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Researchers identify heart defects in progeria patients that may raise risk of arrhythmias, premature death

Researchers at the Centro Nacional de Investigaciones Cardiovasculares Carlos III, working in collaboration with colleagues at other centers in Spain and abroad, have identified defects in the hearts of progeria patients that appear to be related to an elevated risk of arrhythmias and premature death.

2 Nov 2016

New Medgenics data confirms presence of specific genetic mutations in many ADHD children

New data presented at AACAP’s 63rd Annual Meeting (Oct. 24-29, 2016 in New York, NY) confirmed the presence of specific genetic mutations in many children with Attention Deficit Hyperactivity Disorder (ADHD).

2 Nov 2016

Fred Hutchinson opens first-of-its-kind clinic to provide new immunotherapies for cancer patients

Fred Hutchinson Cancer Research Center today announced the official opening of a first-of-its-kind clinic dedicated to providing innovative immunotherapies for cancer patients in clinical trials.

2 Nov 2016

Study shows promise for successful ovarian transplantation in future

Approximately 11% of women worldwide suffer from premature ovarian failure. This can have many different causes: chemotherapy administered for a malignant disease might irreversibly damage the ovaries and, because of the advances in modern cancer therapy, the number of young women surviving cancer is on the increase.

2 Nov 2016

Genetic susceptibility could help identify breast cancer patients at risk of developing VTE

Genetic testing could help identify breast cancer patients with high risk of experiencing venous thromboembolism (VTE), a serious and potentially fatal complication that can occur during cancer treatment.

2 Nov 2016

Researchers identify potential new treatment for brain cancer by targeting genes linked to microcephaly

University of North Carolina Lineberger Comprehensive Cancer Center researchers have identified a potential new treatment for brain cancer by learning from a rare condition that can cause microcephaly.

1 Nov 2016

Research shows way to directly target genes within specific cell type

The cornerstone of genetics is the loss-of-function experiment. In short, this means that to figure out what exactly gene X is doing in a tissue of interest—be it developing brain cells or a pancreatic tumor—you somehow cut out, switch off or otherwise destroy gene X in that tissue and then watch what happens.

1 Nov 2016

Study identifies potential pathway to improve rate at which the body burns calories

Researchers say they have identified a potential pathway in our muscle tissue to improve the rate at which our bodies burn calories.

1 Nov 2016

Illumina donates more than 95,000 human genetic variants to ClinVar database

Illumina, Inc. announced that it has contributed over 95,000 human genetic variants to ClinVar, a public database hosted by the National Center for Biotechnology Information (NCBI).

From Illumina, Inc. 1 Nov 2016

Americans take obesity as seriously as cancer, new survey finds

Americans take obesity as seriously as cancer, and say it's an even bigger health threat than heart disease, the nation's leading killer, yet most do not go beyond traditional diets or involve doctors in their largely unsuccessful personal struggles against the disease, according to a new survey by the American Society for Metabolic and Bariatric Surgery and the independent research organization, NORC at the University of Chicago.

1 Nov 2016

Scientists identify essential enzymes for efficient and precise repair of damaged DNA

Scientists at The Australian National University and Heidelberg University in Germany have found an essential component in the DNA repair process which could open the door to the development of new cancer drugs.

31 Oct 2016

Research shows genetic link between mitochondrial DNA and autism

Cornell University researchers have confirmed a genetic link between mitochondrial DNA (mtDNA), which is passed on from the mother, and some forms of autism spectrum disorder (ASD).

31 Oct 2016

Researchers identify potential approach for preventing neurological problems caused by blast-related TBI

More than 200,000 U.S. soldiers serving in the Middle East have experienced a blast-related traumatic brain injury, making it a common health problem and concern for that population.

31 Oct 2016

Researchers identify drug-resistant superbug in Australian domestic animal

The first evidence of a superbug in a domestic cat that could infect humans and livestock has been discovered in Australia.

31 Oct 2016

New partnership-funded research could lead to better treatment for birdshot

Birdshot uveitis is a rare autoimmune disorder that has the potential to blind. It’s notoriously hard to treat.

31 Oct 2016

Myriad Genetics presents research data that validates accuracy of myPath Melanoma test

Myriad Genetics, Inc., a leader in molecular diagnostics and personalized medicine, today announced it will present two new studies at the American Society of Dermatopathology (ASDP) annual meeting being held Oct. 27-30, 2016 in Chicago, Ill.

31 Oct 2016

Research findings may lead to new treatment option for ovarian cancer

A new study has identified an effective combination therapy for treating ovarian cancer cells.

31 Oct 2016

New study clears “Patient Zero” of responsibility for HIV in US

A new genetic analysis has shown that the French-Canadian flight attendant Gaétan Dugas who was posthumously blamed for spreading HIV across North America, was not the “Patient Zero” of the epidemic. Dugas became notorious as the person responsible for the US AIDS crisis after he slept with men in California and New York during the early 1980s.

28 Oct 2016

NIH researchers identify novel role for Hsp60 protein in tissue regeneration and wound healing

National Institutes of Health researchers have identified a novel role for a gene known as heat shock protein 60 (Hsp60), finding that it is critical in tissue regeneration and wound healing.

27 Oct 2016

Molecular biologist explores simple, innovative methods of developing new antibiotics

Antibiotic-resistant bacteria are a major problem worldwide. Molecular biologist Changsheng Wu explored innovative methods of developing new antibiotics more simply and more easily. He also discovered a new type of antibiotic.

27 Oct 2016

Genetic News and Research

Researchers identify heart defects in progeria patients that may raise risk of arrhythmias, premature death

New Medgenics data confirms presence of specific genetic mutations in many ADHD children

Fred Hutchinson opens first-of-its-kind clinic to provide new immunotherapies for cancer patients

Study shows promise for successful ovarian transplantation in future

Genetic susceptibility could help identify breast cancer patients at risk of developing VTE

Researchers identify potential new treatment for brain cancer by targeting genes linked to microcephaly

Research shows way to directly target genes within specific cell type

Study identifies potential pathway to improve rate at which the body burns calories

Illumina donates more than 95,000 human genetic variants to ClinVar database

Americans take obesity as seriously as cancer, new survey finds

Scientists identify essential enzymes for efficient and precise repair of damaged DNA

Research shows genetic link between mitochondrial DNA and autism

Researchers identify potential approach for preventing neurological problems caused by blast-related TBI

Researchers identify drug-resistant superbug in Australian domestic animal

New partnership-funded research could lead to better treatment for birdshot

Myriad Genetics presents research data that validates accuracy of myPath Melanoma test

Research findings may lead to new treatment option for ovarian cancer

New study clears “Patient Zero” of responsibility for HIV in US

NIH researchers identify novel role for Hsp60 protein in tissue regeneration and wound healing

Molecular biologist explores simple, innovative methods of developing new antibiotics

Genetics & Genomics - Second Edition 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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