Publications associées à Congenital red–green color blindness

Extreme Spatial Dispersion in Nonlocally Resonant Elastic Metamaterials

Romain Christophe Rémy Fleury, Aleksi Antoine Bossart

To date, the vast majority of architected materials have leveraged two physical principles to control wave behavior, namely, Bragg interference and local resonances. Here, we describe a third path: structures that accommodate a finite number of delocalized ...

2023

Two Massive, Compact, and Dust-obscured Candidate z ≃ 8 Galaxies Discovered by JWST

Michaela Hirschmann

We present a search for extremely red, dust-obscured, z > 7 galaxies with JWST/NIRCam+MIRI imaging over the first 20 arcmin(2) of publicly available Cycle 1 data from the COSMOS-Web, CEERS, and PRIMER surveys. Based on their red color in F277W-F444W (simil ...

Iop Publishing Ltd2023

Magic Prints: Image-Changing Prints Observed under Visible and 365 nm UV Light

Petar Pjanic, Marjan Shahpaski

In this paper we propose a novel layered-printing method consisting of superposed visible cmy and invisible fluorescent ultraviolet (UV) rgb inks. Our approach can be used to generate a variety of visual color-alteration effects such as revealing two compl ...

I S & T-SOC IMAGING SCIENCE TECHNOLOGY2019

Color Representation in Deep Neural Networks

Sabine Süsstrunk, Martin Pierre Engilberge, Edo Collins

Convolutional neural networks are top-performers on image classification tasks. Understanding how they make use of color information in images may be useful for various tasks. In this paper we analyze the representation learned by a popular CNN to detect a ...

2017

Anomalous anisotropic exciton temperature dependence in rutile TiO2

Majed Chergui, Edoardo Baldini

Elucidating the details of electron-phonon coupling in semiconductors and insulators is a topic of pivotal interest, as it governs the transport mechanisms and is responsible for various phenomena such as spectral-weight transfers to phonon sidebands and s ...

2017

Retina Color-Opponency Based Pursuit Implemented Through Spiking Neural Networks in the Neurorobotics Platform

Marc-Oliver Gewaltig, Egidio Falotico, Lorenzo Vannucci, Paul Levi, Georg Hinkel, Stefan Ulbrich, Alessandro Ambrosano, Ugo Albanese, Murat Kirtay

The 'red-green' pathway of the retina is classically recognized as one of the retinal mechanisms allowing humans to gather color information from light, by combining information from L-cones and M-cones in an opponent way. The precise retinal circuitry tha ...

Springer Int Publishing Ag2016

Push-pull dioxaborine as fluorescent molecular rotor: far-red fluorogenic probe for ligand-receptor interactions

Iuliia Karpenko

Fluorescent solvatochromic dyes and molecular rotors have attracted considerable attention as fluorogenic probes because of background-free detection of biomolecules in live cells in no-wash conditions. Herein, we introduce a push-pull boron-containing (di ...

Royal Society of Chemistry2016

Origin of the Spectral Shifts among the Early Intermediates of the Rhodopsin Photocycle

Ursula Röthlisberger, Ivano Tavernelli, Pablo Campomanes Ramos, Marilisa Neri, Stefano Vanni, Bruno Araujo Cautiero Horta

A combined strategy based on the computation of absorption energies, using the ZINDO/S semiempirical method, for a statistically relevant number of thermally sampled configurations extracted from QM/MM trajectories is used to establish a one-to-one corresp ...

2014

Extreme Tuning of Redox and Optical Properties of Cationic Cyclometalated Iridium(III) Isocyanide Complexes

Michael Graetzel, Mohammad Khaja Nazeeruddin, Rosario Scopelliti

We report seven heteroleptic cationic iridium(III) complexes with cyclometalating N-arylazoles and alkyl/aryl isocyanides, ((CN)-N-boolean AND)(2)Ir(CNR)(2), and characterize two of them by crystal structure analysis. The complexes are air- and m ...

American Chemical Society2013

Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene

Farah Ouechtati

Complete achromatopsia is a rare autosomal recessive disease associated with CNGA3, CNGB3, GNAT2 and PDE6C mutations. This retinal disorder is characterized by complete loss of color discrimination due to the absence or alteration of the cones function. Th ...

2011