Much research has been conducted over many decades on diseases that are widespread in large parts of the population, such as cancer and heart disease. As a result, treatment methods have improved enormously thanks to long-term ...
Nov 24, 2023
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A new study led by University of Melbourne researchers has discovered a link between a new gene pathway and structural brain anomalies in some people who stutter into adulthood, opening up promising research avenues to enhance ...
Nov 20, 2023
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The cells that make up our bodies are constantly communicating with each other, sometimes directly by physical touch. These interactions allow cells to respond to their neighbors, adapt to their surrounding environment and ...
Nov 16, 2023
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Scientists have examined the gene expression patterns of single cells from 5 human fetal kidneys to create the most complete atlas of the fetal kidney to date. The research will be presented at ASN Kidney Week 2023 November ...
Nov 3, 2023
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The development of sex-specific characteristics is frequently seen in mammals. These characteristics stem from the activation of corresponding genetic programs that until now have been largely undescribed by the scientific ...
Nov 2, 2023
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A team of researchers from the Icahn School of Medicine at Mount Sinai and Yale University School of Medicine has created the first "multiome" atlas of brain cell development in the human cerebral cortex across six broad ...
Oct 12, 2023
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In a recent study published in the journal Genes & Diseases, researchers from University of Electronic Science and Technology of China have uncovered a key relationship between the EMC1 protein and retinal vascular development. ...
Oct 9, 2023
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Blood has long been a symbol of life and health, so it may be surprising that some aspects of blood production (hematopoiesis) remain incompletely understood. One such mystery is the role of a protein called SOX17. Blood ...
Sep 13, 2023
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Concerns about the impact of pharmaceutical agents on fetal development have prompted researchers at Iowa State University to undertake a key study using a placenta-on-a-chip model. The study, focused on the transport of ...
Sep 12, 2023
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Crigler-Najjar syndrome is characterized by hyperbilirubinemia. If it is not treated quickly, the build-up of bilirubin, due to a deficiency in the enzyme UGT1A1 which is responsible for metabolizing it into a substance that ...
Aug 17, 2023
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