By Philip M. Parker
In March 2001, the nationwide Institutes of health and wellbeing issued the subsequent caution: "The variety of websites supplying health-related assets grows each day. Many websites offer precious details, whereas others can have details that's unreliable or misleading." in addition, end result of the fast elevate in Internet-based details, many hours may be wasted looking, identifying, and printing. in view that merely the smallest fraction of knowledge facing cystic fibrosis is listed in se's, reminiscent of www.google.com or others, a non-systematic method of web learn should be not just time eating, but in addition incomplete. This publication was once created for doctors, scholars, and contributors of most of the people who are looking to behavior scientific learn utilizing the main complicated instruments to be had and spending the smallest amount of time doing so.
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Additional resources for Cystic Fibrosis - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
A case-control design will be utilized to test the hypothesis that polymorphisms in innate immune genes may limit CF lung disease. Those innate immune genes encoding the LPS receptor are leading candidates as CF modifier loci, based on the recent finding that CF-specific PA LPS structures have increased inflammatory activity.
Finally, factors that regulate ER biogenesis will be identified using biochemical and genetic approaches. These studies will yield new information concerning UPR-regulated events that control plasma cell development, generate efficient antibody responses, and mediate ER homeostasis. Importantly, the UPR has been linked to a number of physiologically significant processes including pancreatic function, skeletal development, oxidative stress, and macrophage apoptosis in atherosclerotic lesions. In addition, a number of catastrophic disorders including lysosomal storage diseases, cystic fibrosis, and Alzheimer disease have been linked to protein maturation errors in the ER.
The three sub-populations of cells will be assayed for engraftment and differentiation in a model for lung damage by asbestos and in a tracheal explant model. The three sub-populations of cells will be tested for their effectiveness in repairing lung damage in an elastase model for emphysema. In addition, we will attempt to define the mechanisms by which MSCs engraft in lung. MSCs from patients with CF will be engineered to correct the gene defect and then tested to determine whether they can become functional ciliated epithelial cells.
Cystic Fibrosis - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker