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Auteur Li S

Documents disponibles écrits par cet auteur (39)

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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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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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Article

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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Article

BMC Medical Genetics, 18, 1. A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like

Chen Z, Auteur ; Ren Z ; Mei W ; Ma Q ; Shi Y ; Zhang Y ; Li S ; Xiang L ; Zhang J | 2017

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Article

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, 49, 6. Targeted sequencing of maternal plasma for haplotype-based noninvasive prenatal testing of spinal muscular atrophy

Chen M, Auteur ; Lu S ; Lai Z ; Chen C ; Luo K ; Yuan Y ; Wang Y ; Li S ; Gao Y ; Chen F ; Asan ; Chen D | 2017

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Article

Asian journal of endoscopic surgery, 9, 4. Sternotomy versus video-assisted thoracoscopic surgery for thymectomy of myasthenia gravis patients: A meta-analysis

Gung Y, Auteur ; Zhang H ; Li S ; Wang Y | 2016

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Article

Molecular genetics and metabolism, 118, 1. Salmeterol enhances the cardiac response to gene therapy in Pompe disease.

Han SO ; Li S ; Koeberl DD | 2016

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Article

European journal of radiology, 84, 10. The trefoil with single fruit sign in muscle magnetic resonance imaging is highly specific for dystrophinopathies

Zheng Y, Auteur ; Li W ; Du J ; Jin S ; Li S ; Zhao Y ; Xu C ; Wang Z ; Lv H ; Zhang W ; Xiao J ; Yuan Y | 2015

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Article

Human gene therapy, 26, 1. Enhanced Efficacy From Gene Therapy in Pompe Disease Using Coreceptor Blockade

Han SO ; Li S ; Brooks ED ; Masat E ; Leborgne C ; Banugaria S ; Bird A ; Mingozzi F ; Walmann H ; Koeberl D | 2015

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Article

Human gene therapy, 26, 11. Synergistic Efficacy from Gene Therapy with Coreceptor Blockade and a Beta2-Agonist in Murine Pompe Disease

Han SO, Auteur ; Li S ; Bird A ; Koebel D | 2015

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Human molecular genetics, 24, 13. Functional disruption of the dystrophin gene in rhesus monkey using CRISPR/Cas9

Chen Y, Auteur ; Zheng Y ; Kang Y ; Yang W ; Niu Y ; Guo X ; Tu Z ; Si C ; Wang H ; Xing R ; Pu X ; Yang SH ; Li S ; Ji W ; Li XJ | 2015

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Article

FASEB journal (The), 28, 5. Adjunctive beta2-agonist treatment reduces glycogen independently of receptor-mediated acid alpha-glucosidase uptake in the limb muscles of mice with Pompe disease

Farah BL ; Madden L ; Li S ; Nance S ; Bird A ; Bursac N ; Yen PM ; Young SP ; Koeberl DD | 2014

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Détail de l'auteur

Auteur Li S

Documents disponibles écrits par cet auteur (39)

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

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

BMC Medical Genetics, 18, 1. A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology, 49, 6. Targeted sequencing of maternal plasma for haplotype-based noninvasive prenatal testing of spinal muscular atrophy

Asian journal of endoscopic surgery, 9, 4. Sternotomy versus video-assisted thoracoscopic surgery for thymectomy of myasthenia gravis patients: A meta-analysis

Molecular genetics and metabolism, 118, 1. Salmeterol enhances the cardiac response to gene therapy in Pompe disease.

European journal of radiology, 84, 10. The trefoil with single fruit sign in muscle magnetic resonance imaging is highly specific for dystrophinopathies

Human gene therapy, 26, 1. Enhanced Efficacy From Gene Therapy in Pompe Disease Using Coreceptor Blockade

Human gene therapy, 26, 11. Synergistic Efficacy from Gene Therapy with Coreceptor Blockade and a Beta2-Agonist in Murine Pompe Disease

Human molecular genetics, 24, 13. Functional disruption of the dystrophin gene in rhesus monkey using CRISPR/Cas9

FASEB journal (The), 28, 5. Adjunctive beta2-agonist treatment reduces glycogen independently of receptor-mediated acid alpha-glucosidase uptake in the limb muscles of mice with Pompe disease