(Q34394823)

1 August 2017

Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics (English)

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1 August 2017

Tachibana M

1

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1 August 2017

Takeda K

2

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1 August 2017

Nobukuni Y

3

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1 August 2017

Urabe K

4

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1 August 2017

Long JE

5

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1 August 2017

Meyers KA

6

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1 August 2017

Aaronson SA

7

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1 August 2017

Miki T

8

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1 August 2017

language of work or name

English

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publication date

1 September 1996

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1 August 2017

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1 August 2017

14

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1 August 2017

50-54

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1 August 2017

1

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https://scigraph.springernature.com/pub.10.1038/ng0996-50

1 August 2017

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cites work

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

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7 January 2021

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

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7 January 2021

Cochlear disorder associated with melanocyte anomaly in mice with a transgenic insertional mutation

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7 January 2021

Mouse and hamster mutants as models for Waardenburg syndromes in humans

1 reference

7 January 2021

Historical background and evidence for dominant inheritance of the Klein-Waardenburg syndrome (type III)

1 reference

7 January 2021

White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: Possible variant of Waardenburg syndrome

1 reference

7 January 2021

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

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7 January 2021

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

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7 January 2021

Molecular basis of splotch and Waardenburg Pax-3 mutations

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7 January 2021

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7 January 2021

The mutational spectrum in Waardenburg syndrome.

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7 January 2021

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

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7 January 2021

Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3.

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7 January 2021

Temporal bone histopathologic findings of Waardenburg's syndrome: a case report.

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7 January 2021

Expression of a single transfected cDNA converts fibroblasts to myoblasts

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7 January 2021

The myoD Gene Family: Nodal Point During Specification of the Muscle Cell Lineage

1 reference

7 January 2021

ADD1: a novel helix-loop-helix transcription factor associated with adipocyte determination and differentiation

1 reference

7 January 2021

Development of a highly efficient expression cDNA cloning system: application to oncogene isolation

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7 January 2021

Expression of a mouse tyrosinase cDNA in 3T3 Swiss mouse fibroblasts

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7 January 2021

Induction of pigmentation in mouse fibroblasts by expression of human tyrosinase cDNA

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7 January 2021

Conserved cysteine to serine mutation in tyrosinase is responsible for the classical albino mutation in laboratory mice

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7 January 2021

Mammalian tyrosinase. A comparison of tyrosine hydroxylation and melanin formation

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7 January 2021

TFE3: a helix-loop-helix protein that activates transcription through the immunoglobulin enhancer muE3 motif

1 reference

7 January 2021

A helix-loop-helix protein related to the immunoglobulin E box-binding proteins

1 reference

7 January 2021

TFEC, a basic helix-loop-helix protein, forms heterodimers with TFE3 and inhibits TFE3-dependent transcription activation

1 reference

7 January 2021

microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family

1 reference

7 January 2021

A rapid method for viable cell titration and clone production with HeLa cells in tissue culture: the use of X-irradiated cells to supply conditioning factors

1 reference

7 January 2021

Distribution and features of melanocytes during inner ear development in pigmented and albino rats.

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7 January 2021

Cochlear degeneration in aged rats of four strains

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7 January 2021

Melanocyte-specific expression of the human tyrosinase promoter: activation by the microphthalmia gene product and role of the initiator.

1 reference

7 January 2021

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

1 reference

7 January 2021

Growth and differentiation of normal human melanocytes in a TPA-free, cholera toxin-free, low-serum medium and influence of keratinocytes

1 reference

7 January 2021

Molecular control of myogenesis: antagonism between growth and differentiation

1 reference

7 January 2021

Activation and repression of myogenesis in somatic cell hybrids: evidence for trans-negative regulation of MyoD in primary fibroblasts

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7 January 2021

MSX1 inhibits myoD expression in fibroblast x 10T1/2 cell hybrids.

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7 January 2021

Pigment-cell-specific genes from fibroblasts are transactivated after chromosomal transfer into melanoma cells

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7 January 2021

Regulation of melanin synthesis in mammalian cells, as studied by somatic hybridization. I. Evidence for negative control

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7 January 2021

Regulation of melanin synthesis in mammalian cells, as studied by somatic hybridization. II. The level of regulation of 3,4-dihydroxyphenylalanine oxidase

1 reference

7 January 2021

A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1.

1 reference

7 January 2021

Identification of a DNA sequence involved in osteoblast-specific gene expression via interaction with helix-loop-helix (HLH)-type transcription factors

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7 January 2021

atonal is a proneural gene that directs chordotonal organ formation in the Drosophila peripheral nervous system

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7 January 2021

Mammalian achaete-scute homolog 1 is required for the early development of olfactory and autonomic neurons

1 reference

7 January 2021

Transfer of purified herpes virus thymidine kinase gene to cultured mouse cells

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7 January 2021

Identifiers

DOI

10.1038/NG0996-50

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Dimensions Publication ID

1 August 2017

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