(Q52189743)

English

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

scientific article published in January 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

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

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

1 reference

based on heuristic

inferred from title

author name string

Nakayama A

1

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

Nguyen MT

2

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

Chen CC

3

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

Opdecamp K

4

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

Hodgkinson CA

5

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

Arnheiter H

6

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

publication date

1 January 1998

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

Mechanisms of Development

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

70

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

1-2

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

155-166

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of Mutations at the W Locus (c‐kit) on Inner Ear Pigmentation and Function in the Mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel alleles

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

A mouse model for vitiligo.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Embryonic expression of a haematopoietic growth factor encoded by the SI locus and the ligand for c-kit

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene control of mammalian pigmentary differentiation. I. Clonal origin of melanocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Insight into the microphthalmia gene

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Dysgenesis of melanocytes and cochlear dysfunction in mutant microphthalmia (mi) mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Microphthalmia: a new recessive mutation in the Norway rat

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Ultrastructural features of retinal dystrophy in mutant vitiligo mice

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

The eye and skeletal effects of two mutant alleles at the microphthalmia locus of Mus musculus

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Steel factor directs melanocyte development in vitro through selective regulation of the number of c-kit+ progenitors

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

A Dominant Negative form of Transcription Activator mTFE3 Created by Differential Splicing

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

CBP/p300 as a co-factor for the Microphthalmia transcription factor

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

The recessive phenotype displayed by a dominant negative microphthalmia-associated transcription factor mutant is a result of impaired nucleation potential

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Stem cell factor is encoded at the SI locus of the mouse and is the ligand for the c-kit tyrosine kinase receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2897%2900188-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0925-4773(97)00188-3

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9510032

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