Andres Christian R相关文献与解析，生知库

Improving ALS Molecular Diagnosis Through Functional Assays: Reassessment of a SOD1 Variant of Uncertain Significance

通过功能性检测改进ALS分子诊断：重新评估意义未明的SOD1变异体

期刊:International Journal of Molecular Sciences

Bedja-Iacona, Léa; Forget, Arthur; Boisseau, Chloé; Marouillat, Sylviane; Chudinova, Aleksandra; Veyrat-Durebex, Charlotte; Guissart, Claire; Lumbroso, Serge; Raoul, Cédric; Andres, Christian R; Blasco, Hélène; Couratier, Philippe; Corcia, Philippe; Verschueren, Annie; Mouzat, Kevin; Vourc'h, Patrick

Impact of maternal microbiota imbalance during pregnancy on fetal cerebral neurodevelopment: Is there a link to certain autistic disorders?

孕期母体微生物群失衡对胎儿大脑神经发育的影响：与某些自闭症谱系障碍有关联吗？

期刊:Brain Behavior Immunity Health

影响因子:3.5

doi:10.1016/j.bbih.2025.101074

Mavel, Sylvie; Pellé, Léa; Andres, Christian R

scFv intrabody targeting wildtype TDP-43 presents protective effects in a cellular model of TDP-43 proteinopathy.

靶向野生型 TDP-43 的 scFv 胞内抗体在 TDP-43 蛋白病细胞模型中表现出保护作用

期刊:PLoS One

影响因子:2.6

doi:10.1371/journal.pone.0322021

Al Ojaimi Yara, Hergesheimer Rudolf, Chami Anna A, Alarcan Hugo, Augros Johanna, Dangoumau Audrey, Haouari Shanez, Bourgeais JÃ©rÃ´me, Lefevre Antoine, Osman Samira, Emond Patrick, Vourc'h Patrick, Andres Christian R, Corcia Philippe, Herault Olivier, Martineau Pierre, Lanznaster DÃ©bora, Blasco HÃ©lÃ¨ne

细胞生物学

发表日期：2025

文献求助收藏

Contribution of an Ambidirectional Cohort Study on the Epidemiology of 186 Autism Spectrum Disorder Cases in an Algerian Population

一项双向队列研究对阿尔及利亚人群中186例自闭症谱系障碍病例流行病学的贡献

期刊:International Journal of Developmental Neuroscience

影响因子:1.6

doi:10.1002/jdn.70036

Loumi, Ourida; Andres, Christian R

Body Composition and Anthropometric Measurements in Children and Adolescents with Autism Spectrum Disorder: A Case-Control Study in Lebanon

黎巴嫩自闭症谱系障碍儿童和青少年身体成分和人体测量：一项病例对照研究

期刊:Nutrients

影响因子:5

doi:10.3390/nu16060847

Rouphael, Melissa; Sacre, Yonna; Bitar, Tania; Andres, Christian R; Hleihel, Walid

Post-Translational Variants of Major Proteins in Amyotrophic Lateral Sclerosis Provide New Insights into the Pathophysiology of the Disease

肌萎缩侧索硬化症主要蛋白的翻译后修饰变体为该疾病的病理生理学提供了新的见解

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms25168664

Bedja-Iacona, Léa; Richard, Elodie; Marouillat, Sylviane; Brulard, Céline; Alouane, Tarek; Beltran, Stéphane; Andres, Christian R; Blasco, Hélène; Corcia, Philippe; Veyrat-Durebex, Charlotte; Vourc'h, Patrick

发表日期：2024

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Dynamic Expression of Genes Encoding Ubiquitin Conjugating Enzymes (E2s) During Neuronal Differentiation and Maturation: Implications for Neurodevelopmental Disorders and Neurodegenerative Diseases

