Zobrazeno 1 - 10
of 1 599
pro vyhledávání: '"K, Gross"'
Autor:
Roly Megaw, Abigail Moye, Zhixian Zhang, Fay Newton, Fraser McPhie, Laura C. Murphy, Lisa McKie, Feng He, Melissa K. Jungnickel, Alex von Kriegsheim, Peter A. Tennant, Chloe Brotherton, Christine Gurniak, Alecia K. Gross, Laura M. Machesky, Theodore G. Wensel, Pleasantine Mill
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-13 (2024)
Abstract As signalling organelles, cilia regulate their G protein-coupled receptor content by ectocytosis, a process requiring localised actin dynamics to alter membrane shape. Photoreceptor outer segments comprise an expanse of folded membranes (dis
Externí odkaz:
https://doaj.org/article/162f25833a9b438992ccafbff79b3556
Publikováno v:
Frontiers in Ophthalmology, Vol 2 (2022)
The maintenance of intraocular pressure (IOP) is critical to preserving the pristine optics required for vision. Disturbances in IOP can directly impact the optic nerve and retina, and inner retinal injury can occur following acute and chronic IOP el
Externí odkaz:
https://doaj.org/article/5a84dd9cc19e4bff91ede5c12bafac92
Autor:
Paulo E. P. Teixeira, Daniela R. B. Tavares, Kevin Pacheco-Barrios, Luis Castelo Branco, Eric Slawka, Julie Keysor, Virginia F. M. Trevisani, Doug K Gross, Felipe Fregni
Publikováno v:
Biomedicines, Vol 11, Iss 1, p 4 (2022)
The study’s objective was to develop a clinical prediction rule that predicts a clinically significant analgesic effect on chronic knee osteoarthritis pain after transcranial direct current stimulation treatment. This is a secondary analysis from a
Externí odkaz:
https://doaj.org/article/c98f26d8dad9477f82275739dd933cf5
Autor:
Arens Taga, Raha Dastgheyb, Christa Habela, Jessica Joseph, Jean‐Philippe Richard, Sarah K. Gross, Giuseppe Lauria, Gabsang Lee, Norman Haughey, Nicholas J. Maragakis
Publikováno v:
Stem Cells Translational Medicine, Vol 8, Iss 12, Pp 1272-1285 (2019)
Abstract The ability to generate human‐induced pluripotent stem cell (hiPSC)‐derived neural cells displaying region‐specific phenotypes is of particular interest for modeling central nervous system biology in vitro. We describe a unique method
Externí odkaz:
https://doaj.org/article/90f3a373826542afa217b6c5c8f992af
Autor:
T.J. Hollingsworth, Meredith G. Hubbard, Hailey J. Levi, William White, Xiangdi Wang, Raven Simpson, Monica M. Jablonski, Alecia K. Gross
Publikováno v:
Biomolecules, Vol 11, Iss 8, p 1163 (2021)
Retinitis pigmentosa (RP) is a hereditary disease of the retina that results in complete blindness. Currently, there are very few treatments for the disease and those that exist work only for the recessively inherited forms. To better understand the
Externí odkaz:
https://doaj.org/article/51222d457ee84673bc4a2aceedf7499d
Publikováno v:
Science and Technology of Zirconia V ISBN: 9781003421290
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::186847c34952a181c0647af9b452b890
https://doi.org/10.1201/9781003421290-8
https://doi.org/10.1201/9781003421290-8
Autor:
M A M Hammad, D W Barham, T Nguyen, L Jenkins, D Swerdloff, K Gross, G Hatzichristodoulou, J Jones, J Hotaling, I Pearce, H Sadeghi-Nejad, J Simhan, F Yafi, M Gross
Publikováno v:
The Journal of Sexual Medicine. 20
Introduction Inflatable penile prosthesis (IPP) insertion is recommended for the treatment of patients with Peyronie’s Disease (PD) and significant erectile dysfunction (ED). Adjunctive procedures such as modeling, plication, or incision/excision a
Autor:
D Barham, M Hammad, D Swerdloff, K Gross, G Hatzichristodoulou, J Jones, J Hotaling, I Pearce, H Sadeghi-Nejad, J Simhan, F Yafi, M Gross
Publikováno v:
The Journal of Sexual Medicine. 20
Introduction Inflatable penile prosthesis (IPP) can be used in both acute and delayed management of priapism-induced erectile dysfunction. Prolonged priapism may result in corporal fibrosis that makes IPP placement more difficult. The current literat
Akademický článek
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Autor:
T.J. Hollingsworth, Alecia K. Gross
Publikováno v:
Cells, Vol 9, Iss 3, p 630 (2020)
Inherited retinal dystrophies (RDs) are heterogenous in many aspects including genes involved, age of onset, rate of progression, and treatments. While RDs are caused by a plethora of different mutations, all result in the same outcome of blindness.
Externí odkaz:
https://doaj.org/article/380a9f6648ca40378229aa6e90201405