Missense mutations of human homeoboxes: A review
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference117 articles.
1. Pituitary dwarfism in the R271W Pit-1 gene mutation
2. Differential DNA-binding specificity of the engrailed homeodomain: The role of residue 50
3. Autosomal dominant iris hypoplasia is caused by a mutation in the rieger syndrome (rieg/pitx2) gene
4. A transcriptional activating region with two contrasting modes of protein interaction
5. Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome
Cited by 57 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. Investigation of the relationship between hyperacusis and auditory processing difficulties in individuals with normal hearing;European Archives of Oto-Rhino-Laryngology;2023-10-11
2. Study of the Effect of Minimal Sensorineural Hearing Loss on the Central Auditory Processing in Children: A Pilot Study;Indian Journal of Otolaryngology and Head & Neck Surgery;2023-05-14
3. NK2 homeobox gene cluster: Functions and roles in human diseases;Genes & Diseases;2022-10
4. Gene co-expression networks contributing to reproductive development in Holstein-Friesian bull calves;animal;2022-05
5. Pain sensitivity and perceptual sensitivity are associated with severity of emotional dysregulation in children with ADHD: a cross-sectional analysis using the Temperament in Middle Childhood Questionnaire;Disability and Rehabilitation;2022-03-10
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