Articles

  • 1 week ago | news.mit.edu | Anne Trafton

    Researchers from MIT and Dana-Farber Cancer Institute have discovered that a class of peptides expressed in pancreatic cancer cells could be a promising target for T-cell therapies and other approaches that attack pancreatic tumors. Known as cryptic peptides, these molecules are produced from sequences in the genome that were not thought to encode proteins.

  • 1 week ago | news.mit.edu | Anne Trafton

    Inside every human cell, 2 meters of DNA is crammed into a nucleus that is only one-hundredth of a millimeter in diameter. To fit inside that tiny space, the genome must fold into a complex structure known as chromatin, made up of DNA and proteins. The structure of that chromatin, in turn, helps to determine which of the genes will be expressed in a given cell. Neurons, skin cells, and immune cells each express different genes depending on which of their genes are accessible to be transcribed.

  • 1 week ago | news.mit.edu | Anne Trafton

    Tuberculosis, the world’s deadliest infectious disease, is estimated to infect around 10 million people each year, and kills more than 1 million annually. Once established in the lungs, the bacteria’s thick cell wall helps it to fight off the host immune system. Much of that cell wall is made from complex sugar molecules known as glycans, but it’s not well-understood how those glycans help to defend the bacteria. One reason for that is that there hasn’t been an easy way to label them inside cells.

  • 2 weeks ago | news.mit.edu | Anne Trafton

    The composition of bacterial populations living on our faces plays a significant role in the development of acne and other skin conditions such as eczema. Two species of bacteria predominate in most people, but how they interact with each other, and how those interactions may contribute to disease, has been difficult to study.

  • 2 weeks ago | medicalxpress.com | Anne Trafton

    Many diseases are caused by a missing or defective copy of a single gene. For decades, scientists have been working on gene therapy treatments that could cure such diseases by delivering a new copy of the missing genes to the affected cells. Despite those efforts, very few gene therapy treatments have been approved by the FDA.

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