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Home > Retinal Degenerations: Mechanisms and Experimental Therapy > Photoreceptor Degeneration in Pro23His and S334ter Transgenic Rats
Retinal Degenerations: Mechanisms and Experimental Therapy |
Matthew M. LaVail; Joe G. Hollyfield; Robert E. Anderson
Springer US
Retinal Degenerations: Mechanisms and Experimental Therapy
Photoreceptor Degeneration in Pro23His and S334ter Transgenic Rats
Authors

Donald Lee; Scott Geller; Natalie Walsh; Krisztina Valter; Doug Yasumura; Michael Matthes et al.

ARI Id

1674219754654_3329633

Access

Not Available Free

Pages

297-302

DOI

10.1007/978-1-4615-0067-4_36

Chapter URL

https://rd.springer.com/chapter/10.1007/978-1-4615-0067-4_36

Table of Contents of Book
Showing 1 to 20 of 59 entries
Chapters/HeadingsAuthor(s)PagesInfo
Front Matter
i-xvi
Identification of the RP1 and RP10 (IMPDH1) Genes Causing Autosomal Dominant RP
Stephen P. Daiger; Lori S. Sullivan; Sara J. Bowne; Avril Kennan; Peter Humphries; David G. Birch et al.
1-11
On the Role of IMPDH1 in Retinal Degeneration
Avril Kennan; Aileen Aherne; Sara J. Bowne; Stephen P. Daiger; G. Jane Farrar; Paul F. Kenna et al.
13-18
An Integrated Genetic Approach to Identify Candidate Genes for Human Chromosome 6q-Linked Retinal Disorders
Pamela S. Lagali; Radha Ayyagari; Paul W. Wong
19-28
Mouse Genetic Approaches to Access Pathways Important in Retinal Function
Patsy M. Nishina; Jürgen K. Naggert
29-34
Retinal Degenerative Disorders in Southern Africa: A Molecular Genetic Approach
R.S. Ramesar; L. Roberts; G. Rebello; R. Goliath; A. Vorster; A. September et al.
35-40
Comparing Rod and Cone Function with Fundus Autofluorescence Images in Retinitis Pigmentosa
Anthony G. Robson; Catherine Egan; Graham E. Holder; Alan C. Bird; Fred W. Fitzke
41-47
A Modified Protocol for the Assessment of Visual Function in Patients with Retinitis Pigmentosa
N. Lodha; C. A. Westall; M. Brent; M. Abdolell; E. Héon
49-57
Prenatal Human Ocular Degeneration Occurs in Leber’s Congenital Amaurosis
Fernanda B. O. Porto; Isabelle Perrault; David Hicks; Jean-Michel Rozet; Noëlle Hanoteau; Sylvain Hanein et al.
59-68
Leber Congenital Amaurosis — Genotyping Required for Possible Inclusion in a Clinical Trial
Isabelle Perrault; Sylvie Gerber; Sylvain Hanein; Serge Picaud; Jean-Michel Rozet; Jean-Louis Dufier et al.
69-77
Treatment of Cystoid Macular Edema Related to Retinitis Pigmentosa with Intravitreal Triamcinolone Acetonide: Case Report
Juliana M. F. Sallum; Michel E. Farah; Vinicius S. Saraiva
79-81
Proteomic Approaches to Understanding Age-Related Macular Degeneration
Joe G. Hollyfield; Robert G. Salomon; John W. Crabb
83-89
Progressive Pathways in Age-Related Macular Degeneration
Kimberly A. Howes; Jeanne M. Frederick; Alexander Marks; Wolfgang Baehr
91-96
Tissue Inhibitor of Metalloproteinases-3 and Sorsby Fundus Dystrophy
Jian Hua Qi; Quteba Ebrahem; Bela Anand-Apte
97-105
Investigations of RPE Cells of Choriodal Neovascular Membranes from Patients with Age-Related Macula Degeneration
Rita Rosenthal; Olaf Strauß
107-113
Retinal and Choroidal Alterations Following Photodynamic Therapy
Yusuf K. Durlu
115-122
Usher Syndrome: Correlation between Visual Field Size and Maximal ERG Response B-Wave Amplitude
Alessandro Iannaccone
123-131
The Cellular Function of the Usher Gene Product Myosin VIIa is Specified by Its Ligands
Uwe Wolfrum
133-142
Mouse Models for Usher Syndrome 1b
Concepcion Lillo; Junko Kitamoto; Xinran Liu; Elizabeth Quint; Karen P. Steel; David S. Williams
143-150
Screen for Usher Syndrome 1b Mutations in the Ovine Myosin VIIa Gene
Tania Slatter; Sassan M. Azarian; Scott Tebbutt; Marion Maw; David S. Williams
151-155
Chapters/HeadingsAuthor(s)PagesInfo
Showing 1 to 20 of 59 entries
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