The developmental biology of melanocytes and its application to understanding human congenital disorders of pigmentation (Q36716847)

15 August 2017

1 reference

title

The developmental biology of melanocytes and its application to understanding human congenital disorders of pigmentation (English)

1 reference

15 August 2017

0 references

developmental biology

1 reference

Thomas J Hornyak

1

1 reference

15 August 2017

1 January 2006

1 reference

15 August 2017

Advances in dermatology

1 reference

15 August 2017

22

1 reference

15 August 2017

201-218

1 reference

Lineage commitment and fate of neural crest-derived neurogenic cells.

15 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Cellular and molecular biology of neural crest cell lineage determination

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Neural development: crest destiny

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Isolation of a stem cell for neurons and glia from the mammalian neural crest

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Pax-3, a novel murine DNA binding protein expressed during early neurogenesis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

The transcription factor Sox10 is a key regulator of peripheral glial development.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Melanocytes and the microphthalmia transcription factor network

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Structure of the mouse tyrosinase-related protein-2/dopachrome tautomerase (Tyrp2/Dct) gene and sequence of two novel slaty alleles

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Melanocyte-specific expression of dopachrome tautomerase is dependent on synergistic gene activation by the Sox10 and Mitf transcription factors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Direct interaction of Sox10 with the promoter of murine Dopachrome Tautomerase (Dct) and synergistic activation of Dct expression with Mitf

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Pax3 functions at a nodal point in melanocyte stem cell differentiation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Regulation of E- and P-cadherin expression correlated with melanocyte migration and diversification

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Immunological identification of an inward rectifier K+ channel (Kir4.1) in the intermediate cell (melanocyte) of the cochlear stria vascularis of gerbils and rats

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Retinal stem cells in the adult mammalian eye

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

The retinal pigmented epithelium is required for development and maintenance of the mouse neural retina

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Chx10 repression of Mitf is required for the maintenance of mammalian neuroretinal identity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Dominant role of the niche in melanocyte stem-cell fate determination

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Mechanisms of hair graying: incomplete melanocyte stem cell maintenance in the niche

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Hair cycle and hair pigmentation: dynamic interactions and changes associated with aging.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Upper human hair follicle contains a subpopulation of keratinocytes with superior in vitro proliferative potential.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Mouse and hamster mutants as models for Waardenburg syndromes in humans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Linkage of M-CSF signaling to Mitf, TFE3, and the osteoclast defect in Mitf(mi/mi) mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

MAP kinase links the transcription factor Microphthalmia to c-Kit signalling in melanocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

NEW SPLOTCH ALLELES IN THE MOUSE

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Waardenburg syndrome type II: phenotypic findings and diagnostic criteria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

The mutational spectrum in Waardenburg syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

SLUG (SNAI2) deletions in patients with Waardenburg disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Ectopic Pax-3 activates MyoD and Myf-5 expression in embryonic mesoderm and neural tissue

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

Piebaldism with deafness: molecular evidence for an expanded syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YADR.2006.09.002

10.1016/J.YADR.2006.09.002

7 January 2021

Identifiers

DOI

1 reference

15 August 2017

1 reference

PubMed ID

17249303