A. Mengos

发表

Characterization of wild-type and deltaF508 cystic fibrosis transmembrane regulator in human respiratory epithelia.

J. Riordan, L. Rochelle, J. Yankaskas, 2005, Molecular biology of the cell.

Differential Interactions of Nucleotides at the Two Nucleotide Binding Domains of the Cystic Fibrosis Transmembrane Conductance Regulator*

J. Riordan, A. Aleksandrov, L. Aleksandrov, 2001, The Journal of Biological Chemistry.

Removal of multiple arginine-framed trafficking signals overcomes misprocessing of delta F508 CFTR present in most patients with cystic fibrosis.

J. Riordan, L. Cui, A. Aleksandrov, 1999, Molecular cell.

CFTR Delivery to 25% of Surface Epithelial Cells Restores Normal Rates of Mucus Transport to Human Cystic Fibrosis Airway Epithelium

Leatrice N Vogel, P. Collins, R. Boucher, 2009, PLoS biology.

Deletion of the Mitochondrial Protein VWA8 Induces Oxidative Stress and an HNF4a Compensatory Response in Hepatocytes.

J. Finlayson, L. Mandarino, W. Willis, 2019, Biochemistry.

Characterization of the novel protein KIAA0564 (Von Willebrand Domain-containing Protein 8).

J. Finlayson, L. Mandarino, W. Willis, 2017, Biochemical and biophysical research communications.

High Fat Diet-Induced Changes in Hepatic Protein Abundance in Mice

L. Mandarino, A. Mengos, M. Luo, 2012, Journal of proteomics & bioinformatics.

SERCA Pump Inhibitors Do Not Correct Biosynthetic Arrest of (cid:1) F508 CFTR in Cystic Fibrosis

J. Riordan, M. Drumm, S. Randell, 2006 .

The CD14+HLA-DRlo/neg Monocyte: An Immunosuppressive Phenotype That Restrains Responses to Cancer Immunotherapy

M. Gustafson, D. Gastineau, A. Mengos, 2019, Front. Immunol..

SERCA pump inhibitors do not correct biosynthetic arrest of deltaF508 CFTR in cystic fibrosis.

J. Riordan, M. Drumm, S. Randell, 2006, American journal of respiratory cell and molecular biology.

The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon.

J. Riordan, T. Jensen, K. Kunzelmann, 2004, Gastroenterology.

The PDZ-binding Chloride Channel ClC-3B Localizes to the Golgi and Associates with Cystic Fibrosis Transmembrane Conductance Regulator-interacting PDZ Proteins*

J. Riordan, Liying Cui, M. Gentzsch, 2003, The Journal of Biological Chemistry.

Bcr (breakpoint cluster region) protein binds to PDZ-domains of scaffold protein PDZK1 and vesicle coat protein Mint3

J. Riordan, Liying Cui, M. Gentzsch, 2004, Journal of Cell Science.

Identification of a Role for CLASP2 in Insulin Action*

L. Mandarino, Bradlee L. Heckmann, Jun Liu, 2012, The Journal of Biological Chemistry.

Role of N-linked oligosaccharides in the biosynthetic processing of the cystic fibrosis membrane conductance regulator

J. Riordan, A. Aleksandrov, Liying Cui, 2008, Journal of Cell Science.

Role of individual R domain phosphorylation sites in CFTR regulation by protein kinase A.

J. Riordan, A. Aleksandrov, Liying Cui, 2009, Biochimica et biophysica acta.

Early life of cystic fibrosis transmembrane conductance regulator (CFTR) in the cell

J. Riordan, T. Jensen, M. Gentzsch, 2001 .