De novo variants of DEAF1 cause intellectual disability in six Chinese patients-Reference-Cited by-同舟云学术

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De novo variants of DEAF1 cause intellectual disability in six Chinese patients

Published:2021-07 Issue: Volume:518 Page:17-21
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Chen Shimeng,Deng Xiaolu,Xiong Juan,He Fang,Yang Lifen,Chen Baiyu,Chen Chen,Zhang Ciliu,Yang Li,Peng Jing,Yin Fei

Funder

Key Project of Research and Development Plan of Hunan Province

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference30 articles.

1. Molecular cloning, sequence analysis, expression, and tissue distribution of suppressin, a novel suppressor of cell cycle entry;LeBoeuf;J. Biol. Chem.,1998

2. Identification of a nuclear export signal and protein interaction domains in deformed epidermal autoregulatory factor-1 (DEAF-1);Jensik;J. Biol. Chem.,2004

3. Deaf1 isoforms control the expression of genes encoding peripheral tissue antigens in the pancreatic lymph nodes during type 1 diabetes;Yip;Nat. Immunol.,2009

4. Reduced DEAF1 function during type 1 diabetes inhibits translation in lymph node stromal cells by suppressing Eif4g3;Yip;J. Mol. Cell. Biol.,2013

5. Deaf-1 regulates epithelial cell proliferation and side-branching in the mammary gland;Barker;BMC Dev. Biol.,2008

Cited by 3 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. Theoretical Studies of DNA Microarray Present Potential Molecular and Cellular Interconnectivity of Signaling Pathways in Immune System Dysregulation;Genes;2024-03-22

2. Vulto-van Silfhout-de Vries syndrome caused by de novo variants of DEAF1 gene: a case report and literature review;Frontiers in Neurology;2023-11-24

3. Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders;Human Molecular Genetics;2022-08-18

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