Connecting Research and Experts with Journalists

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Scientists at ORNL used neutrons to end a decades-long debate about an enzyme cancer uses. Their findings can support the design of an inhibitor that can target aggressive cancers.

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Comprehensive gene panel testing, one of the exciting new tools in cancer diagnostics, warrants greater scrutiny — as does a federal program aimed at speeding up the review process for proposed new medical technologies. Those are conclusions of Yale medical experts who studied both and published a report in the Journal of the National Cancer Institute on Sept.

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Three Mile Island, the nuclear power plant in Pennsylvania that’s been shuttered since 2019, could come back to life to meet Microsoft’s energy needs. ...

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Vice President Kamala Harris may visit the US-Mexico border on Friday as her campaign looks to close the gap with former President Donald Trump on immigration. ...

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The company said on Monday that this was its “best and final” offer, which would among many things boost general wages by 30% over four years. ...

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Nebraska state Sen. Mike McDonnell announced Monday that he opposes efforts to change how the state allocates its electoral votes before the upcoming 2024 election. ...

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The uninsured rate in Missouri has dropped significantly, according to a new analysis by the Center for Advancing Health Services, Policy & Economics Research at Washington University in St. Louis.

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Un raro trastorno de deterioro cognitivo hereditario conocido como Trastorno Relacionado con CSF1R (CSF1R-RD, por sus siglas en inglés) recibe su nombre debido a mutaciones en el gen CSF1R, descubierto por Mayo Clinic. La pérdida de memoria ocurre a medida que avanza la afección, mientras que los primeros síntomas incluyen cambios de personalidad, ansiedad, depresión y pérdida de inhibición. Las pruebas genéticas se han vuelto más ampliamente disponibles, pero no existe cura para la enfermedad.

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Um transtorno raro de declínio cognitivo hereditário conhecido como Transtorno Relacionado ao CSF1R (CSF1R-RD, sigla em inglês) recebe o seu nome devido a mutações no gene CSF1R, descoberto pela Mayo Clinic. A perda de memória ocorre à medida que a condição avança, enquanto os primeiros sintomas incluem alterações de personalidade, ansiedade, depressão e perda de inibição. Os testes genéticos tornaram-se mais amplamente disponíveis, mas não há cura para a doença.