(Q28276460)

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A candidate gene for the mouse mutation tubby

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A candidate gene for the mouse mutation tubby (English)

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author name string

K Noben-Trauth

1

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J K Naggert

2

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M A North

3

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P M Nishina

4

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publication date

11 April 1996

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380

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6574

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534-8

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Fat (fat) and tubby (tub): two autosomal recessive mutations causing obesity syndromes in the mouse

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Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

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Cochlear and retinal degeneration in the tubby mouse

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Laurence, Moon, Bardet, and Biedl: reflections on a syndrome

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Localization of insulin-2 (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7.

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Efficiency and specificity of gene isolation by exon amplification

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Positional cloning of the nude locus: genetic, physical, and transcription maps of the region and mutations in the mouse and rat

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Basic local alignment search tool

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Identification and characterization of the developmentally regulated pattern of expression in the testis of a mouse gene exhibiting similarity to the family of phosphodiesterases

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2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans

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Cyclic nucleotide phosphodiesterases: functional implications of multiple isoforms

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Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase

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Apoptosis, retinitis pigmentosa, and degeneration

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Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activity

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A workbench for multiple alignment construction and analysis

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