuron dysfunction in humans and neuromuscular junction defects in zebrafish

Rheumatology (Oxford, England) Clinical features, treatments and outcomes of calcinosis in adult patients with dermatomyositis: a single cohort study

Journal of cachexia, sarcopenia and muscle TAK1 inhibition improves myoblast differentiation and alleviates fibrosis in a mouse model of Duchenne muscular dystrophy

Nature communications, 11, 1. CRISPR artificial splicing factors

Journal of cachexia, sarcopenia and muscle A potential therapeutic effect of catalpol in Duchenne muscular dystrophy revealed by binding with TAK1

Mediators of inflammation Soluble IL-2 Receptor in Dermatomyositis: Its Associations with Skin Ulcers and Disease Activity

Rheumatology (Oxford, England) Prognosis of adult idiopathic inflammatory myopathy-associated interstitial lung disease: a retrospective study of 679 adult cases

European journal of obstetrics, gynecology, and reproductive biology, 240. Haplotype-Based noninvasive prenatal diagnosis for duchenne muscular dystrophy: A pilot study in South China.

Molecular therapy. Methods & clinical development, 13. Erratum: Low-Dose Liver-Targeted Gene Therapy for Pompe Disease Enhances Therapeutic Efficacy of ERT via Immune Tolerance Induction

Human gene therapy, 30, 7. Salmeterol with Liver Depot Gene Therapy Enhances the Skeletal Muscle Response in Murine Pompe Disease

Orphanet journal of rare diseases, 13, 1. The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients

Seminars in arthritis and rheumatism, 47, 6. Pregnancy outcomes in adult patients with dermatomyositis and polymyositis

Arthritis care & research, 69, 12. The cutaneous and systemic findings associated with nuclear matrix protein-2 antibodies in adult dermatomyositis patients