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

Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve split-hand/foot malformation type 3

Lbx1/Fgf8基因座基因表达的组合效应可解决3型手足分裂畸形

Giulia Cova #, Juliane Glaser #, Robert Schöpflin, Cesar Augusto Prada-Medina, Salaheddine Ali, Martin Franke, Rita Falcone, Miriam Federer, Emanuela Ponzi, Romina Ficarella, Francesca Novara, Lars Wittler, Bernd Timmermann, Mattia Gentile, Orsetta Zuffardi, Malte Spielmann, Stefan Mundlos

The Search for Molecular Markers in a Gene-Orphan Case Study of a Pediatric Spinal Cord Pilocytic Astrocytoma

在儿童脊髓毛细胞星形细胞瘤基因孤儿病例研究中寻找分子标记

Carolina Martinelli, Fabio Gabriele, Federico Manai, Roberto Ciccone, Francesca Novara, Elisabetta Sauta, Riccardo Bellazzi, Monica Patane, Isabella Moroni, Rosina Paterra, Sergio Comincini

Distinct transcriptional profiles characterize bone microenvironment mesenchymal cells rather than osteoblasts in relationship with multiple myeloma bone disease

独特的转录谱表征了骨微环境间充质细胞而非成骨细胞与多发性骨髓瘤骨病的关系

Katia Todoerti, Gina Lisignoli, Paola Storti, Luca Agnelli, Francesca Novara, Cristina Manferdini, Katia Codeluppi, Simona Colla, Monica Crugnola, Manuela Abeltino, Marina Bolzoni, Valentina Sgobba, Andrea Facchini, Giorgio Lambertenghi-Deliliers, Orsetta Zuffardi, Vittorio Rizzoli, Antonino Neri, N

Generation of mesenchymal stromal cells in the presence of platelet lysate: a phenotypic and functional comparison of umbilical cord blood- and bone marrow-derived progenitors

血小板裂解物存在下间充质基质细胞的产生:脐带血和骨髓来源的祖细胞的表型和功能比较

Maria Antonietta Avanzini, Maria Ester Bernardo, Angela Maria Cometa, Cesare Perotti, Nadia Zaffaroni, Francesca Novara, Livia Visai, Antonia Moretta, Claudia Del Fante, Raffaella Villa, Lynne M Ball, Willem E Fibbe, Rita Maccario, Franco Locatelli

Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood

导致儿童急性淋巴细胞白血病 9p21 缺失的不同分子机制

Francesca Novara, Silvana Beri, Maria Ester Bernardo, Riccardo Bellazzi, Alberto Malovini, Roberto Ciccone, Angela Maria Cometa, Franco Locatelli, Roberto Giorda, Orsetta Zuffardi

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

复发性 15q13.3 微缺失综合征与智力低下和癫痫有关

Andrew J Sharp, Heather C Mefford, Kelly Li, Carl Baker, Cindy Skinner, Roger E Stevenson, Richard J Schroer, Francesca Novara, Manuela De Gregori, Roberto Ciccone, Adam Broomer, Iris Casuga, Yu Wang, Chunlin Xiao, Catalin Barbacioru, Giorgio Gimelli, Bernardo Dalla Bernardina, Claudia Torniero, Rob