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The protein encoded by GIGYF2 interacts with GRB10 and may be involved in the regulation of tyrosine kinase receptor signaling. Additionally we are shipping GIGYF2 Proteins (3) and many more products for this protein.
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Results suggest that the N56S and N457T of GIGYF2 are risk factors for Parkinson's disease in Caucasians, but not in Asians
GIGYF2 and the zinc finger protein 598 (ZNF598) are identifie (show EIF4E Antibodies)d as components of the 4EHP complex.
Our result indicated that SCNA, LRRK2 (show LRRK2 Antibodies), UCHL1 (show UCHL1 Antibodies), HtrA2 (show HTRA2 Antibodies) and GIGYF2 genes' mutations might not be a main reason for Chinese Autosomal dorminant Parkinson's disease
within the Chinese population, the c.297T>C p.Ala99Ala polymorphism of the GIGYF2 gene may be associated with an increased risk of developing Parkinson disease.
These data, together with those recently reported by other groups, suggest that GIGYF2 is unlikely to be the PARK11 gene.
No clearly pathogenic mutations are identified in GIGYF2 and ATP13A2 (show ATP13A2 Antibodies) in Brazilian patients with early-onset Parkinson's disease.
The results of this study did not support a role for GIGYF2 in the genetic etiology of Belgian Parkinson disease.
GIGYF2 is unlikely to play a major role in PD in Japanese patients, similar to other populations.
our findings suggest that GIGYF2 variants are not a frequent cause of Parkinson's disease in the Spanish population, since we found no clearly segregating GIGYF2 variants
GIGYF2 variants are not associated with Parkinson's disease in the mainland Chinese Population.
Negative regulation of Grb10 (show GRB10 Antibodies) Interacting GIGYF2 protein on IGF-1 (show IGF1 Antibodies) receptor signaling pathway caused diabetic mice cognitive impairment.
Disruption of the eukaryotic translation initiation factor 4E (show EIF4E Antibodies) - Gigyf2 complex leads to increased translation and perinatal lethality in mice.
Primary cultured embryo fibroblasts from Gigyf2 null mice exhibit decreased IGF1 (show IGF1 Antibodies) signaling.
identification of proteins linked to insulin (show INS Antibodies)-like growth factor (IGF-I (show IGF1 Antibodies)) receptors by the Grb10 (show GRB10 Antibodies) adapter and modulate IGF-I (show IGF1 Antibodies) signaling
The protein encoded by this gene interacts with GRB10 and may be involved in the regulation of tyrosine kinase receptor signaling. This gene contains CAG repeats, and the encoded protein contains stretches glutamine and glutamic acid residues. Defects in this gene are a cause of Parkinson disease type 11 (PARK11). Multiple transcript variants encoding several different isoforms have been found for this gene.
trinucleotide repeat containing 15
, GRB10 interacting GYF protein 2
, PERQ amino acid-rich with GYF domain-containing protein 2
, PERQ amino acid rich, with GYF domain 3
, Parkinson disease (autosomal recessive, early onset) 11
, trinucleotide repeat-containing gene 15 protein
, GRB10-interacting GYF protein 2