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Molecular Endocrinology (Baltimore, Md.)|May 17, 2008
A novel dwarfism with gonadal dysfunction due to loss-of-function allele of the collagen receptor gene, Ddr2, in the mouseKiyoshi Kano, C Marín de Evsikova, James Young, et al.
Scientific Reports|March 30, 2020
Disruption in murine Eml1 perturbs retinal lamination during early developmentG B Collin, J Won, M P Krebs, et al.
Investigative Ophthalmology & Visual Science|July 13, 2000
Localization of tubby-like protein 1 in developing and adult human retinasA H Milam, A E Hendrickson, M Xiao, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 16, 2008
Full-field electroretinography and marked variability in clinical phenotype of Alström syndromeEva Malm, Vesna Ponjavic, Patsy M Nishina, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 11, 2009
A novel ENU-induced mutation, peewee, causes dwarfism in the mouseBokryeon Lee, Lee Bokryeon, Kiyoshi Kano, et al.
The Journal of Biological Chemistry|October 20, 2010
Prefoldin 5 is required for normal sensory and neuronal development in a murine modelYongSuk Lee, Richard S Smith, Wanda Jordan, et al.
Genomics|June 21, 2001
Genetic analysis of a new mouse model for non-insulin-dependent diabetesJ H Kim, S Sen, C S Avery, et al.
American Journal of Medical Genetics|December 31, 1997
Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional familiesJ D Marshall, M D Ludman, S E Shea, et al.
Genomics|June 2, 2001
Characterization of the murine Lbx2 promoter, identification of the human homologue, and evaluation as a candidate for Alström syndromeF Chen, G B Collin, K C Liu, et al.
Experimental Eye Research|April 22, 2009
Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransductionNeena B Haider, Nissa Mollema, Meghan Gaule, et al.
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