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Research clarifies regulatory impacts of ubiquitin-proteasome system on DNA damage repair

An international research team has clarified the regulatory mechanism of the ubiquitin-proteasome system (*1) in recognizing and repairing DNA that has been damaged by ultraviolet (UV) light.

9 Dec 2020

New method could help resolve unwanted genetic changes associated with CRISPR-Cas9 technique

A research team has used a novel method that could help resolve the issue of unnecessary genetic changes encountered in the CRISPR-Cas9 technique.

7 Dec 2020

Scientists reveal health benefits of clonal hematopoiesis in allogeneic transplants

Clonal hematopoiesis (CH) is a recently identified condition in which mutations associated with blood cancers are detected in the blood of some healthy, usually older, individuals who don't have cancer. People with CH, while asymptomatic, have an elevated risk of developing blood cancers and other negative health outcomes, including heart attacks and strokes.

7 Dec 2020

Research reveals fundamental insights into the causes of severe birth defects

Research by Kai Jiao, M.D., Ph.D., and colleagues at the University of Alabama at Birmingham and in Germany has yielded fundamental insights into the causes of severe birth defects known as CHARGE syndrome cases. These congenital birth defects include severe and life-threatening heart malformations.

3 Dec 2020

A Gene Mutation That Protects Against Disease

Researchers think they have found a fountain of youth, and it is unique to a few French Canadian families.

3 Dec 2020

Scientists unlock new genetic variation in wheat and barley

An international research collaboration, including scientists from the University of Adelaide's Waite Research Institute, has unlocked new genetic variation in wheat and barley - a major boost for the global effort in breeding higher-yielding wheat and barley varieties.

27 Nov 2020

Researchers identify new gene involved in neurodevelopmental disorders

Researchers and physicians constantly search for novel disease genes that can allow them to figure out why medical problems are not diagnosed in patients.

24 Nov 2020

Genetic modification in the ‘coat’ of fatal brain virus may allow it to escape antibodies

A genetic modification in the 'coat' of a brain infection-causing virus may allow it to escape antibodies, according to Penn State College of Medicine researchers.

23 Nov 2020

Researchers identify rare genetic marker that protects against cardiovascular disease

According to researchers from McMaster University and the Montreal Clinical Research Institute, they have identified a “fountain of youth” in a rare genetic marker that is unique to a few French-Canadian families.

20 Nov 2020

Vibrational motions of spike proteins correlate with infectivity, lethality of SARS-CoV-2 virus

When someone struggles to open a lock with a key that doesn't quite seem to work, sometimes jiggling the key a bit will help. Now, new research from MIT suggests that coronaviruses, including the one that causes Covid-19, may use a similar method to trick cells into letting the viruses inside.

From Massachusetts Institute of Technology (MIT) 20 Nov 2020

Study identifies molecular mutation more common in African Americans with late-onset Alzheimer’s

Scientists have identified a molecular mechanism that leads to a “traffic jam” of enzymes, resulting in the accumulation of amyloid-beta.

19 Nov 2020

Somatic mutation acts as natural gene therapy in patients with GATA2 deficiency

Researchers affiliated with the Center for Cell-Based Therapy (CTC) in Ribeirão Preto, Brazil, have identified for the first time a non-hereditary mutation in blood cells from a patient with GATA2 deficiency, a rare autosomal disease caused by inherited mutations in the gene that encodes GATA-binding protein 2 (GATA2).

18 Nov 2020

Study: 95.5% of current entries in GISAID lack relevant COVID-19 patient information

A new study led by Australia's national science agency CSIRO, has found 95.5 per cent of current entries in GISAID, the world's largest novel coronavirus genome database, do not contain relevant patient information -- a critical piece of the puzzle to understand the virus and how it is evolving.

17 Nov 2020

Mutation News and Research

Research clarifies regulatory impacts of ubiquitin-proteasome system on DNA damage repair

New method could help resolve unwanted genetic changes associated with CRISPR-Cas9 technique

Scientists reveal health benefits of clonal hematopoiesis in allogeneic transplants

Research reveals fundamental insights into the causes of severe birth defects

A Gene Mutation That Protects Against Disease

Scientists unlock new genetic variation in wheat and barley

Researchers identify new gene involved in neurodevelopmental disorders

Genetic modification in the ‘coat’ of fatal brain virus may allow it to escape antibodies

Researchers identify rare genetic marker that protects against cardiovascular disease

Vibrational motions of spike proteins correlate with infectivity, lethality of SARS-CoV-2 virus

Study identifies molecular mutation more common in African Americans with late-onset Alzheimer’s

Somatic mutation acts as natural gene therapy in patients with GATA2 deficiency

Study: 95.5% of current entries in GISAID lack relevant COVID-19 patient information

Researchers identify potential genetic target for treating painful, invasive form of endometriosis

Researchers discover new 'hidden' gene in SARS-CoV-2

Mutations in SARS-CoV-2 spike protein may improve monoclonal antibody resistance

Unrelated mutations can lead to false positive results in men with advanced prostate cancer

Study provides key insight to better understand the development of Type 2 diabetes

Developing a new method to reduce antibiotic resistance in waterways

Study shows 1 in 8 cancer patients had inherited cancer-related gene mutation

Driving Support for Pharmaceutical Testing Through Continuous Innovation

From Memory to Metaplasticity: Unraveling the Brain's Secrets

Revolutionizing Mass Spectrometry: A Deep Dive into Plasmion’s SICRIT® Technology

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