Chemical and genetic rescue of an ep300 knockdown model for Rubinstein Taybi Syndrome in zebrafish-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Chemical and genetic rescue of an ep300 knockdown model for Rubinstein Taybi Syndrome in zebrafish

Published:2018-04 Issue:4 Volume:1864 Page:1203-1215
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Babu Aswini,Kamaraj Mageshi,Basu Moumita,Mukherjee Debanjan,Kapoor Shruti,Ranjan Shashi,Swamy Mahadeva M.,Kaypee Stephanie,Scaria Vinod,Kundu Tapas K.,Sachidanandan Chetana

Funder

Council of Scientific and Industrial Research

Jawaharlal Nehru Centre for Advanced Scientific Research

Department of Biotechnology

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference75 articles.

1. Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP;Petrif;Nature,1995

2. Genetic heterogeneity in Rubinstein-Taybi Syndrome: mutations in both the CBP and EP300 genes cause disease;Roelfsema;Am. J. Hum. Genet.,2005

3. Rubinstein-Taybi Syndrome and epigenetic alterations;Korzus,2017

4. Abnormal skeletal patterning in embryos lacking a single Cbp allele: a partial similarity with Rubinstein–Taybisyndrome;Tanaka;Proc. Natl. Acad. Sci.,1997

5. Gene dosage–dependent embryonic development and proliferation defects in mice lacking the transcriptional integrator p300;Yao;Cell,1998

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. O-GlcNAc transferase congenital disorder of glycosylation (OGT-CDG): Potential mechanistic targets revealed by evaluating the OGT interactome;Journal of Biological Chemistry;2024-09

2. KAT3 mutations impair neural crest migration through EMT regulatorssnai1b andsnai2in Rubinstein Taybi Syndrome;2024-05-19

3. Identification of chromosomal abnormalities in miscarriages by CNV-Seq;Molecular Cytogenetics;2024-02-18

4. Epigenetic Modulation to perturb theSYNGAP1Intellectual Disability (ID) that ameliorates synaptic and behavioural deficits;2024-01-03

5. Epigenetic regulation of craniofacial development and disease;Birth Defects Research;2023-11-14

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