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Stress granules in the spinal muscular atrophy and amyotrophic lateral sclerosis: The correlation and promising therapy

Neurobiology of disease, 2022-08, Vol.170, p.105749-105749, Article 105749

2022

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Role of Erythrocyte CD47 in Intracerebral Hematoma Clearance

Stroke (1970), 2016-02, Vol.47 (2), p.505-511

2016

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Nutritional and lipid profile status of children with spinal muscular atrophy in China: A retrospective case-control study

Chinese medical journal, 2024-05, Vol.137 (10), p.1243-1245

2024

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Editorial: Neurogenetic disorders: from the tests to the clinic

Frontiers in neurology, 2023-07, Vol.14, p.1236350-1236350

2023

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Novel EBV LMP1 C-terminal domain binding affibody molecules as potential agents for in vivo molecular imaging diagnosis of nasopharyngeal carcinoma

Applied microbiology and biotechnology, 2021-10, Vol.105 (19), p.7283-7293

2021

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Epidemiological and virological characteristics of respiratory tract infections in children during COVID-19 outbreak

BMC pediatrics, 2021-04, Vol.21 (1), p.195-195, Article 195

2021

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Decreased abundance of Akkermansia after adrenocorticotropic hormone therapy in patients with West syndrome

BMC microbiology, 2021-04, Vol.21 (1), p.126-126, Article 126

2021

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Circ_0007432 promotes non-small cell lung cancer progression and macrophage M2 polarization through SRSF1/KLF12 axis

iScience, 2024-06, Vol.27 (6), p.109861-109861, Article 109861

2024

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Selective capture of silver ions from aqueous solution by series of azole derivatives-functionalized silica nanosheets

Chinese journal of chemical engineering, 2023-05, Vol.57 (5), p.319-328

2023

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Inhibitory effects of a maleimide compound on the virulence factors of Candida albicans

Virulence, 2023-12, Vol.14 (1), p.2230009-2230009

2023

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Quality of life of children with spinal muscular atrophy and their caregivers from the perspective of caregivers: a Chinese cross-sectional study

Orphanet journal of rare diseases, 2021-01, Vol.16 (1), p.7-7, Article 7

2021

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Anxiety and depression in school-age patients with spinal muscular atrophy: a cross-sectional study

Orphanet journal of rare diseases, 2021-09, Vol.16 (1), p.1-385, Article 385

2021

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Functional organoclays for removal of heavy metal ions from water: A review

Journal of molecular liquids, 2021-07, Vol.334, p.116143, Article 116143

2021

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Reversible splenial lesion syndrome in children with benign convulsions associated with mild gastroenteritis: A retrospective study of five cases

Brain & development (Tokyo. 1979), 2019-03, Vol.41 (3), p.271-275

2019

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Health information literacy among children with spinal muscular atrophy and their caregivers

Italian journal of pediatrics, 2024-08, Vol.50 (1), p.157-9

2024

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Optimized MLPA workflow for spinal muscular atrophy diagnosis: identification of a novel variant, NC_000005.10:g.(70919941_70927324)del in isolated exon 1 of SMN1 gene through long-range PCR

BMC neurology, 2024-03, Vol.24 (1), p.93-93, Article 93

2024

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Intestinal bacteria-a powerful weapon for fungal infections treatment

Frontiers in cellular and infection microbiology, 2023-06, Vol.13, p.1187831-1187831

2023

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Core Fucosylation of the T Cell Receptor Is Required for T Cell Activation

Frontiers in immunology, 2018-01, Vol.9, p.78-78

2018

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A comparative analysis of body composition assessment by BIA and DXA in children with type II and III spinal muscular atrophy

Frontiers in neurology, 2022-11, Vol.13, p.1034894-1034894

2022

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Role of Lipocalin-2 in Thrombin-Induced Brain Injury

Stroke (1970), 2016-04, Vol.47 (4), p.1078-1084

2016

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Design of a hyper-numerical-aperture deep ultraviolet lithography objective with freeform surfaces

Chinese optics letters, 2018-03, Vol.16 (3), p.30801

2018

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Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy

Frontiers in genetics, 2021-03, Vol.12, p.605611

2021

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A novel SCN9A gene variant identified in a Chinese girl with paroxysmal extreme pain disorder (PEPD): a rare case report

BMC medical genomics, 2022-07, Vol.15 (1), p.1-159, Article 159

2022

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Somatic KRAS mutation in an infant with linear nevus sebaceous syndrome associated with lymphatic malformations: A case report and literature review

Medicine (Baltimore), 2017-11, Vol.96 (47), p.e8016-e8016

2017

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Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy

Frontiers in genetics, 2021-06, Vol.12, p.684042-684042

2021

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Stress granules in the spinal muscular atrophy and amyotrophic lateral sclerosis: The correlation and promising therapy

Role of Erythrocyte CD47 in Intracerebral Hematoma Clearance

Nutritional and lipid profile status of children with spinal muscular atrophy in China: A retrospective case-control study

Editorial: Neurogenetic disorders: from the tests to the clinic

Novel EBV LMP1 C-terminal domain binding affibody molecules as potential agents for in vivo molecular imaging diagnosis of nasopharyngeal carcinoma

Epidemiological and virological characteristics of respiratory tract infections in children during COVID-19 outbreak

Decreased abundance of Akkermansia after adrenocorticotropic hormone therapy in patients with West syndrome

Circ_0007432 promotes non-small cell lung cancer progression and macrophage M2 polarization through SRSF1/KLF12 axis

Selective capture of silver ions from aqueous solution by series of azole derivatives-functionalized silica nanosheets

Inhibitory effects of a maleimide compound on the virulence factors of Candida albicans

Quality of life of children with spinal muscular atrophy and their caregivers from the perspective of caregivers: a Chinese cross-sectional study

Anxiety and depression in school-age patients with spinal muscular atrophy: a cross-sectional study

Functional organoclays for removal of heavy metal ions from water: A review

Reversible splenial lesion syndrome in children with benign convulsions associated with mild gastroenteritis: A retrospective study of five cases

Health information literacy among children with spinal muscular atrophy and their caregivers

Optimized MLPA workflow for spinal muscular atrophy diagnosis: identification of a novel variant, NC_000005.10:g.(70919941_70927324)del in isolated exon 1 of SMN1 gene through long-range PCR

Intestinal bacteria-a powerful weapon for fungal infections treatment

Core Fucosylation of the T Cell Receptor Is Required for T Cell Activation

A comparative analysis of body composition assessment by BIA and DXA in children with type II and III spinal muscular atrophy

Role of Lipocalin-2 in Thrombin-Induced Brain Injury

Design of a hyper-numerical-aperture deep ultraviolet lithography objective with freeform surfaces

Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy

A novel SCN9A gene variant identified in a Chinese girl with paroxysmal extreme pain disorder (PEPD): a rare case report

Somatic KRAS mutation in an infant with linear nevus sebaceous syndrome associated with lymphatic malformations: A case report and literature review

Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy

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