Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Emily Langron"'
Publikováno v:
British Journal of Pharmacology. 175:3990-4002
BACKGROUND AND PURPOSE: Cystic fibrosis (CF) is a debilitating hereditary disease caused by mutations in the CFTR gene, which encodes an anion channel. WT-CFTR gating is a non-equilibrium process. After ATP binding, CFTR enters a stable open state (O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fac25bd5dcae36ca4dbf8cfd5da1b45
https://doi.org/10.1111/bph.14475
https://doi.org/10.1111/bph.14475
Autor:
Michela I. Simone, David L. Selwood, Jean-Louis Reymond, Clémence Delalande, Paola Vergani, Emily Langron
Publikováno v:
British Journal of Pharmacology. 174:525-539
BACKGROUND AND PURPOSE: Cystic fibrosis (CF) is a debilitating disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which codes for a Cl-/HCO3 - channel. F508del, the most common CF-associated mutation,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a90c8435aa20766497ff5893ebf4ae7
https://doi.org/10.1111/bph.13715
https://doi.org/10.1111/bph.13715
Autor:
Claudio Zamperini, Paola Vergani, Giulia Tagliavini, Miroslava Kissova, Emily Langron, Greta Fontò, Kristina Lanko, Simona Bertoni, Luisa Ragionieri, Simone Palese, Marco Radi, Giovanni Maga, Emmanuele Crespan, Francesca Ravanetti, Elena Dreassi, Sabrina Tassini, Leen Delang, Johan Neyts, Carmen Mirabelli, Carmine Giorgio, Arianna Mancini
Cystic fibrosis (CF) is a multiorgan disease caused by mutations of the cystic fibrosis transmembrane conductance regulator (CFTR). In addition to respiratory impairment due to mucus accumulation, viruses and bacteria trigger acute pulmonary exacerba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99263645f48f3ea20e4668388cbed286
https://lirias.kuleuven.be/handle/123456789/646383
https://lirias.kuleuven.be/handle/123456789/646383
Publikováno v:
Biophysical Journal. 116:172a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2827bcb59b617e680b4010e97f43be8c
https://doi.org/10.1016/j.bpj.2018.11.958
https://doi.org/10.1016/j.bpj.2018.11.958
Autor:
Kalpana M. Merchant, Philip J. Ebert, Leanne Munsie, Terry A. McNearney, Yue-Wei Qian, Daniel Ursu, Wei Zou, Bonnie Fijal, Emanuele Sher, Emily Langron, Adrian J. Mogg, Olivera Grubisha, Cara L. Ruble
Publikováno v:
Molecular Pain
Background: Genetic causes of exaggerated or reduced pain sensitivity in humans are well known. Recently, single\ud nucleotide polymorphisms (SNPs) in the gene P2RX7, coding for the ATP-gated ion channel P2X7, have been\ud described that cause gain-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee85afc674009ef8f4ef75a3f1344656
Autor:
Emanuele Sher, Christian C. Felder, Kalpana M. Merchant, Jingling Li, Antoine Fouillet, Ellen M. Colvin, Matthew G. Schmitt, Adrian J. Mogg, William C. Roell, Lisa M. Broad, Daniel Ursu, Sachin Mathur, Jeffrey L. Dage, Emily Langron, John T.R. Isaac
Publikováno v:
Psychopharmacology. 231(6)
Genetic causes, or predisposition, are increasingly accepted to be part of the ethiopathogenesis of many neuropsychiatric diseases. While genes can be studied in any type of cells, their physiological function in human brain cells is difficult to eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfa3e309beb47eedbbf20c07c63ca516
https://pubmed.ncbi.nlm.nih.gov/24429870
https://pubmed.ncbi.nlm.nih.gov/24429870