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GNAI3 gene

Known as: Guanine Nucleotide Binding Protein (G Protein), Alpha Inhibiting Activity Polypeptide 3 Gene, GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-INHIBITING ACTIVITY POLYPEPTIDE 3, GNAI3 
This gene is involved in signal transduction and neurotransmission.
National Institutes of Health

Related topics

Related topics

6 relations
Environment-to-Cell CommunicationG Protein-Coupled Receptor SignalingGNAI3 protein, humanGTP Binding
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Papers overview

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2019
2019
GNAI1 and GNAI3 Reduce Colitis-Associated Tumorigenesis in Mice by Blocking IL6 Signaling and Down-regulating Expression of GNAI2.
BACKGROUND & AIMS Interleukin 6 (IL6) and tumor necrosis factor contribute to the development of colitis-associated cancer (CAC… Expand
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2019
2019
Guanine and nucleotide binding protein 3 promotes odonto/osteogenic differentiation of apical papilla stem cells via JNK and ERK signaling pathways
Odonto/osteogenic differentiation of stem cells from the apical papilla (SCAPs) is a key process in tooth root formation and… Expand
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2018
2018
Exploring the Key Genes and Pathways of Osteoarthritis in Knee Cartilage in a Rat Model Using Gene Expression Profiling
Purpose To compare differentially expressed genes (DEGs) mediating osteoarthritis (OA) in knee cartilage and in normal knee… Expand
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2017
2017
Role of GATA binding protein 4 (GATA4) in the regulation of tooth development via GNAI3
Transcription factor GATA4 regulates cardiac and osteoblast differentiation. However, its role in tooth development is not clear… Expand
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2017
2017
Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome
Auriculocondylar syndrome, mainly characterized by micrognathia, small mandibular condyle, and question mark ears, is a rare… Expand
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2015
2015
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect
Auriculocondylar syndrome is a rare craniofacial disorder comprising core features of micrognathia, condyle dysplasia and… Expand
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Highly Cited
2012
Highly Cited
2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.
Auriculocondylar syndrome (ACS) is a rare, autosomal-dominant craniofacial malformation syndrome characterized by variable… Expand
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2009
2009
GNAI3, GNAT2, AMPD2, GSTM are clustered in 120 kb of Chinese hamster Chromosome 1q
We studied a polygenic region located on Chromosome (Chr) lq in Chinese hamster cells that is coamplified along with the AMPD2… Expand
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1999
1999
Initiation of DNA replication at the Chinese hamster origin oriGNAI3 relies on local sequences and/or chromatin structures, but not on transcription of the nearby GNAI3 gene.
We recently identified a region of preferential replication initiation, oriGNAI3, near the 3' end of the Chinese hamster GNAI3… Expand
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1994
1994
The highly conserved Chinese hamster GNAI3 gene maps less than 60 kb from the AMPD2 gene and lacks the intronic U6 snRNA present in its human counterpart.
The identity of a gene coamplified with the adenylate deaminase 2 gene (AMPD2) in coformycin-resistant cells was determined by… Expand
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