Genetics News and Research

Latest Genetics News and Research

Single amino acid change in TKTL1 protein underlies greater neuron production in modern humans than Neandertals

Researchers from Dresden uncover a greater neuron production in the frontal lobe during brain development in modern humans than Neandertals, due to the change of a single amino acid in the protein TKTL1.

9 Sep 2022

Study provides some important new clues to age-related memory decline

One of the most upsetting aspects of age-related memory decline is not being able to remember the face that accompanies the name of a person you just talked with hours earlier.

8 Sep 2022

Researchers identify DNA regions associated with physical activity or leisure screen time

In a large international study, researchers at Uppsala University have identified DNA regions that are associated with physical activity or leisure screen time.

7 Sep 2022

High blood pressure may cause bones to age faster

When high blood pressure was induced in young mice, they had bone loss and osteoporosis-related bone damage comparable to older mice, according to new research presented today at the American Heart Association's Hypertension Scientific Sessions 2022 conference, held Sept. 7-10, 2022, in San Diego.

7 Sep 2022

DASH diet plan may be most effective in reducing heart risk in people with hypertension

Among several lifestyle changes that may reduce cardiovascular disease, adopting the DASH (Dietary Approaches to Stop Hypertension) diet may have the greatest impact for young and middle-aged adults with stage 1 hypertension, according to new research presented at the American Heart Association's Hypertension Scientific Sessions 2022, held Sept. 7-10, 2022, in San Diego.

7 Sep 2022

Proposed classification of COPD according to major risk factors

In a recent The Lancet study on COPD, scientists focussed on eliminating the disease by challenging accepted dogma and raising important questions.

7 Sep 2022

Researchers use 3D mapping techniques to identify multiple genes implicated in type 2 diabetes

Researchers from Children's Hospital of Philadelphia used advanced three-dimensional mapping techniques at a microscopic level to identify a multitude of genetic variants and corresponding target gene pairings in the pancreas that are implicated in type 2 diabetes.

6 Sep 2022

Low-dose ketamine is safe and effective to treat children with ADNP syndrome, study suggests

Results of a small, but unique research study, led by researchers from the Seaver Autism Center for Research and Treatment at Mount Sinai and published online in Human Genetics and Genomic Advances, suggest that low-dose ketamine is generally safe, well-tolerated and effective to treat clinical symptoms in children diagnosed with ADNP syndrome (also known as Helsmoortel-VanDerAa syndrome), a rare neurodevelopmental disorder caused by mutations in the activity dependent neuroprotective protein (ADNP) gene.

6 Sep 2022

The existing molecular variance levels in haplotypes of the interferon-alpha-beta receptor gene in Orthopoxviruses

Researchers performed an analysis of molecular variance in 59 haplotypes of the IFNAR gene, departing from monkeypox virus, camelpox virus, buffalopox virus, ectromelia virus, cowpox virus, rabbitpox virus, variola virus, and vaccinia virus.

6 Sep 2022

New method can accurately, quickly predict which antigens will lead to strong immune response

A cell's secrets can be divulged by its surface, decorated with tens to hundreds of thousands of molecules that help immune cells determine friend from foe.

5 Sep 2022

Alternative approaches to functional and phenotypic assays using multi-parameter flow cytometry

Synexa is an industry-leading biomarker and large molecule bio analytic research service provider. In this interview, NewsMedical speaks with Natalie Strickland, a principal scientist at Synexa, about alternative approaches to flow cytometry.

From Synexa Life Sciences BV 5 Sep 2022

Study provides a comprehensive view of the genomics of all childhood ALL subtypes

Scientists have created a roadmap of the genetic mutations present in the most common childhood cancer, acute lymphoblastic leukemia (ALL).

1 Sep 2022

Gene variants associated with blood type may contribute to risk of early stroke

Gene variants associated with a person's blood type may be linked to their risk of early stroke, according to a new meta-analysis published in the August 31, 2022, online issue of Neurology®, the medical journal of the American Academy of Neurology.

1 Sep 2022

Moffitt study uses computer modeling to demonstrate the impact of skin homeostasis on driver and passenger mutations

All normal human tissues acquire mutations over time. Some of these mutations may be driver mutations that promote the development of cancer through increased proliferation and survival, while other mutations may be neutral passenger mutations that have no impact on cancer development.

30 Aug 2022

Genetics News and Research

Latest Genetics News and Research

Single amino acid change in TKTL1 protein underlies greater neuron production in modern humans than Neandertals

Study provides some important new clues to age-related memory decline

Researchers identify DNA regions associated with physical activity or leisure screen time

High blood pressure may cause bones to age faster

DASH diet plan may be most effective in reducing heart risk in people with hypertension

Proposed classification of COPD according to major risk factors

Researchers use 3D mapping techniques to identify multiple genes implicated in type 2 diabetes

Low-dose ketamine is safe and effective to treat children with ADNP syndrome, study suggests

The existing molecular variance levels in haplotypes of the interferon-alpha-beta receptor gene in Orthopoxviruses

New method can accurately, quickly predict which antigens will lead to strong immune response

Alternative approaches to functional and phenotypic assays using multi-parameter flow cytometry

Study provides a comprehensive view of the genomics of all childhood ALL subtypes

Gene variants associated with blood type may contribute to risk of early stroke

Moffitt study uses computer modeling to demonstrate the impact of skin homeostasis on driver and passenger mutations

Popular genetic method is deeply flawed, study reveals

Using deep learning to guide the selection of chemotherapy after surgery for colorectal cancer patients

Genetic screening before pregnancy detects the risk in 44% of couples

Gothenburg scientists discover possible new cancer treatment target

Higher tea intake linked with modestly lower risk of death

Single mutation in Kcnc3 gene causes learning deficits in mice

eBook: Using iPSCs models for human disease research and drug discovery eBook

Real-time Raman monitoring for pharmaceutical hot melt extrusion

Synthetic Psychedelics: A Growing Public Health Concern

How the Vutara VXL simplifies single-molecule imaging