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

Reannotation of cancer mutations based on expressed RNA transcripts reveals functional non-coding mutations in melanoma.

基于表达的 RNA 转录本对癌症突变进行重新注释,揭示了黑色素瘤中的功能性非编码突变

Pepe Daniele, Janssens Xander, Timcheva Kalina, Marrón-Liñares Grecia M, Verbelen Benno, Konstantakos Vasileios, De Groote Dylan, De Bie Jolien, Verhasselt Amber, Dewaele Barbara, Godderis Arne, Cools Charlotte, Franco-Tolsau Mireia, Royaert Jonathan, Verbeeck Jelle, Kampen Kim R, Subramanian Karthik, Cabrerizo Granados David, Menschaert Gerben, De Keersmaecker Kim

Low frequency mutations in ribosomal proteins RPL10 and RPL5 in multiple myeloma

多发性骨髓瘤中核糖体蛋白RPL10和RPL5的低频突变

Hofman, Isabel J F; Patchett, Stephanie; van Duin, Mark; Geerdens, Ellen; Verbeeck, Jelle; Michaux, Lucienne; Delforge, Michel; Sonneveld, Pieter; Johnson, Arlen W; De Keersmaecker, Kim

Copy-number gains of HUWE1 due to replication- and recombination-based rearrangements

由于复制和重组引起的HUWE1拷贝数增加

Froyen, Guy; Belet, Stefanie; Martinez, Francisco; Santos-Rebouças, Cíntia Barros; Declercq, Matthias; Verbeeck, Jelle; Donckers, Lene; Berland, Siren; Mayo, Sonia; Rosello, Monica; Pimentel, Márcia Mattos Gonçalves; Fintelman-Rodrigues, Natalia; Hovland, Randi; Rodrigues dos Santos, Suely; Raymond, F Lucy; Bose, Tulika; Corbett, Mark A; Sheffield, Leslie; van Ravenswaaij-Arts, Conny M A; Dijkhuizen, Trijnie; Coutton, Charles; Satre, Veronique; Siu, Victoria; Marynen, Peter

Dosage-dependent severity of the phenotype in patients with mental retardation due to a recurrent copy-number gain at Xq28 mediated by an unusual recombination

剂量依赖性表型严重程度与由异常重组介导的 Xq28 处复发性拷贝数增加导致的智力低下患者相关

Vandewalle, Joke; Van Esch, Hilde; Govaerts, Karen; Verbeeck, Jelle; Zweier, Christiane; Madrigal, Irene; Mila, Montserrat; Pijkels, Elly; Fernandez, Isabel; Kohlhase, Jürgen; Spaich, Christiane; Rauch, Anita; Fryns, Jean-Pierre; Marynen, Peter; Froyen, Guy