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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
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This gene is involved in signal transduction and neurotransmission.
National Institutes of Health
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Related topics
Related topics
6 relations
Environment-to-Cell Communication
G Protein-Coupled Receptor Signaling
GNAI3 protein, human
GTP Binding
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severity.
A. Nabil
,
Sahar El Shafei
,
+4 authors
F. Alkuraya
European Journal of Medical Genetics
2020
Corpus ID: 214617397
2019
2019
GNAI1 and GNAI3 Reduce Colitis-Associated Tumorigenesis in Mice by Blocking IL6 Signaling and Down-regulating Expression of GNAI2.
Zhi-wei Li
,
Beicheng Sun
,
+41 authors
W. Chu
Gastroenterology
2019
Corpus ID: 73463613
BACKGROUND & AIMS Interleukin 6 (IL6) and tumor necrosis factor contribute to the development of colitis-associated cancer (CAC…
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2018
2018
Guanine and nucleotide binding protein 3 promotes odonto/osteogenic differentiation of apical papilla stem cells via JNK and ERK signaling pathways
Yang Zhang
,
Lichan Yuan
,
+5 authors
Lin Wang
International Journal of Molecular Medicine
2018
Corpus ID: 53431548
Odonto/osteogenic differentiation of stem cells from the apical papilla (SCAPs) is a key process in tooth root formation and…
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2017
2017
Role of GATA binding protein 4 (GATA4) in the regulation of tooth development via GNAI3
Shuyu Guo
,
Yuxin Zhang
,
+4 authors
Junqing Ma
Scientific Reports
2017
Corpus ID: 32953039
Transcription factor GATA4 regulates cardiac and osteoblast differentiation. However, its role in tooth development is not clear…
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2017
2017
Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome
V. R. Romanelli Tavares
,
R. Zechi-Ceide
,
+14 authors
M. Passos-Bueno
American Journal of Medical Genetics. Part A
2017
Corpus ID: 9748262
Auriculocondylar syndrome, mainly characterized by micrognathia, small mandibular condyle, and question mark ears, is a rare…
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2015
2015
Novel variants in GNAI3 associated with auriculocondylar syndrome strengthen a common dominant negative effect
V. L. R. Tavares
,
C. T. Gordon
,
+15 authors
M. Passos-Bueno
European Journal of Human Genetics
2015
Corpus ID: 33275805
Auriculocondylar syndrome is a rare craniofacial disorder comprising core features of micrognathia, condyle dysplasia and…
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Highly Cited
2012
Highly Cited
2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.
M. Rieder
,
G. Green
,
+16 authors
M. Cunningham
American Journal of Human Genetics
2012
Corpus ID: 25719030
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.
F. Toledo
,
A. Lachagès
,
V. Mayau
,
M. Debatisse
Nucleic Acids Research
1999
Corpus ID: 1238874
We recently identified a region of preferential replication initiation, oriGNAI3, near the 3' end of the Chinese hamster GNAI3…
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1996
1996
GNAI3, GNAT2, AMPD2, GSTM are clustered in 120 kb of Chinese hamster Chromosome 1q
B. Baron
,
M. A. Fernandez
,
S. Carignon
,
F. Toledo
,
G. Buttin
,
M. Debatisse
Mammalian Genome
1996
Corpus ID: 11646366
We studied a polygenic region located on Chromosome (Chr) lq in Chinese hamster cells that is coamplified along with the AMPD2…
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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.
B. Baron
,
M. A. Fernandez
,
+5 authors
M. Debatisse
Genomics
1994
Corpus ID: 33578778
The identity of a gene coamplified with the adenylate deaminase 2 gene (AMPD2) in coformycin-resistant cells was determined by…
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