Botta Annalisa相关文献与解析，生知库 | 链接生命科学的每一步

Altered Expression of Cell Cycle Regulators and Factors Released by Aged Cells in Skeletal Muscle of Patients with Bone Fragility: A Pilot Study on the Potential Role of SIRT1 in Muscle Atrophy.

骨骼肌中衰老细胞释放的细胞周期调节因子和因子的表达改变与骨脆症患者骨骼肌的改变：SIRT1 在肌肉萎缩中的潜在作用的初步研究

Falvino Angela, Bonanni Roberto, Gasperini Beatrice, Cariati Ida, Chiavoghilefu Angela, Smakaj Amarildo, Visconti Virginia Veronica, Botta Annalisa, Iundusi Riccardo, Gasbarra Elena, Tancredi Virginia, Tarantino Umberto

细胞生物学

细胞衰老

发表日期：2025

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Cellular Senescence: The Driving Force of Musculoskeletal Diseases

细胞衰老：肌肉骨骼疾病的驱动力

期刊:Biomedicines

影响因子:3.9

doi:10.3390/biomedicines12091948

Falvino, Angela; Gasperini, Beatrice; Cariati, Ida; Bonanni, Roberto; Chiavoghilefu, Angela; Gasbarra, Elena; Botta, Annalisa; Tancredi, Virginia; Tarantino, Umberto

Senescence

发表日期：2024

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In Cis Effect of DMPK Expanded Alleles in Myotonic Dystrophy Type 1 Patients Carrying Variant Repeats at 5' and 3' Ends of the CTG Array

肌强直性营养不良1型患者中DMPK扩增等位基因的顺式效应，这些患者CTG阵列的5'端和3'端携带变异重复序列

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms241210129

Visconti, Virginia Veronica; Macrì, Elisa; D'Apice, Maria Rosaria; Centofanti, Federica; Massa, Roberto; Novelli, Giuseppe; Botta, Annalisa

Association Between DRD2 and DRD4 Polymorphisms and Eating Disorders in an Italian Population

意大利人群中DRD2和DRD4多态性与饮食失调的关联

期刊:Frontiers in Nutrition

影响因子:5.1

doi:10.3389/fnut.2022.838177

Ceccarini, Maria Rachele; Fittipaldi, Simona; Ciccacci, Cinzia; Granese, Erika; Centofanti, Federica; Dalla Ragione, Laura; Bertelli, Matteo; Beccari, Tommaso; Botta, Annalisa

发表日期：2022

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DNA Methylation Signatures of Bone Metabolism in Osteoporosis and Osteoarthritis Aging-Related Diseases: An Updated Review

骨质疏松症和骨关节炎等衰老相关疾病中骨代谢的DNA甲基化特征：最新综述

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms22084244

Visconti, Virginia Veronica; Cariati, Ida; Fittipaldi, Simona; Iundusi, Riccardo; Gasbarra, Elena; Tarantino, Umberto; Botta, Annalisa

Epigenetics of Myotonic Dystrophies: A Minireview

肌强直营养不良的表观遗传学：简述

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms222212594

Visconti, Virginia Veronica; Centofanti, Federica; Fittipaldi, Simona; Macrì, Elisa; Novelli, Giuseppe; Botta, Annalisa

A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles

意大利14年来在DM2基因检测方面的经验：正常和前突变CNBP等位基因的频率和分布

期刊:Frontiers in Genetics

影响因子:2.8

doi:10.3389/fgene.2021.668094

Botta, Annalisa; Visconti, Virginia Veronica; Fontana, Luana; Bisceglia, Paola; Bengala, Mario; Massa, Roberto; Bagni, Ilaria; Cardani, Rosanna; Sangiuolo, Federica; Meola, Giovanni; Antonini, Giovanni; Petrucci, Antonio; Pegoraro, Elena; D'Apice, Maria Rosaria; Novelli, Giuseppe

CNBP

发表日期：2021

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The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bone-related phenotypes

长链五聚蛋白 PTX3：一种新型血清标志物，可提高对骨质疏松症和骨关节炎骨骼相关表型的预测能力

期刊:Journal of Orthopaedic Surgery and Research

影响因子:2.8

doi:10.1186/s13018-021-02440-3

Visconti, Virginia Veronica; Greggi, Chiara; Fittipaldi, Simona; Casamassima, Donato; Tallarico, Mariagrazia; Romano, Francesco; Botta, Annalisa; Tarantino, Umberto

Correction to: The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bonerelated phenotypes

更正：长链五聚蛋白 PTX3：一种新型血清标志物，可改善骨质疏松症和骨关节炎骨相关表型的预测

期刊:Journal of Orthopaedic Surgery and Research

影响因子:2.8

doi:10.1186/s13018-021-02481-8

Visconti, Virginia Veronica; Greggi, Chiara; Fittipaldi, Simona; Casamassima, Donato; Tallarico, Mariagrazia; Romano, Francesco; Botta, Annalisa; Tarantino, Umberto

Mutated sigma-1R disrupts cell homeostasis in dHMN patient cells.

突变的 sigma-1R 会破坏 dHMN 患者细胞的细胞稳态

Altered Expression of Cell Cycle Regulators and Factors Released by Aged Cells in Skeletal Muscle of Patients with Bone Fragility: A Pilot Study on the Potential Role of SIRT1 in Muscle Atrophy.

骨骼肌中衰老细胞释放的细胞周期调节因子和因子的表达改变与骨脆症患者骨骼肌的改变：SIRT1 在肌肉萎缩中的潜在作用的初步研究

Cellular Senescence: The Driving Force of Musculoskeletal Diseases

细胞衰老：肌肉骨骼疾病的驱动力

In Cis Effect of DMPK Expanded Alleles in Myotonic Dystrophy Type 1 Patients Carrying Variant Repeats at 5' and 3' Ends of the CTG Array

肌强直性营养不良1型患者中DMPK扩增等位基因的顺式效应，这些患者CTG阵列的5'端和3'端携带变异重复序列

Association Between DRD2 and DRD4 Polymorphisms and Eating Disorders in an Italian Population

意大利人群中DRD2和DRD4多态性与饮食失调的关联

DNA Methylation Signatures of Bone Metabolism in Osteoporosis and Osteoarthritis Aging-Related Diseases: An Updated Review

骨质疏松症和骨关节炎等衰老相关疾病中骨代谢的DNA甲基化特征：最新综述

Epigenetics of Myotonic Dystrophies: A Minireview

肌强直营养不良的表观遗传学：简述

A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles

意大利14年来在DM2基因检测方面的经验：正常和前突变CNBP等位基因的频率和分布

The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bone-related phenotypes

长链五聚蛋白 PTX3：一种新型血清标志物，可提高对骨质疏松症和骨关节炎骨骼相关表型的预测能力

Correction to: The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bonerelated phenotypes

更正：长链五聚蛋白 PTX3：一种新型血清标志物，可改善骨质疏松症和骨关节炎骨相关表型的预测