| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Lily G Fogg, Stamatina Isari, Jonathan E Barnes, Jagdish Suresh Patel, N Justin Marshall, Walter Salzburger, Fabio Cortesi, Fanny de Busserolle. Deep-sea fish reveal alternative pathway for vertebrate visual development. bioRxiv : the preprint server for biology. 2024-10-17. PMID:39416096. |
through development, these fishes either retain this rod-like cone retina ( |
2024-10-17 |
2024-10-19 |
Not clear |
| Aindrila Saha, Theodore Bucci, Jacob Baudin, Raunak Sinh. Regional tuning of photoreceptor adaptation in the primate retina. Nature communications. vol 15. issue 1. 2024-10-11. PMID:39394185. |
however, little is known about the properties of cone adaptation in the specialized region of the primate central retina called the fovea, which is densely packed with cones and mediates high-acuity central vision. |
2024-10-11 |
2024-10-14 |
monkey |
| Edward V Famigliett. Mammalian Retinal Bipolar Cells: Morphological Identification and Systematic Classification in Rabbit Retina. bioRxiv : the preprint server for biology. 2024-09-30. PMID:39345639. |
the present detailed study of more than 800 bipolar cells in ten golgi-impregnated rabbit retinas indicates that there are 14-16 types of cone bipolar cell and one type of rod bipolar cell in rabbit retina. |
2024-09-30 |
2024-10-02 |
mouse |
| Soo-Young Kim, Christine Haewon Park, Bo-Hyun Moon, Gail K Seabol. Murine Retina Outer Plexiform Layer Development and Transcriptome Analysis of Pre-Synapses in Photoreceptors. Life (Basel, Switzerland). vol 14. issue 9. 2024-09-28. PMID:39337887. |
the transcription factor neural retina leucine zipper (nrl) determines the rod vs. cone photoreceptor cell fate and is critical for rod differentiation. |
2024-09-28 |
2024-10-01 |
Not clear |
| S Supanji, A B I Perdamaian, D K Paramita, R I Jeni. An uncommon case of retinitis pigmentosa patients based on clinical and genetic study. The Medical journal of Malaysia. vol 79. issue Suppl 4. 2024-08-31. PMID:39215425. |
a genetics analysis was conducted in case 1, finding various mutations associated with ird mutation at the cone protein-encoded gene that concentrated at the central and rod protein-encoded gene concentrated at the peripheral retina. |
2024-08-31 |
2024-09-04 |
Not clear |
| Jingjin Xu, Chengtian Zhao, Yunsi Kan. The Formation and Renewal of Photoreceptor Outer Segments. Cells. vol 13. issue 16. 2024-08-28. PMID:39195247. |
in the retina, rod and cone photoreceptor neurons are the initial sites where vision forms. |
2024-08-28 |
2024-08-30 |
Not clear |
| Yeon Jin Kim, Orin Packer, Dennis M Dace. A circuit motif for color in the human foveal retina. Proceedings of the National Academy of Sciences of the United States of America. vol 121. issue 36. 2024-08-27. PMID:39190352. |
the neural pathways that start human color vision begin in the complex synaptic network of the foveal retina where signals originating in long (l), middle (m), and short (s) wavelength-sensitive cone photoreceptor types are compared through antagonistic interactions, referred to as opponency. |
2024-08-27 |
2024-08-30 |
human |
| Yeon Jin Kim, Orin Packer, Dennis M Dace. A circuit motif for color in the human foveal retina. Proceedings of the National Academy of Sciences of the United States of America. vol 121. issue 36. 2024-08-27. PMID:39190352. |
yet linking cone opponency in the nonhuman primate retina to color mechanisms in human vision has proven particularly difficult. |
2024-08-27 |
2024-08-30 |
human |
| Yeon Jin Kim, Orin Packer, Dennis M Dace. A circuit motif for color in the human foveal retina. Proceedings of the National Academy of Sciences of the United States of America. vol 121. issue 36. 2024-08-27. PMID:39190352. |
these two ganglion cell types are postsynaptic to both s-on and l vs. m opponent midget bipolar cells and thus define excitatory pathways in the foveal retina that merge the cardinal red-green and blue-yellow circuits, with the potential for trichromatic cone opponency at the first stage of human vision. |
2024-08-27 |
2024-08-30 |
human |
| Stephanie Niklaus, Stella M K Glasauer, Peter Kovermann, Kulsum F Farshori, Lucia Cadetti, Simon Früh, Nicolas N Rieser, Matthias Gesemann, Jingjing Zang, Christoph Fahlke, Stephan C F Neuhaus. Glutamate transporters are involved in direct inhibitory synaptic transmission in the vertebrate retina. Open biology. vol 14. issue 7. 2024-07-30. PMID:39079673. |
in the zebrafish retina, these transporters are located at the dendritic tips of on-bipolar cells and interact with all four types of cone photoreceptors. |
2024-07-30 |
2024-08-02 |
zebrafish |
