Human diseases caused by germline and somatic abnormalities in microRNA and microRNA-related genes-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Human diseases caused by germline and somatic abnormalities in microRNA and microRNA-related genes

Published:2014-02 Issue:1 Volume:54 Page:12-21
ISSN:0914-3505
Container-title:Congenital Anomalies
language:en
Short-container-title:Congenital Anomalies

Author:

Kawahara Yukio¹

Affiliation:

1. Laboratory of RNA Function; Graduate School of Medicine, Osaka University; Suita Osaka Japan

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Reference84 articles.

1. Sequence variants in SLITRK1 are associated with Tourette's syndrome;Abelson;Science,2005

2. Defective DROSHA processing contributes to downregulation of MiR-15/-16 in chronic lymphocytic leukemia;Allegra;Leukemia,2013

3. An integrated encyclopedia of DNA elements in the human genome;Bernstein;Nature,2012

4. Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome;Boultwood;Blood,2002

5. A synonymous variant in IRGM alters a binding site for miR-196 and causes deregulation of IRGM-dependent xenophagy in Crohn's disease;Brest;Nat Genet,2011

Cited by 40 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. A method for miRNA diffusion association prediction using machine learning decoding of multi-level heterogeneous graph Transformer encoded representations;Scientific Reports;2024-09-03

2. Kernel Bayesian logistic tensor decomposition with automatic rank determination for predicting multiple types of miRNA-disease associations;PLOS Computational Biology;2024-07-08

3. Neuroinflammation and the role of epigenetic-based therapies for Huntington’s disease management: the new paradigm;Inflammopharmacology;2024-04-23

4. MIR204 n.37C>T variant as a cause of chorioretinal dystrophy variably associated with iris coloboma, early‐onset cataracts and congenital glaucoma;Clinical Genetics;2023-06-15

5. miR-181c-5p suppresses neuronal pyroptosis via NLRP1 in Alzheimer’s disease;Behavioural Brain Research;2023-06

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