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New clinical guidelines call for psychosocial support for complex ADHD in children, adolescents

New clinical guidelines call strongly for providing psychosocial supports for children and adolescents with complex attention-deficit/hyperactivity disorder (ADHD). Developed by the Society for Developmental and Behavioral Pediatrics (SDBP), the guideline provides a framework for diagnosing and treating complex ADHD in these age groups.

30 Jan 2020

Study may help develop ibrutinib-based combination therapies for blood cancer

Chronic lymphocytic leukemia (CLL) is the most common form of blood cancer (leukemia) in the Western world, affecting approximately 1.2% of all cancer patients.

30 Jan 2020

Study: 25% of pathogenic bacteria can spread antibiotic resistance directly to peers

Biomedical engineers at Duke University have demonstrated that at least 25 percent of antibiotic-resistant pathogenic bacteria found in clinical settings are capable of spreading their resistance directly to other bacteria.

29 Jan 2020

High intake of dietary flavonols tied to lower risk of Alzheimer's dementia

People who eat or drink more foods with the antioxidant flavonol, which is found in nearly all fruits and vegetables as well as tea, may be less likely to develop Alzheimer's dementia years later, according to a study published in the January 29, 2020, online issue of Neurology, the medical journal of the American Academy of Neurology.

29 Jan 2020

Study shows protective cells reduce lung cancer risk in ex-smokers

A new study could explain how lung cancer risk is reduced by quitting smoking. Published in the journal Nature in January 2020, the study shows that ex-smokers have a greater number of lung cells that have healthy genes compared to current smokers. Healthy genes are less likely to transform into cancerous cells.

29 Jan 2020

Japanese researchers identify genetic variations related to specific dietary habits

Researchers at the RIKEN Center for Integrative Medical Sciences in Japan and colleagues at Osaka University have found genetic variations in humans related to specific dietary habits.

29 Jan 2020

Mount Sinai cardiologists share tips to prevent and lower risk of cardiac events

Heart disease is the leading cause of death among both men and women in the United States, but according to the American Heart Association, it is preventable 80 percent of the time.

29 Jan 2020

New strategy using organoids to study childhood brain tumors

A new study reports the creation of in vitro models of brain tumors in children using organoids derived from stem cells, which will help to screen new drugs for efficacy and thus improve the rate of drug development. The study, titled 'Modeling medulloblastoma in vivo and with human cerebellar organoids,' is published in the journal Nature Communications.

29 Jan 2020

Research uncovers disease-aggravating mutation in mouse model of GRACILE syndrome

The new mitochondrial DNA (mtDNA) variant drastically speeds up the disease progression in a mouse model of GRACILE syndrome. This discovery provides a new tool for studies of mitochondrial diseases.

29 Jan 2020

Study uncovers molecular mechanism that triggers a rare type of muscular dystrophy

A study led by the IBB-UAB has identified the molecular mechanism through which a protein, when carrying genetic mutations associated with a rare disease known as limb-girdle muscular dystrophy, type 1G, accelerates its tendency to form amyloid fibrils and finally triggers the appearance of the disease.

29 Jan 2020

Researchers develop new strategy to study childhood brain tumors

Researchers are at work to find effective treatments to help young patients with brain tumors. Hundreds of brain organoids have been developed in the laboratories of the University of Trento to understand the genetic mechanisms responsible for these hard to treat diseases.

29 Jan 2020

Researchers create new brain cancer model using genetically engineered pluripotent stem cells

Using genetically engineered human pluripotent stem cells, University of California San Diego School of Medicine researchers created a new type of cancer model to study in vivo how glioblastoma, the most common and aggressive form of brain cancer, develops and changes over time.

29 Jan 2020

CDKL5 Deficiency Disorder designated with new disease code in WHO medical classification list

The rare genetic disease CDKL5 Deficiency Disorder has been designated with a new disease code in the International Classification of Diseases, the medical classification list from the World Health Organization.

28 Jan 2020

Widespread screening for islet autoantibodies reduces the occurrence of diabetic ketoacidosis

JDRF, the leading global organization funding type 1 diabetes research, today announced new research that found widespread screening for islet autoantibodies reduced the occurrence of life-threatening diabetic ketoacidosis among children with pre-symptomatic T1D.

28 Jan 2020

Concordia study investigates the link between cognition and hearing or vision loss

There is a long-established and widely recognized link between declines in sensory acuity -- particularly hearing and vision -- and cognition. Data from the Canadian Longitudinal Study on Aging, involving tens of thousands of participants across the country aged 45 to 85, backs this up.

28 Jan 2020

Coronavirus spreads - Australian breakthrough

Novel coronavirus, temporarily named “2019-nCoV”, has affected over 4,600 persons across the world and is spreading at a rapid pace say experts. The World Health Organization and other health organizations have stepped up vigilance to detect and isolate the infection to contain outbreaks.

28 Jan 2020

Successful gene therapy trial in patients with X-linked Chronic Septic Granulomatosis

American and British teams led by Drs Kohn (University of California, Los Angeles), Malech (NIH), Williams (Boston Children's) and Trasher (Great Ormond Street Institute of Child Health) published yesterday in Nature Medicine the conclusive results of a gene therapy trial conducted in the United States and Great Britain in 9 patients with X-linked Chronic Septic Granulomatosis (X-CGD), a rare and severe immune dysfunction. Six of them are free of treatment for complications generated by the disease.

28 Jan 2020

Genetic News and Research

New clinical guidelines call for psychosocial support for complex ADHD in children, adolescents

Study may help develop ibrutinib-based combination therapies for blood cancer

Study: 25% of pathogenic bacteria can spread antibiotic resistance directly to peers

High intake of dietary flavonols tied to lower risk of Alzheimer's dementia

Study shows protective cells reduce lung cancer risk in ex-smokers

Japanese researchers identify genetic variations related to specific dietary habits

Mount Sinai cardiologists share tips to prevent and lower risk of cardiac events

New strategy using organoids to study childhood brain tumors

Research uncovers disease-aggravating mutation in mouse model of GRACILE syndrome

Study uncovers molecular mechanism that triggers a rare type of muscular dystrophy

Researchers develop new strategy to study childhood brain tumors

Researchers create new brain cancer model using genetically engineered pluripotent stem cells

CDKL5 Deficiency Disorder designated with new disease code in WHO medical classification list

Widespread screening for islet autoantibodies reduces the occurrence of diabetic ketoacidosis

Concordia study investigates the link between cognition and hearing or vision loss

Coronavirus spreads - Australian breakthrough

Successful gene therapy trial in patients with X-linked Chronic Septic Granulomatosis

Study on axolotl's ability to regenerate might help find ways to restore damaged tissue in humans

New study of genes in Asian populations may help better understand, treat genetic diseases

Low-protein diet throughout pregnancy and lactation may increase risk of liver damage

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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