Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM (Q24679722)

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scientific article published on November 1, 1992

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English	Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM	scientific article published on November 1, 1992

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Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM (English)

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photoreceptor protein

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human chromosome 11

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Europe PubMed Central

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24 September 2022

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R. A. Bascom

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24 September 2022

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J. García-Heras

2

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24 September 2022

C. L. Hsieh

3

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24 September 2022

D. S. Gerhard

4

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24 September 2022

C. Jones

5

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24 September 2022

U. Francke

6

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24 September 2022

H. F. Willard

7

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24 September 2022

D. H. Ledbetter

8

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24 September 2022

R. R. McInnes

9

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24 September 2022

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November 1992

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https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1415249/?tool=EBI

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24 September 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1415249/pdf/?tool=EBI

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24 September 2022

https://europepmc.org/articles/PMC1682851

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24 September 2022

https://europepmc.org/articles/PMC1682851?pdf=render

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24 September 2022

American Journal of Human Genetics

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51

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5

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1028-35

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

1 reference

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cDNA cloning of human oxysterol-binding protein and localization of the gene to human chromosome 11 and mouse chromosome 19

1 reference

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

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Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin

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

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A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids

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7 April 2017

The gene that encodes the human CD20 (B1) differentiation antigen is located on chromosome 11 near the t(11;14)(q13;q32) translocation site

1 reference

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7 April 2017

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

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7 April 2017

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

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7 April 2017

Chromosome maps of man and mouse, III.

1 reference

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28 September 2017

Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes

1 reference

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28 September 2017

Report of the committee on the genetic constitution of chromosome 11.

1 reference

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28 September 2017

Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11.

1 reference

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28 September 2017

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

1 reference

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28 September 2017

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682851

28 September 2017

Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13

1 reference

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28 September 2017

A radiation hybrid map of the proximal long arm of human chromosome 11 containing the multiple endocrine neoplasia type 1 (MEN-1) and bcl-1 disease loci.

1 reference

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28 September 2017

New insights into genetic eye disease

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Constitutive fragile sites and cancer.

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30 May 2018

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma.

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Isolation of 1001 new markers from human chromosome 11, excluding the region of 11p13-p15.5, and their sublocalization by a new series of radiation-reduced somatic cell hybrids

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A new H-2-linked mutation, rds, causing retinal degeneration in the mouse

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Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization

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A detailed genetic map of the long arm of chromosome 11

1 reference

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inferred from PubMed ID database lookup

Development and degeneration of retina in rds mutant mice: photoreceptor abnormalities in the heterozygotes

1 reference

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Clustering of breakpoints on chromosome 11 in human B-cell neoplasms with the t(11 ; 14) chromosome translocation

1 reference

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based on heuristic

inferred from PubMed ID database lookup

An improved method for G-banding chromosomes after in situ hybridization

1 reference

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inferred from PubMed ID database lookup

Relationships between genes on human chromosome 11 encoding cell-surface antigens

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Development and degeneration of retina in rds mutant mice: light microscopy

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Retinal genetics: a nullifying effect for rhodopsin

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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