B A Stanton
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Explore the profile of B A Stanton including associated specialties, affiliations and a list of published articles.
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92
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2088
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Recent Articles
1.
Madan J, Koestler D, Stanton B, Davidson L, Moulton L, Housman M, et al.
mBio
. 2012 Aug;
3(4).
PMID: 22911969
Unlabelled: Pulmonary damage caused by chronic colonization of the cystic fibrosis (CF) lung by microbial communities is the proximal cause of respiratory failure. While there has been an effort to...
2.
Gifford A, Miller S, Jackson B, Hampton T, OToole G, Stanton B, et al.
Pediatr Pulmonol
. 2010 Oct;
46(2):160-5.
PMID: 20963784
Introduction: This cross-sectional study was conducted to assess the relationship between iron levels in the plasma and sputum of cystic fibrosis (CF) patients. Methods: Demographic, clinical, and iron-related laboratory data...
3.
Loffing-Cueni D, Loffing J, Shaw C, Taplin A, Govindan M, Stanton C, et al.
Am J Physiol Cell Physiol
. 2001 Nov;
281(6):C1889-97.
PMID: 11698247
The DeltaF508 mutation reduces the amount of cystic fibrosis transmembrane conductance regulator (CFTR) expressed in the plasma membrane of epithelial cells. However, a reduced temperature, butyrate compounds, and "chemical chaperones"...
4.
Maitra R, Halpin P, Karlson K, Page R, Paik D, Leavitt M, et al.
Biochem J
. 2001 Apr;
355(Pt 3):617-24.
PMID: 11311122
Previous studies have demonstrated that mitomycin C (MMC) and other DNA cross-linking agents can suppress MDR1 (multidrug resistance 1) gene expression and subsequent functional P-glycoprotein (Pgp) expression, whereas doxorubicin and...
5.
Maitra R, Shaw C, Stanton B, Hamilton J
Am J Physiol Cell Physiol
. 2001 Apr;
280(5):C1031-7.
PMID: 11287314
Cystic fibrosis (CF) is a disease that is caused by mutations within the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The most common mutation, DeltaF508, accounts for 70% of all...
6.
Maitra R, Shaw C, Stanton B, Hamilton J
Cell Physiol Biochem
. 2001 Mar;
11(2):93-8.
PMID: 11275687
Cystic fibrosis is caused by mutations in the CFTR gene. The most common of these mutations, DeltaF508, results in a protein that is not trafficked to the apical plasma membrane...
7.
Milewski M, Mickle J, Forrest J, Stafford D, Moyer B, Cheng J, et al.
J Cell Sci
. 2001 Feb;
114(Pt 4):719-26.
PMID: 11171377
Localization of ion channels and transporters to the correct membrane of polarized epithelia is important for vectorial ion movement. Prior studies have shown that the cytoplasmic carboxyl terminus of the...
8.
Loffing J, Moyer B, Reynolds D, Shmukler B, Alper S, Stanton B
Am J Physiol Cell Physiol
. 2000 Sep;
279(4):C1016-23.
PMID: 11003582
Serous cells secrete Cl(-) and HCO(3)(-) and play an important role in airway function. Recent studies suggest that a Cl(-)/HCO(3)(-) anion exchanger (AE) may contribute to Cl(-) secretion by airway...
9.
Moyer B, Duhaime M, Shaw C, Denton J, Reynolds D, Karlson K, et al.
J Biol Chem
. 2000 Jun;
275(35):27069-74.
PMID: 10852925
Polarization of cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-activated chloride channel to the apical plasma membrane in epithelial cells is critical for vectorial chloride transport. Previously, we reported that...
10.
Ji H, Chalfant M, Jovov B, Lockhart J, Parker S, Fuller C, et al.
J Biol Chem
. 2000 May;
275(36):27947-56.
PMID: 10821834
Epithelial sodium channel (ENaC) and cystic fibrosis transmembrane conductance regulator (CFTR) are co-localized in the apical membrane of many epithelia. These channels are essential for electrolyte and water secretion and/or...