Cloning, expression and characterization of the murine Efemp1, a gene mutated in Doyne-Honeycomb retinal dystrophy. (Q30333281)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Cloning, expression and characterization of the murine Efemp1, a gene mutated in Doyne-Honeycomb retinal dystrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

Julia Ehlermann

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Susanne Weber

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Petra Pfisterer

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 August 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

published in

Gene Expression Patterns

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

441-447

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

Basic local alignment search tool

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Sequence, recombinant expression and tissue localization of two novel extracellular matrix proteins, fibulin-3 and fibulin-4

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Key residues involved in calcium-binding motifs in EGF-like domains

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Calcium binding to fibrillin?

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

The Ensembl genome database project

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Structure and chromosomal assignment of the human S1-5 gene (FBNL) that is highly homologous to fibrillin

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD)

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Prevalence of age-related maculopathy. The Beaver Dam Eye Study

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

An overexpressed gene transcript in senescent and quiescent human fibroblasts encoding a novel protein in the epidermal growth factor-like repeat family stimulates DNA synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Expression of Cdcrel-1 (Pnutl1), a gene frequently deleted in velo-cardio-facial syndrome/DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Aberrant accumulation of EFEMP1 underlies drusen formation in Malattia Leventinese and age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development-matrix components and their homeostasis.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Antagonistic Interactions between FGF and BMP Signaling Pathways: A Mechanism for Positioning the Sites of Tooth Formation

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

SSAHA: a fast search method for large DNA databases

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

The roles of collagen genes in skeletal development and morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Doyne's honeycomb retinal degeneration. Clinical and genetic features

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

A subtractive gene expression screen suggests a role of transcription factor AP-2 alpha in control of proliferation and differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Direct Binding and Activation of Receptor Tyrosine Kinases by Collagen

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Molecular genetic heterogeneity in autosomal dominant drusen

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

The prevalence of age-related maculopathy in the Rotterdam Study

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

Transcription factor gene AP-2 gamma essential for early murine development

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900084-X

7 January 2021

10.1016/S1567-133X(03)00084-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12915309%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference