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

High level of aneuploidy and recurrent loss of chromosome 11 as relevant features of somatotroph pituitary tumors

高度非整倍体和11号染色体反复丢失是生长激素垂体瘤的相关特征

Rymuza, Julia; Kober, Paulina; Maksymowicz, Maria; Nyc, Aleksandra; Mossakowska, Beata J; Woroniecka, Renata; Maławska, Natalia; Grygalewicz, Beata; Baluszek, Szymon; Zieliński, Grzegorz; Kunicki, Jacek; Bujko, Mateusz

Cytogenomic features of Richter transformation

里氏转化的细胞基因组学特征

Woroniecka, Renata; Rymkiewicz, Grzegorz; Bystydzienski, Zbigniew; Pienkowska-Grela, Barbara; Rygier, Jolanta; Malawska, Natalia; Wojtkowska, Katarzyna; Goral, Nikolina; Blachnio, Katarzyna; Chmielewski, Marcin; Bartnik-Glaska, Magdalena; Grygalewicz, Beata

WT1 Gene Mutations, rs16754 Variant, and WT1 Overexpression as Prognostic Factors in Acute Myeloid Leukemia Patients

WT1基因突变、rs16754变异和WT1过表达作为急性髓系白血病患者的预后因素

Koczkodaj, Dorota; Zmorzyński, Szymon; Grygalewicz, Beata; Pieńkowska-Grela, Barbara; Styk, Wojciech; Popek-Marciniec, Sylwia; Filip, Agata Anna

Cryptic MYC insertions in Burkitt lymphoma: New data and a review of the literature.

Burkitt淋巴瘤中的隐匿性MYC插入:新数据和文献综述

Woroniecka Renata, Rymkiewicz Grzegorz, Szafron Lukasz M, Blachnio Katarzyna, Szafron Laura A, Bystydzienski Zbigniew, Pienkowska-Grela Barbara, Borkowska Klaudia, Rygier Jolanta, Kotyl Aleksandra, Malawska Natalia, Wojtkowska Katarzyna, Parada Joanna, Borysiuk Anita, Murcia Pienkowski Victor, Rydzanicz Malgorzata, Grygalewicz Beata

The 11q-Gain/Loss Aberration Occurs Recurrently in MYC-Negative Burkitt-like Lymphoma With 11q Aberration, as Well as MYC-Positive Burkitt Lymphoma and MYC-Positive High-Grade B-Cell Lymphoma, NOS

11q 获得/缺失异常在伴有 11q 异常的 MYC 阴性 Burkitt 样淋巴瘤、MYC 阳性 Burkitt 淋巴瘤以及 MYC 阳性高级别 B 细胞淋巴瘤(未另行分类)中反复出现。

Grygalewicz, Beata; Woroniecka, Renata; Rymkiewicz, Grzegorz; Rygier, Jolanta; Borkowska, Klaudia; Kotyl, Aleksandra; Blachnio, Katarzyna; Bystydzienski, Zbigniew; Nowakowska, Beata; Pienkowska-Grela, Barbara

A novel IGH@ gene rearrangement associated with CDKN2A/B deletion in young adult B-cell acute lymphoblastic leukemia.

在青年成人B细胞急性淋巴细胞白血病中发现一种与CDKN2A/B缺失相关的新型IGH@基因重排

Othman Moneeb A K, Grygalewicz Beata, Pienkowska-Grela Barbara, Rygier Jolanta, Ejduk Anna, Rincic Martina, Melo Joana B, Carreira Isabel M, Meyer Britta, Liehr Thomas

Novel Cryptic Rearrangements in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Involving the MLL Gene.

涉及 MLL 基因的成人 B 细胞前体急性淋巴细胞白血病的新型隐匿性重排

Othman Moneeb A K, Grygalewicz Beata, Pienkowska-Grela Barbara, Rincic Martina, Rittscher Katharina, Melo Joana B, Carreira Isabel M, Meyer Britta, Marzena Watek, Liehr Thomas

An additional human chromosome 21 causes suppression of neural fate of pluripotent mouse embryonic stem cells in a teratoma model

在畸胎瘤模型中,额外的21号人类染色体导致多能性小鼠胚胎干细胞的神经命运受到抑制

Mensah, Afua; Mulligan, Claire; Linehan, Jackie; Ruf, Sandra; O'Doherty, Aideen; Grygalewicz, Beata; Shipley, Janet; Groet, Juergen; Tybulewicz, Victor; Fisher, Elizabeth; Brandner, Sebastian; Nizetic, Dean