Categoría: Noticias
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Broccoli could treat untreatable rare nerve disease, research finds
The secret ingredient for treating a rare nervous system disease could be hiding in the fridge, Swinburne researchers have discovered.
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Telomere-to-telomere brown rat genome could sharpen disease research models
Researchers have created the most complete genetic profile of the brown rat to date, according to a UTHealth Houston-led team, paving the way for scientists to more accurately investigate genetic links to conditions like heart disease, kidney disease, …
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Telomere-to-telomere brown rat genome could sharpen disease research models
Researchers have created the most complete genetic profile of the brown rat to date, according to a UTHealth Houston-led team, paving the way for scientists to more accurately investigate genetic links to conditions like heart disease, kidney disease, …
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Why the body’s inflammatory alarm misfires in familial Mediterranean fever
Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease in which the body’s own immune system overreacts to minimal or inappropriate stimuli, producing recurrent attacks of fever and painful inflammation. The disease is caused by mu…
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Why the body’s inflammatory alarm misfires in familial Mediterranean fever
Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease in which the body’s own immune system overreacts to minimal or inappropriate stimuli, producing recurrent attacks of fever and painful inflammation. The disease is caused by mu…
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From growth to function: Gene helps human heart cells decide when to mature
Understanding how heart muscle cells stop dividing and acquire the characteristics needed to sustain lifelong cardiac function remains one of the greatest challenges in cardiovascular biology. Leveraging human induced pluripotent stem (iPS) cell techno…
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From growth to function: Gene helps human heart cells decide when to mature
Understanding how heart muscle cells stop dividing and acquire the characteristics needed to sustain lifelong cardiac function remains one of the greatest challenges in cardiovascular biology. Leveraging human induced pluripotent stem (iPS) cell techno…
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Gene mutations behind serious bone marrow conditions identified
Inherited bone marrow failure syndrome, or IBMFS, describes a group of disorders in which inherited genetic abnormalities impair the bone marrow’s ability to produce sufficient healthy blood cells. Patients with these disorders are also at increased ri…
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Gene mutations behind serious bone marrow conditions identified
Inherited bone marrow failure syndrome, or IBMFS, describes a group of disorders in which inherited genetic abnormalities impair the bone marrow’s ability to produce sufficient healthy blood cells. Patients with these disorders are also at increased ri…
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Hidden DNA regulators may drive neurodevelopmental disorders by reducing FOXG1 protein
A new study from the laboratory of Gemma Carvill, Ph.D., associate professor in the Ken and Ruth Davee Department of Neurology’s Division of Epilepsy and Clinical Neurophysiology, has uncovered variants in noncoding regulatory regions of the genome tha…