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Items: 15


Blood Pressure Classification Using the Method of the Modular Neural Networks.

Pulido M, Melin P, Prado-Arechiga G.

Int J Hypertens. 2019 Jan 23;2019:7320365. doi: 10.1155/2019/7320365. eCollection 2019.


A Grey Wolf Optimizer for Modular Granular Neural Networks for Human Recognition.

Sánchez D, Melin P, Castillo O.

Comput Intell Neurosci. 2017;2017:4180510. doi: 10.1155/2017/4180510. Epub 2017 Aug 14.


Fuzzy Sets in Dynamic Adaptation of Parameters of a Bee Colony Optimization for Controlling the Trajectory of an Autonomous Mobile Robot.

Amador-Angulo L, Mendoza O, Castro JR, Rodríguez-Díaz A, Melin P, Castillo O.

Sensors (Basel). 2016 Sep 9;16(9). pii: E1458. doi: 10.3390/s16091458.


Fuzzy Index to Evaluate Edge Detection in Digital Images.

Perez-Ornelas F, Mendoza O, Melin P, Castro JR, Rodriguez-Diaz A, Castillo O.

PLoS One. 2015 Jun 26;10(6):e0131161. doi: 10.1371/journal.pone.0131161. eCollection 2015.


The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation.

Rode B, Dirami T, Bakouh N, Rizk-Rabin M, Norez C, Lhuillier P, Lorès P, Jollivet M, Melin P, Zvetkova I, Bienvenu T, Becq F, Planelles G, Edelman A, Gacon G, Touré A.

Hum Mol Genet. 2012 Mar 15;21(6):1287-98. doi: 10.1093/hmg/ddr558. Epub 2011 Nov 25.


Orphan missense mutations in the cystic fibrosis transmembrane conductance regulator: A three-step biological approach to establishing a correlation between genotype and phenotype.

Fresquet F, Clement R, Norez C, Sterlin A, Melin P, Becq F, Kitzis A, Thoreau V, Bilan F.

J Mol Diagn. 2011 Sep;13(5):520-7. doi: 10.1016/j.jmoldx.2011.05.004. Epub 2011 Jun 25.


C terminus of nucleotide binding domain 1 contains critical features for cystic fibrosis transmembrane conductance regulator trafficking and activation.

Billet A, Melin P, Jollivet M, Mornon JP, Callebaut I, Becq F.

J Biol Chem. 2010 Jul 16;285(29):22132-40. doi: 10.1074/jbc.M110.120683. Epub 2010 Apr 30.


Adenovirus 5-fiber 35 chimeric vector mediates efficient apical correction of the cystic fibrosis transmembrane conductance regulator defect in cystic fibrosis primary airway epithelia.

Granio O, Ashbourne Excoffon KJ, Henning P, Melin P, Norez C, Gonzalez G, Karp PH, Magnusson MK, Habib N, Lindholm L, Becq F, Boulanger P, Zabner J, Hong SS.

Hum Gene Ther. 2010 Mar;21(3):251-69. doi: 10.1089/hum.2009.056.


Endosomal SNARE proteins regulate CFTR activity and trafficking in epithelial cells.

Bilan F, Nacfer M, Fresquet F, Norez C, Melin P, Martin-Berge A, Costa de Beauregard MA, Becq F, Kitzis A, Thoreau V.

Exp Cell Res. 2008 Jul 1;314(11-12):2199-211. doi: 10.1016/j.yexcr.2008.04.012. Epub 2008 May 4.


CFTR inhibition by glibenclamide requires a positive charge in cytoplasmic loop three.

Melin P, Hosy E, Vivaudou M, Becq F.

Biochim Biophys Acta. 2007 Oct;1768(10):2438-46. Epub 2007 May 21.


Discovery of alpha-aminoazaheterocycle-methylglyoxal adducts as a new class of high-affinity inhibitors of cystic fibrosis transmembrane conductance regulator chloride channels.

Routaboul C, Norez C, Melin P, Molina MC, Boucherle B, Bossard F, Noel S, Robert R, Gauthier C, Becq F, Décout JL.

J Pharmacol Exp Ther. 2007 Sep;322(3):1023-35. Epub 2007 Jun 19.


Evidence that CFTR is expressed in rat tracheal smooth muscle cells and contributes to bronchodilation.

Vandebrouck C, Melin P, Norez C, Robert R, Guibert C, Mettey Y, Becq F.

Respir Res. 2006 Aug 28;7:113.


Rescue of functional delF508-CFTR channels in cystic fibrosis epithelial cells by the alpha-glucosidase inhibitor miglustat.

Norez C, Noel S, Wilke M, Bijvelds M, Jorna H, Melin P, DeJonge H, Becq F.

FEBS Lett. 2006 Apr 3;580(8):2081-6. Epub 2006 Mar 10.


The cystic fibrosis mutation G1349D within the signature motif LSHGH of NBD2 abolishes the activation of CFTR chloride channels by genistein.

Melin P, Thoreau V, Norez C, Bilan F, Kitzis A, Becq F.

Biochem Pharmacol. 2004 Jun 15;67(12):2187-96.


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