Pages that link to "Q40489429"
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The following pages link to Nonspecific interstitial pneumonia, alveolar proteinosis, and abnormal proprotein trafficking resulting from a spontaneous mutation in the surfactant protein C gene (Q40489429):
Displaying 35 items.
- BRICHOS - a superfamily of multidomain proteins with diverse functions (Q21202152) (← links)
- Interstitial lung disease in children -- genetic background and associated phenotypes (Q24800572) (← links)
- An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy (Q26824718) (← links)
- Genetic disorders of surfactant dysfunction (Q28235256) (← links)
- The Brichos domain-containing C-terminal part of pro-surfactant protein C binds to an unfolded poly-val transmembrane segment (Q28241042) (← links)
- Interstitial lung diseases in children (Q34128163) (← links)
- The surfactant protein C mutation A116D alters cellular processing, stress tolerance, surfactant lipid composition, and immune cell activation (Q34212504) (← links)
- Genetics and early detection in idiopathic pulmonary fibrosis (Q34479395) (← links)
- Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease (Q34618496) (← links)
- Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation (Q34642720) (← links)
- A non-BRICHOS SFTPC mutant (SP-CI73T) linked to interstitial lung disease promotes a late block in macroautophagy disrupting cellular proteostasis and mitophagy (Q34801109) (← links)
- A nonaggregating surfactant protein C mutant is misdirected to early endosomes and disrupts phospholipid recycling. (Q35163057) (← links)
- Surfactant Dysfunction (Q35446540) (← links)
- Genetic Basis of Children's Interstitial Lung Disease (Q35513452) (← links)
- Pulmonary alveolar proteinosis in a cat. (Q35863387) (← links)
- Lost after translation: insights from pulmonary surfactant for understanding the role of alveolar epithelial dysfunction and cellular quality control in fibrotic lung disease (Q36066466) (← links)
- Surfactant Protein C-associated interstitial lung disease; three different phenotypes of the same SFTPC mutation (Q36634161) (← links)
- Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations (Q36695369) (← links)
- Expression of Carcinoembryonic Cell Adhesion Molecule 6 and Alveolar Epithelial Cell Markers in Lungs of Human Infants with Chronic Lung Disease. (Q36774482) (← links)
- Anterograde transport of surfactant protein C proprotein to distal processing compartments requires PPDY-mediated association with Nedd4 ubiquitin ligases (Q37269148) (← links)
- Chronic interstitial lung diseases in children (Q37596284) (← links)
- GM-CSF pathway correction in pulmonary alveolar proteinosis (Q37778844) (← links)
- Contemporary Perspectives on Pediatric Diffuse Lung Disease (Q37925917) (← links)
- Imaging of Childhood Interstitial Lung Disease (Q37983826) (← links)
- A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancy (Q38881731) (← links)
- The biology of the ABCA3 lipid transporter in lung health and disease (Q39057094) (← links)
- Misfolded BRICHOS SP-C mutant proteins induce apoptosis via caspase-4- and cytochrome c-related mechanisms (Q40116328) (← links)
- SFTPC mutations cause SP-C degradation and aggregate formation without increasing ER stress (Q45345359) (← links)
- Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype (Q47949134) (← links)
- Interstitial pulmonary diseases (Q48704888) (← links)
- Surfactant protein C mutations are the basis of a significant portion of adult familial pulmonary fibrosis in a dutch cohort. (Q54418482) (← links)
- Pediatric Case Report on an Interstitial Lung Disease with a Novel Mutation of SFTPC Successfully Treated with Lung Transplantation. (Q54963123) (← links)
- CT features of diffuse lung disease in infancy (Q88142305) (← links)
- Pulmonary alveolar proteinosis (Q95410224) (← links)
- Genetic testing for rare pediatric lung disorders: The promise and the pitfalls (Q98772446) (← links)