Evaluation of NSD2 and NSD3 in overgrowth syndromes-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Evaluation of NSD2 and NSD3 in overgrowth syndromes

Published:2004-10-13 Issue:2 Volume:13 Page:150-153
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Douglas Jenny, ,Coleman Kim,Tatton-Brown Katrina,Hughes Helen E,Temple I Karen,Cole Trevor R P,Rahman Nazneen

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5201298.pdf

Reference15 articles.

1. Cole TR, Hughes HE : Sotos syndrome: a study of the diagnostic criteria and natural history. J Med Genet 1994; 31: 20–32.

2. Douglas J, Hanks S, Temple IK et al: NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes. Am J Hum Genet 2003; 72: 132–143.

3. Nagai T, Matsumoto N, Kurotaki N et al: Sotos syndrome and haploinsufficiency of NSD1: clinical features of intragenic mutations and submicroscopic deletions. J Med Genet 2003; 40: 285–289.

4. Rio M, Clech L, Amiel J et al: Spectrum of NSD1 mutations in Sotos and Weaver syndromes. J Med Genet 2003; 40: 436–440.

5. Turkmen S, Gillesser-Kaesbach G, Meinecke P et al: Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes. Eur J Hum Genet 2003; 11: 858–865.

Cited by 30 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. NSD3 in Cancer: Unraveling Methyltransferase-Dependent and Isoform-Specific Functions;International Journal of Molecular Sciences;2024-01-12

2. Drug Discovery Targeting Nuclear Receptor Binding SET Domain Protein 2 (NSD2);Journal of Medicinal Chemistry;2023-08-14

3. Epigenetic Causes of Overgrowth Syndromes;The Journal of Clinical Endocrinology & Metabolism;2023-07-14

4. Targeting the Nuclear Receptor-Binding SET Domain Family of Histone Lysine Methyltransferases for Cancer Therapy: Recent Progress and Perspectives;Journal of Medicinal Chemistry;2021-09-07

5. Chromatin dysregulation associated with NSD1 mutation in head and neck squamous cell carcinoma;Cell Reports;2021-02

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