نتایج جستجو برای: photoreceptor

تعداد نتایج: 10250  

Journal: :Vision Research 2001
Misha Vorobyev Robert Brandt Dagmar Peitsch Simon B Laughlin Randolf Menzel

Photoreceptor noise sets an absolute limit for the accuracy of colour discrimination. We compared colour thresholds in the honeybee (Apis mellifera) with this limit. Bees were trained to discriminate an achromatic stimulus from monochromatic lights of various wavelengths as a function of their intensity. Signal-to-noise ratios were measured by intracellular recordings in the three spectral type...

2013
Budd A Tucker Robert F Mullins Luan M Streb Kristin Anfinson Mari E Eyestone Emily Kaalberg Megan J Riker Arlene V Drack Terry A Braun Edwin M Stone

Next-generation and Sanger sequencing were combined to identify disease-causing USH2A mutations in an adult patient with autosomal recessive RP. Induced pluripotent stem cells (iPSCs), generated from the patient's keratinocytes, were differentiated into multi-layer eyecup-like structures with features of human retinal precursor cells. The inner layer of the eyecups contained photoreceptor precu...

Journal: :Development 2010
Joseph A Brzezinski Deepak A Lamba Thomas A Reh

Photoreceptors, rods and cones are the most abundant cell type in the mammalian retina. However, the molecules that control their development are not fully understood. In studies of photoreceptor fate determination, we found that Blimp1 (Prdm1) is expressed transiently in developing photoreceptors. We analyzed the function of Blimp1 in the mouse retina using a conditional deletion approach. Dev...

2017
Ayse Sahaboglu Alaa Sharif Lili Feng Enver Secer Eberhart Zrenner François Paquet-Durand

Peripherin (peripherin/rds) is a membrane-associated protein that plays a critical role in the morphogenesis of rod and cone photoreceptor outer segments. Mutations in the corresponding PRPH2 gene cause different types of retinal dystrophies characterized by a loss of photoreceptors. Over activation of poly-ADP-ribose polymerase (PARP) was previously shown to be involved in different animal mod...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Akishi Onishi Guang-Hua Peng Erin M Poth Daniel A Lee Jichao Chen Uel Alexis Jimmy de Melo Shiming Chen Seth Blackshaw

Mutation of rod photoreceptor-enriched transcription factors is a major cause of inherited blindness. We identified the orphan nuclear hormone receptor estrogen-related receptor beta (ERRbeta) as selectively expressed in rod photoreceptors. Overexpression of ERRbeta induces expression of rod-specific genes in retinas of wild-type as well as Nrl(-/-) mice, which lack rod photoreceptors. Mutation...

Journal: :Cell 2000
Joseph R Marszalek Xinran Liu Elizabeth A Roberts Daniel Chui Jamey D Marth David S Williams Lawrence S.B Goldstein

To test whether kinesin-II is important for transport in the mammalian photoreceptor cilium, and to identify its potential cargoes, we used Cre-loxP mutagenesis to remove the kinesin-II subunit, KIF3A, specifically from photoreceptors. Complete loss of KIF3A caused large accumulations of opsin, arrestin, and membranes within the photoreceptor inner segment, while the localization of alpha-trans...

2015
Maria Luisa Rocco Bijorn Omar Balzamino Pamela Petrocchi Passeri Alessandra Micera Luigi Aloe

A number of different studies have shown that neurotrophins, including nerve growth factor (NGF) support the survival of retinal ganglion neurons during a variety if insults. Recently, we have reported that that eye NGF administration can protect also photoreceptor degeneration in a mice and rat with inherited retinitis pigmentosa. However, the evidence that NGF acts directly on photoreceptors ...

Journal: :Mechanisms of Development 1999
Yuki Hirota Masataka Okabe Takao Imai Mitsuhiko Kurusu Atsuyo Yamamoto Sachiyo Miyao Makoto Nakamura Kazunobu Sawamoto Hideyuki Okano

We have examined the roles played by the Drosophila neural RNA-binding protein Musashi (MSI) in eye development. MSI expression was observed in the nuclei of all photoreceptor cells (R1-R8). Although a msi loss-of-function mutation resulted in only weak abnormalities in photoreceptor differentiation, we found that the msi eye phenotype was significantly enhanced in a seven in absentia (sina) ba...

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