Zobrazeno 1 - 10
of 217
pro vyhledávání: '"Thomas W White"'
Autor:
Giacomo Sermonesi, Riccardo Bertelli, Fredric M. Pieracci, Zsolt J. Balogh, Raul Coimbra, Joseph M. Galante, Andreas Hecker, Dieter Weber, Zachary M. Bauman, Susan Kartiko, Bhavik Patel, SarahAnn S. Whitbeck, Thomas W. White, Kevin N. Harrell, Daniele Perrina, Alessia Rampini, Brian Tian, Francesco Amico, Solomon G. Beka, Luigi Bonavina, Marco Ceresoli, Lorenzo Cobianchi, Federico Coccolini, Yunfeng Cui, Francesca Dal Mas, Belinda De Simone, Isidoro Di Carlo, Salomone Di Saverio, Agron Dogjani, Andreas Fette, Gustavo P. Fraga, Carlos Augusto Gomes, Jim S. Khan, Andrew W. Kirkpatrick, Vitor F. Kruger, Ari Leppäniemi, Andrey Litvin, Andrea Mingoli, David Costa Navarro, Eliseo Passera, Michele Pisano, Mauro Podda, Emanuele Russo, Boris Sakakushev, Domenico Santonastaso, Massimo Sartelli, Vishal G. Shelat, Edward Tan, Imtiaz Wani, Fikri M. Abu-Zidan, Walter L. Biffl, Ian Civil, Rifat Latifi, Ingo Marzi, Edoardo Picetti, Manos Pikoulis, Vanni Agnoletti, Francesca Bravi, Carlo Vallicelli, Luca Ansaloni, Ernest E. Moore, Fausto Catena
Publikováno v:
World Journal of Emergency Surgery, Vol 19, Iss 1, Pp 1-35 (2024)
Abstract Background Rib fractures are one of the most common traumatic injuries and may result in significant morbidity and mortality. Despite growing evidence, technological advances and increasing acceptance, surgical stabilization of rib fractures
Externí odkaz:
https://doaj.org/article/ab27c29fa0fe454cb5512281972ddd3d
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e52894 (2012)
The mouse semi-dominant Nm2249 mutation displays variable cataracts in heterozygous mice and smaller lenses with severe cataracts in homozygous mice. This mutation is caused by a Gja8(R205G) point mutation in the second extracellular loop of the Cx50
Externí odkaz:
https://doaj.org/article/4a2e06b66abf4d41a27e9888d42a5a0c
Publikováno v:
PLoS ONE, Vol 5, Iss 9 (2010)
Cataracts, named for any opacity in the ocular lens, remain the leading cause of vision loss in the world. Non-surgical methods for cataract prevention are still elusive. We have genetically tested whether enhanced lens gap junction communication, pr
Externí odkaz:
https://doaj.org/article/f917d4143be44348b9626d8c18495044
Autor:
Thomas W White
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 7, Iss 1, Pp 107-108 (2012)
Externí odkaz:
https://doaj.org/article/66bd685667224b6eb4df9aa0e19242b4
Autor:
Chiara Peres, Caterina Sellitto, Chiara Nardin, Sabrina Putti, Tiziana Orsini, Chiara Di Pietro, Daniela Marazziti, Adriana Vitiello, Arianna Calistri, Mara Rigamonti, Ferdinando Scavizzi, Marcello Raspa, Francesco Zonta, Guang Yang, Thomas W. White, Fabio Mammano
Publikováno v:
EBioMedicine, Vol 89, Iss , Pp 104453- (2023)
Summary: Background: Keratitis ichthyosis deafness (KID) syndrome is a rare disorder caused by hemichannel (HC) activating gain-of-function mutations in the GJB2 gene encoding connexin (Cx) 26, for which there is no cure, or current treatments based
Externí odkaz:
https://doaj.org/article/bd169d1992394aeab17af27a91b30026
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Mutations in five different genes encoding connexin channels cause eleven clinically defined human skin diseases. Keratitis ichthyosis deafness (KID) syndrome is caused by point mutations in the GJB2 gene encoding Connexin 26 (Cx26) which re
Externí odkaz:
https://doaj.org/article/c1607066f032439cbe660364f8f1689b
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
The transparency and refractive properties of the lens are maintained by the cellular physiology provided by an internal microcirculation system that utilizes spatial differences in ion channels, transporters and gap junctions to establish standing e
Externí odkaz:
https://doaj.org/article/98f31cc8d2c14a7fab6d2f2bbb47cf4c
Publikováno v:
Cells, Vol 11, Iss 17, p 2708 (2022)
We have previously shown that the conditional deletion of either the p110α catalytic subunit of phosphatidylinositol 3-kinase (PI3K), or its opposing phosphatase, phosphatase and tensin homolog (PTEN), had distinct effects on lens growth and homeost
Externí odkaz:
https://doaj.org/article/16ef93e50219409f8f8ee6262ff8de60
Autor:
Zhengping Hu, Wen Shi, Manuel A. Riquelme, Qian Shi, Sondip Biswas, Woo-Kuen Lo, Thomas W. White, Sumin Gu, Jean X. Jiang
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract Connexins play essential roles in lens homeostasis and development. Here, we identified a new role for Cx50 that mediates cell-cell adhesion function. Cx50 enhanced the adhesive capability of AQP0. Interestingly, the expression of Cx50 alone
Externí odkaz:
https://doaj.org/article/adbf4e47e6d44d61a17a14eb20b331b8
Publikováno v:
FASEB J
Charged multivesicular-body protein 4b (CHMP4B) is a core sub-unit of the endosomal sorting complex required for transport-III (ESCRT-III) machinery that serves myriad remodeling and scission processes of biological membranes. Mutation of the human C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a21792e59b342599c697118429fa4651
https://doi.org/10.1096/fj.202201368rr
https://doi.org/10.1096/fj.202201368rr