神经元分化和成熟过程中编码泛素结合酶（E2）的基因的动态表达：对神经发育障碍和神经退行性疾病的启示

期刊:Genes

影响因子:2.8

doi:10.3390/genes15111381

Paubel, Agathe; Marouillat, Sylviane; Dangoumau, Audrey; Maurel, Cindy; Haouari, Shanez; Blasco, Hélène; Corcia, Philippe; Laumonnier, Frédéric; Andres, Christian R; Vourc'h, Patrick

Neutrophil to Lymphocyte Ratio as a Prognostic Marker in Amyotrophic Lateral Sclerosis

中性粒细胞与淋巴细胞比值作为肌萎缩侧索硬化症的预后标志物

期刊:Biomolecules

影响因子:4.8

doi:10.3390/biom13121689

Cotet, Camille; Alarcan, Hugo; Hérault, Olivier; Corcia, Philippe; Vourc'h, Patrick; Andres, Christian R; Blasco, Hélène; Veyrat-Durebex, Charlotte

The Roles of NEDD4 Subfamily of HECT E3 Ubiquitin Ligases in Neurodevelopment and Neurodegeneration

NEDD4亚家族HECT E3泛素连接酶在神经发育和神经退行性疾病中的作用

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms23073882

Haouari, Shanez; Vourc'h, Patrick; Jeanne, Médéric; Marouillat, Sylviane; Veyrat-Durebex, Charlotte; Lanznaster, Débora; Laumonnier, Frédéric; Corcia, Philippe; Blasco, Hélène; Andres, Christian R

Exploration of Homocysteine Metabolism and Genetics in Autism Spectrum Disorder

自闭症谱系障碍中同型半胱氨酸代谢和遗传学的研究

Improving ALS Molecular Diagnosis Through Functional Assays: Reassessment of a SOD1 Variant of Uncertain Significance

通过功能性检测改进ALS分子诊断：重新评估意义未明的SOD1变异体

Impact of maternal microbiota imbalance during pregnancy on fetal cerebral neurodevelopment: Is there a link to certain autistic disorders?

孕期母体微生物群失衡对胎儿大脑神经发育的影响：与某些自闭症谱系障碍有关联吗？

scFv intrabody targeting wildtype TDP-43 presents protective effects in a cellular model of TDP-43 proteinopathy.

靶向野生型 TDP-43 的 scFv 胞内抗体在 TDP-43 蛋白病细胞模型中表现出保护作用

Contribution of an Ambidirectional Cohort Study on the Epidemiology of 186 Autism Spectrum Disorder Cases in an Algerian Population

一项双向队列研究对阿尔及利亚人群中186例自闭症谱系障碍病例流行病学的贡献

Body Composition and Anthropometric Measurements in Children and Adolescents with Autism Spectrum Disorder: A Case-Control Study in Lebanon

黎巴嫩自闭症谱系障碍儿童和青少年身体成分和人体测量：一项病例对照研究

Post-Translational Variants of Major Proteins in Amyotrophic Lateral Sclerosis Provide New Insights into the Pathophysiology of the Disease

肌萎缩侧索硬化症主要蛋白的翻译后修饰变体为该疾病的病理生理学提供了新的见解

Dynamic Expression of Genes Encoding Ubiquitin Conjugating Enzymes (E2s) During Neuronal Differentiation and Maturation: Implications for Neurodevelopmental Disorders and Neurodegenerative Diseases

神经元分化和成熟过程中编码泛素结合酶（E2）的基因的动态表达：对神经发育障碍和神经退行性疾病的启示

Neutrophil to Lymphocyte Ratio as a Prognostic Marker in Amyotrophic Lateral Sclerosis

中性粒细胞与淋巴细胞比值作为肌萎缩侧索硬化症的预后标志物

The Roles of NEDD4 Subfamily of HECT E3 Ubiquitin Ligases in Neurodevelopment and Neurodegeneration

NEDD4亚家族HECT E3泛素连接酶在神经发育和神经退行性疾病中的作用