Stock 129.Cg-Pax6<Sey> Tg(Hbb-b1)83Clo/WsH

FESA Number

1589

Strain Name

129.Cg-Pax6<Sey> Tg(Hbb-b1)83Clo/WsH

Mutation Strain Type

Attribution

Gene/Allele Information

Allele Name Allele MGI ID Gene Name Gene MGI ID Chromosome
Pax6<Sey> MGI:1856155 Pax6 MGI:97490 2
Tg(Hbb-b1)83Clo MGI:2655271 3

Phenotypic Description

Reiterated transgene is detectable by DNA in situ hybridisation.

Publications

Displaying 61 - 70 of 141 Stock Publications
Pubmed ID Authors Title Journal
12514213 Stenman J Identification of two distinct progenitor populations in the lateral ganglionic eminence: implications for striatal and olfactory bulb neurogenesis. J Neurosci (2 003) 23:167-74
17953485 Visel A Regulatory pathway analysis by high-throughput in situ hybridization. PLoS Genet (2 007) 3:1867-83
3733894 Lo CW Localization of low abundance DNA sequences in tissue sections by in situ hybridization. J Cell Sci (1 986) 81:143-62
9362466 Cari? D Determination of the migratory capacity of embryonic cortical cells lacking the transcription factor Pax-6. Development (1 997) 124:5087-96
9853907 Dellovade TL Olfactory bulb development is altered in small-eye (Sey) mice. J Comp Neurol (1 998) 402:402-18
9856459 Götz M Pax6 controls radial glia differentiation in the cerebral cortex. Neuron (1 998) 21:1031-44
11731698 Jaskoll T Embryonic submandibular gland morphogenesis: stage-specific protein localization of FGFs, BMPs, Pax6 and Pax9 in normal mice and abnormal SMG phenotypes in FgfR2-IIIc(+/Delta), BMP7(-/-) and Pax6(-/-) mice. Cells Tissues Organs (2 002) 170:83-98
21205789 Matsushima D Combinatorial regulation of optic cup progenitor cell fate by SOX2 and PAX6. Development (2 011) 138:443-54
8600027 Quinn JC Multiple functions for Pax6 in mouse eye and nasal development. Genes Dev (1 996) 10:435-46
12764029 Stoykova A Increase in reelin-positive cells in the marginal zone of Pax6 mutant mouse cortex. Cereb Cortex (2 003) 13:560-71

Pages

Orphanet Categories

Rare developmental defect during embryogenesis
Rare urogenital disease
Rare renal disease
Rare eye disease
Rare endocrine disease
Rare oncologic disease
Rare gynecologic or obstetric disease
Rare neurologic disease

EMMA ID

EM:01891

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