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

JAK2 exon 14 skipping in patients with primary myelofibrosis: a minor splice variant modulated by the JAK2-V617F allele burden.

原发性骨髓纤维化患者的 JAK2 外显子 14 跳跃:一种受 JAK2-V617F 等位基因负荷调节的次要剪接变体

Catarsi Paolo, Rosti Vittorio, Morreale Giacomo, Poletto Valentina, Villani Laura, Bertorelli Roberto, Pedrazzini Matteo, Zorzetto Michele, Barosi Giovanni

No association between the XPD Lys751Gln (rs13181) polymorphism and disease phenotype or leukemic transformation in primary myelofibrosis

XPD Lys751Gln (rs13181) 多态性与原发性骨髓纤维化的疾病表型或白血病转化无关联

Poletto, Valentina; Villani, Laura; Catarsi, Paolo; Campanelli, Rita; Massa, Margherita; Vannucchi, Alessandro M; Rosti, Vittorio; Barosi, Giovanni

A3669G polymorphism of glucocorticoid receptor is a susceptibility allele for primary myelofibrosis and contributes to phenotypic diversity and blast transformation

糖皮质激素受体A3669G多态性是原发性骨髓纤维化的易感基因,并导致表型多样性和原始细胞转化。

Poletto, Valentina; Rosti, Vittorio; Villani, Laura; Catarsi, Paolo; Carolei, Adriana; Campanelli, Rita; Massa, Margherita; Martinetti, Myriam; Viarengo, Gianluca; Malovini, Alberto; Migliaccio, Anna Rita; Barosi, Giovanni