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Auteur Wu W

Documents disponibles écrits par cet auteur (18)

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Article

The European respiratory journal, Epub. Effectiveness and safety of tofacitinib versus calcineurin inhibitor in interstitial lung disease secondary to anti-MDA5-positive dermatomyositis: a multi-centre cohort study

Wu W ; Guo B ; Sun W ; Chen D ; Xu W ; Chen Z ; Fu Y ; Ye Y ; Lyu X ; Xue Z ; Wang K ; Zhao J ; Xie C ; Chen Y ; Ye C ; Dai M ; Fan W ; Li J ; Wang X ; Xue Y ; Wan W ; Sun L ; Wu H ; Luo Q ; Han Q ; Fu Q ; Ye S | 30/01/2025

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Article

Molecular genetics & genomic medicine, 12, 1. Carrier screening for spinal muscular atrophy in 22913 Chinese reproductive age women

Zhang L ; Mo J ; Zhou L ; Xu X ; Xu Z ; Zhang L ; Wu W | 01/2024

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Article

Human molecular genetics The clinical features and TCAP mutation Spectrum in a Chinese cohort of patients with limb-girdle muscular dystrophy R7

Lv X ; Lin F ; Wu W ; Wang H ; Luo Y ; Wang Z ; Yan C ; Lv H ; Luo S ; Lin P | 22/05/2023

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Article

Cytokine, 157. PD-1 inhibitor induces myocarditis by reducing regulatory T cells, activating inflammatory responses, promoting myocardial apoptosis and autophagy

Liu YX ; Song YJ ; Liu XH ; Xu SC ; Kong C ; Chen LF ; Qian H ; Wu W | England | 09/06/2022

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Article

Frontiers in immunology, 12. RNA-Containing Immune Complexes Formed by Anti-Melanoma Differentiation Associated Gene 5 Autoantibody Are Potent Inducers of IFN-α

Wang K ; Zhao J ; Wu W ; Xu W ; Sun S ; Chen Z ; Fu Y ; Guo L ; Du H ; Ye S | 15/10/2021

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Article

Frontiers in immunology, 12. Description and Analysis of a Novel Subtype of the Anti-Synthetase Syndrome Characterized by Frequent Attacks of Fever and Systemic Inflammation in a Single-Center Cohort Study

Sun S ; Chen Z ; Zhang D ; Xu W ; Wu W ; Sun F ; Gu L ; Chen J ; Li J ; Li T ; Wang X ; Ye S | 23/09/2021

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Article

Rheumatology advances in practice, 5, 3. A survey to understand the feelings towards and impact of COVID-19 on the households of juvenile dermato myositis patients from a parent or carer perspective

Wilkinson MGL ; Wu W ; O'Brien K ; Deakin CT ; Wedderburn LR ; Livermore P | 13/09/2021

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Article

Cell reports, 36, 8. The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies

Vignier N ; Chatzifrangkeskou M ; Pinton L ; Wioland H ; Marais T ; Lemaitre M ; Le Dour C ; Peccate C ; Cardoso D ; Schmitt A ; Wu W ; Biferi MG ; Naouar N ; Macquart C ; Beuvin M ; Decostre V ; Bonne G ; Romet-Lemonne G ; Worman HJ ; Tedesco FS ; Jégou A ; Muchir A | 24/08/2021

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Article

Journal of cell science, 134, 6. A lamin A/C variant causing striated muscle disease provides insights into filament organization

Kronenberg-Tenga R ; Tatli M ; Eibauer M ; Wu W ; Shin JY ; Bonne G ; Worman HJ ; Medalia O | 22/03/2021

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Article

Human molecular genetics, 29, 24. Ryanodine receptor remodeling in cardiomyopathy and muscular dystrophy caused by lamin A/C gene mutation

Dridi H ; Wu W ; Reiken SR ; Ofer RM ; Liu Y ; Yuan Q ; Sittenfeld L ; Kushner J ; Muchir A ; Worman HJ ; Marks AR | England | 25/02/2021

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Article

Developmental cell, 51, 5. ERK1/2 Phosphorylation of FHOD Connects Signaling and Nuclear Positioning Alternations in Cardiac Laminopathy

Antoku S ; Wu W ; Joseph LC ; Morrow JP ; Worman HJ ; Gundersen GG | United States | 12/2019

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Article

Bioorganic & medicinal chemistry, 25, 3. Macrocyclic MEK1/2 inhibitor with efficacy in a mouse model of cardiomyopathy caused by lamin A/C gene mutation

