Theeyeless mouse mutation(ey1) removes an alternative start codon from theRx/rax homeobox gene-Reference-Cited by-同舟云学术

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Theeyeless mouse mutation(ey1) removes an alternative start codon from theRx/rax homeobox gene

Published:2001 Issue:1 Volume:31 Page:43-53
ISSN:1526-954X
Container-title:genesis
language:en
Short-container-title:genesis

Author:

Tucker Priscilla,Laemle Lois,Munson Amanda,Kanekar Shami,Oliver Edward R.,Brown Nadean,Schlecht Hans,Vetter Monica,Glaser Tom

Publisher

Wiley

Subject

Cell Biology,Endocrinology,Genetics

Reference79 articles.

1. Role of Xrx1 in Xenopus eye and anterior brain development

2. Microphthalmos

3. The cleavage stage origin of Spemann's Organizer: analysis of the movements of blastomere clones before and during gastrulation in Xenopus

4. Genealogies of mouse inbred strains

5. THE ANOPHTHALMIC MUTANT OF THE MOUSE: I. Genetic Contribution to the Anophthalmic Phenotype

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1. Enhanced maternal behaviors in a mouse model of congenital blindness;Developmental Psychobiology;2023-07-03

2. CRISPR-Cas9 F0 knockout approach using predesigned in vitro transcribed guide RNAs partially recapitulates Rx3 function in eye morphogenesis;Journal of Genetics;2022-12-07

3. Eye and Ear;Pathology of Genetically Engineered and Other Mutant Mice;2021-12-16

4. Conserved roles of Rax/rx3 genes in hypothalamus and pituitary development;The International Journal of Developmental Biology;2021

5. Genetics of Microphthalmia: Global and Indian Perspectives;Essentials in Ophthalmology;2021

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