E-LIB Suche - Ergebnisse für: Moore, T. Anthony

1

Enhanced Learning and Memory in Patients with CRB1 Retinopa..:

Wright, Genevieve A. ; Rodriguez-Martinez, Ana Catalina ; Conn, Hanne...
Genes. 15 (2024) 6 - p. 660 , 2024

2

IMI—Management and Investigation of High Myopia in Infants ..:

Flitcroft, Ian ; Ainsworth, John ; Chia, Audrey...
Investigative Opthalmology & Visual Science. 64 (2023) 6 - p. 3 , 2023

Link: https://doi.org/10.1167/..

3

WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correl..:

Majander, Anna ; Jurkute, Neringa ; Burté, Florence...
American Journal of Ophthalmology. 241 (2022) - p. 9-27 , 2022

Link: https://doi.org/10.1016/..

4

Dominant Cone Rod Dystrophy, Previously Assigned to a Misse..:

Martin-Gutierrez, Maria Pilar ; Schiff, Elena R. ; Wright, Genevieve...
Investigative Opthalmology & Visual Science. 63 (2022) 9 - p. 14 , 2022

Link: https://doi.org/10.1167/..

5

Optogenetic approaches to therapy for inherited retinal deg..:

De Silva, Samantha R. ; Moore, Anthony T.
The Journal of Physiology. 600 (2022) 21 - p. 4623-4632 , 2022

Link: https://doi.org/10.1113/..

6

Multidisciplinary team directed analysis of whole genome se..:

Daich Varela, Malena ; Bellingham, James ; Motta, Fabiana...
Human Molecular Genetics. 32 (2022) 4 - p. 595-607 , 2022

Link: https://doi.org/10.1093/..

7

Contributors:

, In: Clinical Ophthalmic Genetics and Genomics,

Aleman, Tomas S. ; Amati-Bonneau, Patrizia ; Arveiler, Benoît... - p. xi-xiv , 2022

Link: https://doi.org/10.1016/..

8

Allele-specific gene editing to rescue dominant CRX-associa..:

Chirco, Kathleen R. ; Chew, Shereen ; Moore, Anthony T...
Stem Cell Reports. 16 (2021) 11 - p. 2690-2702 , 2021

Link: https://doi.org/10.1016/..

9

Expanding the FDXR-Associated Disease Phenotype: Retinal Dy..:

Jurkute, Neringa ; Shanmugarajah, Priya D. ; Hadjivassiliou, Marios...
Investigative Opthalmology & Visual Science. 62 (2021) 6 - p. 2 , 2021

Link: https://doi.org/10.1167/..

10

Transcription factor overexpression drives reliable differe..:

Dewell, Tessa E. ; Gjoni, Ketrin ; Liu, Angela Z....
Stem Cell Research. 53 (2021) - p. 102368 , 2021

Link: https://doi.org/10.1016/..

11

Beyond factor H: The impact of genetic-risk variants for ag..:

Cipriani, Valentina ; Tierney, Anna ; Griffiths, John R....
The American Journal of Human Genetics. 108 (2021) 8 - p. 1385-1400 , 2021

Link: https://doi.org/10.1016/..

12

Clinical and Genetic Findings in CTNNA1-Associated Macular ..:

Tanner, Alexander ; Chan, Hwei Wuen ; Pulido, Jose S....
Ophthalmology. 128 (2021) 6 - p. 952-955 , 2021

Link: https://doi.org/10.1016/..

13

SSBP1-Disease Update: Expanding the Genetic and Clinical Sp..:

Jurkute, Neringa ; D'Esposito, Fabiana ; Robson, Anthony G....
Investigative Opthalmology & Visual Science. 62 (2021) 15 - p. 12 , 2021

Link: https://doi.org/10.1167/..

14

Variants in PAX6, PITX3 and HSF4 causing autosomal dominant..:

Berry, Vanita ; Ionides, Alex ; Pontikos, Nikolas...
Eye. 36 (2021) 8 - p. 1694-1701 , 2021

Link: https://doi.org/10.1038/..

15

The X-linked retinopathies: Physiological insights, pathoge..:

De Silva, Samantha R. ; Arno, Gavin ; Robson, Anthony G....
Progress in Retinal and Eye Research. 82 (2021) - p. 100898 , 2021

Link: https://doi.org/10.1016/..