Li Q Catalogue en ligne

Détail de l'auteur

Auteur Li Q

Documents disponibles écrits par cet auteur (25)

trié(s) par (Date de parution décroissant(e), Date de parution décroissant(e), Système de projection du document croissant(e)) | Mettre toutes les notices dans le panier | Faire une suggestion | Ajouter un critère de recherche

Article

Chinese medical journal Treatment of SMA type 1 infants using a single-dose AAV9-mediated gene therapy via intrathecal injection of GC101: An open-label, single-arm study

Ma X ; Zhuang L ; Ma W ; Li J ; Wang X ; Li Z ; Jiang X ; Wang Y ; Du Y ; Zhang Y ; He F ; Zhu Z ; Du S ; Xu J ; Gu R ; Zhang Y ; Zhang S ; Li T ; Yang X ; Zhang S ; Zhu L ; Li Q ; Dong X ; Wu X ; Feng Z | 09/07/2024

Plus d'information...

Ajouter au panier

En ligne

Article

Journal of cachexia, sarcopenia and muscle, Epub. Integrated multi-omics approach reveals the role of striated muscle preferentially expressed protein kinase in skeletal muscle including its relationship with myospryn complex

Li Q ; Lin J ; Luo S ; Schmitz-Abe K ; Agrawal R ; Meng M ; Moghadaszadeh B ; Beggs AH ; Liu X ; Perrella MA ; Agrawal PB | 09/05/2024

Plus d'information...

Ajouter au panier

En ligne

Article

Frontiers in medicine, 11. Microbiome features in bronchoalveolar lavage fluid of patients with idiopathic inflammatory myopathy-related interstitial lung disease

Zhang L ; Liu X ; Fan B ; Chen J ; Chen J ; Li Q ; Wu X | 03/04/2024

Plus d'information...

Ajouter au panier

En ligne

Article

bioRxiv : the preprint server for biology Integrated multi-omics approach reveals the role of SPEG in skeletal muscle biology including its relationship with myospryn complex

Li Q ; Lin J ; Luo S ; Schmitz-Abe K ; Agrawal R ; Meng M ; Moghadaszadeh B ; Beggs AH ; Liu X ; Perrella MA ; Agrawal PB | 24/04/2023

Plus d'information...

Ajouter au panier

En ligne

Article

Foods (Basel, Switzerland), 11, 18. Bioactive Components in Whole Grains for the Regulation of Skeletal Muscle Function

Li Q ; Yang H ; Song S ; Liu J ; Wang Z ; Wang J | 07/09/2022

Plus d'information...

Ajouter au panier

En ligne

Article

Journal of applied microbiology Integrating 16S RRNA gene sequencing and metabolomics to evaluate the association between gut microbiota and serum metabolites in patients with myositis

Luo YB ; Liu Y ; Li Q ; Duan H ; Luo Z ; Yang H ; Xu L | England | 20/07/2022

Plus d'information...

Ajouter au panier

En ligne

Article

JCI insight Dynamin-2 reduction rescues the skeletal myopathy of SPEG-deficient mouse model

Li Q ; Lin J ; Widrick JJ ; Luo S ; Li G ; Zhang Y ; Laporte J ; Perrella MA ; Liu X ; Agrawal PB | United States | 28/06/2022

Plus d'information...

Ajouter au panier

En ligne

Article

Frontiers in pediatrics, 10. Establishment of Cutoff Values for Newborn Screening of Six Lysosomal Storage Disorders by Tandem Mass Spectrometry

Li R ; Tian L ; Gao Q ; Guo Y ; Li G ; Li Y ; Sun M ; Yan Y ; Li Q ; Nie W ; Zou H | 28/03/2022

Plus d'information...

Ajouter au panier

En ligne

Article

Clinical rheumatology Myocardial involvement in idiopathic inflammatory myopathies: a multi-center cross-sectional study in the CRDC-MYO Registry

Zhang L ; Zhu H ; Yang P ; Duan X ; Wei W ; Wu Z ; Fang Y ; Li Q ; Liu S ; Shi X ; Li H ; Wu C ; Zhou S ; Leng X ; Zhao J ; Xu D ; Wu Q ; Tian X ; Li M ; Zhao Y ; Wang Q ; Zeng X | Germany | 29/06/2021

Plus d'information...

Ajouter au panier

En ligne

Article

International Journal of molecular sciences, 22, 11. Striated Preferentially Expressed Protein Kinase (SPEG) in Muscle Development, Function, and Disease

Luo S ; Rosen SM ; Li Q ; Agrawal PB | 27/05/2021

Plus d'information...

