Titlebook: Alpha-1 Antitrypsin; Role in Health and D Adam Wanner,Robert A. Sandhaus Book 2016 Springer International Publishing Switzerland 2016 Genet

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Managing the Adaptive Proteostatic Landscape: Restoring Resilience in Alpha-1 Antitrypsin Deficiencially recognized and managed by a sophisticated network mainly composed of folding chaperones (the chaperome) and degradative (ubiquitin and autophagy–lysosome based) components referred to as proteostasis. The .roteostasis .etwork (PN) defines different .uinary states (Q-states) for each protein in

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United States Targeted Detection Program for Alpha-1 Antitrypsin Deficiency, barrier to lifestyle modifications, genetic counseling, and specific treatment. Targeted screening allows for high detection rates and lower costs than population screening. Little is known about the prevalence and demographic and clinical characteristics of individuals with the main AATD genotypes

畢業(yè)典禮

Lung Disease of Alpha-1 Antitrypsin Deficiency, emphysema and/or bronchiectasis (Silverman and Sandhaus, N Engl J Med 360(26):2749–57, 2009). It also represents the most common reason that an adult is tested for AATD (The Alpha 1-Antitrypsin Deficiency Registry Study Group, Chest 106(4):1223–32, 1994). This bias toward testing individuals with l

通情達(dá)理

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cylinder

The Alpha-1 Constellation of Voluntary Health Organizations as a Paradigm for Confronting Rare Disen diseases. Rare disease patients and the clinicians and researchers who serve them lack the benefits of a large patient cohort for studies, federally funded trials and testing, public awareness, and market-driven pharmaceutical and other therapeutic initiatives. They must rely more heavily on a sma

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Book 2016sease in adults and children and is associated with chronic obstructive lung disease in adults. While it is a rare condition, the mechanisms underlying the clinical manifestations of this deficiency have been largely clarified. Treatment, however, is?available only for the lung disease that arises f

Prostatism

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記憶法

https://doi.org/10.1007/978-94-009-8105-8 misfolded ATZ, particularly the autophagic pathway, are believed to play a critical role, and FDA-approved drugs that enhance autophagy and can be repurposed appear to be attractive candidates for treatment. Several other promising drug-, cell-, or gene-based therapeutic strategies are being developed for this liver disease.