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Study indicates that chga may play an important role in nervous system development during the early embryonic stages.
Increased myocardial CgA (show CGA ELISA Kits) glycosylation and impaired CgA (show CGA ELISA Kits) processing to catestatin in heart failure be considered detrimental because CST (show CORT ELISA Kits) reduces diastolic Ca2 (show CA2 ELISA Kits)+ leak via direct CaMKIIdelta inhibition.
performance of CgA (show CGA ELISA Kits)-deficient Chga-KO mice in treadmill exercise was impaired. CgA (show CGA ELISA Kits) deficiency renders the muscle energy deficient, impairs performance in treadmill exercise and prevents regeneration after exercise-induced tissue damage.
dilated mitochondrial cristae, endoplasmic reticulum and Golgi complex, as well as increased synaptic mitochondria, synaptic vesicles and glycogen (show GYS1 ELISA Kits) granules in Chga-knockout mice compared to WT mice.
the presence of ChgA and subsequent activation of ChgA-reactive T cells are essential for the initiation and development of autoimmune diabetes in NOD mice.
Studied leptin (show LEP ELISA Kits) and CST (show CORT ELISA Kits) modulation of SGLT1 (show SLC5A1 ELISA Kits) expression in hyperleptinemic type 2 diabetic mice.
N-terminal additions to the WE14 peptide of chromogranin A create strong autoantigen agonists in type 1 diabetes.
Data indicate that T-cell receptors that react to chromogranin A (ChgA) and islet amyloid polypeptide (show IAPP ELISA Kits) precursor (IAPP (show IAPP ELISA Kits)) autoantigens were impaired when the thymic stromal cells lacked thymus-specific serine protease (TSSP (show PRSS16 ELISA Kits)).
the important roles of CgA and CgB in glucose and cardiovascular homeostasis. This study also unveils the existence of direct implications of Cgs in the control of behaviour and mood.
Chromogranin A (10-19) and chromogranin A (43-52) were identified as antigens for autoreactive CD8 (show CD8A ELISA Kits)(+) T cells in NOD.beta2m(null).HHD mice.
Report QT/heart rate variability in a genomically "humanized" chromogranin a monogenic mouse model with hyperadrenergic hypertension.
Increased myocardial CgA (show CGA ELISA Kits) glycosylation and impaired CgA (show CGA ELISA Kits) processing to catestatin in heart failure be considered detrimental because CST (show GAL3ST1 ELISA Kits) reduces diastolic Ca2 (show CA2 ELISA Kits)+ leak via direct CaMKIIdelta inhibition.
Data suggest pancreastatin, a 49 residue post-translational fragment of chromogranin A, as a routinely tested biomarker in neuroendocrine tumors (NETs) and in particular small bowel NET.
Data indicate that measurement of chromogranin A (CgA) alone is sufficient in the management of patients with neuroendocrine tumours (NETs) and that routine additional measurement of chromogranin B (CgB (show CHGB ELISA Kits)) provides little added value.
Data show that chrysin suppressed cell proliferation and reducing expression of achaete-scute complex-like 1 (ASCL1 (show ASCL1 ELISA Kits)) and the neuroendocrine biomarker chromogranin A (CgA).
In a Japanese population, the Ser (show SIGLEC1 ELISA Kits)-364 allele was associated with elevated systolic blood pressure and pulse pressure, consistent with increased arterial stiffness.
ChrA levels were not effective in predicting outcomes or detecting recurrences of Merkel cell carcinoma.
Decreased CSF (show CSF2 ELISA Kits) levels of chromogranin A were found in Parkinson disease patients with orthostatic hypotension.
In both mice and men the Gly364Ser polymorphism conferred metabolic traits such as elevated HDL (show HSD11B1 ELISA Kits) and lowered norepinephrine levels; it was associated with superior baroreflex function and therefore better response to stress.
In patients with resected pancreatic neuroendocrine tumors, an elevated preoperative CgA (show CGA ELISA Kits) level was negatively associated with disease-free survival and overall survival.
In astrocytes from multiple sclerosis white matter lesions the expression of chromogranin A is increased.
High pancreastatin levels are significantly associated with neuroendocrine tumors.
No circadian pattern was detected for salivary CgA in either spring or autumn, and there were no significant effects of gender or age. However, mean salivary CgA concentrations were significantly higher in the pigs sampled in autumn, compared to spring.
expression and localization of chromogranin A (CgA), chromogranin B (CgB (show CHGB ELISA Kits)), synaptophysin (show SYP ELISA Kits), and insulin (show INS ELISA Kits) were ultrastructurally studied with the immunogold technique in porcine and human pancreatic islet neuroendocrine cells
Vasoconstriction-Inhibiting Factor (VIF (show BTG1 ELISA Kits)), a degradation product of chromogranin A, is a vasoregulatory peptide that modulates the vasoconstrictive effects of angiotensin II by acting on the angiotensin II type 2 receptor (show AGTR2 ELISA Kits).
chromogranin A has a role in the IP(3)-mediated Ca(2 (show CA2 ELISA Kits)+) release mechanism of secretory granules
chromogranin A has a specific site in the N-terminal domain that can bind membrane lipids from different species
role of coupling with the inositol 1,4,5-trisphosphate receptor/Ca2 (show CA2 ELISA Kits)+ channel (InsP3R (show ITPR1 ELISA Kits))in the Ca2 (show CA2 ELISA Kits)+-dependent ciliary movement
involvement of CGA (show CGA ELISA Kits) with other components of the senile plaque
significant species differences in vasoactivity of the N-terminal domain of ChgA
determination of the subcellular distribution of chromogranins A and B in chromaffin cells; results suggest that chromogranins are at the center of intracellular Ca(2 (show CA2 ELISA Kits)+) homeostasis in secretory cells
The protein encoded by this gene is a member of the chromogranin/secretogranin family of neuroendocrine secretory proteins. It is found in secretory vesicles of neurons and endocrine cells. This gene product is a precursor to three biologically active peptides\; vasostatin, pancreastatin, and parastatin. These peptides act as autocrine or paracrine negative modulators of the neuroendocrine system. Other peptides, including chromostatin, beta-granin, WE-14 and GE-25, are also derived from the full-length protein. However, biological activities for these molecules have not been shown.
, chromogranin A
, betagranin (N-terminal fragment of chromogranin A)
, parathyroid secretory protein 1
, pituitary secretory protein I