Identification of a 2 Mb human ortholog of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosa (Q24310728)

GOA release 2020-03-11

1 reference

5

Robert K Koenekoop

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Rob W J Collin

1

object named as

Rob W J Collin

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Frans P M Cremers

11

object named as

Frans P M Cremers

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Anneke den Hollander

10

object named as

Anneke I den Hollander

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author name string

Karin W Littink

2

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B Jeroen Klevering

3

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L Ingeborgh van den Born

4

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Marijke N Zonneveld

6

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Ellen A W Blokland

7

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Tim M Strom

8

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Carel B Hoyng

American Journal of Human Genetics

9

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language of work or name

English

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publication date

November 2008

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published in

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volume

83

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issue

5

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page(s)

594-603

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cites work

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Evaluation of the ELOVL4 gene in families with retinitis pigmentosa linked to the RP25 locus

19 March 2017

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Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene

19 March 2017

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Mutation analysis of GABRR1 and GABRR2 in autosomal recessive retinitis pigmentosa

19 March 2017

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Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

19 March 2017

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SMART, a simple modular architecture research tool: identification of signaling domains

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Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

19 March 2017

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A simple salting out procedure for extracting DNA from human nucleated cells

19 March 2017

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Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs

19 March 2017

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Pals1/Mpp5 is required for correct localization of Crb1 at the subapical region in polarized Muller glia cells

19 March 2017

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Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus

19 March 2017

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Mutation screening of three candidate genes, ELOVL5, SMAP1 and GLULD1 in autosomal recessive retinitis pigmentosa

19 March 2017

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Molecular analysis of RIM1 in autosomal recessive Retinitis pigmentosa

19 March 2017

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Agrin is a chimeric proteoglycan with the attachment sites for heparan sulfate/chondroitin sulfate located in two multiple serine-glycine clusters

19 March 2017

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Cloning, characterization, and chromosome mapping of the human GlcAT-S gene

19 March 2017

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Mutations in the CRB1 gene cause Leber congenital amaurosis

19 March 2017

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Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis

19 March 2017

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A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration

19 March 2017

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19 March 2017

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Prediction, conservation analysis, and structural characterization of mammalian mucin-type O-glycosylation sites

7 April 2017

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Large-scale molecular analysis of a 34 Mb interval on chromosome 6q: major refinement of the RP25 interval

7 April 2017

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Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis

27 September 2017

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Genetic factors modifying clinical expression of autosomal dominant RP.

27 September 2017

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A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

27 September 2017

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Nonsense-mediated decay approaches the clinic

27 September 2017

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Molecular cloning and characterization of human RAB23, a member of the group of Rab GTPases

27 September 2017

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A major locus for autosomal recessive retinitis pigmentosa on 6q, determined by homozygosity mapping of chromosomal regions that contain gamma-aminobutyric acid-receptor clusters

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668042

Standard for clinical electro-oculography. International Society for Clinical Electrophysiology of Vision.

27 September 2017

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Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

27 September 2017

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Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications

27 September 2017

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Linkage validation of RP25 Using the 10K genechip array and further refinement of the locus by new linked families.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668042

Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668042

Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668042

Transforming the architecture of compound eyes

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668042

The agrin/perlecan-related protein eyes shut is essential for epithelial lumen formation in the Drosophila retina

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668042

Exclusion of four candidate genes, KHDRBS2, PTP4A1, KIAA1411 and OGFRL1, as causative of autosomal recessive retinitis pigmentosa.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2668042

A novel genetic study of Chinese families with autosomal recessive retinitis pigmentosa

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18976725

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Novel human pathological mutations. Gene symbol: FRMD7. Disease: congenital motor nystagmus

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.AJHG.2008.10.014

inferred from DOI database lookup

7 January 2021

based on heuristic

Novel human pathological mutations. Gene symbol: FRMD7. Disease: congenital motor nystagmus

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.AJHG.2008.10.014

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2008.10.014

1 reference

1 reference

1 reference

PubMed publication ID

18976725

1 reference