Добірка наукової літератури з теми "Maladie de Hailey-Hailey"
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Статті в журналах з теми "Maladie de Hailey-Hailey":
Alkhalifah, A., H. Montaudié, J. P. Lacour, M. Lantéri-Minet, and T. Passeron. "Maladie de Hailey-Hailey aggravée par topiramate." Annales de Dermatologie et de Vénéréologie 143, no. 12 (December 2016): S260—S261. http://dx.doi.org/10.1016/j.annder.2016.09.365.
Vilmer, C., and L. Dehen. "Forme condylomateuse vulvaire d’une maladie de Hailey-Hailey." Annales de Dermatologie et de Vénéréologie 131, no. 6-7 (June 2004): 607–8. http://dx.doi.org/10.1016/s0151-9638(04)93680-0.
Ferraro, V., H. Adamski, F. Le Gall, and J. Chevrant-Breton. "Efficacité du tacrolimus topique dans la maladie de Hailey-Hailey." Annales de Dermatologie et de Vénéréologie 133, no. 5 (May 2006): 475–76. http://dx.doi.org/10.1016/s0151-9638(06)77567-6.
Collet Villette, A. M., M. A. Richard, F. Fourquet, S. Monestier, C. Gaudy, J. J. Bonerandi, and J. J. Grob. "Traitement de la maladie de Hailey-Hailey par laser ablatif CO2." Annales de Dermatologie et de Vénéréologie 132, no. 8-9 (September 2005): 637–40. http://dx.doi.org/10.1016/s0151-9638(05)79410-2.
Elfatoifi, F. Z., F. Fanian, S. Chiheb, and P. Humbert. "Maladie de Hailey-Hailey : efficacité de l’association doxycycline et vitamine PP." Annales de Dermatologie et de Vénéréologie 144, no. 3 (March 2017): 216–17. http://dx.doi.org/10.1016/j.annder.2016.09.031.
Sellami, K., K. Belhareth, E. Bahloul, A. Ghorbel, S. Boudaya, L. Ayadi, T. Boudaoura, M. Amouri, and H. Turki. "Maladie de Hailey–Hailey de révélation tardive et de siège atypique." Annales de Dermatologie et de Vénéréologie 146, no. 12 (December 2019): A252. http://dx.doi.org/10.1016/j.annder.2019.09.398.
Alsahli, M., C. Girard, B. Guillot, and O. Dereure. "Maladie de Hailey-Hailey des plis : intérêt et limites de la photothérapie dynamique." Annales de Dermatologie et de Vénéréologie 138, no. 12 (December 2011): A179—A180. http://dx.doi.org/10.1016/j.annder.2011.10.139.
Dousset, L., O. Cogrel, E. Imbert, A. Pham-Ledard, M. Beylot-Barry, and M. S. Doutre. "Intérêt de la toxine botulique dans la maladie de Hailey-Hailey : six cas." Annales de Dermatologie et de Vénéréologie 139, no. 6-7 (June 2012): H33—H34. http://dx.doi.org/10.1016/j.annder.2012.04.058.
Bennani, I., J. Ofaiche, C. Uthurriague, F. Fortenfant, L. Lamant, and J. Nougué. "Détection d’anticorps antidesmogléines circulants chez un patient atteint de maladie de Hailey-Hailey." Annales de Dermatologie et de Vénéréologie 139, no. 10 (October 2012): 621–25. http://dx.doi.org/10.1016/j.annder.2012.05.025.
Surinach, C. C., T. Passeron, L. Sillard, and J. P. Lacour. "Traitement de la maladie de Hailey-Hailey par laser Erbium fractionné : deux cas." Annales de Dermatologie et de Vénéréologie 139, no. 12 (December 2012): B226—B227. http://dx.doi.org/10.1016/j.annder.2012.10.394.
Дисертації з теми "Maladie de Hailey-Hailey":
Roy, Anne-Sophie. "Etude du lien fonctionnel entre deux régulateurs de l'homéostasie golgienne du Ca2+ et du Mn2+, TMEM165 et SPCA1, dans un modèle pathologique, la maladie de Hailey-Hailey." Thesis, Lille 1, 2020. http://www.theses.fr/2020LIL1S110.
SPCA1 is a P-type ATPase that transports a Ca2+ ion or a Mn2+ ion from the cytosol to the Golgi lumen by hydrolyzing one molecule of ATP. Another protein seems to be involved in the regulation of Ca2+ and Mn2+ homeostasis, namely TMEM165. Mutations in the ATP2C1 gene, encoding SPCA1 protein, and in the TMEM165 gene, encoding the protein of the same name, cause two different pathologies : a skin disease called Hailey-Hailey and a congenital disorder of glycosylation (CDG), respectively. While nothing seemed to link these two proteins, our results suggest a functional link. We have demonstrated, in two different cell lines (HeLa cells and fibroblasts), that SPCA1 and TMEM165 are close to each other within the Golgi apparatus. In addition, the function of SPCA1 appears to govern the expression of TMEM165. The latter is sensitive to cytosolic Mn2+ concentrations. In fibroblasts and keratinocytes of patients with Hailey-Hailey disease, in the presence of high concentrations of extracellular Mn2+, the expression of TMEM165 is much more sensitive to Mn2+ than in control cells. Using ICP-MS, we measured cellular Mn levels and found greater Mn accumulation in patient cells compared to control cells. Thanks to GPP130, a protein sensitive to the concentrations of Golgi Mn2+ concentrations, we have linked this higher accumulation of Mn2+ in the cells of patients with an increase of the Mn2+ concentration in the cytosol of these cells. In addition, SPCA1 also interacts with Cab45, a protein that binds Ca2+ in the Golgi, and both are involved in a novel way of proteins sorting at the TGN. We have shown, for the first time that the subcellular localization of Cab45 is disturbed in presence of higher concentration of MnCl2 in the culture medium of HHD fibroblasts compared to control fibroblasts. To date, we don’t know the molecular mechanism involved in this loss of Cab45 localization induced by Mn2+.Another evidence is the observation of the increase in the amount of SPCA1 which is concomitant with the degradation of TMEM165 in the presence of high concentrations of MnCl2 in the culture medium of HeLa cells and fibroblasts. This increase is probably due to a transcriptional increase in the ATP2C1 gene. In addition, we have shown that when the expression of one of these proteins is reduced by the CRISPR/Cas9 technique, the expression of the other is disrupted. All of these data tend to suggest a functional link between SPCA1 and TMEM165, two regulators of Mn2+ and Ca2+ homeostasis