@article{1104,
  abstract     = {In the early visual system, cells of the same type perform the same computation in different places of the visual field. How these cells code together a complex visual scene is unclear. A common assumption is that cells of a single-type extract a single-stimulus feature to form a feature map, but this has rarely been observed directly. Using large-scale recordings in the rat retina, we show that a homogeneous population of fast OFF ganglion cells simultaneously encodes two radically different features of a visual scene. Cells close to a moving object code quasilinearly for its position, while distant cells remain largely invariant to the object's position and, instead, respond nonlinearly to changes in the object's speed. We develop a quantitative model that accounts for this effect and identify a disinhibitory circuit that mediates it. Ganglion cells of a single type thus do not code for one, but two features simultaneously. This richer, flexible neural map might also be present in other sensory systems.},
  author       = {Deny, Stephane and Ferrari, Ulisse and Mace, Emilie and Yger, Pierre and Caplette, Romain and Picaud, Serge and Tkacik, Gasper and Marre, Olivier},
  issn         = {20411723},
  journal      = {Nature Communications},
  number       = {1},
  publisher    = {Nature Publishing Group},
  title        = {{Multiplexed computations in retinal ganglion cells of a single type}},
  doi          = {10.1038/s41467-017-02159-y},
  volume       = {8},
  year         = {2017},
}

@inbook{1094,
  abstract     = {Immunogold labeling of freeze-fracture replicas has recently been used for high-resolution visualization of protein localization in electron microscopy. This method has higher labeling efficiency than conventional immunogold methods for membrane molecules allowing precise quantitative measurements. However, one of the limitations of freeze-fracture replica immunolabeling is difficulty in keeping structural orientation and identifying labeled profiles in complex tissues like brain. The difficulty is partly due to fragmentation of freeze-fracture replica preparations during labeling procedures and limited morphological clues on the replica surface. To overcome these issues, we introduce here a grid-glued replica method combined with SEM observation. This method allows histological staining before dissolving the tissue and easy handling of replicas during immunogold labeling, and keeps the whole replica surface intact without fragmentation. The procedure described here is also useful for matched double-replica analysis allowing further identification of labeled profiles in corresponding P-face and E-face.},
  author       = {Harada, Harumi and Shigemoto, Ryuichi},
  booktitle    = {High-Resolution Imaging of Cellular Proteins},
  issn         = {1611-3349},
  pages        = {203 -- 216},
  publisher    = {Springer},
  title        = {{Immunogold protein localization on grid-glued freeze-fracture replicas}},
  doi          = {10.1007/978-1-4939-6352-2_12},
  volume       = {1474},
  year         = {2016},
}