20-Hz Flicker Stimulus Can Isolate the Cone Function in Rat Retina

1998 ◽  
Vol 30 (6) ◽  
pp. 368-373 ◽  
Author(s):  
Yoshinobu Goto ◽  
Tetsujiro Yasuda ◽  
Shozo Tobimatsu ◽  
Motohiro Kato
Keyword(s):  
Rat Retina ◽  
Cone Function ◽  
Flicker Stimulus

The Effects of Two Stereoisomers of N-Acetylcysteine on Photochemical Damage by UVA and Blue Light in Rat Retina

1999 ◽  
Vol 70 (3) ◽  
pp. 353 ◽  
Author(s):  
Eelco M. Busch ◽  
Theo G. M. F. Gorgels ◽  
Joan E. Roberts ◽  
Dirk van Norren
Keyword(s):  
Blue Light ◽  
Rat Retina ◽  
Photochemical Damage

The Mehler-Fock-Clifford transform and pseudo-differential operator on function spaces

Filomat ◽  
2019 ◽  
Vol 33 (8) ◽  
pp. 2457-2469
Author(s):  
Akhilesh Prasad ◽  
S.K. Verma
Keyword(s):  
Differential Operator ◽  
Function Spaces ◽  
Pseudo Differential Operator ◽  
Test Function ◽  
Basic Properties ◽  
Cone Function ◽  
Translation Operators

In this article, weintroduce a new index transform associated with the cone function Pi ??-1/2 (2?x), named as Mehler-Fock-Clifford transform and study its some basic properties. Convolution and translation operators are defined and obtained their estimates under Lp(I, x-1/2 dx) norm. The test function spaces G? and F? are introduced and discussed the continuity of the differential operator and MFC-transform on these spaces. Moreover, the pseudo-differential operator (p.d.o.) involving MFC-transform is defined and studied its continuity between G? and F?.

scholarly journals A Mild Phenotype Caused by Two Novel Compound Heterozygous Mutations in CEP290

Genes ◽  
2020 ◽  
Vol 11 (11) ◽  
pp. 1240
Author(s):  
Agnieszka Rafalska ◽  
Anna M. Tracewska ◽  
Anna Turno-Kręcicka ◽  
Milena J. Szafraniec ◽  
Marta Misiuk-Hojło
Keyword(s):  
Vision Loss ◽  
Compound Heterozygous ◽  
Loss Of Function ◽  
Mild Phenotype ◽  
Cone Function ◽  
Retinal Disorders ◽  
Molecular Inversion Probes ◽  
Disease Experience ◽  
The Individual ◽  
Inherited Retinal Disorders

CEP290 is a ciliary gene frequently mutated in ciliopathies, resulting in a broad range of phenotypes, ranging from isolated inherited retinal disorders (IRDs) to severe or lethal syndromes with multisystemic involvement. Patients with non-syndromic CEP290-linked disease experience profound and early vision loss due to cone-rod dystrophy, as in Leber congenital amaurosis. In this case report, we describe two novel loss-of-function heterozygous alterations in the CEP290 gene, discovered in a patient suffering from retinitis pigmentosa using massive parallel sequencing of a molecular inversion probes library constructed for 108 genes involved in IRDs. A milder phenotype than expected was found in the individual, which serves to prove that some CEP290-associated disorders may display preserved cone function.

Dendritic morphology of alpha ganglion cells in the rat retina

1989 ◽  
Vol 9 ◽  
pp. 174
Author(s):  
Masaki Tauchi ◽  
Yutaka Fukuda ◽  
Katsuko Morigiwa ◽  
Kwok-Fai So
Keyword(s):  
Ganglion Cells ◽  
Dendritic Morphology ◽  
Rat Retina

scholarly journals Vol. 7 (2008) 864–874 Targets of Tyrosine Nitration in Diabetic Rat Retina

2008 ◽  
Vol 7 (6) ◽  
pp. 1188-1189
Author(s):  
Xianquan Zhan ◽  
Yunpeng Du ◽  
John S. Crabb ◽  
Xiaorong Gu ◽  
Timothy S. Kern ◽  
...  
Keyword(s):  
Diabetic Rat ◽  
Tyrosine Nitration ◽  
Rat Retina
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