Regional Fluctuation in the Functional Consequence of LINE-1 Insertion in the Mitf Gene: The Black Spotting Phenotype Arisen from the Mitfmi-bw Mouse Lacking Melanocytes
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference30 articles.
1. LINE-1 Retrotransposition in the Nervous System;CA Thomas;Annu Rev Cell Dev Biol,2012
2. An L1 element intronic insertion in the black-eyed white (Mitfmi-bw) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness;I Yajima;Hum Mol Genet,1999
3. Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein;CA Hodgkinson;Cell,1993
4. A helix-loop-helix transcription factor-like gene is located at the mi locus;MJ Hughes;J Biol Chem,1993
5. Impaired development of melanoblasts in the black-eyed white Mitfmi-bw mouse, a model for auditory-pigmentary disorders;H Hozumi;Genes Cells,2012
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