Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Moran Rubin"'
Autor:
Moran Rubin, Itay Barnea, Yoav N. Nygate, Nir A. Turko, Miki Haifler, Natan T. Shaked, Alon Shalev, Mattan Levi, Simcha K. Mirsky, Gili Dardikman-Yoffe
Publikováno v:
Proceedings of the National Academy of Sciences
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America
Significance We present a method for virtual staining for morphological analysis of individual biological cells based on stain-free digital holography, allowing clinicians and biologists to visualize and analyze the cells as if they have been chemica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b59128a362717d25b855372151c6941a
https://doi.org/10.1073/pnas.1919569117
https://doi.org/10.1073/pnas.1919569117
Publikováno v:
Imaging and Applied Optics 2018 (3D, AO, AIO, COSI, DH, IS, LACSEA, LS&C, MATH, pcAOP).
We suggest new platforms for compressing up to 16 off-axis interferograms into a single interferogram for data compression and real-time 3-D processing and visualization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78218bd7c2794941cc4abac54aae65a4
https://doi.org/10.1364/3d.2018.3w5g.1
https://doi.org/10.1364/3d.2018.3w5g.1
Publikováno v:
Imaging and Applied Optics 2018 (3D, AO, AIO, COSI, DH, IS, LACSEA, LS&C, MATH, pcAOP).
We suggest a new approach for classification of label-free quantitative phase maps of live cells using only a small training set, based on a combination between generative adversarial networks (GANs) and transfer learning.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0174a9407ca3ff00c720b3d7050564dc
https://doi.org/10.1364/cosi.2018.cw2e.7
https://doi.org/10.1364/cosi.2018.cw2e.7
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S130- (2023)
Externí odkaz:
https://doaj.org/article/3a38e44d81d34ad4b1c04d48f2fba20c
Publikováno v:
Optics letters. 42(22)
We present a new holographic concept, named six-pack holography (6PH), in which we compress six off-axis holograms into a single multiplexed off-axis hologram without loss of magnification or resolution. The multiplexed hologram contains straight off
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2d1dc8979105da8b9a81ca1dc0227b1
https://pubmed.ncbi.nlm.nih.gov/29140325
https://pubmed.ncbi.nlm.nih.gov/29140325
Autor:
Saja Fadila, Bertrand Beucher, Iria González Dopeso-Reyes, Anat Mavashov, Marina Brusel, Karen Anderson, Caroline Ismeurt, Ethan M. Goldberg, Ana Ricobaraza, Ruben Hernandez-Alcoceba, Eric J. Kremer, Moran Rubinstein
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 12 (2023)
Dravet syndrome (DS), an intractable childhood epileptic encephalopathy with a high fatality rate, is typically caused by loss-of-function mutations in one allele of SCN1A, which encodes NaV1.1, a 250-kDa voltage-gated sodium channel. In contrast to
Externí odkaz:
https://doaj.org/article/2ad9803b50ee4a45bf9f3b05e52e1d3d
Autor:
Anat Mavashov, Marina Brusel, Jiaxing Liu, Victoria Woytowicz, Haneui Bae, Ying-Hsin Chen, Vardhan S. Dani, Elena Cardenal-Muñoz, Vittoria Spinosa, José Ángel Aibar, Moran Rubinstein
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 17 (2023)
Dravet syndrome (Dravet) is a severe congenital developmental genetic epilepsy caused by de novo mutations in the SCN1A gene. Nonsense mutations are found in ∼20% of the patients, and the R613X mutation was identified in multiple patients. Here we
Externí odkaz:
https://doaj.org/article/a514e71d032547999588604f107d69b1
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Dravet syndrome (Dravet) is a rare and severe form of developmental epileptic encephalopathy. Antiseizure medications (ASMs) for Dravet patients include valproic acid (VA) or clobazam (CLB), with or without stiripentol (STP), while sodium channel blo
Externí odkaz:
https://doaj.org/article/2def9f124f8e4d26b797b4defedf07f4
Autor:
Lucia Mora-Jimenez, Miguel Valencia, Rocio Sanchez-Carpintero, Jan Tønnesen, Saja Fadila, Moran Rubinstein, Manuela Gonzalez-Aparicio, Maria Bunuales, Eva Fernandez-Pierola, Maria Jesus Nicolas, Elena Puerta, Cristina Miguelez, Paula Gimenez Minguez, Sara Lumbreras, Gloria Gonzalez-Aseguinolaza, Ana Ricobaraza, Ruben Hernandez-Alcoceba
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 25, Iss , Pp 585-602 (2021)
Dravet syndrome is a genetic encephalopathy characterized by severe epilepsy combined with motor, cognitive, and behavioral abnormalities. Current antiepileptic drugs achieve only partial control of seizures and provide little benefit on the patient
Externí odkaz:
https://doaj.org/article/d8a21f6b96294c4686222a2f4ad8317e
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Dravet syndrome is severe childhood-onset epilepsy, caused by loss of function mutations in the SCN1A gene, encoding for the voltage-gated sodium channel NaV1.1. The leading hypothesis is that Dravet is caused by selective reduction in the excitabili
Externí odkaz:
https://doaj.org/article/542a7252ad7e454b81ce48af6dff1b54