Three homologs of rds/peripherin in Xenopus laevis photoreceptors that exhibit covalent and non-covalent interactions

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1970 • 253,849 citations

DNA sequencing with chain-terminating inhibitors

1977 • 69,181 citations

Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose.

1980 • 8,711 citations

Purification of Biologically Active Globin Messenger RNA by Chromatography on Oligothymidylic acid-Cellulose

1972 • 6,922 citations

Cleavage of structural proteins during the assemble of the head of bacterio-phage T4

1970 • 5,738 citations

PARTICIPATION OF THE RETINAL PIGMENT EPITHELIUM IN THE ROD OUTER SEGMENT RENEWAL PROCESS

1969 • 1,156 citations

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

1991 • 460 citations

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

1993 • 427 citations

Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

1989 • 399 citations

A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa

1991 • 381 citations

Phenotypic Variation Including Retinitis Pigmentosa, Pattern Dystrophy, and Fundus Flavimaculatus in a Single Family With a Deletion of Codon 153 or 154 of the Peripherin/RDS Gene

1993 • 326 citations

The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein

1991 • 322 citations

Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors: relationship to disk membrane morphogenesis and retinal degeneration.

1992 • 297 citations

Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse.

1991 • 284 citations

Butterfly–shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

1993 • 272 citations

Cloning of the CDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies

1992 • 254 citations

Phylogeny of the major tetrapod groups: Morphological data and divergence dates

1990 • 239 citations

A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens

1993 • 204 citations

A New H‐2‐Linked Mutation, rds, Causing Retinal Degeneration in the Mouse

1978 • 192 citations

Surfaces of rod photoreceptor disk membranes: integral membrane components.

1982 • 175 citations

Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membrane

1990 • 162 citations

The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNA

1991 • 139 citations

The ultrastructure of the rods of the mouse retina

1960 • 138 citations

Complete rescue of photoreceptor dysplasia and degeneration in transgenic retinal degeneration slow (rds) mice

1992 • 123 citations

Heterologous Expression of Photoreceptor Peripherin/rds and Rom-1 in COS-1 Cells: Assembly, Interactions, and Localization of Multisubunit Complexes

1995 • 106 citations

Mouse opsin. Gene structure and molecular basis of multiple transcripts

1990 • 100 citations

Some cytological and initial biochemical observations on photoreceptors in retinas of rds mice.

1983 • 95 citations

Changes in the localization and content of opsin during retinal development in the rds mutant mouse: Immunocytochemistry and immunoassay

1987 • 89 citations

Macular Dystrophy Associated with Mutations at Codon 172 in the Human Retinal Degeneration Slow Gene

1994 • 88 citations

Retinal Degeneration slow (rds) in Mouse Results from Simple Insertion of a t Haplotype-Specific Element into Protein-Coding Exon II

1995 • 83 citations

Immunocytochemical localization of opsin in the inner segment and ciliary plasma membrane of photoreceptors in retinas of rds mutant mice.

1986 • 79 citations

Photoreceptor Outer Segment Development in Xenopus laevis: Influence of the Pigment Epithelium

1994 • 75 citations

Quantitative study of tyrosine hydroxylase mRNA in catecholaminergic neurons and adrenals during development and aging

1990 • 66 citations

A novel Cys-214-Ser mutation in the peripherin/RDS gene in a Japanese family with autosomal dominant retinitis pigmentosa

1993 • 63 citations

RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function.

1994 • 62 citations

Early opsin expression in Xenopus embryos precedes photoreceptor differentiation

1993 • 60 citations

Development and degeneration of retina in rds mutant mice: Ultraimmunohistochemical localization of opsin

1987 • 60 citations

Autosomal dominant retinitis pigmentosa: A novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree

1992 • 51 citations

Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin geneother

1994 • 49 citations

A Novel Mutation (Asn244Lys) in the Peripherin/RDS Gene Causing Autosomal Dominant Retinitis Pigmentosa Associated with Bull's-Eye Maculopathy Detected by Nonradioisotopic SSCP

1994 • 47 citations

Cloning of the human and murine ROM1 genes: genomic organization and sequence conservation

1993 • 40 citations

Resolution of Subcellular Detail in Thick Tissue Sections: Immunohistochemical Preparation and Fluorescence Confocal Microscopy

2002 • 36 citations

Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa

1994 • 36 citations

Structural features of the terminal loop region of frog retinal rod outer segment disk membranes: II. Organization of the terminal loop complex

1987 • 34 citations

Nucleotide and predicted protien sequence of rat retinal degeneration slow (rds)

1990 • 31 citations

Clinical Features of a Previously Undescribed Codon 216 (proline to serine) Mutation in the Peripherin/Retinal Degeneration Slow Gene in Autosomal Dominant Retinitis Pigmentosa

1994 • 29 citations

Retinitis Pigmentosa Associated With a Dominant Mutation in Codon 46 of the Peripherin/RDS Gene (Arginine-46-Stop)

1995 • 26 citations

Chapter 11 Resolution of Subcellular Detail in Thick Tissue Sections: Immunohistochemical Preparation and Fluorescence Confocal Microscopy

1993 • 24 citations

A diurnal rhythm in opsin content of Rana pipiens rod inner segments.

1988 • 23 citations

The cat RDS transcript: candidate gene analysis and phylogenetic sequence analysis

1993 • 19 citations

Cellular site of expression and genetic interaction of the rd and the rds loci in the retina of the mouse.

1987 • 12 citations