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AICARDI-GOUTIERES SYNDROME 4
Known as:
AGS4
National Institutes of Health
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Related topics
Related topics
13 relations
Broader (2)
Autoimmune Diseases of the Nervous System
Congenital neurologic anomalies
Autosomal recessive inheritance
Cerebellar atrophy
Cerebral atrophy
Fetal Growth Retardation
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Regulation of RGS5 GAP activity by GPSM3
P. Zhao
,
P. Chidiac
Molecular and Cellular Biochemistry
2015
Corpus ID: 13529631
Heterotrimeric G protein signaling is limited by intracellular proteins that impede the binding of or accelerate the hydrolysis…
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2015
2015
Regulation of RGS5 GAP activity by GPSM3
P. Zhao
,
P. Chidiac
Molecular and Cellular Biochemistry
2015
Corpus ID: 254799772
Heterotrimeric G protein signaling is limited by intracellular proteins that impede the binding of or accelerate the hydrolysis…
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2010
2010
Reconciling Neuroimaging and Clinical Findings in Aicardi-Goutières Syndrome: An Autoimmune-Mediated Encephalopathy
G. Ramantani
,
Pascal Niggemann
,
T. Bast
,
M. Lee-Kirsch
American Journal of Neuroradiology
2010
Corpus ID: 39624003
In the November-December 2009 issue of the American Journal of Neuroradiology , Uggetti et al[1][1] presented neuroradiologic…
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2009
2009
Interaction of AGS4 and Gialpha1 in living cells
S. Oner
,
B. Breton
,
M. Bouvier
,
J. Blumer
2009
Corpus ID: 87648926
Activator of G Protein Signaling‐4 (AGS4) is one of several receptor independent activators of G‐protein signaling identified in…
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