Wu W ; Chordia MD ; Hart BP ; Kumarasinghe ES ; Ji MK ; Bhargava A ; Lawlor MW ; Shin JY ; Sera F ; Homma S ; Muchir A ; Khire UR ; Worman HJ | 2017

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Article

Human molecular genetics, 25, 11. ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene

Chatzifrangkeskou M, Auteur ; Le Dour C ; Wu W ; Morrow JP ; Joseph LC ; Beuvin M ; Sera F ; Homma S ; Vignier N ; Mougenot N ; Bonne G ; Lipson KE ; Worman HJ ; Muchir A | 2016

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Article

Science translational medicine, 4, 144ra102. Temsirolimus activates autophagy and ameliorates cardiomyopathy caused by lamin A/C gene mutation

Choi JC ; Muchir A ; Wu W ; Iwata S ; Homma S ; Morrow JP ; Worman HJ | 25/02/2012

Accès au résumé PubMed / to PubMed abstract

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Article

Cardiovascular research, 93, 2. Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene

Muchir A ; Reilly SA ; Wu W ; Iwata S ; Homma S ; Bonne G ; Worman HJ | 2012

Accès au résumé PubMed / to PubMed abstract

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Article

Circulation, 123, 1. Mitogen-activated protein kinase inhibitors improve heart function and prevent fibrosis in cardiomyopathy caused by mutation in Lamin A/C gene

Wu W ; Muchir A ; Shan J ; Bonne G ; Worman HJ | 2011

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Article

Inhibition of erk signaling improves cardiomyopathy in emery-dreifuss muscular dystrophy

4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Muchir A ; Wu W ; Bonne G ; Worman H | 2011

Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD) is caused by mutations in the LMNA gene encoding A-type lamins, protein building blocks of the nuclear lamina. EDMD is characterized by muscle weakness and wasting in a humeroperoneal d[...]

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Article

Biochimica et biophysica acta, 1802, 7-8. Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene

Wu W ; Shan J ; Bonne G ; Worman HJ ; Muchir A | 2010

Accès au résumé Pubmed/to pubmed abstract

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Détail de l'auteur

Auteur Wu W

Documents disponibles écrits par cet auteur (18)

The European respiratory journal, Epub. Effectiveness and safety of tofacitinib versus calcineurin inhibitor in interstitial lung disease secondary to anti-MDA5-positive dermatomyositis: a multi-centre cohort study

Molecular genetics & genomic medicine, 12, 1. Carrier screening for spinal muscular atrophy in 22913 Chinese reproductive age women

Human molecular genetics The clinical features and TCAP mutation Spectrum in a Chinese cohort of patients with limb-girdle muscular dystrophy R7

Cytokine, 157. PD-1 inhibitor induces myocarditis by reducing regulatory T cells, activating inflammatory responses, promoting myocardial apoptosis and autophagy

Frontiers in immunology, 12. RNA-Containing Immune Complexes Formed by Anti-Melanoma Differentiation Associated Gene 5 Autoantibody Are Potent Inducers of IFN-α

Frontiers in immunology, 12. Description and Analysis of a Novel Subtype of the Anti-Synthetase Syndrome Characterized by Frequent Attacks of Fever and Systemic Inflammation in a Single-Center Cohort Study

Rheumatology advances in practice, 5, 3. A survey to understand the feelings towards and impact of COVID-19 on the households of juvenile dermato myositis patients from a parent or carer perspective

Cell reports, 36, 8. The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies

Journal of cell science, 134, 6. A lamin A/C variant causing striated muscle disease provides insights into filament organization

Human molecular genetics, 29, 24. Ryanodine receptor remodeling in cardiomyopathy and muscular dystrophy caused by lamin A/C gene mutation

Developmental cell, 51, 5. ERK1/2 Phosphorylation of FHOD Connects Signaling and Nuclear Positioning Alternations in Cardiac Laminopathy

Bioorganic & medicinal chemistry, 25, 3. Macrocyclic MEK1/2 inhibitor with efficacy in a mouse model of cardiomyopathy caused by lamin A/C gene mutation

Human molecular genetics, 25, 11. ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene

Science translational medicine, 4, 144ra102. Temsirolimus activates autophagy and ameliorates cardiomyopathy caused by lamin A/C gene mutation

Cardiovascular research, 93, 2. Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene

Circulation, 123, 1. Mitogen-activated protein kinase inhibitors improve heart function and prevent fibrosis in cardiomyopathy caused by mutation in Lamin A/C gene

Inhibition of erk signaling improves cardiomyopathy in emery-dreifuss muscular dystrophy

Biochimica et biophysica acta, 1802, 7-8. Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene