Genetic News and Research

RSS

Biologists develop new way to inhibit cancer cell cleanup mechanism

The genomes of cancer cells--cells that do not obey signals to stop reproducing--are riddled with genetic mutations, causing them inadvertently to make many dysfunctional proteins.

28 Feb 2017

Study suggests new strategy for treating Alzheimer's disease

Alzheimer's disease (AD) is one of the most common form of dementia. In search for new drugs for AD, the research team, led by Professor Mi Hee Lim of Natural Science at UNIST has developed a metal-based substance that works like a pair of genetic scissors to cut out amyloid-β (Aβ), the hallmark protein of AD.

28 Feb 2017

Genetic variation may be reason for overreaction of immune system to viruses

Researchers at Cardiff University have discovered that genetic variation is the reason why some immune systems overreact to viruses.

28 Feb 2017

KRAS ‘imbalances’ that emerge over time may influence cancer treatment response

Choosing among cancer treatments increasingly involves determining whether tumor cells harbor specific, mutated "oncogenes" that drive abnormal growth and that may also be especially vulnerable or resistant to particular drugs.

28 Feb 2017

Scientists discover how genetic mutation disarms tumor-suppressing BRCA1 proteins in breast cancer

Of the more than 3 million people with breast cancer in the United Stated, about 10 percent carry an inherited mutation in their BRCA1 gene. In health, the gene is responsible for suppressing tumors. In disease, the gene goes terribly awry.

28 Feb 2017

Australian scientists discover genetic clues for degenerative eye disease that leads to blindness

Australian scientists have discovered the first evidence of genes that cause Macular Telangiectasia type 2 (MacTel), a degenerative eye disease which leads to blindness and is currently incurable and untreatable.

28 Feb 2017

Researchers discover rare deafness-dystonia syndrome in a family in Pakistan

A group of researchers from Pakistan, Europe and Singapore have identified and characterised a previously undiscovered rare deafness-dystonia syndrome in a family living in a remote region of Pakistan.

28 Feb 2017

Scientists gain new insight into early brain pathology of schizophrenia using adult skin cells

The skin cells of four adults with schizophrenia have provided an unprecedented "window" into how the disease began while they were still in the womb, according to a recent paper in Schizophrenia Research.

27 Feb 2017

New study aims to better understand major factors affecting African American cancer survivors

The Karmanos Cancer Institute and Wayne State University School of Medicine will launch the nation's largest study of African American cancer survivors to better understand disproportionately high incidence and mortality from cancer and its impact on this specific patient population.

27 Feb 2017

Scientists find link between p53 gene in African American women and breast cancer risk

Scientists at The Wistar Institute in collaboration with Roswell Park Cancer Institute found a significant association between a rare genetic variant of the p53 gene present in African American women and their risk of developing breast cancer in premenopausal age. The study was published online by the journal NPJ Breast Cancer.

27 Feb 2017

Researchers identify genetic variants that may contribute to schizophrenia

New research has identified sections of DNA associated with altered regulation of gene expression underlying schizophrenia.

27 Feb 2017

New research reveals complex role of ‘master gene’ that regulates physical differences between sexes

Physical differences between males and females in species are common, but there remains much to learn about the genetic mechanisms behind these differences.

27 Feb 2017

New York school students help Cornell scientists to monitor invasive species in local waterways

Invasive aquatic species like round goby, Asian carp, and sea lamprey are a growing problem in New York State. Their presence impacts water quality, food supply, recreation and tourism, as well as human and animal health. Early detection is a critical first step in monitoring a species' spread and managing responses.

27 Feb 2017

Study finding suggests new ways in which genetic mutations may cause brain disorders

Many kids say they love their mom and dad equally, but there are times when even the best prefers one parent over the other. The same can be said for how the body's cells treat our DNA instructions. It has long been thought that each copy - one inherited from mom and one from dad - is treated the same. A new study from scientists at the University of Utah School of Medicine shows that it is not uncommon for cells in the brain to preferentially activate one copy over the other.

25 Feb 2017

Alzheimer's drug prescribed off-label could accelerate cognitive decline for some patients

Donepezil, a medication that is approved to treat people with Alzheimer's disease, should not be prescribed for people with mild cognitive impairment without a genetic test.

24 Feb 2017

Scientists unravel mechanism of rare, early phenomenon that can affect human development

The genetic material of an organism encodes the instructions that guide its development. These codes are not written in stone; they can change or mutate any time during the life of the organism.

24 Feb 2017

Pitt study sheds light on shared roots of schizophrenia and rheumatoid arthritis

An in-depth computational analysis of genetic variants implicated in both schizophrenia and rheumatoid arthritis by researchers at the University of Pittsburgh points to eight genes that may explain why susceptibility to one of the disorders could place individuals at lower risk for the other, according to the results of a study published today in the journal npj Schizophrenia.

24 Feb 2017

New humanized model enables better characterization of Alzheimer's pathology

Cells behave differently when removed from their environments, just as cells that develop in cultures do not behave like cells in living creatures.

24 Feb 2017

Newly discovered gene variants increase risk of anxiety disorders

Several newly discovered variants of a gene increase the risk of developing anxiety disorders. A research team aims to derive new therapies from this finding which are better tailored to the individual patients.

24 Feb 2017

Decoding the Exposome Through Breath Biomarkers

The human exposome is probably best defined as “everything that is not the genome.” This is a bit tongue in cheek, but basically, the exposome is comprised of all of the chemicals in your body from the environment, food, consumer products, their metabolites, the endogenous “housekeeping” chemicals, the cellular wastes from energy production, as well as all of the messenger compounds and life supporting chemicals.

From Pittcon 24 Feb 2017

Genetic News and Research

Biologists develop new way to inhibit cancer cell cleanup mechanism

Study suggests new strategy for treating Alzheimer's disease

Genetic variation may be reason for overreaction of immune system to viruses

KRAS ‘imbalances’ that emerge over time may influence cancer treatment response

Scientists discover how genetic mutation disarms tumor-suppressing BRCA1 proteins in breast cancer

Australian scientists discover genetic clues for degenerative eye disease that leads to blindness

Researchers discover rare deafness-dystonia syndrome in a family in Pakistan

Scientists gain new insight into early brain pathology of schizophrenia using adult skin cells

New study aims to better understand major factors affecting African American cancer survivors

Scientists find link between p53 gene in African American women and breast cancer risk

Researchers identify genetic variants that may contribute to schizophrenia

New research reveals complex role of ‘master gene’ that regulates physical differences between sexes

New York school students help Cornell scientists to monitor invasive species in local waterways

Study finding suggests new ways in which genetic mutations may cause brain disorders

Alzheimer's drug prescribed off-label could accelerate cognitive decline for some patients

Scientists unravel mechanism of rare, early phenomenon that can affect human development

Pitt study sheds light on shared roots of schizophrenia and rheumatoid arthritis

New humanized model enables better characterization of Alzheimer's pathology

Newly discovered gene variants increase risk of anxiety disorders

Decoding the Exposome Through Breath Biomarkers

Sequencing & Genomics: Elevating Science and Healthcare eBook

Bringing real-time analytics to downstream bioprocess monitoring

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

Latest News