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Study shows how errors in specific gene can cause growth defects linked to dwarfism

A new study shows how errors in a specific gene can cause growth defects associated with a rare type of dwarfism.

13 Feb 2017

Research shows how protein component of Epstein-Barr virus promotes development of cancer

After an infection with the Epstein-Barr virus (EBV), the virus persists in the body throughout a person's lifetime, usually without causing any symptoms.

13 Feb 2017

Scientists aim to create data mining tools to identify personalized treatment options for cancer

In the laboratories of Institute of Molecular Medicine Finland, drug testing is done ex vivo. That is, various leukemia drugs are tested with patient samples instead of the patients themselves. This enables the researchers to test different drug combinations efficiently and without burdening the patient.

13 Feb 2017

Scientists identify new biomarkers that could guide bowel cancer treatment

Colorectal carcinomas arise in different forms, so all treatments do not work for all patients. OncoTrack, a public-private consortium supported by the Innovative Medicines Initiative Joint Undertaking, has conducted one of Europe's largest collaborative academic-industry research projects to develop and assess novel approaches for identification of new markers for colon cancer.

13 Feb 2017

Cole-Parmer introduces Arcis DNA Prep Kit for fast and convenient DNA or RNA extraction

Cole-Parmer, a leading manufacturer of laboratory equipment, announced today that it has launched the DNA Prep Kit by Arcis Biotechnology for fast and convenient DNA or RNA extraction.

13 Feb 2017

New drug discovered in zebrafish model of pediatric epilepsy shows promising results in clinical study

"Bench-to-bedside" describes research that has progressed from basic science in animal models that has led to therapies used in patients.

13 Feb 2017

USU researchers develop new primer that improves studies into arsenic contamination

A team of Utah State University College of Engineering researchers developed a new primer - a tool used in DNA amplification - that simplifies the process of identifying bacteria found in soil and groundwater samples.

13 Feb 2017

Specific genetic errors that trigger congenital heart disease can be reproduced in common fruit fly

Specific genetic errors that trigger congenital heart disease (CHD) in humans can be reproduced reliably in Drosophila melanogaster - the common fruit fly - an initial step toward personalized therapies for patients in the future.

11 Feb 2017

VIB-KU Leuven researchers identify underlying mechanism in early onset Parkinson's disease

A team of researchers led by Patrik Verstreken have identified an underlying mechanism in early onset Parkinson's.

10 Feb 2017

Research suggests new type of congenital muscular dystrophy

A newly discovered mutation in the INPP5K gene, which leads to short stature, muscle weakness, intellectual disability, and cataracts, suggests a new type of congenital muscular dystrophy.

10 Feb 2017

Expert highlights importance of genetic counseling for cancer patients

"Every cancer diagnosis should come with a referral to genetic counseling," says cancer expert Dr. Antonio Giordano, President of the Sbarro Health Research Organization at Temple University.

9 Feb 2017

MSK researchers publish new review that focuses on genome-driven oncology

Researchers from Memorial Sloan Kettering Cancer Center today published a seminal review of the rapidly evolving field of precision oncology, which allows doctors to recommend therapies based on a genetic understanding of a person's cancer.

9 Feb 2017

Genetic profiling of blood cells can predict response to stem cell transplant for patients with MDS

A single blood test and basic information about a patient's medical status can indicate which patients with myelodysplastic syndrome (MDS) are likely to benefit from a stem cell transplant, and the intensity of pre-transplant chemotherapy and/or radiation therapy that is likely to produce the best results, according to new research by scientists at Dana-Farber Cancer Institute and Brigham and Women's Hospital.

9 Feb 2017

FDA approves new treatment for wide range of patients with Duchenne muscular dystrophy

The U.S. Food and Drug Administration today approved Emflaza (deflazacort) tablets and oral suspension to treat patients age 5 years and older with Duchenne muscular dystrophy (DMD), a rare genetic disorder that causes progressive muscle deterioration and weakness.

9 Feb 2017

Scientists identify vulnerabilities of highly aggressive pancreatic cancer cells

Researchers have identified a gatekeeper protein that prevents pancreatic cancer cells from transitioning into a particularly aggressive cell type and also found therapies capable of thwarting those cells when the gatekeeper is depleted.

9 Feb 2017

Study discovers new form of congenital muscular dystrophy caused by faulty INPP5K gene

A new form of congenital muscular dystrophy has been discovered which is caused by mutations in a previously un-linked gene.

9 Feb 2017

Scientists identify gene variants that predispose children to developing Kawasaki disease

Kawasaki disease (KD) is the most common acquired heart disease in children. Untreated, roughly one-quarter of children with KD develop coronary artery aneurysms -- balloon-like bulges of heart vessels -- that may ultimately result in heart attacks, congestive heart failure or sudden death.

9 Feb 2017

Study suggests new ways to treat neurological symptoms linked to tuberous sclerosis complex

Boston Children's Hospital researchers have uncovered a new molecular pathway that inhibits the myelination of neurons in the brains of patients with the rare genetic disorder tuberous sclerosis complex.

9 Feb 2017

Study explores links between genetic susceptibility and heterogeneous phenotypes of lymphedema

Each year, about 1.38 million women worldwide are diagnosed with breast cancer. Advances in diagnosis and treatment have facilitated a 90-percent, five-year survival rate, among those treated.

9 Feb 2017

Genetic variant encoded in NCF1 linked to increased risk for autoimmune diseases, study shows

Investigators at the Medical University of South Carolina report pre-clinical research showing that a genetic variant encoded in neutrophil cystolic factor 1 (NCF1) is associated with increased risk for autoimmune diseases, including systemic lupus erythematosus (SLE), rheumatoid arthritis, and Sjögren's syndrome, in the January 2017 issue of Nature Genetics.

8 Feb 2017

Genetic News and Research

Study shows how errors in specific gene can cause growth defects linked to dwarfism

Research shows how protein component of Epstein-Barr virus promotes development of cancer

Scientists aim to create data mining tools to identify personalized treatment options for cancer

Scientists identify new biomarkers that could guide bowel cancer treatment

Cole-Parmer introduces Arcis DNA Prep Kit for fast and convenient DNA or RNA extraction

New drug discovered in zebrafish model of pediatric epilepsy shows promising results in clinical study

USU researchers develop new primer that improves studies into arsenic contamination

Specific genetic errors that trigger congenital heart disease can be reproduced in common fruit fly

VIB-KU Leuven researchers identify underlying mechanism in early onset Parkinson's disease

Research suggests new type of congenital muscular dystrophy

Expert highlights importance of genetic counseling for cancer patients

MSK researchers publish new review that focuses on genome-driven oncology

Genetic profiling of blood cells can predict response to stem cell transplant for patients with MDS

FDA approves new treatment for wide range of patients with Duchenne muscular dystrophy

Scientists identify vulnerabilities of highly aggressive pancreatic cancer cells

Study discovers new form of congenital muscular dystrophy caused by faulty INPP5K gene

Scientists identify gene variants that predispose children to developing Kawasaki disease

Study suggests new ways to treat neurological symptoms linked to tuberous sclerosis complex

Study explores links between genetic susceptibility and heterogeneous phenotypes of lymphedema

Genetic variant encoded in NCF1 linked to increased risk for autoimmune diseases, study shows

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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