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pro vyhledávání: '"Mammano, F"'
Akademický článek
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Autor:
Chee, J.M., Lanoue, L., Clary, D., Higgins, K., Bower, L., Flenniken, A., Guo, R., Adams, D.J., Bosch, F., Braun, R.E., Brown, S.D.M., Chin, H.J.G., Dickinson, M.E., Hsu, C.W., Dobbie, M., Gao, X., Galande, S., Grobler, A., Heaney, J.D., Herault, Y., de Angelis, M.H., Mammano, F., Nutter, L.M.J, Parkinson, H., Qin, C., Shiroishi, T., Sedlacek, R., Seong, J.K., Xu, Y., Brooks, B., McKerlie, C., Lloyd, K.C.K., Westerberg, H., Moshiri, A.
BACKGROUND: Microphthalmia, anophthalmia, and coloboma (MAC) spectrum disease encompasses a group of eye malformations which play a role in childhood visual impairment. Although the predominant cause of eye malformations is known to be heritable in n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=mdc______med::49c78b917f4a87b8e4585ceec35f7074
http://edoc.mdc-berlin.de/23140/1/23140oa.pdf
http://edoc.mdc-berlin.de/23140/1/23140oa.pdf
Autor:
Chee, J. M., Lanoue, L., Clary, D., Higgins, K., Bower, L., Flenniken, A., Guo, R., Adams, D. J., Bosch, F., Braun, R. E., Brown, S. D. M., Chin, H. J. G., Dickinson, M. E., Hsu, C. W., Dobbie, M., Gao, X., Galande, S., Grobler, A., Heaney, J. D., Herault, Y., de Angelis, M. H., Mammano, F., Nutter, L. M. J., Parkinson, H., Qin, C., Shiroishi, T., Sedlacek, R., Seong, J. K., Xu, Y., Ackert-Bicknell, C., Adams, D., Adoum, A. T., Aguilar-Pimentel, J. A., Akoma, U., Ali-Hadji, D., Amarie, O. V., André, P., Auburtin, A., Bam’Hamed, C., Beckers, J., Beig, J., Berberovic, Z., Bezginov, A., Birling, M. C., Boroviak, K., Bottomley, J., Bürger, A., Busch, D. H., Butterfield, N. C., Cacheiro, P., Calzada-Wack, J., Cambridge, E. L., Camilleri, S., Champy, M. F., Cater, H., Charles, P., Chesler, E. J., Cho, Y. L., Christiansen, A. E., Cipriani, V., Cockle, N., Codner, G., Creighton, A., Cruz, M., Curry, K. F., D’Souza, A., Danisment, O., Delbarre, D., Dewhurst, H. F., Doe, B., Dorr, A., Giesert, F., Duddy, G., Duffin, K., El Amri, A., Elrick, H., Eskandarian, M., Fray, M., Frost, A., Fuchs, H., Gailus-Durner, V., Gampe, K. K., Ganguly, M., Gannon, D., Garrett, L., Gertsenstein, M., Gleeson, D., Goodwin, L., Graw, J., Grimsrud, K., Haselimashhadi, H., Hobson, L., Hörlein, A., Hölter, S. M., Hong, S. H., Horner, N., Trainor, A. G., Huang, Z., Kane, C., Katsman, Y.
Publikováno v:
BMC Biology. 21
Background Microphthalmia, anophthalmia, and coloboma (MAC) spectrum disease encompasses a group of eye malformations which play a role in childhood visual impairment. Although the predominant cause of eye malformations is known to be heritable in na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9ff3b28f8cd1d8878613ce4e0623d60
https://doi.org/10.1186/s12915-022-01475-0
https://doi.org/10.1186/s12915-022-01475-0
Autor:
Ficarella, R., Di Leva, F., Bortolozzi, M., Ortolano, S., Donaudy, F., Petrillo, M., Melchionda, S., Lelli, A., Domi, T., Fedrizzi, L., Lim, D., Shull, G. E., Gasparini, P., Brini, M., Mammano, F., Carafoli, E.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2007 Jan . 104(5), 1516-1521.
Externí odkaz:
https://www.jstor.org/stable/25426321
Autor:
de Araujo, A. Caterino, Neitzert, E., Mammano, F., Del Mistro, A., De Rossi, A., Chieco-Bianchi, L.
Publikováno v:
European Journal of Epidemiology, 1994 Apr 01. 10(2), 165-171.
Externí odkaz:
https://www.jstor.org/stable/3521216
Publikováno v:
Retrovirology, Vol 6, Iss Suppl 3, p P135 (2009)
Externí odkaz:
https://doaj.org/article/a9d3cb53bf624a24bf9e495fa933a0aa
Akademický článek
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Publikováno v:
In Cell Calcium August 2001 30(2):131-140
Autor:
Johnson, S.L., Ceriani, F., Houston, O., Polishchuk, R., Polishchuk, E., Crispino, G., Zorzi, V., Mammano, F., Marcotti, W.
Publikováno v:
The Journal of Neuroscience
The Journal of neuroscience 37 (2017): 258–268. doi:10.1523/JNEUROSCI.2251-16.2017
info:cnr-pdr/source/autori:Johnson, Stuart L.; Ceriani, Federico; Houston, Oliver; Polishchuk, Roman; Polishchuk, Elena; Crispino, Giulia; Zorzi, Veronica; Mammano, Fabio; Marcotti, Walter/titolo:Connexin-Mediated Signaling in Nonsensory Cells Is Crucial for the Development of Sensory Inner Hair Cells in the Mouse Cochlea/doi:10.1523%2FJNEUROSCI.2251-16.2017/rivista:The Journal of neuroscience/anno:2017/pagina_da:258/pagina_a:268/intervallo_pagine:258–268/volume:37
The Journal of neuroscience 37 (2017): 258–268. doi:10.1523/JNEUROSCI.2251-16.2017
info:cnr-pdr/source/autori:Johnson, Stuart L.; Ceriani, Federico; Houston, Oliver; Polishchuk, Roman; Polishchuk, Elena; Crispino, Giulia; Zorzi, Veronica; Mammano, Fabio; Marcotti, Walter/titolo:Connexin-Mediated Signaling in Nonsensory Cells Is Crucial for the Development of Sensory Inner Hair Cells in the Mouse Cochlea/doi:10.1523%2FJNEUROSCI.2251-16.2017/rivista:The Journal of neuroscience/anno:2017/pagina_da:258/pagina_a:268/intervallo_pagine:258–268/volume:37
Mutations in the genes encoding for gap junction proteins connexin 26 (Cx26) and connexin 30 (Cx30) have been linked to syndromic and nonsyndromic hearing loss in mice and humans. The release of ATP from connexin hemichannels in cochlear nonsensory c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::89a48b9a0de028d22643142979f493de
https://eprints.whiterose.ac.uk/110898/1/258.full.pdf
https://eprints.whiterose.ac.uk/110898/1/258.full.pdf