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RAI1 gene

Known as: KIAA1820, RETINOIC ACID-INDUCED GENE 1, MGC12824 
This gene is involved in transcription, development and behavior.
National Institutes of Health

Related topics

Related topics

7 relations
Biologic DevelopmentHomo sapiensRAI2 geneSmith-Magenis syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Characterization of PTLS-like Phenotypes in a Conditional Rai 1 Transgenic Mouse Model and Study of Rai 1 Molecular Function
of a dissertation at the University of Miami. Dissertation supervised by Professor Katherina Walz. No. of pages in text. (71… 
2017
2017
RAI1 Overexpression Promotes Altered Circadian Gene Expression and Dyssomnia in Potocki–Lupski Syndrome
Abstract Retinoic acid induced 1 (RAI1) encodes a dosage-sensitive gene that when haploinsufficient results in Smith–Magenis… 
2016
2016
Smith-Magenis Syndrome
The Smith-Magenis syndrome is a complex neurobehavioral disorder due to 17p11.2 microdeletion involving the gene RAI1 (retinoic… 
2016
2016
Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics
Smith-Magenis syndrome (SMS) is a developmental disability/multiple congenital anomaly disorder resulting from haploinsufficiency… 
2015
2015
Characterization of PTLS-like Phenotypes in a Conditional Rai 1 Transgenic Mouse Model and Study of Rai 1 Molecular Function
of a dissertation at the University of Miami. Dissertation supervised by Professor Katherina Walz. No. of pages in text. (71… 
2014
2014
Correction: Dietary Regimens Modify Early Onset of Obesity in Mice Haploinsufficient for Rai1
Smith-Magenis syndrome is a complex genomic disorder in which a majority of individuals are obese by adolescence. While an… 
2010
2010
Smith-Magenis syndrome: a mechanistic perspective
Clinical features of Smith–Magenis syndrome (SMS) often correlate with mutations in the gene that encodes RAI1. However, despite… 
2009
2009
Abnormal maternal behavior, altered sociability, and impaired serotonin metabolism in Rai1-transgenic mice
Dup(17)(p11.2) syndrome, consisting of a spectrum of more than 20 clinical features, is associated with increased dosage of the… 
2009
2009
Distorted Mendelian transmission as a function of genetic background in Rai1-haploinsufficient mice.
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