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

Evaluation of potential role of R-loop and G-quadruplex DNA in the fragility of c-MYC during chromosomal translocation associated with Burkitt's lymphoma

评估 R-环和 G-四链体 DNA 在伯基特淋巴瘤相关染色体易位过程中对 c-MYC 脆性的潜在作用

Nitu Kumari, Kohal Das, Shivangi Sharma, Sumedha Dahal, Sagar Sanjiv Desai, Urbi Roy, Anju Sharma, Meghana Manjunath, Vidya Gopalakrishnan, S T Retheesh, Saniya M Javadekar, Bibha Choudhary, Sathees C Raghavan

Type 2 hyper-IgM syndrome with a rare variant of AICDA gene mutation in a young woman

一名年轻女性患有2型高IgM综合征,伴有罕见的AICDA基因突变变异。

Prakash, Prithivi Raaj; Gupta, Gaurav; Aggarwal, Mukul; Baitha, Upendra

SETD2 Haploinsufficiency Enhances Germinal Center-Associated AICDA Somatic Hypermutation to Drive B-cell Lymphomagenesis

SETD2单倍体不足增强生发中心相关AICDA体细胞高频突变,从而驱动B细胞淋巴瘤发生

Wilfred Leung ,Matt Teater ,Ceyda Durmaz ,Cem Meydan ,Alexandra G Chivu ,Amy Chadburn ,Edward J Rice ,Ashlesha Muley ,Jeannie M Camarillo ,Jaison Arivalagan ,Ziyi Li ,Christopher R Flowers ,Neil L Kelleher ,Charles G Danko ,Marcin Imielinski ,Sandeep S Dave ,Scott A Armstrong ,Christopher E Mason ,Ari M Melnick

A Novel AICDA Splice-Site Mutation in Two Siblings with HIGM2 Permits Somatic Hypermutation but Abrogates Mutational Targeting

两名患有HIGM2的兄弟姐妹中发现一种新的AICDA剪接位点突变,该突变允许体细胞高频突变,但消除了突变靶向作用。

Dirks, Johannes; Haase, Gabriele; Cantaert, Tineke; Frey, Lea; Klaas, Moritz; Rickert, Christian H; Girschick, Hermann; Meffre, Eric; Morbach, Henner

Estrogen Reverses HDAC Inhibitor-Mediated Repression of Aicda and Class-Switching in Antibody and Autoantibody Responses by Downregulation of miR-26a

雌激素通过下调 miR-26a 逆转 HDAC 抑制剂介导的 Aicda 抑制以及抗体和自身抗体反应中的类别转换

Paolo Casali ,Tian Shen ,Yijiang Xu ,Zhifang Qiu ,Daniel P Chupp ,John Im ,Zhenming Xu ,Hong Zan

AICDA drives epigenetic heterogeneity and accelerates germinal center-derived lymphomagenesis

AICDA驱动表观遗传异质性并加速生发中心来源的淋巴瘤发生

Matt Teater ,Pilar M Dominguez ,David Redmond ,Zhengming Chen ,Daisuke Ennishi ,David W Scott ,Luisa Cimmino ,Paola Ghione ,Jayanta Chaudhuri ,Randy D Gascoyne ,Iannis Aifantis ,Giorgio Inghirami ,Olivier Elemento ,Ari Melnick ,Rita Shaknovich

Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland

人群分离株中罕见变异的富集:芬兰2型高IgM综合征的致病因素为单个AICDA突变

Trotta, Luca; Hautala, Timo; Hämäläinen, Sari; Syrjänen, Jaana; Viskari, Hanna; Almusa, Henrikki; Lepisto, Maija; Kaustio, Meri; Porkka, Kimmo; Palotie, Aarno; Seppänen, Mikko; Saarela, Janna