Molecular Diagnostics
Single-Cell Analysis Uncovers Regulatory Program in Rare Leukemia
Identifying the causes of human diseases requires deconvolution of abnormal molecular phenotypes spanning DNA accessibility, gene expression and protein abundance. Mixed-phenotype acute leukemia exhibits features of both acute myeloid leukemia and acute lymphoblastic leukemia and, as such, is marked by features of multiple hematopoietic lineages. More...18 Dec 2019
Genetic Biomarkers Associated with Autism Spectrum Disorders Identified
Autism spectrum disorder (ASD) refers to a group of neurodevelopmental conditions resulting in challenges related to communication, social understanding and behavior. Studies show families who have a child with ASD have a 6.9% to 19.5% chance of another child having ASD and a 30% to 40% chance of another child having atypical development. More...17 Dec 2019
Implement Diagnostics System Improves Infectious Disease Testing
A team of scientists recently began using machine-learning tools and assessed them in a prospective clinical trial to determine whether artificial intelligence could perform better than specialists in clinical test interpretation. More...17 Dec 2019
Mutations Causing Loss of Tumor Suppressor Gene Increase Aggressiveness of Rare Bile Duct Cancer
A team of Japanese cancer researchers identified a biomarker, that when absent or reduced, predicts the likely outcome of the rare cancer of the bile duct, intrahepatic cholangiocarcinoma (ICC). More...17 Dec 2019
Childhood Kidney Cancer Arises from Altered Normal Tissue
While kidney cancer in children is rare, the most common type is Wilms tumor, which mostly affects children under the age of five. Most cases of Wilms tumor can be cured through surgery to remove the afflicted kidney in combination with chemotherapy and possibly radiotherapy. More...16 Dec 2019
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In Other News
A Rapid Method for Selecting the Proper Antibiotic to Treat Multidrug Resistant Bacteria
Chronic Comorbidities Are Prevalent Among People with Chagas Disease
A One-step Rapid Point-of-Care Assay for Diagnosis of Celiac Disease
Diagnosis and Monitoring of Patients with Hepatitis C Virus
TP53 Gene Promoter Methylation Impacts Chronic Lymphocytic Leukemia
Three Factors Distinguish MODY, a Rare Diabetes, in Youth
Alzheimer's Disease Gene Expression Varies by Brain Cell Type
Diagnosing Disease Conditions by Analyzing Plasma Protein Expression Patterns
Home Urine Collection for More Accurate Prostate Cancer Detection
Genetic Architectures of Schizophrenia Compared in Different Populations
Marker Panel Detects Early Liver Cancer with Increased Sensitivity
Rare Genetic Variants Associated with Sudden Cardiac Death
CRISPR-based Electrochemical Biosensor Detects Disease-related MicroRNAs
Gene Panel Predicts Failure of Cutaneous Leishmaniasis Treatment
Genetic Locus with Unique Tandem Repeats Linked to Development of Late-onset Alzheimer’s Disease
Multiplex Panel Debuts for Multi-Drug Resistant Infection Screening
Non-coding Regions of the Genome in Microglia Linked to Alzheimer’s Disease Risk
Epigenetic DNA Biomarkers Pinpoint Infertile Men and Predict Potential Success of Treatment
LDL Subclasses Ratio Predicts Cardiovascular Disease Risk More Accurately than LDL-cholesterol Alone
MicroRNA Panel Distinguishes Benign Moles from Melanoma in the Eye
Mycobacterium Infection Found in Gastric Patients’ Stomachs
Novel, High-Accuracy Blood Test Can Screen for Multiple Cancers
Crohn's Disease-Associated Bacteria Tolerate Antibiotics
Genetic Testing channel of LabMedica brings the latest in molecular genetics, cytogenetics, and epigenetics, and methods from PCR to FISH, and more.
