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Study sheds light on how key protein allows hearing to work

Although the basic outlines of human hearing have been known for years – sensory cells in the inner ear turn sound waves into the electrical signals that the brain understands as sound – the molecular details have remained elusive.

29 Jun 2017

Novel micro-cubes can efficiently deliver hydrophobic anti-tumor drug to cancer cells

Many potent anti-cancer drugs have major drawbacks -- they fail to mix with water, which means they will have a limited solubility in blood, and they lack selectivity to cancer cells.

29 Jun 2017

Researchers suggest new strategy to identify germline mutations in men with prostate cancer

Scientists have had limited success at identifying specific inherited genes associated with prostate cancer, despite the fact that it is one of the most common non-skin cancers among men.

29 Jun 2017

Engineers take closer look at mechanical and chemical attributes of heart defect

Elastin and collagen serve as the body's building blocks. They provide tensile strength and elasticity for a number of organs, muscles and tissues. Any genetic mutation short-circuiting their function can have a devastating, and often lethal, health impact.

28 Jun 2017

Mouse brain models reveal insights into genetics of autism

While the definitive causes remain unclear, several genetic and environmental factors increase the likelihood of autism spectrum disorder, or ASD, a group of conditions covering a "spectrum" of symptoms, skills and levels of disability.

28 Jun 2017

Study finds link between gene mutation and retinitis pigmentosa in U.S. Hispanic families

Thirty-six percent of Hispanic families in the U.S. with a common form of retinitis pigmentosa got the disease because they carry a mutation of the arrestin-1 gene, according to a new study from researchers at The University of Texas Health Science Center at Houston School of Public Health.

27 Jun 2017

Elevated levels of suPAR protein combine with genetic mutation to trigger CKD in black people

Between 15 and 20 percent of black people carry a genetic mutation that puts them at risk for certain chronic kidney disease, but only about half of them develop the illness – a variance that long has puzzled researchers.

27 Jun 2017

Study sheds light on night work−cancer link

A new study has offered insights into the association between night shift work and increased cancer risk, as well as pointing towards a potential solution. For several years, scientists have thought that disruption to the body’s natural circadian rhythm is accountable for the increased cancer risk, but the mechanisms behind this have not yet been pinpointed.

27 Jun 2017

Scientists find lack of experimental evidence detailing biologic roles of leptin in metabolism

Discovered more than two decades ago, the hormone leptin has been widely hailed as the key regulator of leanness. Yet, the pivotal experiments that probe the function of this protein and unravel the precise mechanism of its action as a guardian against obesity are largely missing.

24 Jun 2017

Existing drugs could help subgroup of patients with osteosarcoma, suggest scientists

A subgroup of patients with osteosarcoma - a form of bone cancer - could be helped by an existing drug, suggest scientists from the Wellcome Trust Sanger Institute and their collaborators at University College London Cancer Institute and the Royal National Orthopaedic Hospital NHS Trust.

23 Jun 2017

Researchers identify first definitive risk genes for Tourette Syndrome

An international team that just conducted the largest study of Tourette Syndrome has identified genetic abnormalities that are the first definitive risk genes for the disorder.

23 Jun 2017

New approach finds statistical evidence that ancient gene variants contribute to autism

The way you measure things has a lot to do with the value of the results you get. If you want to know how much a blueberry weighs, don't use a bathroom scale; it isn't sensitive enough to register a meaningful result.

22 Jun 2017

Genetic factors play significant role in causing ALS, study reveals

Up to 90 percent of people with amyotrophic lateral sclerosis (ALS) report that they have no family history of the disease.

22 Jun 2017

Could a blood test predict how cancer spreads in children?

Traditionally, we use biopsies to try to predict how cancer spreads. There are a number of molecular markers that are used, but biopsy is a limited approach. Now, the current trend is to use liquid biopsy, which is basically a blood sample.

21 Jun 2017

Finnish researchers find accumulation of gene mutations in some patients with rheumatoid arthritis

Gene mutations accumulating in cells are typical of the development of cancer. Finnish researchers found that a similar accumulation of mutations occurs also in some patients with rheumatoid arthritis.

21 Jun 2017

Faulty BRCA genes and their linkage to breast and ovarian cancer: Study

A new large scale study has focussed on faulty BRCA genes and their linkage to breast and ovarian cancer. The research could help doctors counsel and advise their patients in a more definitive way in terms of treatment as well as lifestyle changes that could minimize cancer risk.

20 Jun 2017

Mutation News and Research

Study sheds light on how key protein allows hearing to work

Novel micro-cubes can efficiently deliver hydrophobic anti-tumor drug to cancer cells

Researchers suggest new strategy to identify germline mutations in men with prostate cancer

Engineers take closer look at mechanical and chemical attributes of heart defect

Mouse brain models reveal insights into genetics of autism

Study finds link between gene mutation and retinitis pigmentosa in U.S. Hispanic families

Elevated levels of suPAR protein combine with genetic mutation to trigger CKD in black people

Study sheds light on night work−cancer link

Scientists find lack of experimental evidence detailing biologic roles of leptin in metabolism

Existing drugs could help subgroup of patients with osteosarcoma, suggest scientists

Researchers identify first definitive risk genes for Tourette Syndrome

New approach finds statistical evidence that ancient gene variants contribute to autism

Genetic factors play significant role in causing ALS, study reveals

Could a blood test predict how cancer spreads in children?

Finnish researchers find accumulation of gene mutations in some patients with rheumatoid arthritis

Faulty BRCA genes and their linkage to breast and ovarian cancer: Study

Japanese scientists develop method to isolate anti-Alzheimer's compounds from plants

Genetic mutation could be cause of severe eczema, research finds

Researchers discover mutations in CARD11 gene that lead to eczema

Mutations identified that enable human transmission of avian flu

Industry Focus eBook - Cell biology (5th edition) eBook

Improving healthcare sustainability through carbon data

Managing vibration in IVF laboratories

A New Approach to Preventing Bladder Cancer Recurrence

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