(Q28211647)

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

CFTR as a cAMP-dependent regulator of sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Cystic fibrosis transmembrane conductance regulator is an epithelial cell receptor for clearance of Pseudomonas aeruginosa from the lung.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

COOH-terminal truncations promote proteasome-dependent degradation of mature cystic fibrosis transmembrane conductance regulator from post-Golgi compartments

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

A Golgi-associated PDZ domain protein modulates cystic fibrosis transmembrane regulator plasma membrane expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

A C-terminal motif found in the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Peptide binding consensus of the NHE-RF-PDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Regulation of cystic fibrosis transmembrane conductance regulator single-channel gating by bivalent PDZ-domain-mediated interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

A macromolecular complex of beta 2 adrenergic receptor, CFTR, and ezrin/radixin/moesin-binding phosphoprotein 50 is regulated by PKA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Association of a novel PDZ domain-containing peripheral Golgi protein with the Q-SNARE (Q-soluble N-ethylmaleimide-sensitive fusion protein (NSF) attachment protein receptor) protein syntaxin 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Identification of a PDZ domain containing Golgi protein, GOPC, as an interaction partner of frizzled

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

PIST: a novel PDZ/coiled-coil domain binding partner for the rho-family GTPase TC10

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

The PDZ-binding chloride channel ClC-3B localizes to the Golgi and associates with cystic fibrosis transmembrane conductance regulator-interacting PDZ proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

CALEB/NGC interacts with the Golgi-associated protein PIST

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

A kinase-regulated PDZ-domain interaction controls endocytic sorting of the beta2-adrenergic receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Membrane trafficking of the cystic fibrosis gene product, cystic fibrosis transmembrane conductance regulator, tagged with green fluorescent protein in madin-darby canine kidney cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Bafilomycins: a class of inhibitors of membrane ATPases from microorganisms, animal cells, and plant cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Multiple proteolytic systems, including the proteasome, contribute to CFTR processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Degradation of CFTR by the ubiquitin-proteasome pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Regulated portals of entry into the cell

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

The dynamin family of mechanoenzymes: pinching in new places

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Induction of mutant dynamin specifically blocks endocytic coated vesicle formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

A novel protein complex linking the delta 2 glutamate receptor and autophagy: implications for neurodegeneration in lurcher mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200

Lack of acrosome formation in mice lacking a Golgi protein, GOPC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308640200