All Relations between retina cone cell and retina photoreceptor rod

Publication Sentence Publish Date Extraction Date Species
Hung-Ju Chiang, Yuko Nishiwaki, Wei-Chieh Chiang, Ichiro Masa. Male germ cell-associated kinase is required for axoneme formation during ciliogenesis in zebrafish photoreceptors. Disease models & mechanisms. vol 17. issue 7. 2024-07-16. PMID:38813692. in mak mutants, both cone and rod photoreceptors completely lacked outer segments and underwent apoptosis. 2024-07-16 2024-07-18 mouse
Héloïse Rach, Ulker Kilic-Huck, Pierre A Geoffroy, Tristan Bourcier, Sophie Braun, Henri Comtet, Elisabeth Ruppert, Laurence Hugueny, Marc Hebert, Eve Reynaud, Patrice Bourgi. The electroretinography to identify biomarkers of idiopathic hypersomnia and narcolepsy type 1. Journal of sleep research. 2024-07-12. PMID:38993053. cone, rod and retinal ganglion cells electrical activity were recorded with flash-electroretinography in non-dilated eye of 31 patients with idiopathic hypersomnia (women 84%, 26.6 ± 5.9 years), 19 patients with narcolepsy type 1 (women 63%, 36.6 ± 12.7 years) and 43 controls (women 58%, 30.6 ± 9.3 years). 2024-07-12 2024-07-14 Not clear
Héloïse Rach, Ulker Kilic-Huck, Pierre A Geoffroy, Tristan Bourcier, Sophie Braun, Henri Comtet, Elisabeth Ruppert, Laurence Hugueny, Marc Hebert, Eve Reynaud, Patrice Bourgi. The electroretinography to identify biomarkers of idiopathic hypersomnia and narcolepsy type 1. Journal of sleep research. 2024-07-12. PMID:38993053. reduced cone a-wave amplitude (p = 0.039) and prolonged cone (p = 0.022) and rod b-wave (p = 0.009) latencies were observed in patients with narcolepsy type 1 as compared with controls, while prolonged photopic negative response-wave latency (retinal ganglion cells activity) was observed in patients with idiopathic hypersomnia as compared with controls (p = 0.033). 2024-07-12 2024-07-14 Not clear
Héloïse Rach, Ulker Kilic-Huck, Pierre A Geoffroy, Tristan Bourcier, Sophie Braun, Henri Comtet, Elisabeth Ruppert, Laurence Hugueny, Marc Hebert, Eve Reynaud, Patrice Bourgi. The electroretinography to identify biomarkers of idiopathic hypersomnia and narcolepsy type 1. Journal of sleep research. 2024-07-12. PMID:38993053. the rod and cone b-wave latency clearly distinguished narcolepsy type 1 from idiopathic hypersomnia and controls (area under the curve > 0.70), and the photopic negative response-wave latency distinguished idiopathic hypersomnia and narcolepsy type 1 from controls with an area under the curve > 0.68. 2024-07-12 2024-07-14 Not clear
Héloïse Rach, Ulker Kilic-Huck, Pierre A Geoffroy, Tristan Bourcier, Sophie Braun, Henri Comtet, Elisabeth Ruppert, Laurence Hugueny, Marc Hebert, Eve Reynaud, Patrice Bourgi. The electroretinography to identify biomarkers of idiopathic hypersomnia and narcolepsy type 1. Journal of sleep research. 2024-07-12. PMID:38993053. narcolepsy type 1 is associated with impaired cone and rod responses, whereas idiopathic hypersomnia is associated with impaired retinal ganglion cells response, suggesting different phototransduction alterations in both hypersomnias. 2024-07-12 2024-07-14 Not clear
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. 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
