Genetic News and Research

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Specific gene mutations may be responsible for how long someone lives with Parkinson's disease

How long someone lives with Parkinson's disease may be down to specific gene mutations, according to new research presented today at the 8th European Academy of Neurology Congress.

26 Jun 2022

Researchers identify orally efficacious antiviral drug against respiratory syncytial virus

An oral antiviral drug that targets a key part of the respiratory syncytial virus (RSV) polymerase and inhibits the synthesis of viral genetic material has been identified, a finding that could provide an effective treatment against RSV disease, according to researchers in the Center for Translational Antiviral Research at Georgia State University.

24 Jun 2022

Study uncovers cryptic vulnerabilities in RET oncogene that could aid in anti-cancer drug design

RET is a receptor protein with tyrosine kinase activity that can transfer a phosphate group from ATP to other molecules modifying their shape and function in signaling pathways that are essential to organogenesis and tissue maintenance.

24 Jun 2022

Novel app can help doctors make better decisions for patients with leukemia.

Researchers at the University of Copenhagen and clinicians at Rigshospitalet have developed an app that can help doctors make better decisions for patients with leukemia.

24 Jun 2022

MD Anderson announces collaborative alliance with Turning Point Therapeutics to advance new treatment options for cancer patients

The University of Texas MD Anderson Cancer Center and Turning Point Therapeutics, Inc., today announced a strategic research and development alliance to expand the evaluation of two of Turning Point's investigational small molecules focusing on precision medicine targets well known in oncology.

24 Jun 2022

Scientists identify new genetic disease that delays children's intellectual development

Scientists have identified a new genetic disease, which causes some children's brains to develop abnormally, resulting in delayed intellectual development.

24 Jun 2022

New nanoparticles effectively stopped the growth and spread of ovarian, liver tumors in mice

As they grow, solid tumors surround themselves with a thick, hard-to-penetrate wall of molecular defenses. Getting drugs past that barricade is notoriously difficult.

24 Jun 2022

"Founder events" that reduced genetic diversity found to be common throughout human history

Human populations have waxed and waned over the millennia, with some cultures exploding and migrating to new areas or new continents, others dropping to such low numbers that their genetic diversity plummeted.

23 Jun 2022

Newly identified gene may be responsible for sex-linked effects on women's heart disease outcomes

When diagnostic tests for the heart were first created, scientists at the time did not fully consider that no two bodies are the same, especially between the sexes.

23 Jun 2022

New method helps unravel three-dimensional structure of the human genome

Weill Cornell Medicine and New York Genome Center researchers, in collaboration with Oxford Nanopore Technologies, have developed a new method to assess on a large scale the three-dimensional structure of the human genome, or how the genome folds.

23 Jun 2022

Study unveils a precise model for the stinging organelle of starlet sea anemone

Summertime beachgoers are all too familiar with the painful reality of a jellyfish sting. But how do the stinging cells of jellyfish and their coral and sea anemone cousins actually work? New research from the Stowers Institute for Medical Research unveils a precise operational model for the stinging organelle of the starlet sea anemone, Nematostella vectensis.

23 Jun 2022

Stanford Medicine launches a diagnostic test for monkeypox

Stanford Medicine's Clinical Virology Laboratory today launched a diagnostic test for the monkeypox virus that has been identified in 42 countries and several U.S. states, including California.

23 Jun 2022

Inherited mutations in the MINAR2 gene lead to sensorineural deafness

Researchers at the John T. Macdonald Department of Human Genetics and John P. Hussman Institute for Human Genomics at the University of Miami Miller School of Medicine have found that inherited mutations in the MINAR2 gene caused deafness in four families.

23 Jun 2022

Genetic News and Research

Specific gene mutations may be responsible for how long someone lives with Parkinson's disease

Researchers identify orally efficacious antiviral drug against respiratory syncytial virus

Study uncovers cryptic vulnerabilities in RET oncogene that could aid in anti-cancer drug design

Novel app can help doctors make better decisions for patients with leukemia.

MD Anderson announces collaborative alliance with Turning Point Therapeutics to advance new treatment options for cancer patients

Scientists identify new genetic disease that delays children's intellectual development

New nanoparticles effectively stopped the growth and spread of ovarian, liver tumors in mice

"Founder events" that reduced genetic diversity found to be common throughout human history

Newly identified gene may be responsible for sex-linked effects on women's heart disease outcomes

New method helps unravel three-dimensional structure of the human genome

Study unveils a precise model for the stinging organelle of starlet sea anemone

Stanford Medicine launches a diagnostic test for monkeypox

Inherited mutations in the MINAR2 gene lead to sensorineural deafness

Molecular tumor profiling in pediatric cancer patients significantly impacts clinical care

U-M researchers reveal how a mutated protein acts as risk factor in Parkinson’s disease

Researchers discover two important novel aspects of APOE4 gene in Alzheimer's patients

Researchers model a complex childhood disease on-a-chip

New funding to help advance scientific understanding of skin disorders in children and young people

Non-traditional pet owners at increased risk of zoonotic diseases

Mutation in SARS-CoV-2 nucleocapsid protein found to enhance replication and pathogenicity

Sequencing & Genomics: Elevating Science and Healthcare eBook

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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