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GJA1 gene
Known as:
ODOD
, GAP JUNCTION PROTEIN, ALPHA-1
, ODD
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This gene is involved in gap junction assembly.
National Institutes of Health
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Related topics
Related topics
11 relations
Connexin 43
GJA1 protein, human
GJA1P1 gene
Homo sapiens
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2016
Highly Cited
2016
Carcinoma-astrocyte gap junctions promote brain metastasis by cGAMP transfer
Qing Chen
,
A. Boire
,
+9 authors
J. Massagué
Nature
2016
Corpus ID: 4467058
Brain metastasis represents a substantial source of morbidity and mortality in various cancers, and is characterized by high…
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Highly Cited
2011
Highly Cited
2011
The muscle-specific microRNA miR-1 regulates cardiac arrhythmogenic potential by targeting GJA1 and KCNJ2
Baofeng Yang
,
Huixian Lin
,
+9 authors
Zhiguo Wang
Nature Network Boston
2011
Corpus ID: 1935811
MicroRNAs (miRNAs) are endogenous noncoding RNAs, about 22 nucleotides in length, that mediate post-transcriptional gene…
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Highly Cited
2011
Highly Cited
2011
Astroglial networks scale synaptic activity and plasticity
U. Pannasch
,
L. Vargova
,
+5 authors
N. Rouach
Proceedings of the National Academy of Sciences…
2011
Corpus ID: 205251852
Astrocytes dynamically interact with neurons to regulate synaptic transmission. Although the gap junction proteins connexin 30…
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Review
2009
Review
2009
GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype
W. Paznekas
,
B. Karczeski
,
+8 authors
E. Wang Jabs
Human Mutation
2009
Corpus ID: 6313930
The predominantly autosomal dominant disorder, oculodentodigital dysplasia (ODDD) has high penetrance with intra‐ and…
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Highly Cited
2007
Highly Cited
2007
Gap junction adhesion is necessary for radial migration in the neocortex
Laura A. B. Elias
,
Doris D. Wang
,
A. Kriegstein
Nature
2007
Corpus ID: 4347739
Radial glia, the neuronal stem cells of the embryonic cerebral cortex, reside deep within the developing brain and extend radial…
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Highly Cited
2005
Highly Cited
2005
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia
A. Flenniken
,
L. Osborne
,
+32 authors
J. Rossant
Development
2005
Corpus ID: 1771336
Oculodentodigital dysplasia (ODDD) is an autosomal dominant disorder characterized by pleiotropic developmental anomalies of the…
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Highly Cited
2003
Highly Cited
2003
Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.
W. Paznekas
,
S. Boyadjiev
,
+8 authors
E. Jabs
American Journal of Human Genetics
2003
Corpus ID: 32883198
Gap junctions are assemblies of intercellular channels that regulate a variety of physiologic and developmental processes through…
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Highly Cited
2003
Highly Cited
2003
Gating and regulation of connexin 43 (Cx43) hemichannels
J. Contreras
,
J. Sáez
,
F. Bukauskas
,
M. Bennett
Proceedings of the National Academy of Sciences…
2003
Corpus ID: 8851008
Connexin 43 (Cx43) nonjunctional or “unapposed” hemichannels can open under physiological or pathological conditions. We…
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Highly Cited
2001
Highly Cited
2001
Connexin 43 hemichannels mediate Ca2+‐regulated transmembrane NAD+ fluxes in intact cells
S. Bruzzone
,
L. Guida
,
E. Zocchi
,
L. Franco
,
A. Flora
The FASEB Journal
2001
Corpus ID: 24037754
A previously unrecognized passive transport for pyridine dinucleotides has been described recently in the plasmamembrane of…
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Highly Cited
1998
Highly Cited
1998
Reversion of the neoplastic phenotype of human glioblastoma cells by connexin 43 (cx43).
R. Huang
,
Yan Fan
,
M. Hossain
,
Ao Peng
,
Ziao Zeng
,
A. Boynton
Cancer Research
1998
Corpus ID: 9051042
Connexins (cx), structural components of gap junction, are believed to play a role in the regulation of cell proliferation and…
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