Whole Exome Sequencing Identifies Novel Genetic Alterations in Patients with Pheochromocytoma/Paraganglioma
Author:
Funder
National Research Foundation of Korea
Publisher
Korean Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://e-enm.org/upload/pdf/enm-2020-756.pdf
Reference32 articles.
1. Updates on the genetics and the clinical impacts on phaeochromocytoma and paraganglioma in the new era
2. New Perspectives on Pheochromocytoma and Paraganglioma: Toward a Molecular Classification
3. Update of Pheochromocytoma Syndromes: Genetics, Biochemical Evaluation, and Imaging
4. Pheochromocytomas and Paragangliomas: New Developments with Regard to Classification, Genetics, and Cell of Origin
Cited by 8 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. Case Report: Aggressive neural crest tumors in a child with familial von Hippel Lindau syndrome associated with a germline VHL mutation (c.414A>G) and a novel KIF1B gene mutation;Frontiers in Endocrinology;2023-07-25
2. Systematic analysis of expression profiles and prognostic significance for MMDS-related iron–sulfur proteins in renal clear cell carcinoma;Scientific Reports;2022-11-16
3. Mass size is a major predictor of hypertensive attack during surgery in patients with paraganglioma of retroperitoneum;Translational Cancer Research;2022-10
4. Mutations of 1p genes do not consistently abrogate tumor suppressor functions in 1p-intact neuroblastoma;BMC Cancer;2022-06-30
5. A case of juvenile-onset pheochromocytoma with <i>KIF1B</i> p.V1529M germline mutation;Endocrine Journal;2022
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