Gene News and Research

Latest Gene News and Research

Researchers identify genetic switch that may be potential target for Alzheimer's disease

A team at the MRC Clinical Sciences Centre, based at Imperial College London, has found an important part of the machinery that switches on a gene known to protect against Alzheimer's Disease.

20 Sep 2016

Mice study explains why antidepressants don't work in some patients

SSRI antidepressants (Selective Serotonin Reuptake Inhibitors, the best known being Prozactm) are amongst the most commonly taken medicines.

20 Sep 2016

Scientists begin research work at new £650 million Francis Crick Institute building

The first scientists have moved into the new £650 million Francis Crick Institute building in London and are starting work in their purpose-built labs.

20 Sep 2016

CBN neuroscientists awarded NIMH grant to develop novel genome engineering research tools

The Center for Behavioral Neuroscience at Georgia State University has received a two-year, exploratory grant from the National Institute of Mental Health to develop transformative genome engineering research tools.

20 Sep 2016

Researchers discover gene variants linked to thoracic aortic dissections

On Super Bowl Sunday, Tina Wilkins was relaxing in her recliner while she chatted on the phone with her mother and waited for the game to begin. She had recently lost 63 pounds and was in better shape than she had been in years.

20 Sep 2016

Sarepta Therapeutics wins accelerated approval from FDA for Duchenne muscular dystrophy drug

The U.S. Food and Drug Administration today approved Exondys 51 (eteplirsen) injection, the first drug approved to treat patients with Duchenne muscular dystrophy (DMD).

19 Sep 2016

Researchers use computer modelling to identify mechanism behind aggressive brain tumours

Researchers at Uppsala University have used computer modelling to study how brain tumours arise.

19 Sep 2016

Researchers identify mutant traits in mouse for many human disease genes

About one-third of all genes in the mammalian genome are essential for life. An international, multi-institutional research collaboration identified, for the first time, mutant traits in the mouse for 52 human disease genes, which significantly contributes to the understanding of the genetic bases for some human diseases, including cardiovascular defects, spina bifida, and metabolic disorders, among many others. The study was published this week in Nature.

19 Sep 2016

Memory of heart attack can be stored in genes through epigenetic changes, study shows

Both heredity and environmental factors influence our risk of cardiovascular disease. A new study, by researches at Uppsala University, shows now that the memory of a heart attack can be stored in our genes through epigenetic changes.

19 Sep 2016

Researchers find switch that helps restore damaged axons

Researchers at the University of Wisconsin-Madison have found a switch that redirects helper cells in the peripheral nervous system into "repair" mode, a form that restores damaged axons.

16 Sep 2016

Researchers explain novel approach for analyzing diverse immune responses

The response to infection is highly variable from one individual to another. The Milieu Intérieur consortium, coordinated by Prof. Matthew Albert (Immunobiology of dendritic cells Unit, Institut Pasteur / Inserm) and Dr Lluis Quintana-Murci (Human Evolutionary Genetics Unit, Institut Pasteur / CNRS) seek to establish the parameters that characterize the immune system of healthy individuals and its natural variability.

16 Sep 2016

Chromatrap reports benefits of using ChIP-seq kit for histone methylation applications

Chromatrap reports on the advantages of using its Chromatin Immunoprecipitation Sequencing (ChIP-seq) assay kits for histone methylation applications.

From Chromatrap® - Porvair Sciences Ltd 16 Sep 2016

Research findings point to potential new targeted therapy for SMA

For the first time, scientists found that in spinal muscular atrophy (SMA), the affected nerve cells that control muscle movement, or motor neurons, have defects in their mitochondria, which generate energy used by the cell.

15 Sep 2016

Columbia researchers find way to reawaken potent cancer-fighting molecule in tumor cells

A potent cancer-fighting molecule in our cells can be reawakened by reducing levels of a protein - called SET - that's often found in excess in cancer cells, a new study from Columbia University's Herbert Irving Comprehensive Cancer Center has found.

15 Sep 2016

Mood stabilizers may decrease negative symptoms in psychiatric patients with specific genotype

A drug prescribed to many patients with schizophrenia or bipolar disorder may decrease negative symptoms for people with a certain variant of the COMT gene, suggests a new study from researchers at Columbia University Medical Center.

14 Sep 2016

Pathologists to collaborate on promise, challenges of immunotherapy at CAP16

At the College of American Pathologists annual meeting this month, more than 1,300 pathologists will collaborate on the promise, challenges, and questions surrounding immunotherapy—the subject of the opening Scientific Plenary at CAP16 - The Pathologists' Meeting in Las Vegas on Sept. 25.

14 Sep 2016

Research findings may pave way for innovative treatments of multiple sclerosis

Researchers at the Research Center for Immunotherapy and the Focus Program Translational Neurosciences of Johannes Gutenberg University Mainz have identified a new mechanism that is involved in the development of autoimmune diseases.

14 Sep 2016

Discovery of immune antibody could lead to development of improved influenza vaccines

Dana-Farber Cancer Institute investigators report they have discovered a type of immune antibody that can rapidly evolve to neutralize a wide array of influenza virus strains - including those the body hasn't yet encountered.

14 Sep 2016

BET inhibitors could be powerful new therapeutic strategy for ovarian cancer

Few effective treatments have been approved to treat ovarian cancer, the deadliest of all cancers affecting the female reproductive system.

14 Sep 2016

New study identifies potential therapeutic option for treatment of Huntington's disease

A new scientific study reveals one way to stop proteins from triggering an energy failure inside nerve cells during Huntington's disease. Huntington's disease is an inherited genetic disorder caused by mutations in the gene that encodes huntingtin protein.

14 Sep 2016

Gene News and Research

Latest Gene News and Research

Researchers identify genetic switch that may be potential target for Alzheimer's disease

Mice study explains why antidepressants don't work in some patients

Scientists begin research work at new £650 million Francis Crick Institute building

CBN neuroscientists awarded NIMH grant to develop novel genome engineering research tools

Researchers discover gene variants linked to thoracic aortic dissections

Sarepta Therapeutics wins accelerated approval from FDA for Duchenne muscular dystrophy drug

Researchers use computer modelling to identify mechanism behind aggressive brain tumours

Researchers identify mutant traits in mouse for many human disease genes

Memory of heart attack can be stored in genes through epigenetic changes, study shows

Researchers find switch that helps restore damaged axons

Researchers explain novel approach for analyzing diverse immune responses

Chromatrap reports benefits of using ChIP-seq kit for histone methylation applications

Research findings point to potential new targeted therapy for SMA

Columbia researchers find way to reawaken potent cancer-fighting molecule in tumor cells

Mood stabilizers may decrease negative symptoms in psychiatric patients with specific genotype

Pathologists to collaborate on promise, challenges of immunotherapy at CAP16

Research findings may pave way for innovative treatments of multiple sclerosis

Discovery of immune antibody could lead to development of improved influenza vaccines

BET inhibitors could be powerful new therapeutic strategy for ovarian cancer

New study identifies potential therapeutic option for treatment of Huntington's disease

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