Ajouter au panier

En ligne

Article

Human molecular genetics SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins

Luo S ; Li Q ; Lin J ; Murphy Q ; Marty I ; Zhang Y ; Kazerounian S ; Agrawal PB | England | 23/12/2020

Plus d'information...

Ajouter au panier

En ligne

Article

Annals of clinical and translational neurology Systematic review of CMTX1 patients with episodic neurological dysfunction

Tian D ; Zhao Y ; Zhu R ; Li Q ; Liu X | United States | 12/12/2020

Plus d'information...

Ajouter au panier

En ligne

Article

Frontiers in neurology, 11. Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center

Luo YB ; Peng Y ; Lu Y ; Li Q ; Duan H ; Bi F ; Yang H | 15/09/2020

Plus d'information...

Ajouter au panier

En ligne

Article

Cell Research Dosage effect of multiple genes accounts for multisystem disorder of myotonic dystrophy type 1

Yin Q ; Wang H ; Li N ; Ding Y ; Xie Z ; Jin L ; Li Y ; Wang Q ; Liu X ; Xu L ; Li Q ; Ma Y ; Cheng Y ; Wang K ; Zhong C ; Yu Q ; Tang W ; Chen W ; Yang W ; Zhang F ; Ding C ; Bao L ; Zhou B ; Hu P ; Li J | England | 12/2019

Plus d'information...

Ajouter au panier

En ligne

Article

Drug safety, 42, 7. Long-Term Safety and Efficacy of Fecal Microbiota Transplant in Active Ulcerative Colitis

Ding X, Auteur ; Li Q ; Li P ; Zhang T ; Cui B ; Ji G ; Lu X ; Zhang F | New Zealand | 07/2019

Plus d'information...

Ajouter au panier

En ligne

Article

European journal of neurology Clinical analysis of Chinese anti-low-density-lipoprotein-receptor-associated protein 4 antibodies in patients with myasthenia gravis

Li M, Auteur ; Han J ; Zhang Y ; Lv J ; Zhang J ; Zhao X ; Ren L ; Fang H ; Yang J ; Zhang Y ; Cui X ; Zhang Q ; Li Q ; Du Y ; Gao F | 02/05/2019

Plus d'information...

Ajouter au panier

En ligne

Article

Cells, 8, 5. Overexpression of miR-29 Leads to Myopathy that Resemble Pathology of Ullrich Congenital Muscular Dystrophy

Liu C ; Li L ; Ge M ; Gu L ; Wang M ; Zhang K ; Su Y ; Zhang Y ; Liu C ; Lan M ; Yu Y ; Wang T ; Li Q ; Zhao Y ; Yu Z ; Li N ; Meng Q | 2019

Plus d'information...

Ajouter au panier

En ligne

Article

Molecular genetics and metabolism reports, 16. Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency

Fan X, Auteur ; Fan X ; Xie B ; Zou J ; Luo J ; Qin Z ; D'Gama AM ; Shi J ; Yi S ; Yang Q ; Wang J ; Luo S ; Chen S ; Agrawal PB ; Li Q ; Shen Y | 2018

Plus d'information...

Ajouter au panier

En ligne

Article

International journal of neuroscience, 124, 1. Modeling induced pluripotent stem cells from fibroblasts of Duchenne muscular dystrophy patients

Luo Y ; Fan Y ; Chen X ; Yue L ; Yu B ; Li Q ; Chen Y ; Sun X | 2014

Plus d'information...

Ajouter au panier

Article

International journal of neuroscience, 120, 11. Vocal cord paresis and probable X-linked Charcot-Marie-Tooth disease with novel GJB1 mutation

Li Q ; Chen M ; Liu K ; Lin X ; Chui D | 2010

Accès au résumé PubMed / to PubMed abstract

Plus d'information...

Ajouter au panier

Article

Nature medicine, 13, 6. Restoration of cone vision in a mouse model of achromatopsia

Alexander JJ ; Umino Y ; Everhart D ; Chang BS ; Min SH ; Li Q ; Timmers AM ; Hawes NL ; Pang JJ ; Barlow RB ; Hauswirth WW | 06/2007

Accès au résumé PubMed / to PubMed abstract

Plus d'information...

Ajouter au panier

Article

Journal of peking university. Health sciences, 38, 1. Prenatal molecular diagnosis of Duchenne and Becker muscular dystrophy

Li Q ; Li SY ; Hu D ; Sun X ; Chen D ; Zhang C ; Jiang W | 18/02/2006

Accès au résumé PubMed / to PubMed abstract

Plus d'information...

