Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome (Q28298470)

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R Reiter

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N J Leysens

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K W Small

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N A Datson

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J Siegel-Bartelt

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D Bierke-Nelson

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P Bitoun

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B U Zabel

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J C Carey

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J C Murray

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome

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language of work or name

English

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publication date

December 1996

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published in

Nature Genetics

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volume

14

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issue

4

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page(s)

392-9

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cites work

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A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

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A human MSX1 homeodomain missense mutation causes selective tooth agenesis

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P-OTX: a PIT-1-interacting homeodomain factor expressed during anterior pituitary gland development

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Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

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Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. The Treacher Collins Syndrome Collaborative Group

21 April 2017

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Hox genes in vertebrate development

21 January 2018

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Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

21 January 2018

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Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

21 January 2018

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Interpreting cDNA sequences: some insights from studies on translation

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1296-392

DNA specificity of the bicoid activator protein is determined by homeodomain recognition helix residue 9

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1296-392

Control of type-D GABAergic neuron differentiation by C. elegans UNC-30 homeodomain protein

21 January 2018

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Specific DNA recognition and intersite spacing are critical for action of the bicoid morphogen

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1296-392

A chicken homeobox gene related to Drosophila paired is predominantly expressed in the developing limb

21 January 2018

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Expression patterns of the paired-related homeobox genes MHox/Prx1 and S8/Prx2 suggest roles in development of the heart and the forebrain

21 January 2018

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The gene for the homeodomain-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development.

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1296-392

Identification by differential RT-PCR of a novel paired homeodomain protein specifically expressed in sensory neurons and a subset of their CNS targets

21 January 2018

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Developmental expression of a novel murine homeobox gene (Chx10): evidence for roles in determination of the neuroretina and inner nuclear layer

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1296-392

Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

Good genes in bad neighbourhoods.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

RNA recognition and translational regulation by a homeodomain protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

Use of restriction enzymes to detect potential gene sequences in mammalian DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

Detection of messenger RNA by in situ hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

Linkage of an X-chromosome cleft palate gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

Positional cloning moves from perditional to traditional

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Rieger syndrome revisited: experimental approaches using pharmacologic and antisense strategies to abrogate EGF and TGF-alpha functions resulting in dysmorphogenesis during embryonic mouse craniofacial morphogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Characterization of the human HOX 7 cDNA and identification of polymorphic markers

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Ptx1, a bicoid-related homeo box transcription factor involved in transcription of the pro-opiomelanocortin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Molecular genetics of aristaless, a prd-type homeo box gene involved in the morphogenesis of proximal and distal pattern elements in a subset of appendages in Drosophila.

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

The organization of 3' splice-site sequences in mammalian introns

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Pituitary cell phenotypes involve cell-specific Pit-1 mRNA translation and synergistic interactions with other classes of transcription factors

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Autosomal dominant transmission of isolated growth hormone deficiency in iris-dental dysplasia (Rieger's syndrome).

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

The homeodomain: a new face for the helix-turn-helix?

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Evolutionary conservation of the AU-rich 3' untranslated region of messenger RNA.

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Degradation of mRNA in eukaryotes

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Iris dysgenesis with other anomalies

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

The Axenfeld syndrome and the Rieger syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

The major locus for multifactorial nonsyndromic cleft lip maps to mouse chromosome 11

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Transforming growth factor-beta 3 is required for secondary palate fusion

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021

Appendix G: In Situ Hybridization: An Improved Whole-Mount Method for Xenopus Embryos

1 reference

https://api.crossref.org/works/10.1038%2FNG1296-392

7 January 2021