Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Khaoula, Talbi"'
Autor:
Karl Kunzelmann, Raquel Centeio, Jiraporn Ousingsawat, Khaoula Talbi, Ursula Seidler, Rainer Schreiber
Publikováno v:
Channels, Vol 17, Iss 1 (2023)
ABSTRACTSLC26A9 is one out of 11 proteins that belong to the SLC26A family of anion transporters. Apart from expression in the gastrointestinal tract, SLC26A9 is also found in the respiratory system, in male tissues and in the skin. SLC26A9 has gaine
Externí odkaz:
https://doaj.org/article/4fe0fe1fe0f14cb381bb1534fce08f9c
Autor:
Ghada Bouguerra, Khaoula Talbi, Nawel Trabelsi, Dorra Chaouachi, Imen Boudriga, Salem Abbès, Samia Menif
Publikováno v:
Cellular Physiology and Biochemistry, Vol 55, Iss 6, Pp 761-772 (2021)
Externí odkaz:
https://doaj.org/article/4d4de2fd699147ba90815c868eb7ed21
Publikováno v:
Membranes, Vol 11, Iss 9, p 723 (2021)
Regulation of the Ca2+-activated Cl− channel TMEM16A by Ca2+/calmodulin (CAM) is discussed controversially. In the present study, we compared regulation of TMEM16A by Ca2+/calmodulin (holo-CAM), CAM-dependent kinase (CAMKII), and CAM-dependent phos
Externí odkaz:
https://doaj.org/article/5e0882f327974cd7ae8d780429728ead
Autor:
JinHeng Lin, Sean M. Gettings, Khaoula Talbi, Rainer Schreiber, Michael J. Taggart, Matthias Preller, Karl Kunzelmann, Mike Althaus, Michael A. Gray
Publikováno v:
Pflügers Archiv: European Journal of Physiology
Pflugers Arch-Eur J Physiol 475, 167–179 (2023)
Pflugers Arch-Eur J Physiol 475, 167–179 (2023)
The cystic fibrosis transmembrane conductance regulator (CFTR) anion channel and the epithelial Na+ channel (ENaC) play essential roles in transepithelial ion and fluid transport in numerous epithelial tissues. Inhibitors of both channels have been i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dce82df3ee85d7e50006e23e06b319ed
https://pub.h-brs.de/files/6457/s00424-022-02758-9.pdf
https://pub.h-brs.de/files/6457/s00424-022-02758-9.pdf
Autor:
Sungwoo Jo, Raquel Centeio, Jinhong Park, Jiraporn Ousingsawat, Dong‐kyu Jeon, Khaoula Talbi, Rainer Schreiber, Kunhi Ryu, Kristin Kahlenberg, Veronika Somoza, Livia Delpiano, Michael A. Gray, Margarida D. Amaral, Violeta Railean, Jeffrey M. Beekman, Lisa W. Rodenburg, Wan Namkung, Karl Kunzelmann
Publikováno v:
The FASEB Journal. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84df78702cc97c0ab313559f457294ee
https://doi.org/10.1096/fj.202200313rr
https://doi.org/10.1096/fj.202200313rr
Autor:
Sungwoo, Jo, Raquel, Centeio, Jinhong, Park, Jiraporn, Ousingsawat, Dong-Kyu, Jeon, Khaoula, Talbi, Rainer, Schreiber, Kunhi, Ryu, Kristin, Kahlenberg, Veronika, Somoza, Livia, Delpiano, Michael A, Gray, Margarida D, Amaral, Violeta, Railean, Jeffrey M, Beekman, Lisa W, Rodenburg, Wan, Namkung, Karl, Kunzelmann
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental BiologyREFERENCES. 36(11)
The solute carrier 26 family member A9 (SLC26A9) is an epithelial anion transporter that is assumed to contribute to airway chloride secretion and surface hydration. Whether SLC26A9 or CFTR is responsible for airway Cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c3cea7d2fcdf1a23111e7c3069f6e1a5
https://pubmed.ncbi.nlm.nih.gov/36183361
https://pubmed.ncbi.nlm.nih.gov/36183361
Autor:
Raquel Centeio, Jiraporn Ousingsawat, Khaoula Talbi, Isaac Cohen, Rainer Schreiber, Kris De Boeck, Inês Cabrita, Tereza Doušová, Karl Kunzelmann, Roberta Benedetto, Eric Verbeken
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 15
International Journal of Molecular Sciences, Vol 22, Iss 7852, p 7852 (2021)
Volume 22
Issue 15
International Journal of Molecular Sciences, Vol 22, Iss 7852, p 7852 (2021)
Activation of the Ca2+ activated Cl- channel TMEM16A is proposed as a treatment in inflammatory airway disease. It is assumed that activation of TMEM16A will induce electrolyte secretion, and thus reduce airway mucus plugging and improve mucociliary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c0c9f0520a9d82538f3086e8ceb43b9
https://epub.uni-regensburg.de/46060/
https://epub.uni-regensburg.de/46060/
Autor:
Kathrin Skoczynski, Khaoula Talbi, Inês Cabrita, Rainer Schreiber, Karl Kunzelmann, Bjoern Buchholz, Sascha Hofmann, Andre Kraus
Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the development of bilateral renal cysts which enlarge continuously, leading to compression of adjacent intact nephrons. The growing cysts lead to a progressive decline in renal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc6240745b00ecfc89254d9d394d2764
Publikováno v:
Cell calcium. 97
In polycystic kidney disease (PKD) multiple bilateral renal cysts gradually enlarge causing a decline in renal function. Transepithelial chloride secretion through cystic fibrosis transmembrane conductance regulator (CFTR) and TMEM16A (anoctamin 1) d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9cfb2859633ade33788f1e5396c0e788
https://pubmed.ncbi.nlm.nih.gov/33915319
https://pubmed.ncbi.nlm.nih.gov/33915319
Publikováno v:
Cell Calcium. 97:102413
In polycystic kidney disease (PKD) multiple bilateral renal cysts gradually enlarge causing a decline in renal function. Transepithelial chloride secretion through cystic fibrosis transmembrane conductance regulator (CFTR) and TMEM16A (anoctamin 1) d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd7ebb2d2f73f8a2a67d1c4ae5374844
https://doi.org/10.1016/j.ceca.2021.102413
https://doi.org/10.1016/j.ceca.2021.102413