(Q40585958)

21 September 2017

title

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

1 reference

21 September 2017

Noriko Esumi

1

1 reference

21 September 2017

Yuji Oshima

2

1 reference

21 September 2017

Yuanyuan Li

3

1 reference

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

published in

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21 September 2017

volume

279

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21 September 2017

issue

18

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21 September 2017

page(s)

19064-19073

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

21 September 2017

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21 January 2018

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21 January 2018

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

21 January 2018

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21 January 2018

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

21 January 2018

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Structure-function analysis of the bestrophin family of anion channels

21 January 2018

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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

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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

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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

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Rostrocaudal gradient of transgene expression in adult skeletal muscle

21 January 2018

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A novel function for Hedgehog signalling in retinal pigment epithelium differentiation

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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

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MyoD1 promoter autoregulation is mediated by two proximal E-boxes

21 January 2018

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

21 January 2018

1 reference

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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

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OTX2 activates the molecular network underlying retina pigment epithelium differentiation

21 January 2018

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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

1 reference