Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,391,230 papers from all fields of science
Search
Sign In
Create Free Account
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
Expand
This gene is involved in signal transduction and neurotransmission.
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
6 relations
Environment-to-Cell Communication
G Protein-Coupled Receptor Signaling
GNAI3 protein, human
GTP Binding
Expand
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.
Amira Nabil
,
Sahar El Shafei
,
+4 authors
F. Alkuraya
European Journal of Medical Genetics
2020
Corpus ID: 214617397
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…
Expand
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…
Expand
2016
2016
GNAI3: Another Candidate Gene to Screen in Persons with Ocular Albinism
A. Young
,
Uma Dandekar
,
+4 authors
D. Farber
PLoS ONE
2016
Corpus ID: 751877
Ocular albinism type 1 (OA), caused by mutations in the OA1 gene, encodes a G-protein coupled receptor, OA1, localized in…
Expand
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
2012
2012
Erratum: A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome ((The American Journal of Human Genetics (2012) 90 (907-914))
M. Rieder
,
G. Green
,
+16 authors
M. Cunningham
2012
Corpus ID: 90134407
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. Lachages
,
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…
Expand
1998
1998
Twelve genes, including the unassigned proteasome ζ subunit gene, ordered within the human 1p13 region
V. Mayau
,
B. Baron
,
G. Buttin
,
M. Debatisse
Mammalian Genome
1998
Corpus ID: 10732911
Using a coamplification mapping technique, we previously established the map of a cluster of genes located on Chinese hamster…
Expand
1996
1996
GNAI3, GNAT2, AMPD2, GSTM are clustered in 120 kb of Chinese hamster Chromosome 1q
B. Baron
,
M. Fernández
,
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…
Expand
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. 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…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE