(Q37467748)

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Disease-causing mutations in the cystic fibrosis transmembrane conductance regulator determine the functional responses of alveolar macrophages

scientific article published on December 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Disease-causing mutations in the cystic fibrosis transmembrane conductance regulator determine the functional responses of alveolar macrophages (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

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cystic fibrosis

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transmembrane protein

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author name string

Ludmila V Deriy

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Erwin A Gomez

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Guangping Zhang

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Daniel W Beacham

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Jessika A Hopson

5

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Alexander J Gallan

6

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Pavel D Shevchenko

7

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Vytautas P Bindokas

8

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Deborah J Nelson

9

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Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

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publication date

1 December 2009

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Europe PubMed Central

PMC publication ID

20 August 2017

Journal of Biological Chemistry

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Europe PubMed Central

PMC publication ID

20 August 2017

284

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Europe PubMed Central

PMC publication ID

20 August 2017

51

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

35926-35938

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2791021/fullTextXML

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inferred from PubMed Central ID database lookup

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1 reference

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Ceramide accumulation mediates inflammation, cell death and infection susceptibility in cystic fibrosis

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G551D and G1349D, two CF-associated mutations in the signature sequences of CFTR, exhibit distinct gating defects

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1 reference

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Secretory lysosomes

1 reference

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pH Homeostasis of cellular organelles

1 reference

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Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung

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Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations.

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Lack of acidification in Mycobacterium phagosomes produced by exclusion of the vesicular proton-ATPase

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Co-localization of hydrolytic enzymes with widely disparate ph optima: Implications for the regulation of lysosomal ph

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CFTR Expression in human neutrophils and the phagolysosomal chlorination defect in cystic fibrosis

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Cystic fibrosis transmembrane conductance regulator-independent phagosomal acidification in macrophages

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Macrophages use different internalization mechanisms to clear apoptotic and necrotic cells

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Priming of insulin granules for exocytosis by granular Cl(-) uptake and acidification

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Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels

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The dynamics of exocytosis in human neutrophils

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Ca(2+)-independent F-actin assembly and disassembly during Fc receptor-mediated phagocytosis in mouse macrophages.

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Direct recruitment of H+-ATPase from lysosomes for phagosomal acidification.

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Burkholderia cenocepacia-induced delay of acidification and phagolysosomal fusion in cystic fibrosis transmembrane conductance regulator (CFTR)-defective macrophages

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Macrophages directly contribute to the exaggerated inflammatory response in cystic fibrosis transmembrane conductance regulator-/- mice

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CFTR regulates phagosome acidification in macrophages and alters bactericidal activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/19837664

12 December 2020

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Macrophage Activation Downregulates the Degradative Capacity of the Phagosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19837664

12 December 2020

based on heuristic

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Identifiers

10.1074/JBC.M109.057372

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

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