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

Identification of the HMGA2::CIBAR1-DT fusion transcript in two lipomas with chromosomal rearrangements involving chromosomes 8 and 12

在两例伴有8号和12号染色体重排的脂肪瘤中鉴定出HMGA2::CIBAR1-DT融合转录本

Brunetti, Marta; Andersen, Kristin; Lobmaier, Ingvild; Micci, Francesca

Complex Genetic Evolution and Treatment Challenges in Myeloid Neoplasms: A Case of Persistent t(2;3)(p15~23;q26)/MECOM Rearrangement, SF3B1 Mutation, and Transient TNIP1::PDGFRB Chimera

髓系肿瘤的复杂遗传演变和治疗挑战:一例持续性t(2;3)(p15~23;q26)/MECOM重排、SF3B1突变和短暂性TNIP1::PDGFRB嵌合体病例

Andersen, Kristin; Tjønnfjord, Geir E; Hestdalen, Malu Lian; Spetalen, Signe; Panagopoulos, Ioannis

Novel FRMD6::PTH chimera in tumorous bone lesion carrying a t(4;11;14;12)(q35;p15;q22;q13)

肿瘤性骨病变中发现新型 FRMD6::PTH 嵌合体,携带 at(4;11;14;12)(q35;p15;q22;q13)

Panagopoulos, Ioannis; Andersen, Kristin; Lloret, Isabel; Gorunova, Ludmila; Lobmaier, Ingvild

Sodium-Permeable Ion Channels TRPM4 and TRPM5 are Functional in Human Gastric Parietal Cells in Culture and Modulate the Cellular Response to Bitter-Tasting Food Constituents

钠通透性离子通道 TRPM4 和 TRPM5 在培养的人胃壁细胞中发挥作用,并调节细胞对苦味食物成分的反应

Phil Richter, Gaby Andersen, Kristin Kahlenberg, Alina Ulrike Mueller, Philip Pirkwieser, Valerie Boger, Veronika Somoza

Cell surface marker heterogeneity in human myeloma cell lines for modeling of disease and therapy.

人类骨髓瘤细胞系中细胞表面标志物的异质性及其在疾病和治疗建模中的应用

Behsen Alenka Djarmila, Holien Toril, Micci Francesca, Rye Morten, Rasmussen Jenny Malm, Andersen Kristin, Hess Eli Svorkdal, Børset Magne, Keats Jonathan, Våtsveen Thea Kristin, Misund Kristine

NUP214 fusion genes in acute leukemias: genetic characterization of rare cases

急性白血病中的NUP214融合基因:罕见病例的基因特征

Brunetti, Marta; Andersen, Kristin; Spetalen, Signe; Lenartova, Andrea; Osnes, Liv Toril Nygård; Vålerhaugen, Helen; Heim, Sverre; Micci, Francesca

Molecular genetic characterization of myeloid neoplasms with idic(X)(q13) and i(X)(q10)

具有idic(X)(q13)和i(X)(q10)的髓系肿瘤的分子遗传学特征

Brunetti, Marta; Andersen, Kristin; Trøen, Gunhild; Micci, Francesca; Spetalen, Signe; Lenartova, Andrea; Tandsæther, Maren Randi; Panagopoulos, Ioannis

Genetic Characterization of Pediatric Mixed Phenotype Acute Leukemia (MPAL)

儿童混合表型急性白血病(MPAL)的基因特征分析

Panagopoulos, Ioannis; Andersen, Kristin; Johannsdottir, Inga Maria Rinvoll; Tandsæther, Maren Randi; Micci, Francesca; Heim, Sverre

Fusion of Platelet Derived Growth Factor Receptor Alpha (PDGFRA) With Ubiquitin Specific Peptidase 8 (USP8) in a Calcified Chondroid Mesenchymal Neoplasm Harboring t(4;15)(q12;q21) as a Sole Aberration

在以t(4;15)(q12;q21)为唯一异常的钙化软骨样间充质肿瘤中,血小板衍生生长因子受体α (PDGFRA) 与泛素特异性肽酶8 (USP8) 发生融合

Panagopoulos, Ioannis; Andersen, Kristin; Gorunova, Ludmila; Lobmaier, Ingvild

Germline MYOF1::WNK4 and VPS25::MYOF1 Chimeras Generated by the Constitutional Translocation t(17;19)(q21;p13) in Two Siblings With Myelodysplastic Syndrome

两名患有骨髓增生异常综合征的同胞中,由体细胞易位t(17;19)(q21;p13)产生的种系MYOF1::WNK4和VPS25::MYOF1嵌合体

Panagopoulos, Ioannis; Andersen, Kristin; Stavseth, Vidar; Torkildsen, Synne; Heim, Sverre; Tandsæther, Maren Randi