Decreased DGCR8 Expression and miRNA Dysregulation in Individuals with 22q11.2 Deletion Syndrome-Reference-Cited by-同舟云学术

Decreased DGCR8 Expression and miRNA Dysregulation in Individuals with 22q11.2 Deletion Syndrome

Published:2014-08-01 Issue:8 Volume:9 Page:e103884
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Sellier Chantal,Hwang Vicki J.,Dandekar Ravi,Durbin-Johnson Blythe,Charlet-Berguerand Nicolas,Ander Bradley P.,Sharp Frank R.,Angkustsiri Kathleen,Simon Tony J.,Tassone Flora

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference80 articles.

1. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population;LD Botto;Pediatrics,2003

2. A population study of chromosome 22q11 deletions in infancy;J Goodship;Arch Dis Child,1998

3. Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden;S Oskarsdottir;Archives of Disease in Childhood,2004

4. Prevalence of 22q11 microdeletion;S Tezenas Du Montcel;J Med Genet,1996

5. DiGeorge syndrome: part of CATCH 22;DI Wilson;J Med Genet,1993

Cited by 67 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. MicroRNA miR-92b-3p regulation of a cardiovascular gene regulatory network in the developing branchial arches;2024-07-29

2. Epigenetic factors in the 22q11.2 deletion syndrome in relation to stress and schizophrenia;2024-06-24

3. Next-generation sequencing profiling of miRNAs in individuals with 22q11.2 deletion syndrome revealed altered expression of miR-185-5p;Human Genomics;2024-06-13

4. MicroRNAs in maxillofacial bone modeling and remodeling: implications for malocclusion development and orthodontic treatment;Frontiers in Cell and Developmental Biology;2024-03-13

5. Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors;Genes;2024-02-29