RERE deficiency contributes to the development of orofacial clefts in humans and mice
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
RERE deficiency contributes to the development of orofacial clefts in humans and mice
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 30, Issue 7, Pages 595-602
Publisher
Oxford University Press (OUP)
Online
2021-03-19
DOI
10.1093/hmg/ddab084
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- PAX 7 nucleotide variants and the risk of non‐syndromic orofacial clefts in the Polish population
- (2019) Agnieszka Gaczkowska et al. ORAL DISEASES
- Genotype-phenotype correlations in individuals with pathogenic RERE variants
- (2018) Valerie K. Jordan et al. HUMAN MUTATION
- RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects
- (2018) Bum Jun Kim et al. Disease Models & Mechanisms
- De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions
- (2016) Brieana Fregeau et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate
- (2016) Elisabeth Mangold et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Identification of Functional Variants for Cleft Lip with or without Cleft Palate in or near PAX7, FGFR2, and NOG by Targeted Sequencing of GWAS Loci
- (2015) Elizabeth J. Leslie et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Retinoic acid controls body axis extension by directly repressing Fgf8 transcription
- (2014) S. Kumar et al. DEVELOPMENT
- Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development
- (2013) Myriam Peyrard-Janvid et al. AMERICAN JOURNAL OF HUMAN GENETICS
- An Allelic Series of Mice Reveals a Role for RERE in the Development of Multiple Organs Affected in Chromosome 1p36 Deletions
- (2013) Bum Jun Kim et al. PLoS One
- Median facial clefts in Xenopus laevis: Roles of retinoic acid signaling and homeobox genes
- (2012) Allyson E. Kennedy et al. DEVELOPMENTAL BIOLOGY
- Palatogenesis: morphogenetic and molecular mechanisms of secondary palate development
- (2011) J. O. Bush et al. DEVELOPMENT
- Rere controls retinoic acid signalling and somite bilateral symmetry
- (2010) Gonçalo C. Vilhais-Neto et al. NATURE
- Prdm16 is required for normal palatogenesis in mice
- (2009) Bryan C. Bjork et al. HUMAN MOLECULAR GENETICS
- Atrophin recruits HDAC1/2 and G9a to modify histone H3K9 and to determine cell fates
- (2008) Lei Wang et al. EMBO REPORTS
- Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation
- (2008) A. Battaglia et al. PEDIATRICS
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search