Ajouter au panier

Article

Journal of biological chemistry (The), 280, 16. A minimal structural analogue of cyclic ADP-ribose: synthesis and calcium release activity in mammalian cells.

Guse AH ; Gu X ; Weber K ; Kramer E ; Yang Z ; Jin H ; Li Q ; Carrier L ; Zhang L | 2005

Accès au résumé PubMed / to PubMed abstract

Plus d'information...

Ajouter au panier

Article

Development, 131, 21. Accordion, a zebrafish behavioral mutant, has a muscle relaxation defect due to a mutation in the ATPase CA2+ pump SERCA1

Hirata H ; Saint-Amant L ; Waterbury J ; Cui W ; Wei Z ; Li Q ; Goldman D ; Granato M ; Kuwada JY | 2004

Accès au résumé PubMed / to PubMed abstract

Plus d'information...

Ajouter au panier

Article

Journal of virology, 69, 4. Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses

Yang YP ; Li Q ; Wilson JM | 1995

"Journal of Virology" n'est pas enregistré car je ne connais pas l'écriture courte...

Plus d'information...

Ajouter au panier

MYOBASE

Newsletters

Bibliographies

Portail documentaire sur les maladies neuromusculaires

Se connecter

Accueil

Sélection de la langue

Adresse

Détail de l'auteur

Auteur Li Q

Documents disponibles écrits par cet auteur (25)

Chinese medical journal Treatment of SMA type 1 infants using a single-dose AAV9-mediated gene therapy via intrathecal injection of GC101: An open-label, single-arm study

Journal of cachexia, sarcopenia and muscle, Epub. Integrated multi-omics approach reveals the role of striated muscle preferentially expressed protein kinase in skeletal muscle including its relationship with myospryn complex

Frontiers in medicine, 11. Microbiome features in bronchoalveolar lavage fluid of patients with idiopathic inflammatory myopathy-related interstitial lung disease

bioRxiv : the preprint server for biology Integrated multi-omics approach reveals the role of SPEG in skeletal muscle biology including its relationship with myospryn complex

Foods (Basel, Switzerland), 11, 18. Bioactive Components in Whole Grains for the Regulation of Skeletal Muscle Function

Journal of applied microbiology Integrating 16S RRNA gene sequencing and metabolomics to evaluate the association between gut microbiota and serum metabolites in patients with myositis

JCI insight Dynamin-2 reduction rescues the skeletal myopathy of SPEG-deficient mouse model

Frontiers in pediatrics, 10. Establishment of Cutoff Values for Newborn Screening of Six Lysosomal Storage Disorders by Tandem Mass Spectrometry

Clinical rheumatology Myocardial involvement in idiopathic inflammatory myopathies: a multi-center cross-sectional study in the CRDC-MYO Registry

International Journal of molecular sciences, 22, 11. Striated Preferentially Expressed Protein Kinase (SPEG) in Muscle Development, Function, and Disease

Human molecular genetics SPEG binds with desmin and its deficiency causes defects in triad and focal adhesion proteins

Annals of clinical and translational neurology Systematic review of CMTX1 patients with episodic neurological dysfunction

Frontiers in neurology, 11. Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center

Cell Research Dosage effect of multiple genes accounts for multisystem disorder of myotonic dystrophy type 1

Drug safety, 42, 7. Long-Term Safety and Efficacy of Fecal Microbiota Transplant in Active Ulcerative Colitis

European journal of neurology Clinical analysis of Chinese anti-low-density-lipoprotein-receptor-associated protein 4 antibodies in patients with myasthenia gravis

Cells, 8, 5. Overexpression of miR-29 Leads to Myopathy that Resemble Pathology of Ullrich Congenital Muscular Dystrophy

Molecular genetics and metabolism reports, 16. Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency

International journal of neuroscience, 124, 1. Modeling induced pluripotent stem cells from fibroblasts of Duchenne muscular dystrophy patients

International journal of neuroscience, 120, 11. Vocal cord paresis and probable X-linked Charcot-Marie-Tooth disease with novel GJB1 mutation

Nature medicine, 13, 6. Restoration of cone vision in a mouse model of achromatopsia

Journal of peking university. Health sciences, 38, 1. Prenatal molecular diagnosis of Duchenne and Becker muscular dystrophy

Journal of biological chemistry (The), 280, 16. A minimal structural analogue of cyclic ADP-ribose: synthesis and calcium release activity in mammalian cells.

Development, 131, 21. Accordion, a zebrafish behavioral mutant, has a muscle relaxation defect due to a mutation in the ATPase CA2+ pump SERCA1

Journal of virology, 69, 4. Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses