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Top Russian Scientist Fired After He Claims Ancestral Sins Shortened Human Lifespan

He claimed that sin was the cause of mutations in genetic diseases harming modern man.

Belarus generalFyodor lukyanovAlexander kudryavtsevThird international scientificRussian academy of sciencesRussian academy of science vavilov instituteInstitute of geneticsRussian academyVavilov instituteGeneral geneticsTheological conferenceBiblical floodSins of our ancestorsHuman lifespanTop russian scientistDr alexander kudryavtsev

Leveraging Science to Unlock Progress in Advanced Prostate Cancer

Leveraging Science to Unlock Progress in Advanced Prostate Cancer
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United statesNew yorkEl metnawyMatthew cotterFizazik talazoparibAmerican cancer societyGlobal medical affairsImpact beyond the labCenters for diseaseNational comprehensive cancer networkPfizer incAmerican society of clinical oncology educational bookDrug administrationVice presidentProstate cancerGenetic mutations

Mapping Genetic Mutations to Customize Preterm Birth Therapy

Explore how tracing genetic mutations in pregnant women could help provide effective preterm birth therapeutics.

United statesCheng wangJingjing liEdythe broad centerStanford universityDepartment of neurologyStem cell researchScience advancesRegenerative medicineStem cellEffective treatmentPreterm birth theAfrican americanGenetic mutationsReterm birth therapyPregnant woman

Every cancer is unique – why different cancers require different treatments, and how evolution drives drug resistance

There is no one-size-fits-all approach to treating cancer. Understanding how cancer cells evolve could help researchers develop more effective drugs.

Monika joshiDavid degraffJoshua warrickDrug administrationPenn stateCancer cellsProstate cancerThyroid cancersPancreatic cancerTesticular cancerSkin cancerGenetic mutationsColon cancer

Surprising Molecular Pattern in Fragile X Syndrome Revealed

Fragile X Syndrome is linked to significant DNA misfolding leading to gene silencing, affecting synaptic and connective tissues.

Ravi boyaKen chandradossJennifer phillips creminsLou gehrigThomas malachowskiEpigenetics institute at penn medicineCenters for diseaseFragilex syndromeDisease controlEpigenetics institutePenn medicineFragilex messenger ribonucleoproteinRepeat expansion anchoring contactingGenetic mutations