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A blood-based genome testing service provides accurate results within 72 hours

Blood-Based Genome Testing Feasible for Rapid Mutation Assay

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Mutation results available within 72 hours for 94 percent of non-small-cell lung CA samples evaluated

T2DM Risk Cut by Variant in Sulfonylurea Receptor Encoder

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Missense variant in ABCC8 gene also linked to reduced risk of coronary heart disease
A gene therapy strategy can be applied to retinitis pigmentosa

Gene Therapy Strategy Feasible for Retinitis Pigmentosa

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Reprogramming rod to cone-like photoreceptors by inactivation of Nrl or Nr2e3 restores visual function
Circulating exosomes have a distinct RNA profile in relapsing-remitting multiple sclerosis

Circulating Exosomes Have Distinct RNA Profile in MS

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Serum exosomal expression of four microRNAs significantly decreased during relapse
The Runt-related transcription factor 1 gene may play a role in human proliferative diabetic retinopathy

RUNX1 May Play Role in Proliferative Diabetic Retinopathy

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RUNX1 upregulated in CD31+ vascular endothelial cells from human PDR fibrovascular membranes
Close to half of breast cancer patients who choose to have a double mastectomy after genetic testing may not have the gene mutations known to raise the risk of additional cancers

Misunderstanding of BRCA Test Results Affects Mastectomy Rates

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Half of average-risk patients with variants of uncertain significance may undergo bilateral mastectomy
Many survivors of childhood cancer have mutations in cancer-associated genes

AACR: Genetic Mutations Seen in Many Childhood Cancer Survivors

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One in four children who lived through cancer developed another cancer by age 45, researchers say
Angiopoietin-like 3 deficiency is associated with reduced risk of coronary artery disease

ANGPTL3 Deficiency Linked to Reduced CAD Risk

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Heterozygous carriers of ANGPTL3 loss-of-function mutations have reductions in TGs, LDL-C
BRCA testing has shifted from being primarily used in cancer patients to being used in unaffected women

BRCA Mutation Testing Shifts to Unaffected Women

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From 2004 to 2014, greater percent of testing in unaffected women versus cancer patients
Genetic predisposition to hyperglycemia raises the odds of coronary artery disease (CAD)

Genetic Hyperglycemia Raises Risk of Coronary Artery Disease

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Increased risk of coronary artery disease is separate from diabetes risk