Gene News and Research

Latest Gene News and Research

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

Researchers identify link between neuronal proteins and frontotemporal lobar degeneration

Frontotemporal lobar degeneration is a type of dementia characterized by personality changes, language dysfunction, and abnormal behavior. It has an earlier onset than Alzheimer's disease, and is associated with a buildup of the tau protein in affected nerve cells (neurons).

13 Feb 2017

Scientists discover 'Achilles' heel' of tumor-suppressing protein that drives prostate cancer metastasis

Researchers at Cold Spring Harbor Laboratory have discovered that a protein called Importin-11 protects the anti-cancer protein PTEN from destruction by transporting it into the cell nucleus. A study they publish today in The Journal of Cell Biology suggests that the loss of Importin-11 may destabilize PTEN, leading to the development of lung, prostate, and other cancers.

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

Reprogramming liver cells to become pancreatic cells may help diabetic patients

It is now possible to reprogram cells from the liver into the precursor cells that give rise to the pancreas by altering the activity of a single gene.

13 Feb 2017

LMU study shows crucial role of microRNAs in protecting precursors of neurons

Programmed cell death is an integral part of embryonic development. Exploring the regulation of the process, Ludwig-Maximilians-Universitaet in Munich researchers have shown that so-called microRNAs protect the precursors of neurons from 'precocious' elimination.

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

New study aims to better understand long-term neurologic effects of mild TBI

An ambitious U.S. federally funded study is enrolling at least 1,100 service members and veterans who fought in Iraq or Afghanistan to learn more about mild traumatic brain injury (TBI) and how it can be best evaluated, and perhaps prevented and treated.

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

New kit for DNA library preparation released by PCR company

Bioline, The PCR Company, a whollyowned subsidiary of Meridian Bioscience, Inc., announced the expansion of the JetSeq™ DNA Library Preparation portfolio for Next Generation Sequencing (NGS) sample preparation.

9 Feb 2017

Gene News and Research

Latest Gene 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

Researchers identify link between neuronal proteins and frontotemporal lobar degeneration

Scientists discover 'Achilles' heel' of tumor-suppressing protein that drives prostate cancer metastasis

Scientists identify new biomarkers that could guide bowel cancer treatment

Reprogramming liver cells to become pancreatic cells may help diabetic patients

LMU study shows crucial role of microRNAs in protecting precursors of neurons

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

New study aims to better understand long-term neurologic effects of mild TBI

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

New kit for DNA library preparation released by PCR company

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