| Mingchao Li, Yuexuan Wang, Huiyun Gao, Zhengwang Xia, Chaofan Zeng, Kun Huang, Zhaoqi Zhu, Jianfeng Lu, Qiang Chen, Xiaoyan Ke, Weiwei Zhan. Exploring autism via the retina: Comparative insights in children with autism spectrum disorder and typical development. Autism research : official journal of the International Society for Autism Research. 2024-07-30. PMID:39075780. |
our findings present potential novel characteristics of asd: the thickness of the ellipsoid zone (ez) with cone photoreceptors was significantly increased in asd; the large-caliber arteriovenous of the inner retina was significantly reduced in asd; these changes in the ez and arteriovenous were more significant in the left eye than in the right eye. |
2024-07-30 |
2024-08-02 |
Not clear |
| Fenglan Wang, Wenhui Zhong, Jun Zhan. Investigating Retinal Circuits and Molecular Localization by Pre-Embedding Immunoelectron Microscopy. Journal of visualized experiments : JoVE. issue 209. 2024-07-29. PMID:39072644. |
to better investigate retinal circuits and cross-talk, such as the link between cone and rod pathways, and precise molecular localization (neurotransmitters or neuropeptides), such as the presence of substance p-like immunoreactivity in the mouse retina, we employed a pre-embedding immunoelectron microscopy (immuno-em) method to explore synaptic connections and organization. |
2024-07-29 |
2024-08-02 |
mouse |
| Deepayan Kar, Ramya Singireddy, Yeon Jin Kim, Orin Packer, Richard Schalek, Dongfeng Cao, Kenneth R Sloan, Andreas Pollreisz, Dennis M Dacey, Christine A Curci. Unusual morphology of foveal Müller glia in an adult human born pre-term. Frontiers in cellular neuroscience. vol 18. 2024-07-12. PMID:38994326. |
the fovea of the human retina, a specialization for acute and color vision, features a high concentration of cone photoreceptors. |
2024-07-12 |
2024-07-14 |
human |
| Adree Songco-Aguas, William N Grimes, Fred Riek. Rod-cone signal interference in the retina shapes perception in primates. Frontiers in ophthalmology. vol 3. 2024-07-10. PMID:38983027. |
here we relate circuit-level processing of rod and cone signals in the non-human primate retina to a known break in the normal seamlessness of human vision - a surprising inability to see high contrast flickering lights under specific conditions. |
2024-07-10 |
2024-07-12 |
mouse |
| Riley Ferguson, Kiyoharu J Miyagishima, Francisco M Nadal-Nicolas, Wei L. Characterizing the rod pathway in cone-dominated thirteen-lined ground squirrels. Frontiers in ophthalmology. vol 3. 2024-07-08. PMID:38974057. |
this contrasts with the mouse retina, where they significantly contribute to cone signaling pathways. |
2024-07-08 |
2024-07-11 |
mouse |
| Riley Ferguson, Kiyoharu J Miyagishima, Francisco M Nadal-Nicolas, Wei L. Characterizing the rod pathway in cone-dominated thirteen-lined ground squirrels. Frontiers in ophthalmology. vol 3. 2024-07-08. PMID:38974057. |
therefore, the aii's original function is likely that of a 'rod' amacrine cell, and its role in cone pathways in the mouse retina might be an adaptive feature stemming from its rod dominance. |
2024-07-08 |
2024-07-11 |
mouse |
| Prakash Adhikari, Samir Uprety, Beatrix Feigl, Andrew J Zel. Melanopsin-mediated amplification of cone signals in the human visual cortex. Proceedings. Biological sciences. vol 291. issue 2023. 2024-05-29. PMID:38808443. |
although melanopsin and cone photoresponses can be mediated via separate pathways, the connectivity of melanopsin cells across all levels of the retina enables them to modify cone signals. |
2024-05-29 |
2024-06-03 |
human |
| Prakash Adhikari, Samir Uprety, Beatrix Feigl, Andrew J Zel. Melanopsin-mediated amplification of cone signals in the human visual cortex. Proceedings. Biological sciences. vol 291. issue 2023. 2024-05-29. PMID:38808443. |
by increasing the melanopsin activation, a reverse response pattern was observed with cone signals being supressed in the retina by 27% ( |
2024-05-29 |
2024-06-03 |
human |
| Joseph Kreis, Joseph Carrol. Applications of Adaptive Optics Imaging for Studying Conditions Affecting the Fovea. Annual review of vision science. 2024-04-18. PMID:38635871. |
the fovea is a highly specialized region of the central retina, defined by an absence of inner retinal layers and the accompanying vasculature, an increased density of cone photoreceptors, a near absence of rod photoreceptors, and unique private-line photoreceptor to midget ganglion cell circuitry. |
2024-04-18 |
2024-04-21 |
Not clear |
| Rumi Kawashima, Kenji Matsushita, Kenji Mandai, Yuko Sugita, Tomohiko Maruo, Kiyohito Mizutani, Yoshihiro Midoh, Akiko Oguchi, Yasuhiro Murakawa, Kazuki Kuniyoshi, Ryohei Sato, Takahisa Furukawa, Kohji Nishida, Yoshimi Taka. Necl-1/CADM3 regulates cone synapse formation in the mouse retina. iScience. vol 27. issue 4. 2024-04-16. PMID:38623325. |
necl-1/cadm3 regulates cone synapse formation in the mouse retina. |
2024-04-16 |
2024-04-18 |
mouse |