Leukemia in Severe Congenital Neutropenia: Defective Proteolysis Suggests New Pathways to Malignancy and Opportunities for Therapy
Author:
Publisher
Informa UK Limited
Subject
Cancer Research,Oncology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1081/CNV-120022378
Reference65 articles.
1. Infantile genetic agranulocytosis, morbus Kostmann: Presentation of six cases from the original "Kostmann family" and a review
2. Congenital Dysgranulopoietic Neutropenia in Two Siblings: Clinical, Ultrastructural, and in Vitro Bone Marrow Culture Studies
3. Dominantly inherited severe congenital neutropenia
Cited by 21 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
1. High yield expression in Pichia pastoris of human neutrophil elastase fused to cytochrome B5;Protein Expression and Purification;2023-06
2. Exosomes derived from mesenchymal stem cells improved function and survival of neutrophils from severe congenital neutropenia patients in vitro;Human Immunology;2019-12
3. A Novel Peptide-Based SILAC Method to Identify the Posttranslational Modifications Provides Evidence for Unconventional Ubiquitination in the ER-Associated Degradation Pathway;International Journal of Proteomics;2013-02-03
4. ELANE Mutations in Cyclic and Severe Congenital Neutropenia;Hematology/Oncology Clinics of North America;2013-02
5. Glycosaminoglycans Modify Elastase ActionIn Vitroand Enhance Elastase-Induced Cell Death in Cultured Fibroblasts;ISRN Cell Biology;2012-11-22
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