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

High-plex imaging of hepatoblastoma and adjacent liver in pediatric patients reveals a predominant myeloid infiltrate expressing immune-checkpoints

对儿童肝母细胞瘤及其邻近肝组织进行高通量成像显示,以表达免疫检查点的髓系浸润为主。

Krijgsman, Daniëlle; Schubert, Stephanie A; Kraaier, Lianne J; Lu, Yuyan; van Avondt, Kristof; Verdonschot, Meggy E L; Leusen, Jeanette H W; van den Heuvel, Marius C; de Kleine, Ruben H; de Meijer, Vincent E; Kraal, Kathelijne C J; de Krijger, Ronald R; Zsiros, József; Peng, Weng Chuan; Vercoulen, Yvonne

Divergent WNT signaling and drug sensitivity profiles within hepatoblastoma tumors and organoids.

肝母细胞瘤肿瘤和类器官中 WNT 信号传导和药物敏感性特征的差异

Kluiver Thomas A, Lu Yuyan, Schubert Stephanie A, Kraaier Lianne J, Ringnalda Femke, Lijnzaad Philip, DeMartino Jeff, Megchelenbrink Wouter L, Amo-Addae Vicky, Eising Selma, de Faria Flavia W, Münter Daniel, van de Wetering Marc, Kerl Kornelius, Duiker Evelien, van den Heuvel Marius C, de Meijer Vincent E, de Kleine Ruben H, Molenaar Jan J, Margaritis Thanasis, Stunnenberg Hendrik G, de Krijger Ronald R, Zsiros József, Clevers Hans, Peng Weng Chuan

Germline NPAT inactivating variants as cause of hereditary colorectal cancer

生殖系NPAT失活变异是遗传性结直肠癌的病因

Terradas, Mariona; Schubert, Stephanie A; Viana-Errasti, Julen; Ruano, Dina; Aiza, Gemma; Nielsen, Maartje; Marciel, Paula; Tops, Carli M; Parra, Genís; Morreau, Hans; Torrents, David; van Leerdam, Monique E; Capellá, Gabriel; de Miranda, Noel F C C; Valle, Laura; van Wezel, Tom

Germline biallelic Mcm8 variants are associated with early-onset Lynch-like syndrome

生殖系双等位基因Mcm8变异与早发性林奇样综合征相关。

Golubicki, Mariano; Bonjoch, Laia; Acuña-Ochoa, José G; Díaz-Gay, Marcos; Muñoz, Jenifer; Cuatrecasas, Miriam; Ocaña, Teresa; Iseas, Soledad; Mendez, Guillermo; Cisterna, Daniel; Schubert, Stephanie A; Nielsen, Maartje; van Wezel, Tom; Goldberg, Yael; Pikarsky, Eli; Robbio, Juan; Roca, Enrique; Castells, Antoni; Balaguer, Francesc; Antelo, Marina; Castellví-Bel, Sergi

The missing heritability of familial colorectal cancer

家族性结直肠癌遗传性的缺失

Schubert, Stephanie A; Morreau, Hans; de Miranda, Noel F C C; van Wezel, Tom

Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer

家族性结直肠癌中MSH6和MUTYH变异的双基因遗传

Schubert, Stephanie A; Ruano, Dina; Tiersma, Yvonne; Drost, Mark; de Wind, Niels; Nielsen, Maartje; van Hest, Liselotte P; Morreau, Hans; de Miranda, Noel F C C; van Wezel, Tom

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

染色体 1q 位点与结直肠肿瘤易感性之间存在遗传关联的证据

Schubert, Stephanie A; Ruano, Dina; Elsayed, Fadwa A; Boot, Arnoud; Crobach, Stijn; Sarasqueta, Arantza Farina; Wolffenbuttel, Bruce; van der Klauw, Melanie M; Oosting, Jan; Tops, Carli M; van Eijk, Ronald; Vasen, Hans Fa; Vossen, Rolf Ham; Nielsen, Maartje; Castellví-Bel, Sergi; Ruiz-Ponte, Clara; Tomlinson, Ian; Dunlop, Malcolm G; Vodicka, Pavel; Wijnen, Juul T; Hes, Frederik J; Morreau, Hans; de Miranda, Noel Fcc; Sijmons, Rolf H; van Wezel, Tom