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G6PC3 encodes the catalytic subunit of glucose-6-phosphatase (G6Pase). 再加上，我们可以发G6PC3 蛋白 (3) 和 和数多这个蛋白质的别的产品。
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these results indicated that coronin3 is significantly dysregulated in hepatocellular carcinoma tumor tissues, and may exert its function via regulating G6PC3 expression.
mir (显示 MLXIP 抗体)-122 and its targets G6PC3, ALDOA (显示 ALDOA 抗体) and CS play roles in the hypoxia responses that regulate glucose and energy metabolism and can serve as hypoxia biomarkers.
classic features of SCN (显示 SRI 抗体) IV found to share an identical inherited canonical splice-site mutation of the G6PC3 gene (c.218+1G>A).
Multilineage involvement of immune system occurs in G6PC3 deficiency in addition to the previously described neutropenia and multiple abnormalities.
G6PC3 defects should be considered in any case of congenital, unexplained neutropenia regardless of the clinical phenotype.
functional characterization of 16 of the 19 known missense mutations in severe congenital neutropenia syndrome caused by glucose-6-phosphatase-beta deficiency;14 missense mutations completely abolish G6Pase-beta activity while the p.S139I and p.R189Q mutations retain 49% and 45%, respectively of wild type activity
Severe congenital neutropenia with autosomal recessive G6PC3 mutations is associated with considerable clinical heterogeneity.
A role for G6PC3 in testicular differentiation and formation.
G6PC3 mutation is associated with severe congenital neutropenia.
Glucose 6 phosphatase catalytic subunit-3 deficiency due to mutation is a heterogenous disorder characterized by severe congenital neutropenia.
Survival and differentiation defects contribute to neutropenia in glucose-6-phosphatase-beta (G6PC3) deficiency in a model of mouse neutrophil granulocyte differentiation.
G-CSF (显示 CSF3 抗体) improves G6pc3(-/-) neutrophil survival by modulating apoptotic mediators and rectifies function by enhancing energy homeostasis.
in nonapoptotic neutrophils, G6PC3 is essential for normal energy homeostasis. A G6PC3 deficiency prevents recycling of ER glucose to the cytoplasm, leading to neutrophil dysfunction
UGRP/G6Pase (显示 G6PC 抗体) is the major glucose-6-phosphatase (显示 G6PC 抗体) of physiological importance for glucose homeostasis in vivo.
The absence of G6Pase-beta led to neutropenia
This gene encodes the catalytic subunit of glucose-6-phosphatase (G6Pase). G6Pase is located in the endoplasmic reticulum (ER) and catalyzes the hydrolysis of glucose-6-phosphate to glucose and phosphate in the last step of the gluconeogenic and glycogenolytic pathways. Mutations in this gene result in autosomal recessive severe congenital neutropenia. Multiple transcript variants have been found for this gene, only one of which is expected to express a protein.
, G6Pase 3
, glucose-6-phosphatase 3
, glucose-6-phosphatase catalytic subunit 3
, ubiquitous glucose-6-phosphatase catalytic subunit-related protein
, ubiquitously expressed G6Pase catalytic subunit-related protein
, glucose-6-phosphatase catalytic subunit-related