Scientists at the Francis Crick Institute have found that using immunotherapy alongside a drug that blocks a common gene mutation in lung cancer could be a promising new combination therapy for certain types of lung tumors.
Jul 20, 2022
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Researchers led by the Francis Crick Institute have found that blocking a particular protein could offer a new way to target leukemic stem cells without causing harm to healthy stem cells.
Jun 23, 2022
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Researchers at the Francis Crick Institute have developed an imaging technique to capture information about the structure and function of brain tissue at subcellular level—a few billionths of a meter, while also capturing ...
May 25, 2022
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An international team of researchers has identified DNA mutations in a gene that senses viral RNA, as a cause of the autoimmune disease lupus, with the finding paving the way for the development of new treatments.
Apr 27, 2022
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Researchers at the Francis Crick Institute have identified structural changes in COVID-19 variants which provide clues to how the virus evolved to have greater levels of infectivity.
Mar 4, 2022
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Researchers at the Francis Crick Institute have uncovered how a process involved in the regeneration of tissue damaged by radiation can aid the spread of cancer.
Feb 24, 2022
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Researchers at the Francis Crick Institute and King's College London have identified how specialist immune cells, called gamma delta T cells (γδ T cells), sense the body's status quo, enabling them to assess the health ...
Feb 15, 2022
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Researchers at the Francis Crick Institute and King's College London have shown that the length of nerve cells is intimately connected with their function. Their accurate model allows the study of structural and functional ...
Feb 7, 2022
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Nearly 50 percent of blood cancer patients do not have detectable levels of antibodies able to neutralize the omicron SARS-CoV-2 variant after a third vaccine dose, according to new laboratory data from the Francis Crick ...
Jan 26, 2022
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Researchers at the Francis Crick Institute have pieced together genetic and molecular changes that lead to a rare progressive neurodegenerative condition called ataxia with oculomotor apraxia 2.
Jan 20, 2022
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