Dominic W H Shayler, Kevin Stachelek, Linda Cambier, Sunhye Lee, Jinlun Bai, Mark W Reid, Daniel J Weisenberger, Bhavana Bhat, Jennifer G Aparicio, Yeha Kim, Mitali Singh, Maxwell Bay, Matthew E Thornton, Eamon K Doyle, Zachary Fouladian, Stephan G Erberich, Brendan H Grubbs, Michael A Bonaguidi, Cheryl Mae Craft, Hardeep P Singh, David Cobrini. Single cell transcriptomics reveals early photoreceptor states, cell-specific transcript isoforms, and cancer-predisposing features. bioRxiv : the preprint server for biology. 2024-06-25. PMID:38915659. the analyses revealed early post-mitotic cone- and rod-directed populations characterized by higher thrb or nrl regulon activities, an immature photoreceptor precursor population with concurrent cone and rod gene and regulon expression, and distinct early and late cone and rod maturation states distinguished by maturation-associated declines in rax regulon activity. 2024-06-25 2024-06-27 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
Tomoko Sato, Kazuki Kuniyoshi, Takaaki Hayashi, Hirokazu Nishiwaki, Kei Mizobuchi, Shunji Kusak. Clinical course of two siblings with potassium voltage-gated channel modifier subfamily V member 2 (KCNV2)-associated retinopathy. Documenta ophthalmologica. Advances in ophthalmology. 2024-04-17. PMID:38630375. kcnv2-associated retinopathy causes a phenotype reported as "cone dystrophy with nyctalopia and supernormal rod responses (cdsrr; omim# 610356)," featuring pathognomonic findings on electroretinography (erg). 2024-04-17 2024-04-19 Not clear
Busra Yen, Mukaddes Damla Ciftci, Filiz Afrashi, Huseyin Onay, Damla Gokse. A CASE OF ALSTRÖM SYNDROME WITH A NOVEL VARIANT IN ALMS1 GENE PRESENTING WITH CONE ROD DYSTROPHY AS FIRST FINDING. Retinal cases & brief reports. 2024-04-03. PMID:38569205. a case of alstrÖm syndrome with a novel variant in alms1 gene presenting with cone rod dystrophy as first finding. 2024-04-03 2024-04-06 Not clear
Imran H Yusuf, Thomas Burgoyne, Ahmed Salman, Michelle E McClements, Robert E MacLaren, Peter Charbel Iss. Rescue of cone and rod photoreceptor function in a CDHR1-model of age-related retinal degeneration. Molecular therapy : the journal of the American Society of Gene Therapy. 2024-03-20. PMID:38504520. biallelic variants in cdhr1 - a specialised protocadherin highly expressed in cone and rod photoreceptors - result in blindness from shortened photoreceptor outer segments and progressive photoreceptor cell death. 2024-03-20 2024-03-23 mouse
Jiali Liu, Melvin R Hayden, Ying Yang. Research progress of RP1L1 gene in disease. Gene. 2024-03-14. PMID:38485037. to date, rp1l1 variants have been associated with occult macular dystrophy (cone degeneration) and retinitis pigmentosa (rod disease). 2024-03-14 2024-03-17 Not clear
Izarbe Aísa-Marín, Quirze Rovira, Noelia Díaz, Laura Calvo-López, Juan M Vaquerizas, Gemma Marfan. Specific photoreceptor cell fate pathways are differentially altered in NR2E3-associated diseases. Neurobiology of disease. 2024-03-14. PMID:38485095. mutations in nr2e3, a gene encoding an orphan nuclear transcription factor, cause two retinal dystrophies with a distinct phenotype, but the precise role of nr2e3 in rod and cone transcriptional networks remains unclear. 2024-03-14 2024-03-17 mouse
Izarbe Aísa-Marín, Quirze Rovira, Noelia Díaz, Laura Calvo-López, Juan M Vaquerizas, Gemma Marfan. Specific photoreceptor cell fate pathways are differentially altered in NR2E3-associated diseases. Neurobiology of disease. 2024-03-14. PMID:38485095. overall, our results shed light on the role of nr2e3 in modulating photoreceptor differentiation towards cone and rod fates and explain how different mutations in nr2e3 lead to distinct visual disorders in humans. 2024-03-14 2024-03-17 mouse
