Genetic Information News and Research

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High fat diet during pregnancy increases breast cancer susceptibility in female progeny, mice study finds

Feeding pregnant female mice a diet high in fat derived from common corn oil resulted in genetic changes that substantially increased breast cancer susceptibility in three generations of female offspring, reports a team of researchers led by scientists at Georgetown Lombardi Comprehensive Cancer Center.

3 Jul 2017

Safe under the ACA, patients with preexisting conditions now fear bias

Cheasanee Huette, a 20-year-old college student in Northern California, is worried. Two years ago, knowing she was protected by the Affordable Care Act's guarantees of coverage for preexisting conditions, she decided to find out if she carried the same genetic mutation that eventually killed her mother.

29 Jun 2017

PNNL-OHSU scientists part of NCI effort to study about role of proteins in cancer biology

The Department of Energy's Pacific Northwest National Laboratory is part of a nationwide effort to learn more about the role of proteins in cancer biology and to use that information to benefit cancer patients.

28 Jun 2017

Existing drugs could help subgroup of patients with osteosarcoma, suggest scientists

A subgroup of patients with osteosarcoma - a form of bone cancer - could be helped by an existing drug, suggest scientists from the Wellcome Trust Sanger Institute and their collaborators at University College London Cancer Institute and the Royal National Orthopaedic Hospital NHS Trust.

23 Jun 2017

Philips introduces new web-based informatics platform to hasten drug research and biomarker discovery

Royal Philips, a global leader in health technology, today announced the launch of its Xplore web-based informatics platform for drug research and biomarker discovery.

From Philips Healthcare 20 Jun 2017

Study explores factors, patterns that predict use of restrictive feeding for children

In the preschool years, children begin to learn from their environment about self-regulation--both in regards to food choices and how to deal with their emotions.

16 Jun 2017

Viral vectors for gene transfer can travel to distant areas in the brain, study shows

Gene transfer is seen as a hopeful therapy for Alzheimer's and Parkinson's patients. The approach involves using harmless laboratory-produced viruses to introduce important genes into the brain cells.

16 Jun 2017

New genomic sequencing approach could be first step toward blood tests for early cancer detection

In a study of 124 patients with advanced breast, lung, and prostate cancers, a new, high-intensity genomic sequencing approach detected circulating tumor DNA at a high rate.

5 Jun 2017

Researchers make significant advance in treatment of bowel cancer

New research led by Queen's University Belfast has discovered how a genomic approach to understanding bowel (colorectal) cancer could improve the prognosis and quality of life for patients.

31 May 2017

Prolaris becomes first genetic test to receive Medicare coverage for favorable intermediate and low-risk prostate cancer

Myriad Genetics, Inc., a leader in molecular diagnostics and personalized medicine, today announced that Palmetto GBA, a Medicare Administrative Contractor that assesses molecular diagnostic technologies, has issued a positive final Local Coverage Determination to expand Medicare coverage of the Prolaris test.

29 May 2017

Obesity causes poorer cardiovascular health in young adults

Copenhagen, Denmark: Higher than normal body mass index (BMI) is known to lead to cardiovascular ill-health in mid-to-late life, but there has been limited investigation of its effect in young, apparently healthy, adults.

27 May 2017

Open-access BRCA testing for inherited breast cancer enables identification of missed carriers

Ashkenazi Jewish women are known to have a predisposition to the inherited breast cancers BRCA1 and BRCA2, but currently genetic testing in this group is limited to women affected by breast and ovarian cancers and those who are unaffected but have a family history of the disease.

27 May 2017

Researchers discover cardioprotective genetic variant in isolated Greek population

A genetic variant that protects the heart against cardiovascular disease has been discovered by researchers at the Wellcome Trust Sanger Institute and their collaborators.

26 May 2017

Preliminary study: Co-occurrence of COMT and BRCA 1/2 variants may reduce breast cancer incidence

Research looking at genomic data from women with a genetic risk for breast cancer, who may never develop cancer, found their cancer-free state may be related to a second genetic variation.

25 May 2017

Study provides new understanding of silent gene changes and genetic complexity of cystic fibrosis

Cystic fibrosis is a common life-shortening inherited disease that affects over 70,000 people worldwide, the majority of whom are children and young adults.

18 May 2017

KU Leuven researchers identify vital role of TET1 protein in earliest stages of embryonic development

In the earliest stages of embryonic development, a protein known as TET1 may be the factor that tips the balance toward health or disease.

18 May 2017

FDA expands approval for cystic fibrosis drug to treat additional rare gene mutations

The U.S. Food and Drug Administration today expanded the approved use of Kalydeco (ivacaftor) for treating cystic fibrosis.

18 May 2017

Scientists identify gene linked to incurable bowel disorders

A key gene that helps to explain an underlying cause of incurable bowel disorders such as Crohn's disease has been identified by scientists.

17 May 2017

Scientists develop world's first smartphone app to collect large data for people with MS

What if a single smartphone app could help solve the enigma of multiple sclerosis and move new treatments ahead at lightning speed? That was the bold idea that led Keck Medicine of USC neurologist Daniel Pelletier, MD, professor of neurology at the Keck School of Medicine of USC and division chief of the Neuro-Immunology and USC Multiple Sclerosis Center, to develop myMS, the world's first smartphone app capable of collecting large amounts of clinical, imaging and genetic data for people with MS. Enrollment is now underway for a pilot study of the app.

16 May 2017

Discovery of steroid hormone in fruit flies may shed new light on maternal hypothyroidism

University of Oregon researchers using Drosophila have identified a steroid hormone that triggers a vital transition in early brain development in which neural stem cells properly change gears to produce different kinds of neurons.

15 May 2017

Genetic Information News and Research

High fat diet during pregnancy increases breast cancer susceptibility in female progeny, mice study finds

Safe under the ACA, patients with preexisting conditions now fear bias

PNNL-OHSU scientists part of NCI effort to study about role of proteins in cancer biology

Existing drugs could help subgroup of patients with osteosarcoma, suggest scientists

Philips introduces new web-based informatics platform to hasten drug research and biomarker discovery

Study explores factors, patterns that predict use of restrictive feeding for children

Viral vectors for gene transfer can travel to distant areas in the brain, study shows

New genomic sequencing approach could be first step toward blood tests for early cancer detection

Researchers make significant advance in treatment of bowel cancer

Prolaris becomes first genetic test to receive Medicare coverage for favorable intermediate and low-risk prostate cancer

Obesity causes poorer cardiovascular health in young adults

Open-access BRCA testing for inherited breast cancer enables identification of missed carriers

Researchers discover cardioprotective genetic variant in isolated Greek population

Preliminary study: Co-occurrence of COMT and BRCA 1/2 variants may reduce breast cancer incidence

Study provides new understanding of silent gene changes and genetic complexity of cystic fibrosis

KU Leuven researchers identify vital role of TET1 protein in earliest stages of embryonic development

FDA expands approval for cystic fibrosis drug to treat additional rare gene mutations

Scientists identify gene linked to incurable bowel disorders

Scientists develop world's first smartphone app to collect large data for people with MS

Discovery of steroid hormone in fruit flies may shed new light on maternal hypothyroidism

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