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Genetics news
Oncology & Cancer
CRISPR screen identifies new regulator of androgen receptor in prostate cancer
A poorly characterized protein, historically thought to be a chaperon or enzyme, may actually be a key player in prostate cancer. In a systematic CRISPR screen, scientists from Arc Institute, UCSF, and the Fred Hutchinson ...
3 hours ago
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Genetics
Reactivating a fetal gene enables adult heart cells to regenerate after injury
Around the globe, heart disease remains one of the top causes of death. Once patients begin to suffer from serious heart problems, like heart attacks and heart failure, the heart muscles become damaged and are difficult to ...
21 hours ago
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Hidden nuclear droplets link multiple leukemias and reveal a new therapeutic target
A hidden structure inside the cell is rewriting how scientists understand leukemia. Beneath the microscope, what looked like disorder turned out to follow a simple physical rule—one that connects several major mutations ...
21 hours ago
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Japanese public expresses strong reluctance to donate cells for human brain organoid research
Research on human brain organoids (HBOs) is directly challenging how biobanks and biomedical institutes recruit volunteers. That is what a new study by Japanese researchers in Frontiers in Genetics concludes after finding ...
19 hours ago
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Protein plays unexpected dual role in protecting brain from oxidative stress damage
New research from Johns Hopkins Medicine shows that the enzyme biliverdin reductase A (BVRA) plays a direct protective role against oxidative stress in neurons, independent of its role producing the yellow pigment bilirubin.
Nov 3, 2025
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A new tool for understanding chromosome abnormalities in the eggs of older women
Human egg cells are often prone to chromosomal errors. As women age, the error rate increases sharply—and can contribute to infertility, pregnancy loss, and genetic disorders. Yet why this sudden rise happens remains unknown.
Nov 3, 2025
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Genomic identification method provides diagnoses for 145 families with rare conditions
A new genomic method has enabled multiple people with rare conditions to receive diagnoses that were previously unattainable by identifying complex structural genetic changes that are often missed by standard tests.
Nov 3, 2025
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Safe new target against acute myeloid leukemia discovered
Targeting a specialized group of histones is safe and opens new therapeutic opportunities for treating blood cancers. This is the main finding of the latest research by Dr. Marcus Buschbeck and Dr. René Winkler, researchers ...
Nov 3, 2025
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Specific human gene can help the heart repair itself from heart attack or heart failure
A naturally occurring gene called Cyclin A2 (CCNA2), which turns off after birth in humans, can actually make new, functioning heart cells and help the heart repair itself from injury, including a heart attack or heart failure, ...
Nov 3, 2025
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Gene CEP76 sheds light on cause of rare ciliopathy disorders
A Northwestern Medicine-led study has identified mutations in the gene CEP76 as a new cause of ciliopathies, shedding light on a complex group of disorders that affect multiple body systems, according to a study published ...
Nov 3, 2025
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How a tiny RNA molecule in the kidney triggers a deadly autoimmune disease
Researchers at the University Hospital Bonn (UKB) and the University of Bonn have discovered how a small, naturally occurring RNA molecule in the kidney activates a mutated immune receptor, triggering a chain reaction.
Nov 3, 2025
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Abnormal transport signal on mutant UBTF gene drives high-risk acute myeloid leukemia
Acute myeloid leukemia driven by tandem duplications within the UBTF gene (UBTF-TD AML) is a high-risk pediatric cancer in urgent need of novel therapeutic options. To better understand this disease and how to treat it, St. ...
Nov 3, 2025
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Common gene variant linked to higher heart disease risk in people with African ancestry
Dilated cardiomyopathy (DCM), a leading cause of heart failure, is twice as common in Black individuals as in white individuals. This excess risk is not fully explained by known risk factors such as high blood pressure or ...
Nov 2, 2025
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Scientists find the genetic clues that let humans walk on two legs
Two small changes in human DNA may have played a big role in helping our ancestors walk upright, researchers say.
Nov 2, 2025
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New clue to ALS and FTD: Faulty protein disrupts brain's 'brake' system
A new Northwestern University study using patient nervous tissue and lab-grown human neurons has uncovered how a key disease protein, TDP-43, drives overactive nerve cells in the neurodegenerative diseases amyotrophic lateral ...
Oct 31, 2025
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Genes, personality, and family may predict alcohol drinking in teens
Examining genetic, family, and personality characteristics may help identify those who are at high risk for drinking and drinking problems as teenagers. A study, published in Alcohol: Clinical and Experimental Research, found ...
Oct 31, 2025
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BRCA2 research reveals a novel mechanism behind chemoresistance
One of the biggest challenges in cancer treatment is chemoresistance: Tumors that initially respond well to chemotherapy become resistant over time. When that happens, treatment options are often limited.
Oct 30, 2025
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Genes associated with obesity shared across ancestries, researchers find
Obesity is a global epidemic affecting millions of people every day and is associated with comorbidities ranging from heart disease and type 2 diabetes to osteoarthritis and social stigma. While lifestyle factors, like diet ...
Oct 30, 2025
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Study links genetic variants to higher 'bad' cholesterol and heart attack risk
An international team led by a University of Pittsburgh School of Medicine scientist has created a first-of-its-kind resource to identify those with a genetic risk for elevated "bad" cholesterol—a major contributor to heart ...
Oct 30, 2025
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Tying protein to fraying DNA solves mystery of illness for patients around the world
New research from the University of Wisconsin–Madison reveals that dysfunction in a protein essential to maintaining stability in our chromosomes may be responsible for serious—and sometimes deadly—diseases.
Oct 30, 2025
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Genetic mechanisms reveal how toxic substances damage balance cells in the inner ear
The vestibular system is responsible for the sense of balance in the inner ear. Prolonged use of toxic substances, such as certain antibiotics or anticancer drugs, can damage the hair cells that form part of this system, ...
Oct 30, 2025
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Transcription factor drives chemotherapy resistance in ovarian cancer
Northwestern Medicine scientists have discovered how a specific transcription factor promotes genetic reprogramming and chemotherapy resistance in ovarian cancer cells, findings that may inform new targeted treatment approaches ...
Oct 30, 2025
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Mutation yields hot new clues for treating immune 'cold' tumors
Immune checkpoint inhibitors (ICIs) emerged in the US about 15 years ago as an exciting class of cancer treatments that have achieved complete and durable remissions for thousands of people with end-stage metastatic cancers. ...
Oct 29, 2025
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Changing the 'packaging' of DNA in neurons can turn memories on or off in mice
Our experiences leave traces in the brain, stored in small groups of cells called engrams. Engrams are thought to hold the information of a memory and are reactivated when we remember, which makes them very interesting for ...
Oct 29, 2025
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Common genetic causes across motor neuron diseases identified
Motor neuron diseases, such as amyotrophic lateral sclerosis (ALS) and hereditary spastic paraplegia (HSP), share physical similarities but have been largely viewed as genetically distinct. However, an analysis led by investigators ...
Oct 29, 2025
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