Malena Daich Varela, Mira Dixit, Angelos Kalitzeos, Michel Michaelide. Adaptive Optics Retinal Imaging in RDH12-Associated Early Onset Severe Retinal Dystrophy. Investigative ophthalmology & visual science. vol 65. issue 3. 2024-03-11. PMID:38466282. adaptive optics scanning light ophthalmoscopy (aoslo) enables resolution of individual rod and cone photoreceptors in the retina. 2024-03-11 2024-03-14 Not clear
Pablo A Barrionuevo, María L Sandoval Salinas, José M Fanchin. Are ipRGCs involved in human color vision? Hints from physiology, psychophysics, and natural image statistics. Vision research. vol 217. 2024-03-08. PMID:38458004. in comparison with the transient and adaptive nature of cone and rod signals, iprgcs' signaling might provide an ecological advantage to different attributes of color vision. 2024-03-08 2024-03-11 human
Andrea Bighinati, Elisa Adani, Agnese Stanzani, Sara D'Alessandro, Valeria Marig. Molecular mechanisms underlying inherited photoreceptor degeneration as targets for therapeutic intervention. Frontiers in cellular neuroscience. vol 18. 2024-02-19. PMID:38370034. retinitis pigmentosa (rp) is a form of retinal degeneration characterized by primary degeneration of rod photoreceptors followed by a secondary cone loss that leads to vision impairment and finally blindness. 2024-02-19 2024-02-21 Not clear
Chengjie He, Jingyi Peng, Jiayi Jin, Wanwen Shao, Yongxin Zheng, Liuxueying Zhon. Comparison of retinal parameters between rhesus and cynomolgus macaques. Experimental animals. vol 73. issue 1. 2024-02-14. PMID:37460311. dark-adapted 3.0 oscillatory potentials (reflection of amacrine cell activity) and light-adapted 30-hz flicker erg (a sensitive cone-pathway-driven response) waveforms of the ff-erg were similar in both species, while the times to peaks in dark-adapted 0.01 erg (the rod-driven response of bipolar cells) and dark-adapted 3.0 erg (combined rod and cone system responses) as well as the implicit times of the a- and b-waves in light-adapted 3.0 erg (the single-flash cone response) were substantially different. 2024-02-14 2024-02-17 monkey
Michalis Georgiou, Anthony G Robson, Kaoru Fujinami, Thales A C de Guimarães, Yu Fujinami-Yokokawa, Malena Daich Varela, Nikolas Pontikos, Angelos Kalitzeos, Omar A Mahroo, Andrew R Webster, Michel Michaelide. Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, leber congenital amaurosis, and cone dysfunction syndromes. Progress in retinal and eye research. 2024-01-26. PMID:38278208. herein we present in a comprehensive and concise manner: (i) macular dystrophies (stargardt disease (abca4), x-linked retinoschisis (rs1), best disease (best1), prph2-associated pattern dystrophy, sorsby fundus dystrophy (timp3), and autosomal dominant drusen (efemp1)), (ii) cone and cone-rod dystrophies (guca1a, prph2, abca4, kcnv2 and rpgr), (iii) predominant rod or rod-cone dystrophies (retinitis pigmentosa, enhanced s-cone syndrome (nr2e3), bietti crystalline corneoretinal dystrophy (cyp4v2)), (iv) leber congenital amaurosis/early-onset severe retinal dystrophy (gucy2d, cep290, crb1, rdh12, rpe65, tulp1, aipl1 and nmnat1), (v) cone dysfunction syndromes (achromatopsia (cnga3, cngb3, pde6c, pde6h, gnat2, atf6), x-linked cone dysfunction with myopia and dichromacy (bornholm eye disease; opn1lw/opn1mw array), oligocone trichromacy, and blue-cone monochromatism (opn1lw/opn1mw array). 2024-01-26 2024-01-29 Not clear