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Rat NaV1.7 loss-of-function genetic model: Deficient nociceptive and neuropathic pain behavior with retained olfactory function and intra-epidermal nerve fibers

Molecular pain, 2019, Vol.15, p.1744806919881846-1744806919881846

2019

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Rab1 Recruitment of p115 into a cis-SNARE Complex: Programming Budding COPII Vesicles for Fusion

Science (American Association for the Advancement of Science), 2000-07, Vol.289 (5478), p.444-448

2000

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Discovery of a selective, state-independent inhibitor of NaV1.7 by modification of guanidinium toxins

Scientific reports, 2020-09, Vol.10 (1), p.14791-14791, Article 14791

2020

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Functional and molecular characterization of an anion exchanger in airway serous epithelial cells

American Journal of Physiology: Cell Physiology, 2000-10, Vol.279 (4), p.C1016-C1023

2000

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Rab1 Interaction with a GM130 Effector Complex Regulates COPII Vesicle cis‐Golgi Tethering

Traffic (Copenhagen, Denmark), 2001-04, Vol.2 (4), p.268-276

2001

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Rat Na V 1.7 loss-of-function genetic model: Deficient nociceptive and neuropathic pain behavior with retained olfactory function and intra-epidermal nerve fibers

Molecular pain, 2019-01, Vol.15, p.1744806919881846

2019

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Discovery and hit-to-lead evaluation of piperazine amides as selective, state-dependent NaV1.7 inhibitors

MedChemComm, 2017-04, Vol.8 (4), p.744-754

2017

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Discovery and hit-to-lead evaluation of piperazine amides as selective, state-dependent Na V 1.7 inhibitors

MedChemComm, 2017-04, Vol.8 (4), p.744-754

2017

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A PDZ-interacting domain in CFTR is an apical membrane polarization signal

The Journal of clinical investigation, 1999-11, Vol.104 (10), p.1353-1361

1999

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The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane

The Journal of biological chemistry, 2000-09, Vol.275 (35), p.27069-27074

2000

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[1] Structural basis for rab function: An overview

Methods in Enzymology, 2001, Vol.329, p.3-6

2001

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Membrane Trafficking of the Cystic Fibrosis Gene Product, Cystic Fibrosis Transmembrane Conductance Regulator, Tagged with Green Fluorescent Protein in Madin-Darby Canine Kidney Cells

The Journal of biological chemistry, 1998-08, Vol.273 (34), p.21759-21768

1998

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Adenosine inhibits arginine vasopressin-stimulated chloride secretion in a mouse IMCD cell line (mIMCD-K2)

American journal of physiology. Renal physiology, 1995-12, Vol.269 (6), p.884-F891

1995

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Expression of wild-type and mutant green fluorescent protein-Rab1 for fluorescence microscopy analysis

Methods in enzymology, 2001, Vol.329, p.6-14

2001

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A PDZ-binding motif is essential but not sufficient to localize the C terminus of CFTR to the apical membrane

Journal of cell science, 2001-02, Vol.114 (Pt 4), p.719-726

2001

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Butyrate increases apical membrane CFTR but reduces chloride secretion in MDCK cells

American journal of physiology. Renal physiology, 1999-08, Vol.277 (2), p.F271-F276

1999

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Traffic Pattern of Cystic Fibrosis Transmembrane Regulator through the Early Exocytic Pathway

Traffic (Copenhagen, Denmark), 2000-11, Vol.1 (11), p.852-870

2000

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Exocytosis is not involved in activation of Cl- secretion via CFTR in Calu-3 airway epithelial cells

American Journal of Physiology: Cell Physiology, 1998-10, Vol.275 (4), p.C913-C920

1998

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PBA increases CFTR expression but at high doses inhibits Cl- secretion in Calu-3 airway epithelial cells

American journal of physiology. Lung cellular and molecular physiology, 1999-10, Vol.277 (4), p.700-L708

1999

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Discovery of a selective, state-independent inhibitor of Na V 1.7 by modification of guanidinium toxins

Scientific reports, 2020-09, Vol.10 (1), p.14791

2020

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Functional and molecular characterization of an anion exchanger in airway serous epithelial cells

American Journal of Physiology: Cell Physiology, 2000-10, Vol.48 (4), p.1016-1023

2000

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Endoplasmic Reticulum Retention, Degradation, and Aggregation of Olfactory G‐Protein Coupled Receptors

Traffic (Copenhagen, Denmark), 2003-06, Vol.4 (6), p.416-433

2003

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A Golgi-associated PDZ Domain Protein Modulates Cystic Fibrosis Transmembrane Regulator Plasma Membrane Expression

The Journal of biological chemistry, 2002-02, Vol.277 (5), p.3520-3529

2002

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Non-conventional Trafficking of the Cystic Fibrosis Transmembrane Conductance Regulator through the Early Secretory Pathway

The Journal of biological chemistry, 2002-03, Vol.277 (13), p.11401-11409

2002

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Rat NaV1.7 loss-of-function genetic model: Deficient nociceptive and neuropathic pain behavior with retained olfactory function and intra-epidermal nerve fibers

Rab1 Recruitment of p115 into a cis-SNARE Complex: Programming Budding COPII Vesicles for Fusion

Discovery of a selective, state-independent inhibitor of NaV1.7 by modification of guanidinium toxins

Functional and molecular characterization of an anion exchanger in airway serous epithelial cells

Rab1 Interaction with a GM130 Effector Complex Regulates COPII Vesicle cis‐Golgi Tethering

Rat Na V 1.7 loss-of-function genetic model: Deficient nociceptive and neuropathic pain behavior with retained olfactory function and intra-epidermal nerve fibers

Discovery and hit-to-lead evaluation of piperazine amides as selective, state-dependent NaV1.7 inhibitors

Discovery and hit-to-lead evaluation of piperazine amides as selective, state-dependent Na V 1.7 inhibitors

A PDZ-interacting domain in CFTR is an apical membrane polarization signal

The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane

[1] Structural basis for rab function: An overview

Membrane Trafficking of the Cystic Fibrosis Gene Product, Cystic Fibrosis Transmembrane Conductance Regulator, Tagged with Green Fluorescent Protein in Madin-Darby Canine Kidney Cells

Adenosine inhibits arginine vasopressin-stimulated chloride secretion in a mouse IMCD cell line (mIMCD-K2)

Expression of wild-type and mutant green fluorescent protein-Rab1 for fluorescence microscopy analysis

A PDZ-binding motif is essential but not sufficient to localize the C terminus of CFTR to the apical membrane

Butyrate increases apical membrane CFTR but reduces chloride secretion in MDCK cells

Traffic Pattern of Cystic Fibrosis Transmembrane Regulator through the Early Exocytic Pathway

Exocytosis is not involved in activation of Cl- secretion via CFTR in Calu-3 airway epithelial cells

PBA increases CFTR expression but at high doses inhibits Cl- secretion in Calu-3 airway epithelial cells

Discovery of a selective, state-independent inhibitor of Na V 1.7 by modification of guanidinium toxins

Functional and molecular characterization of an anion exchanger in airway serous epithelial cells

Endoplasmic Reticulum Retention, Degradation, and Aggregation of Olfactory G‐Protein Coupled Receptors

A Golgi-associated PDZ Domain Protein Modulates Cystic Fibrosis Transmembrane Regulator Plasma Membrane Expression

Non-conventional Trafficking of the Cystic Fibrosis Transmembrane Conductance Regulator through the Early Secretory Pathway

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