Acquired copy-neutral loss of heterozygosity of chromosome 1p as a molecular event associated with marrow fibrosis in MPL-mutated myeloproliferative neoplasms

Author:

Rumi Elisa12,Pietra Daniela2,Guglielmelli Paola3,Bordoni Roberta4,Casetti Ilaria1,Milanesi Chiara2,Sant’Antonio Emanuela1,Ferretti Virginia2,Pancrazzi Alessandro3,Rotunno Giada3,Severgnini Marco4,Pietrelli Alessandro4,Astori Cesare2,Fugazza Elena2,Pascutto Cristiana2,Boveri Emanuela5,Passamonti Francesco6,De Bellis Gianluca4,Vannucchi Alessandro3,Cazzola Mario12

Affiliation:

1. Department of Molecular Medicine, University of Pavia, Pavia, Italy;

2. Department of Hematology Oncology, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy;

3. Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy;

4. Institute for Biomedical Technologies, National Research Council of Italy, Segrate, Italy;

5. Anatomic Pathology Section, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; and

6. Division of Hematology, Department of Internal Medicine, Ospedale di Circolo e Fondazione Macchi, Varese, Italy

Abstract

Key Points In MPL exon 10–mutated myeloproliferative neoplasms, the MPL-mutant allele burden varies considerably from about 1% to almost 100%. High mutation burdens originate from acquired copy-neutral loss of heterozygosity of chromosome 1p and are associated with marrow fibrosis.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Cited by 81 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3