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

Interplay between WNT/PI3K-mTOR axis and the microbiota in APC-driven colorectal carcinogenesis: data from a pilot study and possible implications for CRC prevention

WNT/PI3K-mTOR 轴与 APC 驱动的肠道致癌作用中的微生物群相互作用:一项初步研究的数据及其对 CRC 预防的可能影响

Floriana Jessica Di Paola #, Chiara Alquati #, Gabriele Conti #, Giulia Calafato, Silvia Turroni, Federica D'Amico, Claudio Ceccarelli, Francesco Buttitta, Alice Bernardi, Dajana Cuicchi, Gilberto Poggioli, Daniela Turchetti, Simona Ferrari, Renato Cannizzaro, Stefano Realdon, Patrizia Brigidi, Luig

Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders

甲状旁腺疾病中的新型胶质细胞缺失-2 (GCM2) 变异

Lucie Canaff, Vito Guarnieri, Yoojung Kim, Betty Y L Wong, Alexis Nolin-Lapalme, David E C Cole, Salvatore Minisola, Cristina Eller-Vainicher, Filomena Cetani, Andrea Repaci, Daniela Turchetti, Sabrina Corbetta, Alfredo Scillitani, David Goltzman

Pathogenic Mitochondrial DNA Mutation Load Inversely Correlates with Malignant Features in Familial Oncocytic Parathyroid Tumors Associated with Hyperparathyroidism-Jaw Tumor Syndrome

致病性线粒体 DNA 突变负荷与与甲状旁腺功能亢进-颌骨肿瘤综合征相关的家族性嗜酸细胞性甲状旁腺肿瘤的恶性特征呈负相关

Monica De Luise, Luisa Iommarini, Lorena Marchio, Greta Tedesco, Camelia Alexandra Coadă, Andrea Repaci, Daniela Turchetti, Maria Lucia Tardio, Nunzio Salfi, Uberto Pagotto, Ivana Kurelac, Anna Maria Porcelli, Giuseppe Gasparre

PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis

PTEN 错构瘤综合征:皮肤表现及其分子发病机制的见解

Giovanni Innella, Elena Bonora, Iria Neri, Annalucia Virdi, Alba Guglielmo, Laura Maria Pradella, Claudio Ceccarelli, Laura Benedetta Amato, Anna Lanzoni, Sara Miccoli, Giuseppe Gasparre, Roberta Zuntini, Daniela Turchetti

An Analysis of Clinical, Surgical, Pathological and Molecular Characteristics of Endometrial Cancer According to Mismatch Repair Status. A Multidisciplinary Approach

根据错配修复状态分析子宫内膜癌的临床、手术、病理和分子特征。多学科方法

Giulia Dondi, Sara Coluccelli, Antonio De Leo, Simona Ferrari, Elisa Gruppioni, Alessandro Bovicelli, Lea Godino, Camelia Alexandra Coadă, Alessio Giuseppe Morganti, Antonio Giordano, Donatella Santini, Claudio Ceccarelli, Daniela Turchetti, Pierandrea De Iaco, Anna Myriam Perrone

Primary constitutional MLH1 epimutations: a focal epigenetic event

原发性体质性 MLH1 表观突变:局灶性表观遗传事件

Estela Dámaso, Adela Castillejo, María Del Mar Arias, Julia Canet-Hermida, Matilde Navarro, Jesús Del Valle, Olga Campos, Anna Fernández, Fátima Marín, Daniela Turchetti, Juan de Dios García-Díaz, Conxi Lázaro, Maurizio Genuardi, Daniel Rueda, Ángel Alonso, Jose Luis Soto, Megan Hitchins, Marta Pine

BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype

BRCA1 p.His1673del 是一种与主要卵巢癌表型相关的致病突变

Roberta Zuntini, Laura Cortesi, Daniele Calistri, Tommaso Pippucci, Pier Luigi Martelli, Rita Casadio, Elisa Capizzi, Donatella Santini, Sara Miccoli, Veronica Medici, Rita Danesi, Isabella Marchi, Valentina Zampiga, Michelangelo Fiorentino, Simona Ferrari, Daniela Turchetti

A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype

PAK3 突变具有双重分子效应,导致 RAS/MAPK 通路失调,并导致 X 连锁综合征表型

Pamela Magini, Tommaso Pippucci, I-Chun Tsai, Simona Coppola, Emilia Stellacci, Anna Bartoletti-Stella, Daniela Turchetti, Claudio Graziano, Giovanna Cenacchi, Iria Neri, Duccio Maria Cordelli, Valentina Marchiani, Rosalba Bergamaschi, Giuseppe Gasparre, Giovanni Neri, Laura Mazzanti, Annalisa Patri

MLH1 constitutional and somatic methylation in patients with MLH1 negative tumors fulfilling the revised Bethesda criteria

符合修订版 Bethesda 标准的 MLH1 阴性肿瘤患者的 MLH1 体质和体细胞甲基化

Francesca Crucianelli, Rossella Tricarico, Daniela Turchetti, Greta Gorelli, Francesca Gensini, Roberta Sestini, Laura Giunti, Monica Pedroni, Maurizio Ponz de Leon, Serenella Civitelli, Maurizio Genuardi