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

International research to address the challenges of metastatic breast cancer: the AURORA Program (BIG 14-01)

应对转移性乳腺癌挑战的国际研究:AURORA计划(BIG 14-01)

Caballero, Carmela; Irrthum, Alexandre; Goulioti, Theodora; Cameron, David; Norton, Larry; Piccart, Martine

Genomic and Transcriptomic Analyses of Breast Cancer Primaries and Matched Metastases in AURORA, the Breast International Group (BIG) Molecular Screening Initiative

AURORA(乳腺癌国际协作组 (BIG) 分子筛查计划)中乳腺癌原发灶及其匹配转移灶的基因组和转录组分析

Aftimos, Philippe; Oliveira, Mafalda; Irrthum, Alexandre; Fumagalli, Debora; Sotiriou, Christos; Gal-Yam, Einav Nili; Robson, Mark E; Ndozeng, Justin; Di Leo, Angelo; Ciruelos, Eva M; de Azambuja, Evandro; Viale, Giuseppe; Scheepers, Elsemieke D; Curigliano, Giuseppe; Bliss, Judith M; Reis-Filho, Jorge S; Colleoni, Marco; Balic, Marija; Cardoso, Fatima; Albanell, Joan; Duhem, Caroline; Marreaud, Sandrine; Romagnoli, Dario; Rojas, Beatriz; Gombos, Andrea; Wildiers, Hans; Guerrero-Zotano, Angel; Hall, Peter; Bonetti, Andrea; Larsson, Karolina Fs; Degiorgis, Martina; Khodaverdi, Silvia; Greil, Richard; Sverrisdóttir, Ásgerdur; Paoli, Marta; Seyll, Ethel; Loibl, Sibylle; Linderholm, Barbro; Zoppoli, Gabriele; Davidson, Nancy E; Johannsson, Oskar Th; Bedard, Philippe L; Loi, Sherene; Knox, Susan; Cameron, David A; Harbeck, Nadia; Montoya, Maite Lasa; Brandão, Mariana; Vingiani, Andrea; Caballero, Carmela; Hilbers, Florentine S; Yates, Lucy R; Benelli, Matteo; Venet, David; Piccart, Martine J

The AURORA pilot study for molecular screening of patients with advanced breast cancer-a study of the breast international group

AURORA 试点研究:晚期乳腺癌患者分子筛查——国际乳腺癌研究组的研究

Maetens, Marion; Brown, David; Irrthum, Alexandre; Aftimos, Philippe; Viale, Giuseppe; Loibl, Sibylle; Laes, Jean-François; Campbell, Peter J; Thompson, Alastair; Cortes, Javier; Seiler, Sabine; Vinnicombe, Sara; Oliveira, Mafalda; Rothé, Françoise; Bareche, Yacine; Fumagalli, Debora; Zardavas, Dimitrios; Desmedt, Christine; Piccart, Martine; Loi, Sherene; Sotiriou, Christos

Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema

VEGFR3信号通路突变可解释36%的家族性淋巴水肿病例。

Mendola, A; Schlögel, M J; Ghalamkarpour, A; Irrthum, A; Nguyen, H L; Fastré, E; Bygum, A; van der Vleuten, C; Fagerberg, C; Baselga, E; Quere, I; Mulliken, J B; Boon, L M; Brouillard, P; Vikkula, M

Myelin-derived lipids modulate macrophage activity by liver X receptor activation

髓鞘衍生脂质通过激活肝脏 X 受体调节巨噬细胞活性

Jeroen F J Bogie, Silke Timmermans, Vân Anh Huynh-Thu, Alexandre Irrthum, Hubert J M Smeets, Jan-Åke Gustafsson, Knut R Steffensen, Monique Mulder, Piet Stinissen, Niels Hellings, Jerome J A Hendriks

MicroRNAs profiling in murine models of acute and chronic asthma: a relationship with mRNAs targets

在急性和慢性哮喘小鼠模型中microRNA谱分析:与mRNA靶标的关系

Nancy Garbacki ,Emmanuel Di Valentin, Vân Anh Huynh-Thu, Pierre Geurts, Alexandre Irrthum, Céline Crahay, Thierry Arnould, Christophe Deroanne, Jacques Piette, Didier Cataldo, Alain Colige

Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase

由VEGFR3酪氨酸激酶失活突变引起的先天性遗传性淋巴水肿

Irrthum, A; Karkkainen, M J; Devriendt, K; Alitalo, K; Vikkula, M

A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22

导致遗传性皮肤静脉畸形(“血管球瘤”)的基因位于1p21-22染色体上。

Boon, L M; Brouillard, P; Irrthum, A; Karttunen, L; Warman, M L; Rudolph, R; Mulliken, J B; Olsen, B R; Vikkula, M