Analysis of the VMD2 promoter and implication of E-box binding factors in its regulation (Q40585958)

21 September 2017

Analysis of the VMD2 promoter and implication of E-box binding factors in its regulation (English)

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21 September 2017

Noriko Esumi

1

1 reference

21 September 2017

Yuji Oshima

2

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21 September 2017

Yuanyuan Li

3

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21 September 2017

Peter A Campochiaro

4

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21 September 2017

Donald J Zack

5

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21 September 2017

language of work or name

English

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publication date

24 February 2004

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Journal of Biological Chemistry

21 September 2017

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21 September 2017

279

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21 September 2017

18

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21 September 2017

19064-19073

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Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat

21 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Risk factors for age-related macular degeneration: Pooled findings from three continents.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Mutations in RPE65 cause Leber's congenital amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Identification of the gene responsible for Best macular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

The vitelliform macular dystrophy protein defines a new family of chloride channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Structure-function analysis of the bestrophin family of anion channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

The upstream region of the Rpe65 gene confers retinal pigment epithelium-specific expression in vivo and in vitro and contains critical octamer and E-box binding sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Expression and promoter activation of the Rpe65 gene in retinal pigment epithelium cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Transcriptional regulation of cellular retinaldehyde-binding protein in the retinal pigment epithelium. A role for the photoreceptor consensus element

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Expression of the mouse tyrosinase gene during embryonic development: recapitulation of the temporal regulation in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Functional analysis of microphthalmia-associated transcription factor in pigment cell-specific transcription of the human tyrosinase family genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Microphthalmia-associated transcription factor as a regulator for melanocyte-specific transcription of the human tyrosinase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein

21 January 2018

1 reference

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Mitf and Tfe3, two members of the Mitf-Tfe family of bHLH-Zip transcription factors, have important but functionally redundant roles in osteoclast development

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Microphthalamia-associated transcription factor: a critical regulator of pigment cell development and survival.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Mutations in microphthalmia, the mouse homolog of the human deafness gene MITF, affect neuroepithelial and neural crest-derived melanocytes differently.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

MatInd and MatInspector: new fast and versatile tools for detection of consensus matches in nucleotide sequence data

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Unusual topography of bovine rhodopsin promoter-lacZ fusion gene expression in transgenic mouse retinas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

ARPE-19, a human retinal pigment epithelial cell line with differentiated properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Extension of life-span by introduction of telomerase into normal human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

A novel chromosome abnormality in human neuroblastoma and antifolate-resistant Chinese hamster cell lives in culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

The bZIP transcription factor Nrl stimulates rhodopsin promoter activity in primary retinal cell cultures

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Identification of a novel isoform of microphthalmia-associated transcription factor that is enriched in retinal pigment epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Structural organization of the human microphthalmia-associated transcription factor gene containing four alternative promoters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Molecular cloning of cDNA encoding a novel microphthalmia-associated transcription factor isoform with a distinct amino-terminus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Mitf-D, a newly identified isoform, expressed in the retinal pigment epithelium and monocyte-lineage cells affected by Mitf mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Isoforms of mi transcription factor preferentially expressed in cultured mast cells of mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

The identification and functional characterization of a novel mast cell isoform of the microphthalmia-associated transcription factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Histochemical techniques for locating Escherichia coli beta-galactosidase activity in transgenic organisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Rostrocaudal gradient of transgene expression in adult skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

A novel function for Hedgehog signalling in retinal pigment epithelium differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Comparative proteome analysis of native differentiated and cultured dedifferentiated human RPE cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

MyoD binds cooperatively to two sites in a target enhancer sequence: occupancy of two sites is required for activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Two adjacent E box elements and a M-CAT box are involved in the muscle-specific regulation of the rat acetylcholine receptor beta subunit gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

MyoD1 promoter autoregulation is mediated by two proximal E-boxes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Cooperative E-box regulation of human GLI1 by TWIST and USF

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

An L1 element intronic insertion in the black-eyed white (Mitf[mi-bw]) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

OTX2 activates the molecular network underlying retina pigment epithelium differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

Two adjacent MyoD1-binding sites regulate expression of the acetylcholine receptor α-subunit gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309881200

21 January 2018

Identifiers

DOI

10.1074/JBC.M309881200

1 reference

21 September 2017

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