Single Nucleotide Polymorphisms News and Research

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The Genetic Secret Behind Human Skull Morphology

Researchers at the Universities of Helsinki, Barcelona, and Tokyo Medical and Dental University (TMDU) have discovered a single nucleotide alteration that is crucial to the evolution of human skull morphology and influences the expression of the TBX1 gene and the formation of the skull base.

18 Apr 2024

Key Insights into LAR-RPTP's Synaptic Regulation via Microexon Molecular Codes

The Synapse Diversity and Specificity Regulation Research Team (Director: Jaewon Ko) at DGIST (President Kunwoo Lee) reported on Tuesday the 27th that they have profiled the molecular code that constitutes brain neural circuits and discovered that it regulates specific excitatory synapse characteristics that contribute to memory of new object locations.

30 Mar 2024

Genes may be Responsible for Third of Complex Regional Pain Syndrome Cases

But the condition is less common in men, even though they are more likely to have the 4 genetic variations implicated in heightened risk, suggesting that there may be sex specific causes, say the researchers.

11 Oct 2023

Canine DNA Database Provides Unprecedented Look at Dog Evolution

A global collaboration of scientists is leveraging an exceptionally extensive canine DNA database to conduct an impartial exploration into the evolutionary processes that have given rise to the diverse breeds of our canine companions.

8 Sep 2023

Understanding the Origins of Human Disease Using the Power of Evolutionary Genomics

Hundreds of scientific studies have been conducted over the years to find the genes underlying common human traits, from eye color to intelligence and physical and mental illnesses.

28 Apr 2023

New signals of natural selection in humans identified

A team of global experts has discovered new signals of natural selection in humans.

2 Mar 2023

Gaining insights into human disease biology through CRISPR platforms

In this interview, we speak with Laralynne Przybyla about how she is utilizing CRISPR platforms to understand human disease biology in greater detail.

From Society for Laboratory Automation and Screening (SLAS) 7 Feb 2023

Blending multiple maps uncover new genetic causes of blindness

In a new study, Ran Elkon and Ruth Ashery-Padan of Tel Aviv University, Israel, and colleagues discovered a new genetic risk factor for adult-onset macular degeneration (AMD) by combining a map of gene regulatory sites with disease-associated loci.

18 Jan 2023

Insights into the evolution of banana domestication

People on the island of New Guinea are said to have domesticated bananas 7,000 years ago. However, the history of banana domestication is convoluted, and their categorization is widely discussed, as the boundaries between species and subspecies are frequently ambiguous.

10 Oct 2022

Genome of domesticated banana varieties contains traces of three unknown ancestors

Bananas are thought to have been first domesticated by people 7,000 years ago on the island of New Guinea.

10 Oct 2022

Genomics plays a major role in psychedelic drugs behavior

It can be crippling for those who suffer from conditions like depression, anxiety, and cluster headaches. In clinical research, psychedelic substances have demonstrated benefits as therapies for several ailments, but not in all cases.

1 Aug 2022

Research highlights the new genetic variations and pediatric NAFLD severity

A multidisciplinary group of researchers at the University of California San Diego School of Medicine have advanced investigations into the genetic causes of NAFLD in children.

1 Jul 2022

Scientists determine drug-resistant mold that infects human lungs

According to a recent study conducted by Imperial College London, drug-resistant mold is disseminated from the environment and affects the lungs of those who are susceptible.

29 Apr 2022

Study uncovers the genetic risk factors for premature aging in pediatric cancer survivors

Variants in two genes have been linked to premature aging in childhood cancer survivors, according to researchers at St. Jude Children’s Research Hospital.

23 Mar 2022

New tools for measuring the biological ages of various organ systems

It's common to say that someone looks either younger or older than their chronological age, but aging is more than skin deep.

9 Mar 2022

Analysis reveals novel insights into Indian genetic heritage of people living in present-day Thailand

A new genetic analysis reveals novel insights into the genetic heritage of people living in Thailand in the present day, which suggest the potential importance of past migrations in spreading Indian culture to the region.

18 Feb 2022

Oligodendrocyte plays major role in the development of multiple sclerosis, says study

A team of international researchers revealed that oligodendrocytes, a kind of central nervous system cell, may play a different function in the progression of MS.

2 Feb 2022

Study elucidates the role of genomics in obsessive-compulsive disorder

According to recent research carried out by the researchers from the Icahn School of Medicine at Mount Sinai, both rare and commonly seen differences in the DNA letters threaded along an individual’s chromosomes can elucidate about a third of the risk for being diagnosed with obsessive-compulsive disorder (OCD).

19 Nov 2021

New research center brings advancements in genomic medicine to admixed individuals

One way to make health care more personalized is to use a person's DNA sequence -; or genome -; to predict their risk of disease. But as the field of precision medicine grows, so have concerns that we may be leaving a large fraction of Americans out.

From UC San Diego 13 Oct 2021

Study identifies C9orf72 repeat expansion using novel genetic marker

Research offers a new genetic tool to pinpoint C9orf72 repeat expansion-carrying frontotemporal lobar degeneration from huge population-based cohorts.

25 Aug 2021