The Family of Crumbs Genes and Human Disease (Q28080033)

Crossref

language of work or name

1 reference

October 2016

1 reference

published in

Molecular syndromology

1 reference

volume

7

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issue

5

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page(s)

274-281

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Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa

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Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination

20 March 2017

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CRB1 gene mutations are associated with keratoconus in patients with leber congenital amaurosis

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CRB1 mutation spectrum in inherited retinal dystrophies

20 March 2017

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Deficiency in Crumbs homolog 2 (Crb2) affects gastrulation and results in embryonic lethality in mice

20 March 2017

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Expansion of phenotype and genotypic data in CRB2-related syndrome

20 March 2017

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Cilia in the choroid plexus: their roles in hydrocephalus and beyond.

29 September 2017

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Common and distinctive localization patterns of Crumbs polarity complex proteins in the mammalian eye

29 September 2017

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CRB2 mutations produce a phenotype resembling congenital nephrosis, Finnish type, with cerebral ventriculomegaly and raised alpha-fetoprotein

29 September 2017

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Defects of CRB2 cause steroid-resistant nephrotic syndrome.

29 September 2017

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Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins

29 September 2017

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Whole exome sequencing identifies CRB1 defect in an unusual maculopathy phenotype

29 September 2017

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The CRB1 and adherens junction complex proteins in retinal development and maintenance.

29 September 2017

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Microarray and morphological analysis of early postnatal CRB2 mutant retinas on a pure C57BL/6J genetic background

29 September 2017

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Complexities of Crumbs function and regulation in tissue morphogenesis

29 September 2017

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CRB1 mutations in inherited retinal dystrophies

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Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model

29 September 2017

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The Crumbs complex: from epithelial-cell polarity to retinal degeneration

29 September 2017

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29 September 2017

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Composition and function of the Crumbs protein complex in the mammalian retina

29 September 2017

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Gene therapy into photoreceptors and Müller glial cells restores retinal structure and function in CRB1 retinitis pigmentosa mouse models

29 September 2017

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Spatial-temporal expressions of Crumbs and Nagie oko and their interdependence in zebrafish central nervous system during early development

2 June 2018

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oko meduzy and related crumbs genes are determinants of apical cell features in the vertebrate embryo.

2 June 2018

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Characterization of the Crumbs homolog 2 (CRB2) gene and analysis of its role in retinitis pigmentosa and Leber congenital amaurosis.

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Isolation of Crb1, a mouse homologue of Drosophila crumbs, and analysis of its expression pattern in eye and brain

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Expanding the phenotype of CRB2 mutations - A new ciliopathy syndrome?

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Crumbs 2 prevents cortical abnormalities in mouse dorsal telencephalon.

27 November 2018

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CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice

27 November 2018

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Sticking together the Crumbs - an unexpected function for an old friend

27 November 2018

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Mutation in MPDZ causes severe congenital hydrocephalus.

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Homozygosity mapping identifies the Crumbs homologue 1 (Crb1) gene as responsible for a recessive syndrome of retinitis pigmentosa and nanophthalmos.

27 November 2018

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Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.

27 November 2018

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A reverse genetic screen in the zebrafish identifies crb2b as a regulator of the glomerular filtration barrier

27 November 2018

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Mutation screening of 299 Spanish families with retinal dystrophies by Leber congenital amaurosis genotyping microarray

27 November 2018

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Crb1 is a determinant of retinal apical Müller glia cell features

27 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/27867342

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/27867342

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

0 references

PubMed publication ID

27867342

1 reference