M. Krouse

发表

Inhibition of airway surface fluid absorption by cholinergic stimulation

Jae Young Choi, N. Joo, J. Wine, 2016, Scientific Reports.

Doxorubicin selection for MDR1/P-glycoprotein reduces swelling-activated K+ and Cl- currents in MES-SA cells.

B. Sikic, J. Wine, M. Krouse, 1996, The American journal of physiology.

Selection for MDR1/P-glycoprotein enhances swelling-activated K+ and Cl- currents in NIH/3T3 cells.

J. Wine, M. Krouse, D. Luckie, 1994, The American journal of physiology.

Optical method for quantifying rates of mucus secretion from single submucosal glands.

N. Joo, J. Wine, M. Krouse, 2001, American journal of physiology. Lung cellular and molecular physiology.

Mucus Secretion from Single Submucosal Glands of Pig

N. Joo, J. Wine, M. Krouse, 2002, The Journal of Biological Chemistry.

Most basal I(SC) in Calu-3 human airway cells is bicarbonate-dependent Cl- secretion.

J. Wine, M. Krouse, M. Singh, 1997, The American journal of physiology.

Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.

Jae Young Choi, N. Joo, J. Wine, 2007, The Journal of clinical investigation.

Calcium-stimulated Cl-secretion in Calu-3 human airway cells requires CFTR.

J. Wine, M. Krouse, S. Moon, 1997, American journal of physiology. Lung cellular and molecular physiology.

An Inwardly Rectifying Potassium Channel in Apical Membrane of Calu-3 Cells*

N. Joo, J. Wine, M. Krouse, 2004, Journal of Biological Chemistry.

Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process.

Jae Young Choi, N. Joo, J. Wine, 2009, The Journal of clinical investigation.

Measurement of fluid secretion from intact airway submucosal glands.

Jae Young Choi, N. Joo, J. Wine, 2011, Methods in molecular biology.

Acinar origin of CFTR-dependent airway submucosal gland fluid secretion.

J. Wine, M. Krouse, Jin V. Wu, 2007, American journal of physiology. Lung cellular and molecular physiology.

Two novel mutations in a cystic fibrosis patient of Chinese origin

J. Wine, R. Moss, J. Wagner, 1999, Human Genetics.

Properties of substance P-stimulated mucus secretion from porcine tracheal submucosal glands.

Jae Young Choi, N. Joo, J. Wine, 2011, American journal of physiology. Lung cellular and molecular physiology.

Cystic fibrosis gene expression is not correlated with rectifying Cl- channels.

J. Wine, R. Kopito, D. Gruenert, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Acid and base secretion in the Calu-3 model of human serous cells.

N. Joo, J. Talbott, J. Wine, 2004, American journal of physiology. Lung cellular and molecular physiology.

Cystic Fibrosis Transmembrane Conductance Regulator Gating Requires Cytosolic Electrolytes*

N. Joo, J. Wine, M. Krouse, 2001, The Journal of Biological Chemistry.

A "virtual gland" method for quantifying epithelial fluid secretion.

N. Joo, J. Wine, M. Krouse, 2004, American journal of physiology. Lung cellular and molecular physiology.

A large anion-selective channel has seven conductance levels

P. Gage, M. Krouse, Mauri E. Krouse, 1986, Nature.

CFTR and MDR: ABC Transporters with Homologous Structure but Divergent Function

M. Krouse, D. Luckie, J. Wilterding, 2003 .

Delta F508-CFTR channels: kinetics, activation by forskolin, and potentiation by xanthines.

H. Wakelee, J. Wine, M. Krouse, 1996, The American journal of physiology.

Glycerol Reverses the Misfolding Phenotype of the Most Common Cystic Fibrosis Mutation (*)

J. Wine, R. Kopito, M. Krouse, 1996, The Journal of Biological Chemistry.

Cystic fibrosis, the CFTR, and rectifying Cl- channels.

David J Brayden, J. Wine, J. Widdicombe, 1991, Advances in experimental medicine and biology.

CFTR channels in immortalized human airway cells.

J. Wine, D. Gruenert, M. Krouse, 1992, The American journal of physiology.

Comparison with Reversibly Bound Agonists at Electrophorus Electrop laques

H. Lester, M. M. Nass, M. Krouse, 1980 .

Rates and equilibria for a photoisomerizable antagonist at the acetylcholine receptor of Electrophorus electroplaques

H. Lester, M. Krouse, B. Erlanger, 1985, The Journal of general physiology.

Light-activated drug confirms a mechanism of ion channel blockade

H. Lester, M. M. Nass, M. Krouse, 1979, Nature.

Response of acetylcholine receptors to photoisomerizations of bound agonist molecules.

H. Lester, M. M. Nass, M. Krouse, 1978, Biophysical journal.

Swelling and Ca2+-activated Anion Conductances in C127 Epithelial Cells Expressing WT and ΔF508-CFTR

J. Wine, M. Krouse, Y. Xia, 1996, The Journal of Membrane Biology.

Dissociation of depolarization-activated and swelling-activated Cl- channels.

J. Wine, M. Krouse, C. Haws, 1994, The American journal of physiology.

Stilbenes stimulate T84 Cl- secretion by elevating Ca2+.

David J Brayden, J. Wine, M. Krouse, 1993, The American journal of physiology.

Cystic Fibrosis: Does CFTR Malfunction Alter pH Regulation?

M. Krouse, D. Luckie, 2013 .

32 Properties of a novel F508del-CFTR corrector FDL169

M. Krouse, A. Deshpande, A. Kolodziej, 2016 .

Evidence that CFTR Channels Can Regulate the Open Duration of other CFTR Channels: Cooperativity

J. Wine, M. Krouse, 2001, The Journal of Membrane Biology.

Ion channels in normal human and cystic fibrosis sweat gland cells.

J. Wine, M. Krouse, N. Lewiston, 1989, The American journal of physiology.

Is Cystic Fibrosis Lung Disease Caused by Abnormal Ion Composition or Abnormal Volume?

M. Krouse, 2001, The Journal of general physiology.

Electrophysiological Experiments With Photoisomerizable Cholinergic Compounds: Review and Progress Report *

H. Lester, J. Nerbonne, M. M. Nass, 1980, Annals of the New York Academy of Sciences.

HCO3- transport in relation to mucus secretion from submucosal glands.

N. Joo, J. Wine, A. Verkman, 2001, JOP : Journal of the pancreas.