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CTF along with NTAP and Sage announce first-ever open data portal for neurofibromatosis

The Children's Tumor Foundation, together with the Neurofibromatosis Therapeutic Acceleration Program and Sage Bionetworks, has announced the first-ever open data portal for scientific research results in the field of neurofibromatosis.

17 Dec 2018

Folate deficiency creates more damaging chromosomal abnormalities than previously known

Folate deficiency creates more problems in connection with DNA replication than researchers had hitherto assumed, researchers from the University of Copenhagen show in a new study.

14 Dec 2018

New computer model helps predict course of the disease in prostate cancer patients

How does a normal cell turn into a deadly cancer? Seeking an answer to this question, and working alongside other international working groups, researchers from Charité - Universitätsmedizin Berlin examined the tumor genomes of nearly 300 prostate cancer patients.

14 Dec 2018

Shining new light on neuron firing

Scientists have plenty of ways to watch as individual neurons in a brain fire, sending electrical signals from one to the next, but they all share a basic problem.

14 Dec 2018

Scientists discover rules that determine precision of CRISPR/Cas9 genome editing in human cells

Scientists at the Francis Crick Institute have discovered a set of simple rules that determine the precision of CRISPR/Cas9 genome editing in human cells.

14 Dec 2018

New research lays out potential path for treatment of Huntington’s disease

New research gives scientists a clearer picture of what is happening in the brains of people with Huntington's disease and lays out a potential path for treatment.

14 Dec 2018

UA scientists uncover biological processes leading to rare brain disorder in babies

Babies born with pontocerebellar hypoplasia type Ib often do not survive past one year. Born with an underdeveloped brain, infants struggle to move, feed and even breathe.

14 Dec 2018

Genetic marker, predictor of early relapse in common childhood cancer discovered

Nova Southeastern University researchers recently discovered that by testing the level of NER (nucleotide excision repair) gene expression, pediatric oncologists can determine the likelihood of early relapse (less than three years) in their acute lymphoblastic leukemia patients.

14 Dec 2018

Acne could have a genetic basis find researchers promising new cure

In one of the pioneering genetic studies of acne, it has been seen that the condition that affects millions of teenagers and adults could have a genetic basis. This genetic study can also pave the way for new and accurate treatment for acne promise researchers. The study results are published in the latest issue of the journal Nature Communications.

13 Dec 2018

Study finds drug targets for Ebola, Dengue, and Zika viruses

No drugs are currently available to treat Ebola, Dengue, or Zika viruses, which infect millions of people every year and result in severe illness, birth defects, and even death. New research from the Gladstone Institutes and UC San Francisco may finally change that. Scientists identified key ways the three viruses hijack the body's cells, and they found at least one potential drug that can disrupt this process in human cells.

13 Dec 2018

Study uncovers new genetic clues to frontotemporal dementia

Unlike the more common Alzheimer's disease, frontotemporal dementia tends to afflict young people. It accounts for an estimated 20 percent of all cases of early-onset dementia.

13 Dec 2018

Scientists perform lung lavage as new approach for tuberculosis diagnosis in rhinoceros

Conventional immunological tests for tuberculosis in rhinoceros are substantially insecure and bear high risk of false negative or false positive diagnosis with sometimes fatal consequences for the animal.

13 Dec 2018

Genetic study reveals new insights into underlying causes of moderate-to-severe asthma

The largest-ever genetic study of people with moderate-to-severe asthma has revealed new insights into the underlying causes of the disease which could help improve its diagnosis and treatment.

13 Dec 2018

New discovery will improve the safety and predictability of CRISPR

Scientists have discovered a simple set of rules that can be used to precisely predict how DNA will be modified by the CRISPR gene editing technique.

13 Dec 2018

Chronic rhinitis associated with hospital readmissions for asthma and COPD patients

Patients hospitalized for either asthma or chronic obstructive pulmonary disease have a higher risk of being readmitted for a hospital stay within 30 days of release if they also suffer from chronic rhinitis, according to a trio of researchers at the University of Cincinnati.

13 Dec 2018

UAlberta scientists identify biomarkers for detecting Alzheimer's disease in saliva samples

University of Alberta scientists have identified three biomarkers for detecting mild cognitive impairment and Alzheimer's disease in saliva samples. The research has promising results for application in a clinical setting.

13 Dec 2018

Recent findings on rare genetic disorder may help develop new treatment options

Fresh discoveries about a rare genetic disorder that affects mainly boys may inform the development of therapies to treat the condition.

13 Dec 2018

New findings throw light on natural sex selection process

For nearly 100 years biologists have argued about how exactly natural selection can possibly work. If nature selects the individuals with the best genes then why aren't all organisms the same?

13 Dec 2018

Blood test helps identify distinct molecular signatures in children with cystic fibrosis

Researchers at Stanley Manne Children's Research Institute at Ann & Robert H. Lurie Children's Hospital of Chicago, and colleagues, used a blood test and microarray technology to identify distinct molecular signatures in children with cystic fibrosis.

12 Dec 2018

Intellectually active lifestyle confers protection against neurodegeneration in Huntington's patients

Researchers from the Cognition and Brain Plasticity research group of the Bellvitge Biomedical Research Institute and the University of Barcelona, in collaboration with several hospitals, have discovered that an intellectually active lifestyle confers protection against neurodegeneration in people with Huntington's disease, delaying the onset of symptoms and loss of grey matter in the brain.

12 Dec 2018

Genetic News and Research

CTF along with NTAP and Sage announce first-ever open data portal for neurofibromatosis

Folate deficiency creates more damaging chromosomal abnormalities than previously known

New computer model helps predict course of the disease in prostate cancer patients

Shining new light on neuron firing

Scientists discover rules that determine precision of CRISPR/Cas9 genome editing in human cells

New research lays out potential path for treatment of Huntington’s disease

UA scientists uncover biological processes leading to rare brain disorder in babies

Genetic marker, predictor of early relapse in common childhood cancer discovered

Acne could have a genetic basis find researchers promising new cure

Study finds drug targets for Ebola, Dengue, and Zika viruses

Study uncovers new genetic clues to frontotemporal dementia

Scientists perform lung lavage as new approach for tuberculosis diagnosis in rhinoceros

Genetic study reveals new insights into underlying causes of moderate-to-severe asthma

New discovery will improve the safety and predictability of CRISPR

Chronic rhinitis associated with hospital readmissions for asthma and COPD patients

UAlberta scientists identify biomarkers for detecting Alzheimer's disease in saliva samples

Recent findings on rare genetic disorder may help develop new treatment options

New findings throw light on natural sex selection process

Blood test helps identify distinct molecular signatures in children with cystic fibrosis

Intellectually active lifestyle confers protection against neurodegeneration in Huntington's patients

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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