Categoría: Noticias
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Genetic mapping identifies new hope for bone diseases
In a global breakthrough published in Nature Genetics, researchers have successfully mapped the cells and genes that regulate bone formation and loss at an unprecedented scale and discovered the critical role that blood vessel cells play in bone health.
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Autism research finds Phelan-McDermid syndrome may affect 1 in 7,300 people: More common than previously thought
New research, led by scientists from the Seaver Autism Center for Research and Treatment at Mount Sinai and published in Autism Research, has estimated that Phelan-McDermid syndrome (PMS) affects approximately 1 in 7,300 people, making it far more comm…
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Genome editing in rats enables more accurate estrogen receptor-positive breast cancer models
Rat disease models have played an integral role in scientific discovery and cancer research, including Nobel Prize–winning work from Charles Huggins on hormone therapy for prostate cancer in 1966. However, technical challenges in genetic engineering of…
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Researchers discover new form of hereditary prostate cancer
Researchers at the University of British Columbia have identified a new form of hereditary prostate cancer that, while rare, can cause aggressive disease at a young age. The discovery paves the way for genetic testing programs that could help identify …
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Genetic study links IBS to lipid metabolism and triglyceride regulation
Irritable bowel syndrome (IBS) is a common condition that affects more than 10% of the general population, causing recurrent abdominal pain, bloating, constipation and diarrhea. IBS is considered a disorder of gut-brain interaction, and previous resear…
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New approach to gene correction for iron storage disease
Hereditary primary hemochromatosis is caused by a single faulty building block in a gene. This leads to iron overload, which can have serious consequences for organs and joints. In preclinical studies, researchers have already successfully treated this…
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Liver-directed gene therapy shows preclinical efficacy for severe inherited metabolic disorder
Genespire, in collaboration with researchers at the San Raffaele Telethon Institute for Gene Therapy (SR-TIGET), announced the publication of preclinical data supporting the potential of its liver-directed immune-shielded lentiviral gene therapy approa…
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Genetic insights into a fluid-related brain condition in newborns
Early detection and treatment of congenital cerebral ventriculomegaly (CCV)—when a fetus’s fluid-filled brain ventricles swell due to a condition called hydrocephalus—can help clinicians prevent developmental or neurological disabilities in affected in…
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A long‑standing mystery in the deadliest breast cancer just yielded 81 new treatment targets
Researchers have solved a long-standing mystery of how abnormal chromosomes drive cancer, identifying 81 new genes involved in aggressive breast cancer. The discovery expands understanding of the cellular processes behind the disease and opens new aven…
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New platform combines precision gene targeting with brain-wide delivery
A new study describes a gene therapy strategy that uses the brain’s own glymphatic transport system to distribute engineered viral vectors throughout the brain. The approach addresses two major challenges in neurological medicine—reaching therapeutic t…