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

De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay

一名患有轻度智力低下和语言发育迟缓的患者,其8p22区域存在1Mb的新发间质缺失。

Piovani, Giovanna; Savio, Giulia; Traversa, Michele; Pilotta, Alba; De Petro, Giuseppina; Barlati, Sergio; Magri, Chiara

Effects of miR-193a and sorafenib on hepatocellular carcinoma cells.

miR-193a和索拉非尼对肝细胞癌细胞的影响

Salvi Alessandro, Conde Isabel, Abeni Edoardo, Arici Bruna, Grossi Ilaria, Specchia Claudia, Portolani Nazario, Barlati Sergio, De Petro Giuseppina

Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections

三兄弟因DOCK8和CLEC7A基因联合突变导致免疫缺陷,并出现腹泻、湿疹和感染等症状。

Dinwiddie, Darrell L; Kingsmore, Stephen F; Caracciolo, Sonia; Rossi, Giuseppe; Moratto, Daniele; Mazza, Cinzia; Sabelli, Cristiano; Bacchetta, Rosa; Passerini, Laura; Magri, Chiara; Bell, Callum J; Miller, Neil A; Hateley, Shannon L; Saunders, Carol J; Zhang, Lu; Schroth, Gary P; Barlati, Sergio; Badolato, Raffaele

Functional characterisation of human cells harbouring a novel t(2p;7p) translocation involving TNS3 and EXOC6B genes

对携带涉及TNS3和EXOC6B基因的新型t(2p;7p)易位的人类细胞进行功能表征

Ludwig, Desiree; Carter, Jessica; Smith, James R; Borsani, Giuseppe; Barlati, Sergio; Hafizi, Sassan

Effects of neuroinflammation on the regenerative capacity of brain stem cells

神经炎症对脑干细胞再生能力的影响

Russo, Isabella; Barlati, Sergio; Bosetti, Francesca

Altered mRNA editing and expression of ionotropic glutamate receptors after kainic acid exposure in cyclooxygenase-2 deficient mice

环氧合酶-2缺陷小鼠暴露于红藻氨酸后,mRNA编辑和离子型谷氨酸受体的表达发生改变。

Caracciolo, Luca; Barbon, Alessandro; Palumbo, Sara; Mora, Cristina; Toscano, Christopher D; Bosetti, Francesca; Barlati, Sergio

Gallus gallus NEU3 sialidase as model to study protein evolution mechanism based on rapid evolving loops

以鸡NEU3唾液酸酶为模型,基于快速进化环研究蛋白质进化机制

Giacopuzzi, Edoardo; Barlati, Sergio; Preti, Augusto; Venerando, Bruno; Monti, Eugenio; Borsani, Giuseppe; Bresciani, Roberto

BDNF Val66Met polymorphism and protein levels in amniotic fluid.

BDNF Val66Met 多态性与羊水中蛋白质水平

Cattaneo Annamaria, Bocchio-Chiavetto Luisella, Zanardini Roberta, Marchina Eleonora, Bellotti Daniela, Milanesi Elena, Moraschi Stefania, Calabrese Francesca, Barlati Sergio, Riva Marco Andrea, Gennarelli Massimo

Arterial tortuosity syndrome in two Italian paediatric patients

两例意大利儿科患者的动脉迂曲综合征

Ritelli, Marco; Drera, Bruno; Vicchio, Mariano; Puppini, Giovanni; Biban, Paolo; Pilati, Mara; Prioli, Maria Antonia; Barlati, Sergio; Colombi, Marina

Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients

Loeys-Dietz综合征I型和II型:两名意大利患者的临床表现和新突变

Drera, Bruno; Ritelli, Marco; Zoppi, Nicoletta; Wischmeijer, Anita; Gnoli, Maria; Fattori, Rossella; Calzavara-Pinton, Pier Giacomo; Barlati, Sergio; Colombi, Marina