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Amplified Sciences secures $400,000 grant to develop pancreatic cancer diagnostic test

Health care providers and their patients could know with greater confidence whether pancreatic cysts are benign or potentially malignant, and if surgery is required to remove them, by using a new diagnostic test currently in development.

12 Jul 2023

Self-reported long COVID symptoms not identified in diagnostic tests

Researchers describe chronic symptoms related to physical or mental functioning following SARS-CoV-2 infection.

12 Jul 2023

New research finds COPD diagnosis gap in African Americans

Recently published research suggests that despite showing clear symptoms of chronic obstructive pulmonary disease (COPD), many African Americans are not officially diagnosed with the disease due to flaws in diagnosis methods.

11 Jul 2023

£1.5 million funding boost awarded for revolutionary test to improve early detection of Alzheimer's

A significant NIHR grant will enable researchers at the universities of Bath and Bristol, in collaboration with Cumulus Neuroscience, to develop revolutionary technology to help expand early dementia diagnosis.

11 Jul 2023

Photon-counting CT protocol shows promise for lung imaging

New CT technology allows for a comprehensive, simultaneous evaluation of lung structure and function, something not possible with standard CT, according to a study published in Radiology, a journal of the Radiological Society of North America.

11 Jul 2023

mAb-based bELISA developed to detect SARS-CoV-2 antibodies in a broad spectrum of animal species

Researchers developed a mAb-based blocking enzyme-linked immunosorbent assay (bELISA) to detect SARS-CoV-2 in animals.

11 Jul 2023

Fibromyalgia patients may be at increased risk of death

Fibromyalgia, a condition that causes persistent widespread pain and fatigue, may be linked to a heightened risk of death as a result of vulnerability to accidents, infections, and especially suicide, suggests a pooled data analysis of the available evidence, published in the open access journal RMD Open.

10 Jul 2023

REDH database provides insights into RNA editing in hematopoietic cells

The process of converting DNA to proteins through an RNA is far from straightforward. Of the several types of RNA involved in the process of protein synthesis, a few may be edited mid-way.

10 Jul 2023

AMP releases consensus recommendations for CYP3A4 and CYP3A5 genotyping assays

The Association for Molecular Pathology (AMP), the premier global molecular diagnostic professional society, today published consensus recommendations to aid in the design and validation of clinical CYP3A4 and CYP3A5 genotyping assays, promote standardization of testing across different laboratories, and improve patient care.

10 Jul 2023

Lollipop-based saliva collection system shows promise for more enjoyable, accurate diagnostic testing

A lollipop might be a sweet reward for a kid who's endured a trip to the doctor's office, but now, this candy could make diagnostic testing during a visit less invasive and more enjoyable.

10 Jul 2023

Biomarkers in the brain could redefine mental health conditions

The study of biomarkers in the brain - powered by cutting-edge machine learning techniques - could redefine the way mental health conditions are categorized and diagnosed and lead to more effective, personalized treatments.

10 Jul 2023

New technique could help identify rare genetic disorders while preserving privacy

Macquarie University researchers have demonstrated a new way of linking personal records and protecting privacy. The first application is in identifying cases of rare genetic disorders. There are many other potential applications across society.

10 Jul 2023

PacBio's Revio long-read sequencing system to help Bioscientia solve complex genetic cases

PacBio, a leading developer of high-quality, highly accurate sequencing solutions, today announced that Bioscientia is using its Revio long-read sequencing system to expand its genomics research projects and sequence several thousand human genomes per year.

10 Jul 2023

PrecisionLife licenses OXEGENE dataset to develop personalized treatments for endometriosis

PrecisionLife, a leading techbio company driving precision medicine in complex chronic diseases, announced today a data access agreement with the University of Oxford to license the Oxford Endometriosis Gene (OXEGENE) dataset with the aim to develop new personalised treatments for endometriosis patients.

10 Jul 2023

Study uncovers three previously unknown membrane proteins in ovarian cancer

A study led by Nagoya University in Japan has identified three previously unknown membrane proteins in ovarian cancer.

7 Jul 2023

MRI may be more effective than CT with CTA in patients with dizziness

According to an accepted manuscript published in the American Journal of Roentgenology (AJR), patients discharged from the emergency department (ED) after CT with CTA alone could have benefitted from an alternative or additional MRI evaluation, including using a specialized abbreviated protocol for the modality.

7 Jul 2023

Drug-resistant pathogen found in ears of stray dogs, raising concerns about spread to humans

Scientists at McMaster University and India's University of Delhi have discovered and isolated the first live culture of the drug-resistant pathogen Candida auris from an animal, specifically from the ear canals of stray dogs.

7 Jul 2023

Unique blood protein patterns in long COVID patients could reveal potential drug targets

Recently published in The Journal of Translational Medicine, a team at Lawson Health Research Institute has discovered unique patterns of blood plasma proteins in patients with long COVID that could reveal potential drug targets to improve patient outcomes.

7 Jul 2023

AI tool can rapidly decode brain tumor DNA during surgery

Scientists have designed an AI tool that can rapidly decode a brain tumor's DNA to determine its molecular identity during surgery - critical information that under the current approach can take a few days and up to a few weeks.

7 Jul 2023

New molecular pathway identified for early onset coronary artery disease

A novel molecular pathway to explain how a mutation in the gene ACTA2 can cause individuals in their 30s – with normal cholesterol levels and no other risk factors - to develop coronary artery disease has been identified, according to researchers with UTHealth Houston.

7 Jul 2023

Diagnostic News and Research

Amplified Sciences secures $400,000 grant to develop pancreatic cancer diagnostic test

Self-reported long COVID symptoms not identified in diagnostic tests

New research finds COPD diagnosis gap in African Americans

£1.5 million funding boost awarded for revolutionary test to improve early detection of Alzheimer's

Photon-counting CT protocol shows promise for lung imaging

mAb-based bELISA developed to detect SARS-CoV-2 antibodies in a broad spectrum of animal species

Fibromyalgia patients may be at increased risk of death

REDH database provides insights into RNA editing in hematopoietic cells

AMP releases consensus recommendations for CYP3A4 and CYP3A5 genotyping assays

Lollipop-based saliva collection system shows promise for more enjoyable, accurate diagnostic testing

Biomarkers in the brain could redefine mental health conditions

New technique could help identify rare genetic disorders while preserving privacy

PacBio's Revio long-read sequencing system to help Bioscientia solve complex genetic cases

PrecisionLife licenses OXEGENE dataset to develop personalized treatments for endometriosis

Study uncovers three previously unknown membrane proteins in ovarian cancer

MRI may be more effective than CT with CTA in patients with dizziness

Drug-resistant pathogen found in ears of stray dogs, raising concerns about spread to humans

Unique blood protein patterns in long COVID patients could reveal potential drug targets

AI tool can rapidly decode brain tumor DNA during surgery

New molecular pathway identified for early onset coronary artery disease

Bringing real-time analytics to downstream bioprocess monitoring

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

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