Genetic News and Research

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People who have a parent, sibling, or child with blood cancer have higher risk of disease

New data suggest that people who have a parent, sibling, or child with blood cancer have a higher likelihood of being diagnosed with the disease.

9 Aug 2019

Neuronal gene malfunction is behind seizures associated with long QT syndrome, study suggests

Most people with a medical condition called long QT syndrome have a mutation in a gene that causes bouts of fast, chaotic heartbeats.

9 Aug 2019

New genomic module facilitates more personalized forms of medicine

Researchers from the HSE Epilepsy Lighthouse Project and FutureNeuro, the SFI Research Centre for Chronic and Rare Neurological Diseases hosted by RCSI, have developed a new genomics module in the Irish National Epilepsy Electronic Patient Record system.

9 Aug 2019

New insights into emergent evolutionary potential and generative phenotype

In the cover photo, nature photographer Andreas Kay has captured one of the most striking examples of Batesian Mimicry in nature--first reported by Henry Walter Bates in 1861.

9 Aug 2019

Researchers test new drug to treat patients with chylomicronemia syndrome

People with familial chylomicronemia syndrome are born with a genetic mutation that means they can't produce an enzyme called lipoprotein lipase.

9 Aug 2019

Individual differences in pleasure are due to genetic variation, research suggests

Differences in how our brains respond when we're anticipating a financial reward are due, in part, to genetic differences, according to research with identical and fraternal twins published in Psychological Science, a journal of the Association for Psychological Science.

9 Aug 2019

New technique finds medically and ecologically relevant bacteria groups

Identifying species among plants and animals has been a full-time occupation for some biologists, but the task is even more daunting for the myriad microbes that inhabit the planet.

9 Aug 2019

Moffitt study uncovers subtypes of squamous cell lung cancer

Lung cancer is the number one cause of cancer-related deaths in the United States, with squamous cell lung cancer (SCC) being one of the common types.

8 Aug 2019

Internet may help diagnose people with rare disorders

A team of researchers at the Wake Forest Baptist Medical Center found that information found on the internet can serve as good means to diagnose individuals who suspect they have a rare disorder that has not been identified by their doctors.

8 Aug 2019

Whole genome sequencing could give officials a powerful weapon to track disease outbreaks

Whole genome sequencing technology may give epidemiologists and healthcare workers a powerful weapon in tracking and, possibly, controlling outbreaks of serious diseases, according to a team of researchers.

8 Aug 2019

Study aims to reduce therapy for subsets of patients with intermediate-risk neuroblastoma

Each year, approximately 750 patients are diagnosed with neuroblastoma in North America, the most common form of cancer in infants less than one year old.

8 Aug 2019

Atrial fibrillation is common and incurable, but can be controlled

One of the most common problems cardiologists handle is atrial fibrillation, also called AFib or AF. AFib is an abnormal or irregular heartbeat that can lead to blood clots, stroke, heart failure and other heart-related complications.

7 Aug 2019

New 'liquid biopsy' blood test for breast cancer could help avoid unnecessary surgeries

A new type of blood test for breast cancer could help avoid thousands of unnecessary surgeries and otherwise precisely monitor disease progression, according to a study led by the Translational Genomics Research Institute and Mayo Clinic in Arizona.

7 Aug 2019

Researchers identify gene mutation combo linked to endometrial cancer

Michigan State University researchers, in collaboration with the Van Andel Institute, have identified a combination of two gene mutations that is linked to endometrial cancer.

7 Aug 2019

New improved model for cancer wasting syndrome cachexia

A new model of cancer-related cachexia promises to help scientists understand why patients with cancer show severe wasting, which in turn may drive the development of better therapies.

7 Aug 2019

New discovery using fungi could lead to the development of effective radioprotective drugs

Thanks to fungi, researchers have made a new discovery that could lead to the development of effective radioprotective drugs for workers cleaning up nuclear contamination zones, like Fukushima and Chernobyl.

7 Aug 2019

Genome editing strategy opens new perspectives in the treatment of cystic fibrosis

The approach adopted by the team of the University of Trento, led by Anna Cereseto, opens new perspectives in the treatment of cystic fibrosis, a genetic disease for which no cure is currently available.

7 Aug 2019

Statement related to data inaccuracies with newly approved gene therapy

As a public health agency, we believe that it is critical to facilitate the development of innovative safe and effective medical products, like the cellular and gene therapy products that have shown enormous potential to treat previously untreatable diseases.

7 Aug 2019

Pitt researchers first to grow genetically modified miniature human livers in the lab

Researchers at the University of Pittsburgh School of Medicine are the first to grow genetically modified miniature human livers in the laboratory, to emulate human liver disease progression and test therapeutics.

7 Aug 2019

Freiburg start-up company takes over publicly traded company ‘CELLINK AB’

The idea of developing a laboratory instrument that handles and sorts individual, viable cells has been realized by researchers in the Laboratory for MEMS Applications in the Department of Microsystems Engineering at the University of Freiburg.

7 Aug 2019

Genetic News and Research

People who have a parent, sibling, or child with blood cancer have higher risk of disease

Neuronal gene malfunction is behind seizures associated with long QT syndrome, study suggests

New genomic module facilitates more personalized forms of medicine

New insights into emergent evolutionary potential and generative phenotype

Researchers test new drug to treat patients with chylomicronemia syndrome

Individual differences in pleasure are due to genetic variation, research suggests

New technique finds medically and ecologically relevant bacteria groups

Moffitt study uncovers subtypes of squamous cell lung cancer

Internet may help diagnose people with rare disorders

Whole genome sequencing could give officials a powerful weapon to track disease outbreaks

Study aims to reduce therapy for subsets of patients with intermediate-risk neuroblastoma

Atrial fibrillation is common and incurable, but can be controlled

New 'liquid biopsy' blood test for breast cancer could help avoid unnecessary surgeries

Researchers identify gene mutation combo linked to endometrial cancer

New improved model for cancer wasting syndrome cachexia

New discovery using fungi could lead to the development of effective radioprotective drugs

Genome editing strategy opens new perspectives in the treatment of cystic fibrosis

Statement related to data inaccuracies with newly approved gene therapy

Pitt researchers first to grow genetically modified miniature human livers in the lab

Freiburg start-up company takes over publicly traded company ‘CELLINK AB’

eBook: Using iPSCs models for human disease research and drug discovery 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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