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Examples
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FTLD cases that are characterized by TDP-43 inclusions can be passed from one generation to the next, as a result of mutations in another protein called progranulin (GRN).
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FTLD cases that are characterized by TDP-43 inclusions can be passed from one generation to the next, as a result of mutations in another protein called progranulin (GRN).
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FTLD cases that are characterized by TDP-43 inclusions can be passed from one generation to the next, as a result of mutations in another protein called progranulin (GRN).
Science Blog BJS 2010
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FTLD cases that are characterized by TDP-43 inclusions can be passed from one generation to the next, as a result of mutations in another protein called progranulin (GRN).
THE MEDICAL NEWS Editors 2010
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FTLD cases that are characterized by TDP-43 inclusions can be passed from one generation to the next, as a result of mutations in another protein called progranulin (GRN).
PhysOrg.com - latest science and technology news stories 2010
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FTLD cases that are characterized by TDP-43 inclusions can be passed from one generation to the next, as a result of mutations in another protein called progranulin (GRN).
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Further scientific research is needed to determine how a shortage of progranulin can be restored to normal.
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They predicted that people with these hereditable defects produce only half of the normal amount of progranulin.
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New results indicate that progranulin also plays a role in the death of brain cells in other diseases of the brain, such as Alzheimer's disease and Amyotrophic Lateral Sclerosis (ALS).
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This finding also offers prospects for the early detection of FTD caused by a shortage of progranulin.
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