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

Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA.

恶性周围神经鞘瘤 (MPNST) 的基因组模式演变与临床结果相关,并且可以在无细胞 DNA 中检测到

Cortes-Ciriano Isidro, Steele Christopher D, Piculell Katherine, Al-Ibraheemi Alyaa, Eulo Vanessa, Bui Marilyn M, Chatzipli Aikaterini, Dickson Brendan C, Borcherding Dana C, Feber Andrew, Galor Alon, Hart Jesse, Jones Kevin B, Jordan Justin T, Kim Raymond H, Lindsay Daniel, Miller Colin, Nishida Yoshihiro, Proszek Paula Z, Serrano Jonathan, Sundby R Taylor, Szymanski Jeffrey J, Ullrich Nicole J, Viskochil David, Wang Xia, Snuderl Matija, Park Peter J, Flanagan Adrienne M, Hirbe Angela C, Pillay Nischalan, Miller David T

Circulating tumour DNA sequencing to determine therapeutic response and identify tumour heterogeneity in patients with paediatric solid tumours

循环肿瘤DNA测序用于确定儿童实体瘤患者的治疗反应并识别肿瘤异质性

Stankunaite, Reda; George, Sally L; Gallagher, Lewis; Jamal, Sabri; Shaikh, Ridwan; Yuan, Lina; Hughes, Debbie; Proszek, Paula Z; Carter, Paul; Pietka, Grzegorz; Heide, Timon; James, Chela; Tari, Haider; Lynn, Claire; Jain, Neha; Portela, Laura Rey; Rogers, Tony; Vaidya, Sucheta J; Chisholm, Julia C; Carceller, Fernando; Szychot, Elwira; Mandeville, Henry; Angelini, Paola; Jesudason, Angela B; Jackson, Michael; Marshall, Lynley V; Gatz, Susanne A; Anderson, John; Sottoriva, Andrea; Chesler, Louis; Hubank, Michael

The Spectrum and Clinical Impact of Epigenetic Modifier Mutations in Myeloma

多发性骨髓瘤中表观遗传修饰因子突变的谱系和临床影响

Pawlyn, Charlotte; Kaiser, Martin F; Heuck, Christoph; Melchor, Lorenzo; Wardell, Christopher P; Murison, Alex; Chavan, Shweta S; Johnson, David C; Begum, Dil B; Dahir, Nasrin M; Proszek, Paula Z; Cairns, David A; Boyle, Eileen M; Jones, John R; Cook, Gordon; Drayson, Mark T; Owen, Roger G; Gregory, Walter M; Jackson, Graham H; Barlogie, Bart; Davies, Faith E; Walker, Brian A; Morgan, Gareth J

Mutational Spectrum, Copy Number Changes, and Outcome: Results of a Sequencing Study of Patients With Newly Diagnosed Myeloma

突变谱、拷贝数变化和预后:一项针对新诊断多发性骨髓瘤患者的测序研究结果

Walker, Brian A; Boyle, Eileen M; Wardell, Christopher P; Murison, Alex; Begum, Dil B; Dahir, Nasrin M; Proszek, Paula Z; Johnson, David C; Kaiser, Martin F; Melchor, Lorenzo; Aronson, Lauren I; Scales, Matthew; Pawlyn, Charlotte; Mirabella, Fabio; Jones, John R; Brioli, Annamaria; Mikulasova, Aneta; Cairns, David A; Gregory, Walter M; Quartilho, Ana; Drayson, Mark T; Russell, Nigel; Cook, Gordon; Jackson, Graham H; Leleu, Xavier; Davies, Faith E; Morgan, Gareth J

A molecular diagnostic approach able to detect the recurrent genetic prognostic factors typical of presenting myeloma

一种能够检测多发性骨髓瘤典型复发性遗传预后因素的分子诊断方法

Boyle, Eileen M; Proszek, Paula Z; Kaiser, Martin F; Begum, Dil; Dahir, Nasrin; Savola, Suvi; Wardell, Christopher P; Leleu, Xavier; Ross, Fiona M; Chiecchio, Laura; Cook, Gordon; Drayson, Mark T; Owen, Richard G; Ashcroft, John M; Jackson, Graham H; Anthony Child, James; Davies, Faith E; Walker, Brian A; Morgan, Gareth J