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BioWorld - Saturday, April 25, 2026
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Home » Topics » BioWorld Science, Biomarkers

BioWorld Science, Biomarkers
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ESC Congress 2022

GRP78 serum levels predict mortality in patients with coronary artery disease

Sep. 1, 2022
Researchers from University Hospital Bonn presented data from a study that aimed to evaluate the significance of serum levels of the endoplasmic-reticulum-stress chaperone GRP78 in patients undergoing coronary angiography for suspected coronary artery disease (CAD).
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Multiple myeloma illustration
2022 International Myeloma Workshop

Circulating miR-27b-3p may aid in the diagnosis and prognosis of multiple myeloma

Sep. 1, 2022
The crosstalk between immune cells and multiple myeloma (MM) cells is an important determinant of MM progression, but the mechanisms behind this have not been fully defined.
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Vascular system
ESC Congress 2022

Anti-CCP antibodies behind the progression of aortic stenosis

Sep. 1, 2022
There is a lack of biomarkers for disease activity in aortic stenosis (AS). On the other hand, citrullination is involved in many chronic inflammatory processes and citrullinated proteins have been found within atherosclerotic plaque.
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Neurology/Psychiatric

Target ALS and ADDF award grants to support biomarker research for neurodegenerative diseases

Aug. 31, 2022
Target ALS Foundation Inc. and the Alzheimer's Drug Discovery Foundation LLC (ADDF) have announced the first four award recipients in a new initiative to identify and develop biomarkers for neurodegenerative diseases, including Alzheimer's disease, amyotrophic lateral sclerosis (ALS) and frontotemporal degeneration (FTD).
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Biomarkers

CSMD1 expression is linked to poor prognosis in patients with glioma

Aug. 30, 2022
The prognostic role of complement inhibitor CSMD1 was assessed in 1,507 patients with glioma from three different datasets. Results of the bioinformatical analysis suggested that high expression of CSMD1 was associated with increased overall survival and disease-free survival, as well as lower tumor grade.
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Variation in the TMEM163 gene tied to hypomyelinating leukodystrophy

Aug. 26, 2022
Hypomyelinating leukodystrophy is a genetic disorder characterized by deficient myelination of the central nervous system white matter. An international team of researchers has published a case report of 4 unrelated families with a hypomyelinating leukodystrophy phenotype.
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Plasma GFAP and UCHL1 predict functional recovery after traumatic brain injury

Aug. 23, 2022
The usefulness of glial fibrillary acidic protein (GFAP) and ubiquitin C-terminal hydrolase L1 (UCHL1) for the early prediction of long-term traumatic brain injury (TBI) outcomes has not been well investigated.
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Mutation in the ADIPOQ gene found in family with diabetes and renal disease

Aug. 22, 2022
Adiponectin (ADIPOQ) is an adipocyte-derived hormone that promotes insulin sensitivity, inhibits cell death and decreases inflammation. Previous studies identified common variants in the ADIPOQ gene that have been associated with aberrant adiponectin levels, obesity, type 2 diabetes and diabetic kidney disease. In a recent study, the first multigenerational family was identified as harboring a protein-truncating mutation in the ADIPOQ gene, p.Gly93GlufsTer73, that cosegregated with diabetes and end-stage renal disease.
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TRAF3 mutations increase the risk of immunodeficiency and autoimmunity in humans

Aug. 19, 2022
Tumor necrosis factor receptor-associated factor 3 (TRAF3) is a cytoplasmic protein that controls signal transduction from different receptor families, and plays a key role in regulating immunity.
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CXCL9 predicts the risk of hip osteoporotic fracture in men

Aug. 19, 2022
Chemokines are small signaling cytokines that are involved in many physiological processes such as host immune responses, wound healing and bone remodeling, with two of these chemokines, C-X-C motif chemokine 9 (CXCL9) and CXCL10, being involved in different osteoimmuno-modulating pathways.
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