Mutation News and Research

RSS

New drug shows promising results for treating spinal muscular atrophy

A drug developed by an Iowa State University biomedical researcher as a potential treatment for spinal muscular atrophy showed promising results in a recently published study.

26 Aug 2017

Researchers aim to develop dynamic therapeutics for combating antiviral drug resistance

Antiviral drug resistance has long been a problem in modern society. As viruses evolve, they develop resistance to antiviral drugs, which become less effective at treating diseases such as influenza.

24 Aug 2017

Researchers uncover how mutations in single gene lead to rare kidney and liver disease

In a joint international study, researchers from Osaka University have partnered with research groups from the United States and Spain to uncover how mutations in a single gene called PKHD1 lead to symptoms associated with a rare kidney and liver disease, ARPKD (autosomal recessive polycystic kidney disease).

24 Aug 2017

Researchers describe mechanism linking HPV infection and cancer

Infection with human papillomavirus (HPV) is the primary cause of cervical cancer and a subset of head and neck cancers worldwide.

23 Aug 2017

New clinical trial to test cancer drug in patients with advanced solid tumors

A clinical trial to test a new cancer drug in patients with advanced solid tumors, launches in four centers across the UK today (Wednesday), through Cancer Research UK's Center for Drug Development.

23 Aug 2017

Scientists identify genetic variation that promotes longevity in men

Researchers have found a mutation in the gene for the growth hormone receptor that promotes longevity, increasing men's lifespan by an average of 10 years.

22 Aug 2017

Researchers develop quick and easy-to-use test for detecting rare immunodeficiency

Researchers at the University of Basel have developed a test to quickly and reliably diagnose a rare and severe immune defect, hepatic veno-occlusive disease with immunodeficiency. They reported on their findings in the Journal of Clinical Immunology.

22 Aug 2017

Women with a medical history of breast or ovarian cancer often fail to test for inherited genetic changes

A new study conducted by the UCLA Fielding School of Public Health, states that among nearly 4 million women in the United States who possess a medical history of ovarian cancer or breast cancer, 1.5 million have an increased risk of bearing some kinds of genetic mutations, which might increase the probability of causing additional cancers in the future.

21 Aug 2017

Study: More than 80% of women at risk for breast, ovarian cancer have not taken simple genetic test

Of the nearly 4 million women in the United States who have had either breast cancer or ovarian cancer, at least 1.5 million have a high risk of carrying certain types of genetic mutations that could increase their risk for additional cancers in the future.

21 Aug 2017

Study provides insight into development of red blood cells

Every cell in the body, whether skin or muscle or brain, starts out as a generic cell that acquires its unique characteristics after undergoing a process of specialization. Nowhere is this process more dramatic than it is in red blood cells.

18 Aug 2017

Eggshell-like mineral layer on avian flu viruses may be cause for human infections

Avian flu can be transmitted from birds to humans; transmission among humans, however, is limited. The reason may be an eggshell-like mineral layer that the virus acquires due to the high calcium concentration in the intestines of birds.

18 Aug 2017

New research suggests cell immortalization as more complicated process than originally thought

A mutation that helps make cells immortal is critical to the development of a tumor, but new research at the University of California, Berkeley suggests that becoming immortal is a more complicated process than originally thought.

18 Aug 2017

Impaired DNA replication may lead to trans-generational inheritance of epigenetic changes

Scientists reveal that a fault in the process that copies DNA during cell division can cause epigenetic changes that may be inherited for up-to five generations.

17 Aug 2017

Scientists identify basic biological mechanism that kills neurons in ALS

A team led by scientists at St. Jude Children's Research Hospital and Mayo Clinic has identified a basic biological mechanism that kills neurons in amyotrophic lateral sclerosis (ALS) and in a related genetic disorder, frontotemporal dementia (FTD), found in some ALS patients.

16 Aug 2017

Lab-grown miniature blood vessels mimic rare Hutchinson-Gilford Progeria Syndrome

Biomedical engineers have grown miniature human blood vessels that exhibit many of the symptoms and drug reactions associated with Hutchinson-Gilford Progeria Syndrome -- an extremely rare genetic disease that causes symptoms resembling accelerated aging in children.

16 Aug 2017

Mayo Clinic researchers discover new cause of treatment resistance in prostate cancer

Mayo Clinic researchers have identified a new cause of treatment resistance in prostate cancer. Their discovery also suggests ways to improve prostate cancer therapy. The findings appear in Nature Medicine.

14 Aug 2017

Counteracting premature aging

Aging is the continuing process of such stress exposures, and with advancing age (normal aging), we must carry lots of senescent cells within our bodies. Senescent cells also often provide some ‘bad influences’ to surrounding healthy cells; such as chronic inflammation and tumorigenesis

14 Aug 2017

Mutation News and Research

New drug shows promising results for treating spinal muscular atrophy

Researchers aim to develop dynamic therapeutics for combating antiviral drug resistance

Researchers uncover how mutations in single gene lead to rare kidney and liver disease

Researchers describe mechanism linking HPV infection and cancer

New clinical trial to test cancer drug in patients with advanced solid tumors

Scientists identify genetic variation that promotes longevity in men

Researchers develop quick and easy-to-use test for detecting rare immunodeficiency

Women with a medical history of breast or ovarian cancer often fail to test for inherited genetic changes

Study: More than 80% of women at risk for breast, ovarian cancer have not taken simple genetic test

Study provides insight into development of red blood cells

Eggshell-like mineral layer on avian flu viruses may be cause for human infections

New research suggests cell immortalization as more complicated process than originally thought

Impaired DNA replication may lead to trans-generational inheritance of epigenetic changes

Scientists identify basic biological mechanism that kills neurons in ALS

Lab-grown miniature blood vessels mimic rare Hutchinson-Gilford Progeria Syndrome

Mayo Clinic researchers discover new cause of treatment resistance in prostate cancer

Counteracting premature aging

Highly sensitive blood test holds potential for quickly tracking cancer growth and spread

Newly discovered immunodeficiency can make people seriously ill from chickenpox virus

Mount Sinai experts offer tips on knowing risks and detecting symptoms of ovarian cancer

Improving healthcare sustainability through carbon data

Managing vibration in IVF laboratories

A New Approach to Preventing Bladder Cancer Recurrence

Latest News