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Serina Therapeutics and AgeX Therapeutics Enter into Merger Agreement

Merger to result in NYSE American-listed company focused on developing therapeutics based on Serina’s proprietary POZ Platform™ delivery technology Lead program of the combined company will.

United statesJ milton harrisMilton harrisRandall moreadithJoannem hackettGregory baileyRichard marshallTechnology advancement remy grossSerina therapeutics incBradley arant boult cummingsDrug administrationDunn crutcherBuck institute for aging viceExchange commissionHudsonalpha institute of biotechnologyAgex therapeutics inc

AgeX Therapeutics (AGE) and Serina Therapeutics to Merge

AgeX Therapeutics (AGE) and Serina Therapeutics to Merge
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United statesMilton harrisJ milton harrisJoannem hackettRandall moreadithRichard marshallGregory baileyTechnology advancement remy grossExchange commissionSerina therapeutics incDrug administrationHudsonalpha institute of biotechnologyBradley arant boult cummingsBuck institute for aging viceJuvenescence limitedAgex therapeutics inc

HudsonAlpha hires Carr to lead economic development for Wiregrass

HudsonAlpha Institute of Biotechnology has named Ann Marie Carr as its new economic development associate for the Wiregrass.

United statesCity of dothanAnn marie carrHudsonalpha wiregrassDean mitchellAnn marieHudsonalpha institute of biotechnologyAlpha instituteSoutheast alabamaCarter wellsSoutheast alabamaworksJob marketHe economy

State of Alabama allocates $20M to Wiregrass Innovation Center

State legislatures made their way to the Circle City Monday morning to present the City of Dothan with a check, allocating $20M to the building of the Wiregrass Innovation Center.

Mark salibaPaul leeInnovation centerWiregrass foundationWiregrass innovation centerHudsonalpha institute of biotechnologyDothan mayor markCircle city mondayWiregrass innovationHudsonalpha instituteRepresentative paul lee20 million

AI algorithm accurately detects disease-causing variants in infants with rare diseases

Fabric Genomics and Rady Children's Institute for Genomic Medicine today announced the publication of a retrospective study in Genome Medicine showing that across six leading genomic centers and hospitals, researchers were able to detect more than 90% of disease-causing variants in infants with rare diseases using the Fabric GEM AI algorithm and whole-genome and whole-exome data from previously diagnosed newborns and rare disease patients at Rady Children's Hospital - San Diego and other clinical sites.

United statesSan diegoStephen kingsmoreMark yandellMartin reeseEmily hendersonTartu university hospitalRady children institute for genomic medicineStudy coTranslational genomics research institute tgenUniversity of utahHudsonalpha institute of biotechnologyChristian albrechts university of kiel hospital schleswig holsteinRady childrenGenome medicineStudy co author