日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

[Corrigendum] Lithium chloride induces mesenchymal‑to‑epithelial reverting transition in primary colon cancer cell cultures

【更正】氯化锂诱导原代结肠癌细胞培养物发生间质-上皮逆转转化

期刊:International Journal of Oncology
影响因子:4.9
doi:10.3892/ijo.2025.5800
Costabile, Valeria; Duraturo, Francesca; Delrio, Paolo; Rega, Daniela; Pace, Ugo; Liccardo, Raffaella; Rossi, Giovanni Battista; Genesio, Rita; Nitsch, Lucio; Izzo, Paola; De Rosa, Marina
肿瘤
肠癌
肿瘤免疫
Cell Culture
细胞生物学
发表日期：2025
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Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression

唐氏综合征胎儿成纤维细胞内体运输可能由于SYNJ1过度表达而发生改变

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2022.867989
De Rosa, Laura; Fasano, Dominga; Zerillo, Lucrezia; Valente, Valeria; Izzo, Antonella; Mollo, Nunzia; Amodio, Giuseppina; Polishchuk, Elena; Polishchuk, Roman; Melone, Mariarosa Anna Beatrice; Criscuolo, Chiara; Conti, Anna; Nitsch, Lucio; Remondelli, Paolo; Pierantoni, Giovanna Maria; Paladino, Simona
细胞生物学
成纤维细胞
发表日期：2022
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Microdeletion of pseudogene chr14.232.a affects LRFN5 expression in cells of a patient with autism spectrum disorder

假基因 chr14.232.a 的微缺失影响自闭症谱系障碍患者细胞中 LRFN5 的表达

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-019-0430-5
Cappuccio, Gerarda; Attanasio, Sergio; Alagia, Marianna; Mutarelli, Margherita; Borzone, Roberta; Karali, Marianthi; Genesio, Rita; Mormile, Angela; Nitsch, Lucio; Imperati, Floriana; Esposito, Annalisa; Banfi, Sandro; Del Giudice, Ennio; Brunetti-Pierri, Nicola
细胞生物学
自闭症
神经科学
发表日期：2019
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Pioglitazone Improves Mitochondrial Organization and Bioenergetics in Down Syndrome Cells

吡格列酮改善唐氏综合征细胞的线粒体组织和生物能量学

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2019.00606
Mollo, Nunzia; Nitti, Maria; Zerillo, Lucrezia; Faicchia, Deriggio; Micillo, Teresa; Accarino, Rossella; Secondo, Agnese; Petrozziello, Tiziana; Calì, Gaetano; Cicatiello, Rita; Bonfiglio, Ferdinando; Sarnataro, Viviana; Genesio, Rita; Izzo, Antonella; Pinton, Paolo; Matarese, Giuseppe; Paladino, Simona; Conti, Anna; Nitsch, Lucio
细胞生物学
线粒体
发表日期：2019
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MON-620 Autoimmune Thyroiditis, Benign Nodular Thyroid Disease and Adipokines Levels

MON-620 自身免疫性甲状腺炎、良性结节性甲状腺疾病和脂肪因子水平

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0027648
Frezzetti, Daniela; Reale, Carla; Calì, Gaetano; Nitsch, Lucio; Fagman, Henrik; Nilsson, Ola; Scarfò, Marzia; De Vita, Gabriella; Di Lauro, Roberto; Neves, Celestino; Neves, João Sérgio; Castro Oliveira, Sofia; Sokhatska, Oksana; Pereira, Miguel; Oliveira, Ana; Medina, José Luís; Delgado, Luís; Carvalho, Davide
免疫/内分泌
发表日期：2019
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Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations

内体运输的改变与SYNJ1基因突变引起的早发性帕金森病有关。

期刊:Cell Death & Disease
影响因子:9.6
doi:10.1038/s41419-018-0410-7
Fasano, Dominga; Parisi, Silvia; Pierantoni, Giovanna Maria; De Rosa, Anna; Picillo, Marina; Amodio, Giuseppina; Pellecchia, Maria Teresa; Barone, Paolo; Moltedo, Ornella; Bonifati, Vincenzo; De Michele, Giuseppe; Nitsch, Lucio; Remondelli, Paolo; Criscuolo, Chiara; Paladino, Simona
帕金森
神经科学
发表日期：2018
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Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report

产前诊断的远端16p11.2微缺失与先天性膈疝的新关联：病例报告

期刊:Clinical Case Reports
影响因子:0.6
doi:10.1002/ccr3.1369
Genesio, Rita; Maruotti, Giuseppe Maria; Saccone, Gabriele; Mormile, Angela; Conti, Anna; Cicatiello, Rita; Sarnataro, Viviana; Sirico, Angelo; Izzo, Antonella; Martinelli, Pasquale; Nitsch, Lucio
发表日期：2018
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New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants

阵列比较基因组杂交（array-CGH）解读的新见解：自闭症谱系障碍和智力障碍家族史阳性可预测致病变异的检出

期刊:Italian Journal of Pediatrics
影响因子:3.1
doi:10.1186/s13052-016-0246-7
Cappuccio, Gerarda; Vitiello, Francesco; Casertano, Alberto; Fontana, Paolo; Genesio, Rita; Bruzzese, Dario; Ginocchio, Virginia Maria; Mormile, Angela; Nitsch, Lucio; Andria, Generoso; Melis, Daniela
自闭症
神经科学
发表日期：2016
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Erratum to: In vivo role of different domains and of phosphorylation in the transcription factor Nkx2-1

勘误：转录因子Nkx2-1中不同结构域和磷酸化的体内作用

期刊:BMC Developmental Biology
影响因子:
doi:10.1186/s12861-016-0130-0
Silberschmidt, Daniel; Rodriguez-Mallon, Alina; Mithboakar, Prathiba; Calì, Gaetano; Amendola, Elena; Sanges, Remo; Zannini, Mariastella; Scarfò, Marzia; De Luca, Pasquale; Nitsch, Lucio; Di Lauro, Roberto; De Felice, Mario
信号转导
磷酸化
发表日期：2016
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Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocation

身材矮小和原发性卵巢功能不全可能是由于平衡的X;1易位中的染色体位置效应所致。

期刊:Molecular Cytogenetics
影响因子:1.4
doi:10.1186/s13039-015-0154-3
Genesio, Rita; Mormile, Angela; Licenziati, Maria Rosaria; De Brasi, Daniele; Leone, Graziella; Balzano, Sara; Izzo, Antonella; Bonfiglio, Ferdinando; Conti, Anna; Fioretti, Gennaro; Lenta, Selvaggia; Poggiano, Maria Rita; Siani, Paolo; Nitsch, Lucio
发表日期：2015
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